Your activity: 16 p.v.

Nutrition in pregnancy: Dietary requirements and supplements

Nutrition in pregnancy: Dietary requirements and supplements
Author:
Christine D Garner, PhD, RD, CLC
Section Editors:
Charles J Lockwood, MD, MHCM
David Seres, MD
Deputy Editor:
Vanessa A Barss, MD, FACOG
Literature review current through: Dec 2022. | This topic last updated: Apr 14, 2022.

INTRODUCTION — The intense fetal growth and development during pregnancy requires maternal physiologic adaptation and a change in nutritional needs. Adequate maternal intake of macronutrients and micronutrients promotes normal embryonic and fetal development [1], while undernutrition and overnutrition (eg, an obesogenic environment) may be associated with adverse maternal, pregnancy, and newborn outcomes, including miscarriage, some congenital anomalies, hypertensive disorders of pregnancy, gestational diabetes, preterm birth, small for gestational age newborn, and suboptimal neurocognitive development [2-9]. Furthermore, the developmental model for the origins of disease (ie, Barker hypothesis) hypothesizes that the fetal environment, which is affected by maternal nutritional and metabolic status, causes epigenetic modifications that impact gene expression and thereby influence subsequent development of disease in offspring, both in childhood and adulthood [10]. Seminal studies of the health status of adult offspring of a cohort of females who were pregnant during the Dutch famine in World War II support this hypothesis [11,12]. More recently, epigenetic changes (altered gene methylation) related to periconception obesity have been associated with an increased risk for metabolic syndrome in offspring [13].

Importantly, maternal nutritional status is a modifiable risk factor that can be evaluated, monitored, and, when appropriate, improved. Beginning this process before conception is important since addressing diet during pregnancy can impact some outcomes (eg, gestational weight gain), but may not be sufficiently early to affect others, such as occurrence of gestational diabetes related to obesity [9,14]. Ideally, individuals should be at a healthy body mass index (BMI) and have optimal nutritional status when they conceive; however, in reality, approximately 50 percent of females in high-income countries are overweight or obese at the time of conception and many have inadequate micronutrient status, particularly for iron and folate [9,15]. (See "The preconception office visit", section on 'Core interventions'.)

It is also important to note the limitations of available evidence. Although some relationships between nutrients and pregnancy outcomes are clear (such as the timing and dose of folic acid needed to prevent neural tube defects [NTDs]), many questions remain unanswered due to the many challenges of performing high-quality research in pregnancy [16]. These challenges include the often unknown critical windows when nutrition may impact development, the many physiologic changes that occur over the course of normal pregnancy, the large individual differences in maternal adaptation to pregnancy, difficulties with accurately measuring maternal diet, ethical and practical issues of experimenting with pregnant people, challenges with determining effects of specific nutrients in the context of the entire diet, and the lack of a good animal model that can be directly extrapolated to humans. Thus, many recommendations for intake are based on observational studies and expert consensus, and lack randomized trials to support them. Nevertheless, the preponderance of evidence supports a relationship between maternal diet and health of both mother and offspring.

This topic will discuss basic nutritional requirements in pregnancy, primarily for pregnant people living in middle- and high-income countries. Assessment of maternal diet and counseling about dietary issues in these areas are reviewed separately. (See "Nutrition in pregnancy: Assessment and counseling".)

The evaluation and management of undernutrition in pregnancy in resource-limited areas are also reviewed separately. (See "Undernutrition in pregnancy: Evaluation, management, and outcome in resource-limited areas".)

GENERAL DIETARY PRINCIPLES FOR OPTIMAL PREGNANCY OUTCOME — The key components of healthy eating during pregnancy include [17,18] (see "Nutrition in pregnancy: Assessment and counseling", section on 'General principles of a healthy diet during pregnancy'):

Following a healthy dietary pattern, including consumption of [18]:

Vegetables of all types: dark green, red, and orange vegetables; beans, peas, and lentils; starchy vegetables; other vegetables

Fruits, especially whole fruits

Grains, at least half of which should be whole grains

Dairy, including fat-free or low-fat milk, yogurt, and cheese, and/or lactose-free versions and fortified soy beverages and yogurt as alternatives

Protein foods, including lean meats, poultry, and eggs; seafood; beans, peas, and lentils; and nuts, seeds, and soy products

Oils, including vegetable oils and oils in food, such as in seafood and nuts

A variety of primarily whole, unprocessed foods and beverages should be consumed in appropriate amounts to allow adequate, but not excessive, gestational weight gain.

Limiting consumption of added sugars, saturated fat, and sodium – Pregnant people (and others) typically exceed recommended limits for these substances, and this may have negative health consequences. They should focus on increasing intake of high-quality, nutrient-dense foods and attempt to limit intake of processed "empty-calorie" foods and beverages. Avoiding or limiting consumption of highly processed foods is an important means of decreasing consumption of sugar, saturated fat, and sodium.

Appropriate vitamin and mineral supplementation – (See 'Dietary requirements' below.)

Appropriate gestational weight gain – Weight gain is routinely monitored throughout pregnancy. The National Academy of Medicine (formerly the Institute of Medicine [IOM]) has published widely used goals for gestational weight gain (table 1) [19].

Prepregnancy body mass index (BMI) and gestational weight gain have independent, but cumulative, effects on birth weight, maternal weight retention long after delivery, and possibly gestational duration and risk of childhood obesity; BMI is considered to have the stronger effect. The incidence of pregnancy complications is higher at the upper and lower extremes of weight gain. (See "Gestational weight gain".)

Avoiding alcohol and other known or potential harmful substances (eg, mercury) – (See "Alcohol intake and pregnancy" and "Fish consumption and marine omega-3 fatty acid supplementation in pregnancy", section on 'Methylmercury in fish'.)

Limiting caffeine intake to less than 200 to 300 mg per day. (See "Caffeine: Effects on reproductive outcomes in females".)

Safe food handling – (See "Nutrition in pregnancy: Assessment and counseling", section on 'Food safety'.)

DIETARY REQUIREMENTS

Background — In 2020, the Dietary Guidelines Advisory Committee of the United States Department of Health and Human Services and United States Department of Agriculture (USDA) published a scientific report of Dietary Guidelines for Americans, which included nutritional guidance for pregnant individuals for the first time [18]. The guidelines incorporated evidence from the most recent research with guidelines from prior sources, including the 1990 Institute of Medicine (IOM, now the National Academy of Medicine) report on nutrition in pregnancy [6], the 2009 IOM report on weight gain in pregnancy [20], the 2006 IOM publication Dietary Reference Intakes: The Essential Guide to Nutrient Requirements [21], and some updates of the dietary reference intakes [22].

The following discussion focuses on the general obstetric population. Other populations, such as those with medical disorders affecting nutrition or residing in severely resource-limited areas, may require additional nutritional considerations.

Recommended dietary allowances (RDAs) are levels of nutrients recommended by an expert IOM panel based on extensive evaluation of available scientific evidence and mathematically adjusted to meet the needs of 97 percent of the population.

Energy intake — Energy intake (also called caloric intake) is a key nutritional factor in determining birth weight. In the first trimester, pregnant people typically do not need to increase their caloric intake. In the second and third trimesters, most pregnant individuals will need to increase their caloric consumption to promote appropriate weight gain. However, the old adage "eating for two" neither accurately nor appropriately depicts the increased needs of pregnant people.

Additional energy requirements for pregnancy differ by body mass index (BMI) class:

Normal BMI range: An additional 340 and 450 kcal/day is suggested for the second and third trimesters, respectively [23], or a total of between 2200 and 2900 kcal/day [24].

Underweight BMI range: An additional intake above 340 and 450 kcal/day is suggested to support adequate weight gain, individualized depending on the patients baseline BMI [25].

Overweight BMI range: An additional 260 to 360 kcal/day is suggested, which is less than the 340 and 450 kcal/day suggested for those with a normal BMI [25].

Obese BMI range: These patients may not need any additional calories, but data have been inadequate to make strong recommendations [24]. Evidence from a small, novel, observational study that used indirect calorimetry to measure energy balance during pregnancy among individuals with prepregnancy obesity showed that those who gained within the recommended ranges did not increase caloric consumption, suggesting that individuals with obesity may not require increased caloric consumption to promote appropriate weight gain; rather, fat stores are mobilized and used to promote fetal growth [26]. However, more and larger studies are needed to validate these. (See "Gestational weight gain", section on 'Overweight and obese pregnant people'.)

Macronutrients

Protein — The fetal/placental unit utilizes approximately 1000 g of protein, with most of this requirement in the last six months.

Recommended intake – The Dietary Guidelines for Americans recommend a minimum daily nutritional goal of 71 g/day (1.1 g/kg/day) (table 2), which is higher than the recommendation for nonpregnant people (46 g/day or 0.8 g/kg/day) [18,27]. The increase in protein consumption should be proportional to total calories, as the percent of calories from protein remains at 10 to 35 percent total kcal for both pregnant and nonpregnant individuals. Some experts have recommended keeping protein consumption below 25 percent kcal [28].

Reported total protein intake among pregnant individuals in resource-abundant countries is between 14.7 and 16.1 percent, thus falling within these recommendations.

Sources – Healthy protein sources include lean meats, poultry and eggs, seafood, beans, peas, lentils, nuts, seeds, and soy products. Highly processed meats are not recommended. In the United States, pregnant individuals typically consume excess meats, poultry, and eggs, while consumption of seafood, beans, peas and lentils are below recommendations [18].

We discourage use of special protein powders and high-protein supplements. In pregnant people, especially those who likely have adequate protein intake, high-protein supplements have no measurable benefits and may have harmful effects, such as lower birth weight and higher risk of small for gestational age, although data are not definitive [6,29]. For example:

In analyses of randomized trials of undernourished pregnant people, protein supplementation alone (in contrast to balanced energy and protein supplementation) did not improve clinically important pregnancy outcomes [30-32].

In an observational study of >91,000 pregnant people in Japan, maternal protein intake had an inverse U-curve: Birth weight was highest and risk of small for gestational age was lowest when protein consumption was approximately 12 percent of kcals [33].

In a study of >120,000 pregnant people in Denmark and Norway, high-protein intake did not appear to affect mean birth weight or incidence of low birth weight; however, it was associated with a modest increased risk of preterm birth [34]. (See "Undernutrition in pregnancy: Evaluation, management, and outcome in resource-limited areas", section on 'Balanced energy and protein supplementation'.)

Carbohydrate and fiber

Recommended intake – Carbohydrate requirements increase to 175 g/day in pregnancy, up from 130 g/day in nonpregnant females [18,27]. The Dietary Guidelines for Americans recommend 45 to 65 percent of kcals from carbohydrate for both pregnant and nonpregnant individuals (table 2) [18] since the increase in the carbohydrate requirement is proportional to the increase in pregnancy caloric requirements.

Fiber intake of 28 to 36 g/day is recommended in pregnancy (table 2), which, along with adequate fluid intake, may help prevent or reduce constipation [18]. High fiber consumption prior to conception was associated with a decreased risk of preeclampsia and dyslipidemia in an observational study [35]. High fiber intake may also have favorable effects on blood glucose. (See "Healthy diet in adults", section on 'Fiber'.)

Sources – The focus should be on consuming several servings of whole foods: fruits, vegetables, and whole grains. Highly processed carbohydrates should be minimized to help manage weight gain and avoid high postprandial blood glucose levels, particularly among those with or at high risk of diabetes.

Fat

Recommended intake – The Dietary Guidelines for Americans set daily nutritional goals for pregnant individuals as 20 to 35 percent of total energy intake from fats, <10 percent of total energy from saturated fat, and daily goals for essential fatty acids of 13 g/day of linoleic acid (18:2) and 1.4 g/day of linolenic acid (18:3) (table 2) [18]. These goals are consistent with a healthy dietary pattern.

Approximately 75 percent of pregnant people exceed the recommended limit for saturated fat (that from animal products such as meat and dairy, and coconut, palm, and palm kernel oil) [18], which may have negative metabolic consequences.

Sources – Consumption of healthy fats and limiting of saturated fats are recommended. Dietary patterns that provide a healthy profile of fats consistent with the Dietary Guidelines for Americans include the Mediterranean diet (see "Healthy diet in adults", section on 'Mediterranean diet') and the Dietary Approaches to Stop Hypertension (DASH) diet (see "Healthy diet in adults", section on 'DASH diet'). In these diets, plant-derived fats, such as olive oil and nuts, and two to three servings per week of fish comprise the majority of fat intake.

Long-chain polyunsaturated fatty acids — Docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA) are two n-3 (also known as omega-3) long-chain polyunsaturated fatty acids (n-3 LCPUFAs) derived primarily from fish or marine-based sources. DHA is necessary for normal development of the fetal brain and retina, and seafood consumption during pregnancy has also been associated with favorable cognitive development in offspring [36]. N-3 PUFAs have anti-inflammatory effects, which have been associated with a reduction in preterm birth and an increase in mean duration of gestation [37].

Recommended intake – The Dietary Guidelines for Americans recommend that pregnant individuals consume 8 to 12 ounces of seafood per week [18]. The number of weekly servings of fish needed to achieve the DHA intake goal of 200 to 300 mg/day depends on the type of fish, as shown in the table (table 3). Importantly, pregnant people (and those planning to conceive) should choose fish that are low in mercury and other contaminants; a chart to help consumers make appropriate choices is available online. (See "Nutrition in pregnancy: Assessment and counseling", section on 'Guidelines for safe seafood consumption'.)

Sources – Consumption of fish and other marine-based sources is recommended. For pregnant people who are not able or willing to consume fish or adequate amounts of fish, supplementation with n-3 LCPUFAs and consumption of other food sources of n-3 LCPUFA are recommended to achieve an intake of 200 to 300 mg/day of DHA. A number of foods fortified with DHA are available, including yogurt, milk, and eggs. DHA supplements are available either from fish oil or synthesized by algae. Some prenatal vitamins also contain DHA/EPA. (See "Fish consumption and marine omega-3 fatty acid supplementation in pregnancy".)

Lipid-based nutrient supplements are a good source of macro- and micronutrients and have been used to address nutrient requirements in areas where maternal undernutrition is prevalent. (See "Undernutrition in pregnancy: Evaluation, management, and outcome in resource-limited areas", section on 'Lipid-based nutrient supplements'.)

Micronutrients

Overview — Requirements for most micronutrients increase during pregnancy. Requirements for several nutrients (calcium, magnesium, phosphorus, potassium, zinc, and vitamins A, C, and K) vary by maternal age. Recommendations for daily intake of vitamins and minerals during pregnancy for specific age groups are shown in the table (table 2).

Ideally, all or most nutrients can be obtained by eating a diet consisting of nutrient-dense and fortified whole and unprocessed foods and beverages. However, some nutrients (eg, calcium, vitamin D, potassium, fiber, folate/folic acid, iron, iodine, choline) are consistently under-consumed in the United States population.

Multiple-micronutrient supplements

Evidence – In a Cochrane meta-analysis of randomized trials conducted in low- and middle-income countries where the prevalence of micronutrient deficiencies is high, multiple-micronutrient (MMN) supplements in pregnancy appeared to modestly reduce rates of low birth weight (risk ratio [RR] 0.88, 95% CI 0.85-0.91) and small for gestational age (RR 0.92, 95% CI 0.88-0.97), and possibly preterm birth (RR 0.95, 95% CI 0.90-1.01) compared with iron supplementation with/without folic acid [38]. Maternal anemia was reduced when compared with placebo but not when compared with iron supplementation with/without folic acid. There were no demonstrable benefits for several other maternal and pregnancy outcomes: miscarriage, congenital anomalies, maternal mortality, perinatal mortality.

Candidates for MMNs – Most trials of MMNs have been conducted in low-income countries and are not generalizable to high-income countries. Because of a lack of high-quality evidence of the efficacy of MMNs in well-nourished pregnant people, recommendations in high-income countries vary [39]. In the absence of a careful evaluation by a nutritionist, we believe that it is prudent to recommend MMN supplement: Prenatal vitamins are the standard approach.

National health authorities in the United Kingdom do not recommend routine prescription of MMNs for pregnant persons but do recommend specific supplements, such as folic acid and vitamin D [40].

In the United States, the National Academy of Medicine (formerly the Institute of Medicine [IOM]), American College of Obstetricians and Gynecologists (ACOG), and the Centers for Disease Control and Prevention (CDC) recommend MMN supplements for pregnant people who do not consume an adequate diet [41-43]. In high-income countries, such as the United States, groups at increased risk for micronutrient deficiencies include those carrying a multiple gestation, heavy smokers, adolescents, complete vegetarians (ie, vegans), substance abusers, and individuals who have had bariatric surgery or who have gastrointestinal conditions that cause malabsorption (eg, Crohn disease, bowel resection) [44-47]. These groups can benefit from consultation with dietitians who specialize in maternal nutrition. (See "Nutrition in pregnancy: Assessment and counseling", section on 'Indications for referral to a nutrition professional'.)

Well-nourished individuals may not need MMN supplements to satisfy daily requirements; instead, specific supplements would be prescribed to meet individual needs. For example, United States data indicate that while 10 to 48 percent of pregnant people taking MMNs had a total usual intake that was less than the estimated average requirement for some micronutrients, 3 to 48 percent exceeded the adequate intake or the tolerable upper intake level for some micronutrients [48].

World Health Organization (WHO) guidelines recommend use of MMNs in pregnant people receiving antenatal care in any healthcare facility or community-based setting, in the context of rigorous research [49]. Because the evidence for this recommendation was mainly derived from low- and middle-income countries, they state that applicability to high-income countries or to populations not at risk of micronutrient (eg, adequate diet, food fortification programs) is unclear. The evidence was derived from trials using MMNs containing 13 to 15 micronutrients (including iron and folic acid) and the widely available United Nations International Multiple Micronutrient Antenatal Preparation (UNIMMAP), which contains 15 micronutrients (folic acid: 400 mcg, vitamin A: 800 mcg, vitamin D: 200 international units, vitamin E: 10 mg, vitamin B1: 1.4 mg, vitamin B6: 1.9 mg, vitamin B12: 2.6 mcg, niacin: 18 mg, vitamin C: 70 mg, zinc: 15 mg, iron: 30 mg, selenium: 65 mcg, copper: 2 mg, iodine: 150 mcg [50]).

Recommended intake and source – Prenatal vitamins and UNIMMAP account for the majority of MMN supplements taken by pregnant people. The content varies depending on the product used. At a minimum, the daily supplement should contain key vitamins/minerals that are often not met by diet alone, such as iron, calcium, folic acid, vitamin D, and iodine (table 2). In addition to these key vitamins/minerals, the supplement should contain adequate amounts of vitamins A, E, and C; B vitamins; and zinc.

Specific micronutrients are discussed in more detail below.

Iron

Evidence – Iron is necessary for fetal brain and placental development and to expand the maternal red cell mass. Iron deficiency, which is the most prevalent single-nutrient deficiency worldwide [51] and a major cause of anemia, is estimated to occur in 19 percent of pregnant people in the United States, ranging from 7 percent in the first trimester to 30 percent in the third trimester [52].

Although systematic reviews have observed that routine iron supplementation in pregnancy consistently results in a reduction in the frequency of iron deficiency anemia at term (eg, RR 0.29, 95% CI 0.17-0.49) [53], clear benefits for mothers or offspring have not been consistently demonstrated for a variety of other outcomes [53,54], even among pregnant people with iron deficiency anemia [55]. However, available evidence is generally of low quality. (See "Anemia in pregnancy", section on 'Treatment of iron deficiency' and "Anemia in pregnancy", section on 'How to screen for iron deficiency'.)

Recommended intake – Dietary reference values for iron in pregnancy vary worldwide [56]. The CDC recommend iron intake of 27 mg/day during pregnancy (up from 18 mg/day in nonpregnant/non-lactating people) to prevent iron deficiency anemia (table 2) [57]. The WHO recommends daily oral iron supplementation with 30 to 60 mg of elemental iron [58]. This amount is readily met by most prenatal vitamin formulations and is adequate supplementation for non-anemic individuals. European and United Kingdom authorities have concluded that additional dietary iron is not needed during pregnancy, provided that iron stores at conception are adequate [59-61]. Of note, in the United States, mean dietary iron intake among pregnant individuals is 17 mg/day from foods alone, and 38 mg/day from foods plus supplements [48]. Importantly, 36 percent of pregnant people consume less than the requirement.

For pregnant people with iron deficiency anemia (first- or third-trimester hemoglobin [Hb] <11 g/dL or second-trimester Hb <10.5 g/dL and low serum ferritin [<40 ng/mL]), an additional iron supplement (30 to 120 mg/day) is required until the anemia is corrected [58,62]. One option is 65 mg of elemental iron (325 mg ferrous sulfate) every other day [63]. Iron absorption decreases with increasing dose, thus larger supplementation amounts are best split into several doses during the day. Intermittent iron supplementation (one to three times per week) appears to be as effective as daily supplementation for preventing anemia at term and is better tolerated and may result in better compliance [60,64]. The tolerable upper limit of 45 mg/day set by the National Academy of Medicine (formerly the Institute of Medicine [IOM]) based on gastrointestinal side effects is much lower than international recommendations [65] and has been challenged [66]. Of note, iron absorption increases substantially with advancing gestational age [67,68]. Evidence suggests, however, that this increase is blunted in overweight mothers [69].

For individuals who do not tolerate oral iron, iron can be administered safely and effectively intravenously [70-72]. (See "Anemia in pregnancy", section on 'Treatment of iron deficiency'.)

Dietary sources – Dietary sources of iron are shown in the table (table 4). There are two dietary forms of iron: heme and non-heme. The most bioavailable form is heme iron, which is found in meat, poultry, and fish. Non-heme iron, which comprises 60 percent of iron in animal foods and all of the iron in plant foods, fortified grains, and supplements, is less bioavailable. Absorption of non-heme iron is enhanced by vitamin-C-rich foods or muscle tissue (meats, poultry, and seafood) [73], and inhibited by consumption of dairy products and coffee/tea/cocoa. (See "Overview of dietary trace elements", section on 'Iron'.)

Calcium and vitamin D

Calcium

Evidence – Low calcium and vitamin D levels have been associated with adverse health outcomes in mother and child, but it is unclear whether low levels are the causal factor or a marker of poor maternal health. These issues are discussed in detail separately. (See "Vitamin D and extraskeletal health", section on 'Pregnancy outcomes' and "Vitamin D deficiency in adults: Definition, clinical manifestations, and treatment", section on 'Pregnancy' and "Clinical manifestations, diagnosis, and treatment of osteomalacia", section on 'Pregnancy'.)

Fetal skeletal development requires approximately 30 g of calcium across pregnancy, primarily in the last trimester. This total is a relatively small percentage of total maternal body calcium and is easily mobilized from maternal stores, if necessary. Intestinal absorption and renal retention of calcium increase progressively throughout gestation [74].

For pregnant people with low baseline dietary calcium intake (particularly in non-United States populations), high-dose calcium supplementation may reduce the risk of developing a hypertensive disorder of pregnancy [75]. Calcium supplementation does not appear to reduce this risk in healthy, nulliparous pregnant people in whom baseline dietary calcium intake is adequate. Although there may be a benefit for preeclampsia prevention in high-risk populations, further study is required since available information is based upon small numbers of patients and heterogeneity in study populations. These data are reviewed separately. (See "Preeclampsia: Prevention", section on 'Calcium supplementation'.)

Calcium supplementation does not appear to reduce the risk of spontaneous preterm birth or low birth weight [76].

Recommended intake – In the United States, the recommended daily allowance for calcium is 1000 to 1300 mg/day in pregnant and lactating individuals, depending on age (table 2) [77].

Of note, average calcium consumption among pregnant people in the United States is 1090 mg/day from foods and 1300 mg/day from foods plus supplements. An estimated 21 percent of pregnant people consume less than 800 mg/day from foods alone [48].

Sources – Calcium content of selected foods can be found online from the USDA National Nutrient Database.

Vitamin D

Evidence – In addition to its role in calcium and bone homeostasis, vitamin D potentially regulates many other cellular functions. Poor vitamin D status in the perinatal period may have short- or long-term consequences on bone, the immune system, and general health, but the precise threshold for optimal vitamin D status during pregnancy and the effects of high-dose supplementation (4000 to 5000 international units daily) on pregnancy outcomes are not well defined [78-82]. These data are reviewed in detail separately. (See "Vitamin D and extraskeletal health", section on 'Pregnancy outcomes'.)

Recommended intake – The Dietary Guidelines for Americans recommend daily intake of 600 international units per day during pregnancy [18]. Vitamin D deficiency is estimated to affect between 40 and 98 percent of pregnant individuals worldwide [83].

Most prenatal vitamins contain 400 international units of vitamin D, but some preparations contain as little as 200 or as much as 1000 to 1200 international units. The safe upper limit of vitamin D has not been well studied but was conservatively set at 4000 international units in a 2011 guideline [84]. (See "Vitamin D deficiency in adults: Definition, clinical manifestations, and treatment", section on 'Pregnancy'.)

Sources – Supplements often specify the type of vitamin D they contain. Most prescription prenatal vitamins contain cholecalciferol (D3), but some contain ergocalciferol (D2), and some contain a mixture. Many commercial nonprescription products labeled "vitamin D" (multivitamin supplements, fortified milk, and bread) contain D2 rather than D3. D3 is more readily converted to active forms of vitamin D and is more effective at increasing serum 25-hydroxyvitamin D.

Dermal synthesis after exposure to sunlight is the major natural source of the vitamin. Very few foods naturally contain vitamin D (fatty fish livers are the exception). (See "Overview of vitamin D", section on 'Sources'.)

Folate/folic acid

Evidence – The body of evidence supports the efficacy of folic acid supplementation and dietary fortification to decrease the occurrence and recurrence of neural tube defects (NTDs) by at least 70 percent. These data are reviewed in detail separately. (See "Folic acid supplementation in pregnancy", section on 'Folic acid supplementation for prevention of neural tube defects'.)

Folic acid supplementation, usually as part of a multivitamin, has also been associated with a variety of other benefits, including a reduction in risk of hypertensive disorders during pregnancy and occurrence of congenital anomalies other than NTDs. (See "Folic acid supplementation in pregnancy", section on 'Effect of folic acid supplementation on other pregnancy outcomes'.)

Recommended intake – The Dietary Guidelines for Americans recommends 0.6 mg/day of folate for pregnant people (table 2) [18]. In addition to consuming a diet rich in folate, the United States Preventive Services Task Force (USPSTF) recommends a supplement containing 0.4 to 0.8 mg of folic acid one month before and for the first two to three months after conception to reduce the risk of open NTDs [85,86]. An RDA of 0.6 mg is recommended thereafter to meet the growth needs of the fetus and placenta [41]. Continuing folic acid supplementation after the first trimester prevents the decline in serum folate and rise in homocysteine concentrations that occur when supplementation is discontinued [87]. (See "Folic acid supplementation in pregnancy", section on 'Dose and administration'.)

For pregnant people at high risk (eg, history of NTD, use of some antiseizure medications), folic acid recommendations are higher (4 mg/day) and are reviewed separately. (See "Folic acid supplementation in pregnancy", section on 'Females who may benefit from higher dose folic acid supplementation'.)

Sources – Dietary sources of folic acid (fortified foods) and folate are shown in the table (table 5). While intake of folate from foods on average meets the recommended daily intake, food folate intake is inadequate in at least 36 percent of pregnant individuals [48], which supports routine supplementation of all females of reproductive age. (See "Folic acid supplementation in pregnancy", section on 'Sources'.)

Other micronutrients

Choline

Evidence – Choline is a component of acetylcholine, sphingomyelin, and phosphatidylcholine, thus it is important in the development of the fetal central nervous system and cognition [88]. In a systematic review of studies on the relationship between choline, neurological development, and brain function during the first 1000 days of life (38 animal studies, 16 human studies), choline supplementation was associated with faster information processing in infants and improvement in memory tasks [88]. The authors suggested that choline supplementation supported normal brain development, and high doses may protect against neural and metabolic insults, such as fetal exposure to alcohol.

Recommended intake – In the United States, pregnant people should consume 450 mg/day of choline from food and supplemental sources (table 2) [89]. US National Health and Nutrition Examination Survey (NHANES) data indicate that usual choline intake among pregnant individuals was 319 mg/day, and only 8.5 percent consumed at or above the recommended amount [90].

Sources – Most prenatal supplements contain between 0 and 50 mg of choline, which is substantially less than the recommended daily amount. Thus, the daily requirement is best met by consumption of good choline sources, such as eggs, meats, poultry, seafood, and dairy. Plant sources, such as navy beans, Brussels sprouts, broccoli, and spinach contain lower amounts of choline; therefore, vegetarians and vegans should seek out supplemental sources of choline.

Zinc

Evidence – Zinc has a role in many biological functions, including normal fetal growth and neuronal development. However, in a 2021 systematic review of 25 randomized trials of zinc versus no zinc/placebo supplementation in pregnancy (>18,000 pregnant people and their offspring), zinc supplementation did not significantly improve any maternal, fetal, or newborn outcome (eg, preterm birth, stillbirth, neonatal death, birthweight, low birthweight, small for gestational age), but the evidence was generally low quality [91].

Recommended intake – In the United States, the recommended daily allowance for zinc is 11 to 12 mg/day during pregnancy (table 2) [92]. Data from the National Health and Nutrition Examination Survey (2011 to 2014) indicate that mean zinc intake among pregnant individuals is 10.3 mg/day from food alone and 18.4 mg/day from food plus supplements [93]. However, an estimated 11 percent of pregnant people consume less than recommended [48].

Management of pregnant people who are at risk for severe zinc deficiency (eg, active inflammatory bowel disease, acrodermatitis enteropathica, pica) is discussed separately. (See "Zinc deficiency and supplementation in children" and "Pica in pregnancy".)

Sources – Food sources of zinc include meat, poultry, and certain types of seafood (oysters, crab, lobster). Whole grains, cereals, and legumes are also good sources of zinc, but bioavailability is lower due to phytates that bind to and decrease its absorption [94].

Iodine

Evidence – Iodine is an essential mineral necessary for production of thyroid hormones. Deficiency has potentially harmful effects, such as maternal and fetal/neonatal hypothyroidism. A 2017 systematic review that examined routine iodine supplementation found insufficient data to reach any clinically useful conclusions on its benefits and harms of preconception, during pregnancy, or postpartum [95]. A 2020 systematic review came to a similar conclusion regarding iodine supplementation for pregnant people residing in areas of mild to moderate iodine deficiency [96], presumably because they are able to physiologically adapt to mildly low iodine intakes and draw from intrathyroidal iodine stores to maintain fetal euthyroidism and enable normal neurodevelopment [97].

Recommended intake – The National Academy of Medicine recommends daily iodine intake of 220 mcg during pregnancy (table 2) and 290 mcg during lactation [98]; the WHO recommends daily iodine intake of 250 mcg for both pregnant and lactating people [99]. The American Thyroid Association recommends that individuals who are planning pregnancy, are pregnant, or are lactating supplement their diet with a daily oral multivitamin supplement that contains 150 mcg of iodine in the form of potassium iodide [100].

Excessive intake can be harmful [101]. (See 'Supplements and dietary intake that can be harmful' below.)

Sources – Many prenatal vitamins contain no iodine since requirements are often met with dietary sources, such as iodized salt. In the United States, data suggest that 23 to 56 percent of pregnant people have intake below recommended levels based on urinary iodine concentrations [102,103]. Similar findings have been reported in the United Kingdom and in Sweden [104]. Declining intakes of iodine may be related to increased intake of non-iodized salt from processed foods and in the home (such as sea salt, which contains less iodine than iodized salt). Although pregnant individuals should not be encouraged to start using table salt if they do not already do so, pregnant people should be encouraged to use iodized salt (contains 95 mcg iodine per one-quarter teaspoon) rather than non-iodized, and/or consume cooked seafood that is naturally rich in iodine to attain adequate intake.

Vitamin B12

EvidenceVitamin B12 functions closely with folate and homocysteine and is involved in DNA synthesis and cellular metabolism. Few randomized trials have examined the effects of B12 supplementation in pregnancy on maternal or neonatal outcomes. One systematic review of longitudinal cohort studies reported that lower maternal vitamin B12 plasma levels were associated with higher risk of preterm birth, particularly with vitamin B12 deficiency [105]. No association was found with birth weight.

Recommended intake – In the United States, the recommended daily allowance for vitamin B12 is 2.6 mcg/day in pregnancy and 2.8 mcg/day during lactation (table 2) [106]. The majority of pregnant people in the United States meet vitamin B12 requirements, with mean intake from foods of 5.6 mcg/day (more than two times RDA).

Sources Only animal source foods, such as fish, meat, poultry, eggs, and dairy products, contain vitamin B12; thus, individuals who consume a vegetarian or vegan diet are at higher risk of B12 deficiency and should take a supplement [107].

Vitamin A

EvidenceVitamin A is important in cell division, fetal organ and skeletal growth, maintenance of the immune system, fetal visual development, and maintenance of maternal vision [108]. However, supplementation in nondeficient subjects has not been shown to improve pregnancy outcomes and may increase risk of toxicity.

A pregnant person with moderate deficiency is at higher risk for night blindness, particularly in the third trimester when fetal growth is accelerated, because the fetus will obtain sufficient vitamin A at the expense of maternal stores [108-110]. In some resource-limited countries, vitamin A deficiency is a concern; in addition to maternal night blindness, deficiency puts pregnant people at risk of xerophthalmia, anemia, and susceptibility to infection [111]. By contrast, in resource-abundant countries, excessive intake of vitamin A is the primary concern.

Recommended intakeVitamin A utilization increases slightly during pregnancy; thus, recommended intake is increased to 750 to 770 mcg retinol equivalents (2500 to 2560 international units) per day in pregnancy (versus 700 mcg retinol equivalents [approximately 2330 international units] per day in nonpregnant females) (table 2) [112]. Supplements containing high doses of preformed vitamin A should be avoided (see 'Preformed vitamin A in supplements' below). In the United States, mean daily intake of vitamin A among pregnant individuals is 696 mcg retinol equivalents from foods alone and 1283 mcg retinol equivalents from foods plus supplements [48]. An estimated 15 percent of pregnant people consume less than recommended.

Where vitamin A deficiency is endemic, such as Southeast Asia and sub-Saharan Africa, a daily supplement containing less than 3000 mcg retinol equivalents (10,000 international units) or a weekly supplement less than 8500 mcg retinol equivalents (25,000 international units) appears to have some maternal and fetal/neonatal health benefits (eg, reduction in maternal anemia and night blindness) with no evidence of teratogenicity [113,114], but does not reduce maternal or perinatal mortality [115], which was suggested by some early studies.

SourcesVitamin A is found in moderate amounts (300 to 770 mcg retinol equivalents) in many prenatal vitamins, often in the form of beta-carotene (provitamin A).

Vitamin A is present in a variety of foods, and requirements can be met by consuming foods such as milk, fish, eggs, carrots, leafy greens, broccoli, cantaloupe, and squash. Some groups recommend avoiding liver because of its high vitamin A content. (see 'Vitamin A in liver' below).

SUPPLEMENTS AND DIETARY INTAKE THAT CAN BE HARMFUL — The use of self-prescribed over-the-counter supplements is commonplace and has led to numerous case reports of vitamin or mineral toxicities due to overuse. Excessive maternal consumption of some foods can also be potentially toxic to the fetus.

Preformed vitamin A in supplements — Consumption of vitamin supplements containing high doses of preformed vitamin A (greater than 10,000 international units per day [1 international unit = 0.3 retinol equivalents]) appears to be teratogenic [113,116]. In the absence of severe deficiency, pregnant people should avoid consuming multivitamin or prenatal supplements that contain more than 5000 international units (1500 mcg retinol equivalents) of vitamin A. Most supplements contain beta-carotene rather than retinol; high beta-carotene intakes have not been associated with an increased risk for congenital anomalies [117].

Vitamin A in liver — Some foods are fortified with vitamin A and others are rich in vitamin A (eg, liver). For this reason, some groups (eg, Finnish Food Safety Authority Evira, National Health Service) recommend avoiding liver consumption during pregnancy [118-123]. Limiting the intake of liver and liver products during the first trimester is likely prudent, particularly in high-income countries where vitamin A deficiency is rare.

For pregnant people who commonly consume liver, we advise checking local food composition databases as vitamin A content of livers from different animals vary. For example, in the United States Department of Agriculture (USDA) Nutrient Database [124], vitamin A content of liver and liver products varies from 4900 international units in one raw chicken liver to 59,500 international units in 3 ounces of cooked New Zealand beef liver.

Iodine in nutritional supplements and seaweed — Excessive intake of iodine can cause fetal goiter [125-127], but the safe upper limit of iodine intake in pregnancy is unclear. Congenital hypothyroidism has been reported in offspring of pregnant people ingesting 2.3 to 12.5 mg iodine daily (greater than 10 times the recommended dietary allowances [RDA] of 220 mcg, and greater than two times the upper limit of 1100 mcg) (table 2) [125,127]. The cases from the United States were related to excess iodine ingestion from nutritional supplements, and those from Japan were related to diets containing large quantities of kombu, other seaweeds, and instant kombu soups. Nevertheless, excessive iodine intake in the United States is uncommon (<1 percent) [103].

Processed trans fatty acids — Processed trans fatty acids (TFAs) should be minimized or preferably avoided. They may have adverse effects on fetal growth and development by interfering with essential fatty acid metabolism, by direct effects on membrane structures or metabolism, or by replacing maternal intake of the cis essential fatty acids [128]. (See "Dietary fat", section on 'Trans fatty acids'.)

TFAs were previously ubiquitous in processed foods in the United States food supply, but are no longer considered "Generally Recognized As Safe" (GRAS) by the FDA and no longer permitted for use in the United States [129]. They are still present in some items with long shelf-lives, and they are still used in some countries. The World Health Organization (WHO) set a goal to eliminate TFAs from the world's food supply by 2023 [130].

SUPPLEMENTS WITH NO OR UNCERTAIN PREGNANCY BENEFITS

Vitamin E — In a systematic review of randomized trials, vitamin E supplementation during pregnancy in combination with vitamin C or other supplements or drugs did not improve rates of stillbirth, preterm birth, preeclampsia, or low birth weight [131]. Prior evidence [132] suggested that vitamin E increased self-reported abdominal pain and prelabor rupture of membranes at term; however, preterm prelabor rupture of membranes was not increased [131].

Vitamin C — In a systematic review of randomized trials, vitamin C supplementation during pregnancy either alone or in combination with other supplements had no beneficial or harmful effects [133]. No effects were observed on prevention of stillbirth, preterm birth, preeclampsia, or low birth weight. Vitamin C supplementation alone resulted in a decreased risk of preterm prelabor rupture of membranes; however, the quality of evidence was poor.

Vitamin B6 — Vitamin B6 (pyridoxine) is a coenzyme for more than 100 enzymes in the body, including those involved in metabolism of amino acids, carbohydrates, and lipids and synthesis of neurotransmitters. The majority of pregnant individuals consume an adequate amount of B6 through foods and safely exceed the requirement through a combination of foods plus supplements [48]. A 2015 Cochrane review that included four small trials that examined B6 supplementation during pregnancy found no evidence of clinical benefits [134]. Vitamin B6 has been shown to improve mild to moderate nausea during pregnancy. (See "Nausea and vomiting of pregnancy: Treatment and outcome", section on 'Pyridoxine (vitamin B6) monotherapy'.)

Probiotics — Consumption of probiotic supplements is increasingly popular. Some evidence suggests that probiotic use (combinations of certain Lactobacillus and Bifidobacterium strains) during pregnancy may have beneficial maternal effects, such as reduced risk of inflammatory events and preeclampsia and improved maternal glucose metabolism [135,136]. However, a 2020 Cochrane review of probiotic treatment for patients with gestational diabetes concluded available evidence was too limited to inform practice due to the high variability of products used and small sample sizes in trials [137].

Studies of probiotic use during pregnancy have not reported increased risk of adverse fetal outcomes, but these data are also limited. A 2018 Cochrane review of maternal oral probiotic supplementation for prevention of morbidity and mortality in preterm infants did not find appreciable benefit or harm to neonates as a result of supplementation of pregnant people at low risk for preterm birth or mothers of preterm infants after birth [138].

FLUID REQUIREMENTS

Water and other fluids — During pregnancy, adequate fluid intake from consumption of beverages (water and other liquids) is estimated to be approximately 2.3 L/day (76 fluid ounces or approximately 10 cups) [139]. Additional water is consumed in foods other than beverages to meet the total adequate intake of 3 L/day. Numerous factors (eg, ambient temperature, humidity, physical activity, exercise influence) also influence total water needs.

Fluoride — Fluoride supplementation during pregnancy is unnecessary, even though pregnant people who live in areas where water is not fluoridated or who consume only unfluoridated bottled water may not achieve adequate intake of fluoride. (See "Nutrition in pregnancy: Assessment and counseling", section on 'Consumption of nonfluoridated bottled or tap water'.)

SPECIAL POPULATIONS

Multiple gestation — Nutritional requirements and weight gain recommendations are higher in multiple gestations. Guidelines are provided separately. (See "Twin pregnancy: Routine prenatal care", section on 'Nutrition and supplements' and "Twin pregnancy: Routine prenatal care", section on 'Gestational weight gain' and "Triplet pregnancy", section on 'Weight gain'.)

Pregnant patients with diabetes — Medical nutritional therapy for patients with pregestational or gestational diabetes are reviewed separately. (See "Pregestational (preexisting) diabetes mellitus: Antenatal glycemic control", section on 'Medical nutrition therapy' and "Gestational diabetes mellitus: Glucose management and maternal prognosis", section on 'Medical nutritional therapy'.)

Postpartum and breastfeeding — An adequate, balanced diet is believed to be important for replenishment of maternal stores that are expended during the pregnancy, for promoting loss of excess weight, and for nourishing the breastfed infant. Maternal nutrition in the postpartum period, including during lactation, are discussed separately. (See "Maternal nutrition during lactation" and "Overview of the postpartum period: Disorders and complications", section on 'Postpartum weight retention'.)

Pregnant people with undernutrition living in resource-limited areas — Pregnant people with potentially severe undernutrition living in resource-limited areas require careful assessment and a different approach to treatment, which is reviewed separately. (See "Undernutrition in pregnancy: Evaluation, management, and outcome in resource-limited areas".)

Pregnant people with self-imposed dietary restraints and other dietary issues — (See "Nutrition in pregnancy: Assessment and counseling", section on 'Issues regarding self-imposed dietary restraints' and "Nutrition in pregnancy: Assessment and counseling", section on 'Other dietary issues'.)

RESOURCES — The Food and Information Center of the United States Department of Agriculture provides several online resources for pregnant people, including information on folic acid, food safety, foods to avoid, and nutrition.

SOCIETY GUIDELINE LINKS — Links to society and government-sponsored guidelines from selected countries and regions around the world are provided separately. (See "Society guideline links: Nutrition and supplements in pregnancy".)

INFORMATION FOR PATIENTS — UpToDate offers two types of patient education materials, "The Basics" and "Beyond the Basics." The Basics patient education pieces are written in plain language, at the 5th to 6th grade reading level, and they answer the four or five key questions a patient might have about a given condition. These articles are best for patients who want a general overview and who prefer short, easy-to-read materials. Beyond the Basics patient education pieces are longer, more sophisticated, and more detailed. These articles are written at the 10th to 12th grade reading level and are best for patients who want in-depth information and are comfortable with some medical jargon.

Here are the patient education articles that are relevant to this topic. We encourage you to print or e-mail these topics to your patients. (You can also locate patient education articles on a variety of subjects by searching on "patient info" and the keyword(s) of interest.)

Basics topics (see "Patient education: Nutrition before and during pregnancy (The Basics)" and "Patient education: Health and nutrition during breastfeeding (The Basics)" and "Patient education: Vegetarian diet (The Basics)")

Beyond the Basics topic (see "Patient education: Health and nutrition during breastfeeding (Beyond the Basics)")

SUMMARY AND RECOMMENDATIONS

Clinical significance – Nutrition is a key modifiable factor that may affect birth outcomes and has long-term effects on the health of offspring. (See 'Introduction' above.)

Key components of healthy eating – The key components of recommended healthy eating, based on consensus guidelines, during pregnancy include (see 'General dietary principles for optimal pregnancy outcome' above):

Appropriate gestational weight gain

Consumption of a variety of primarily whole, unprocessed foods in appropriate amounts to allow adequate, but not excessive, gestational weight gain

Appropriate vitamin and mineral supplementation

Avoidance of alcohol and other known or potentially harmful substances

Safe food handling

Recommended intake – Daily nutritional goals for macronutrients, micronutrients, and vitamins during pregnancy are shown in the table (table 2). (See 'Dietary requirements' above.)

In the first trimester, pregnant people typically do not need to increase their caloric intake. In the second and third trimesters, energy requirements differ by prepregnancy body mass index (BMI) classification and trimester. (See 'Energy intake' above.)

Adequate fluid intake from consumption of beverages (water and other liquids) is estimated to be approximately 2.3 L/day (76 fluid ounces or approximately 10 cups). (See 'Water and other fluids' above.)

Supplements/dietary intake that can be harmful – Consumption of vitamin supplements containing high doses of preformed vitamin A (greater than 10,000 international units per day [1 international unit = 0.3 retinol equivalents]) appears to be teratogenic. Excessive intake of liver and liver products can also result in excessive intake of vitamin A. (See 'Preformed vitamin A in supplements' above and 'Vitamin A in liver' above.)

Excess iodine ingestion can cause fetal goiter. Iodine is present in nutritional supplements and kombu and other seaweeds. (See 'Iodine in nutritional supplements and seaweed' above.)

ACKNOWLEDGMENT — The UpToDate editorial staff acknowledges Edmund F Funai, MD, Jonathan Gillen-Goldstein, MD, Henry Roque, MD, MS, and Jean M Ruvel, RD, CDE, CDN who contributed to an earlier version of this topic review.

  1. Finnell RH, Shaw GM, Lammer EJ, et al. Gene-nutrient interactions: importance of folates and retinoids during early embryogenesis. Toxicol Appl Pharmacol 2004; 198:75.
  2. Feodor Nilsson S, Andersen PK, Strandberg-Larsen K, Nybo Andersen AM. Risk factors for miscarriage from a prevention perspective: a nationwide follow-up study. BJOG 2014; 121:1375.
  3. Shaw GM, Wise PH, Mayo J, et al. Maternal prepregnancy body mass index and risk of spontaneous preterm birth. Paediatr Perinat Epidemiol 2014; 28:302.
  4. Ramakrishnan U, Grant F, Goldenberg T, et al. Effect of women's nutrition before and during early pregnancy on maternal and infant outcomes: a systematic review. Paediatr Perinat Epidemiol 2012; 26 Suppl 1:285.
  5. American College of Obstetricians and Gynecologists. ACOG Committee opinion no. 549: obesity in pregnancy. Obstet Gynecol 2013; 121:213.
  6. Nutrition during pregnancy: Part 1: Weight gain, Part 2: Nutrient supplements. Institute of Medicine. Available at: http://nationalacademies.org/hmd/reports/1990/nutrition-during-pregnancy-part-i-weight-gain-part-ii-nutrient-supplements.aspx (Accessed on April 05, 2016).
  7. Gete DG, Waller M, Mishra GD. Effects of maternal diets on preterm birth and low birth weight: a systematic review. Br J Nutr 2020; 123:446.
  8. Raghavan R, Dreibelbis C, Kingshipp BL, et al. Dietary patterns before and during pregnancy and maternal outcomes: a systematic review. Am J Clin Nutr 2019; 109:705S.
  9. Stephenson J, Heslehurst N, Hall J, et al. Before the beginning: nutrition and lifestyle in the preconception period and its importance for future health. Lancet 2018; 391:1830.
  10. Barker DJ, Thornburg KL. The obstetric origins of health for a lifetime. Clin Obstet Gynecol 2013; 56:511.
  11. Ravelli AC, van der Meulen JH, Michels RP, et al. Glucose tolerance in adults after prenatal exposure to famine. Lancet 1998; 351:173.
  12. Roseboom T, de Rooij S, Painter R. The Dutch famine and its long-term consequences for adult health. Early Hum Dev 2006; 82:485.
  13. Dunford AR, Sangster JM. Maternal and paternal periconceptional nutrition as an indicator of offspring metabolic syndrome risk in later life through epigenetic imprinting: A systematic review. Diabetes Metab Syndr 2017; 11 Suppl 2:S655.
  14. Muktabhant B, Lawrie TA, Lumbiganon P, Laopaiboon M. Diet or exercise, or both, for preventing excessive weight gain in pregnancy. Cochrane Database Syst Rev 2015; :CD007145.
  15. Ng M, Fleming T, Robinson M, et al. Global, regional, and national prevalence of overweight and obesity in children and adults during 1980-2013: a systematic analysis for the Global Burden of Disease Study 2013. Lancet 2014; 384:766.
  16. Robinson S, Baird J, Godfrey KM. Eating for two? The unresolved question of optimal diet in pregnancy. Am J Clin Nutr 2014; 100:1220.
  17. Kaiser L, Allen LH, American Dietetic Association. Position of the American Dietetic Association: nutrition and lifestyle for a healthy pregnancy outcome. J Am Diet Assoc 2008; 108:553.
  18. Dietary Guidelines for Americans, 2020-2025 9th Edition. U.S. Department of Agriculture and U.S. Department of Health and Human Services, 2020. https://www.dietaryguidelines.gov/sites/default/files/2021-03/Dietary_Guidelines_for_Americans-2020-2025.pdf
  19. Institute of Medicine. Weight gain during pregnancy: Reexamining the guidelines http://iom.edu/Reports/2009/Weight-Gain-During-Pregnancy-Reexamining-the-Guidelines.aspx (Accessed on June 18, 2015).
  20. Institute of Medicine. Weight gain during pregnancy: Reexamining the guidelines. http://iom.edu/Reports/2009/Weight-Gain-During-Pregnancy-Reexamining-the-Guidelines.aspx (Accessed on April 05, 2016).
  21. https://fnic.nal.usda.gov/sites/fnic.nal.usda.gov/files/uploads/DRIEssentialGuideNutReq.pdf (Accessed on April 21, 2016).
  22. https://fnic.nal.usda.gov/dietary-guidance/dri-nutrient-reports/vitamin-d-and-calcium (Accessed on April 21, 2016).
  23. Weight Gain During Pregnancy: Reexamining the Guidelines, Institute of Medicine (US) and National Research Council (US) Committee to Reexamine IOM Pregnancy Weight Guidelines. (Ed), National Academies Press (US) 2009.
  24. Most J, Dervis S, Haman F, et al. Energy Intake Requirements in Pregnancy. Nutrients 2019; 11.
  25. Thomas DM, Navarro-Barrientos JE, Rivera DE, et al. Dynamic energy-balance model predicting gestational weight gain. Am J Clin Nutr 2012; 95:115.
  26. Most J, Amant MS, Hsia DS, et al. Evidence-based recommendations for energy intake in pregnant women with obesity. J Clin Invest 2019; 129:4682.
  27. Institute of Medicine. Dietary reference intakes: The essential guide to nutrient requirements. National Academies Press; Washington, DC 2006.
  28. Mousa A, Naqash A, Lim S. Macronutrient and Micronutrient Intake during Pregnancy: An Overview of Recent Evidence. Nutrients 2019; 11.
  29. Blumfield ML, Collins CE. High-protein diets during pregnancy: healthful or harmful for offspring? Am J Clin Nutr 2014; 100:993.
  30. Ota E, Tobe-Gai R, Mori R, Farrar D. Antenatal dietary advice and supplementation to increase energy and protein intake. Cochrane Database Syst Rev 2012; :CD000032.
  31. Kramer MS, Kakuma R. Energy and protein intake in pregnancy. Cochrane Database Syst Rev 2003; :CD000032.
  32. Lindmark G. Energy and protein intake in pregnancy: RHL commentary (last revised: 31 October 2003). The WHO Reproductive Health Library; Geneva, 2003.
  33. Morisaki N, Nagata C, Yasuo S, et al. Optimal protein intake during pregnancy for reducing the risk of fetal growth restriction: the Japan Environment and Children's Study. Br J Nutr 2018; 120:1432.
  34. Halldorsson TI, Birgisdottir BE, Brantsæter AL, et al. Old Question Revisited: Are High-Protein Diets Safe in Pregnancy? Nutrients 2021; 13.
  35. Qiu C, Coughlin KB, Frederick IO, et al. Dietary fiber intake in early pregnancy and risk of subsequent preeclampsia. Am J Hypertens 2008; 21:903.
  36. Scientific Report of the 2020 Dietary Guidelines Advisory Committee: Advisory Report to the Secretary of Agriculture and the Secretary of Health and Human Services. U.S. Department of Agriculture, Agricultural Research Service. Available at: https://www.dietaryguidelines.gov/2020-advisory-committee-report (Accessed on July 20, 2021).
  37. Middleton P, Gomersall JC, Gould JF, et al. Omega-3 fatty acid addition during pregnancy. Cochrane Database Syst Rev 2018; 11:CD003402.
  38. Keats EC, Haider BA, Tam E, Bhutta ZA. Multiple-micronutrient supplementation for women during pregnancy. Cochrane Database Syst Rev 2019; 3:CD004905.
  39. Wolf HT, Hegaard HK, Huusom LD, Pinborg AB. Multivitamin use and adverse birth outcomes in high-income countries: a systematic review and meta-analysis. Am J Obstet Gynecol 2017; 217:404.e1.
  40. Vitamin supplementation in pregnancy. Drug Ther Bull 2016; 54:81.
  41. Institute of Medicine, Food and Nutrition Board, Committee on Nutritional Status During Pregnancy. Part II: Dietary intake and nutrient supplements. National Academy Press; Washington, DC 1990.
  42. Moos MK, Dunlop AL, Jack BW, et al. Healthier women, healthier reproductive outcomes: recommendations for the routine care of all women of reproductive age. Am J Obstet Gynecol 2008; 199:S280.
  43. Dietary reference intakes for calcium and vitamin D. www.iom.edu/vitamind (Accessed on December 03, 2010).
  44. Sebastiani G, Herranz Barbero A, Borrás-Novell C, et al. The Effects of Vegetarian and Vegan Diet during Pregnancy on the Health of Mothers and Offspring. Nutrients 2019; 11.
  45. Goodnight W, Newman R, Society of Maternal-Fetal Medicine. Optimal nutrition for improved twin pregnancy outcome. Obstet Gynecol 2009; 114:1121.
  46. Shawe J, Ceulemans D, Akhter Z, et al. Pregnancy after bariatric surgery: Consensus recommendations for periconception, antenatal and postnatal care. Obes Rev 2019; 20:1507.
  47. Ghishan FK, Kiela PR. Vitamins and Minerals in Inflammatory Bowel Disease. Gastroenterol Clin North Am 2017; 46:797.
  48. Bailey RL, Pac SG, Fulgoni VL 3rd, et al. Estimation of Total Usual Dietary Intakes of Pregnant Women in the United States. JAMA Netw Open 2019; 2:e195967.
  49. WHO antenatal care recommendations for a positive pregnancy experience. Nutritional interventions update: Multiple micronutrient supplements during pregnancy. Last updated July 26, 2020. World Health Organization. (Available online at: https://www.who.int/publications/i/item/9789240007789).
  50. World Health Organization, United Nations University, United Nations Children’s Fund. Composition of a multi-micronutrient supplement to be used in pilot programmes among pregnant women in developing countries: report of a United Nations Children’s Fund (UNICEF), World Health Organization (WHO) and United Nations University workshop. New York: UNICEF; 1999.
  51. McLean E, Cogswell M, Egli I, et al. Worldwide prevalence of anaemia, WHO Vitamin and Mineral Nutrition Information System, 1993-2005. Public Health Nutr 2009; 12:444.
  52. Mei Z, Cogswell ME, Looker AC, et al. Assessment of iron status in US pregnant women from the National Health and Nutrition Examination Survey (NHANES), 1999-2006. Am J Clin Nutr 2011; 93:1312.
  53. Cantor AG, Bougatsos C, Dana T, et al. Routine iron supplementation and screening for iron deficiency anemia in pregnancy: a systematic review for the U.S. Preventive Services Task Force. Ann Intern Med 2015; 162:566.
  54. Peña-Rosas JP, De-Regil LM, Garcia-Casal MN, Dowswell T. Daily oral iron supplementation during pregnancy. Cochrane Database Syst Rev 2015; :CD004736.
  55. Reveiz L, Gyte GM, Cuervo LG, Casasbuenas A. Treatments for iron-deficiency anaemia in pregnancy. Cochrane Database Syst Rev 2011; :CD003094.
  56. Fairweather-Tait S. How much iron does a healthy pregnant woman require? Am J Clin Nutr 2022; 115:985.
  57. Recommendations to prevent and control iron deficiency in the United States. Centers for Disease Control and Prevention. MMWR Recomm Rep 1998; 47:1.
  58. Daily iron and folic acid supplementation during pregnancy. World Health Organization. Available at: https://www.who.int/elena/titles/guidance_summaries/daily_iron_pregnancy/en/ (Accessed on August 10, 2021).
  59. Scientific Advisory Committee on Nutrition. Iron and health report - GOV.UK. [Internet]. Norwich, UK: The Stationery Office; 2011. Available from: https://www.gov.uk/government/publications/sacn-iron-and-health-report.
  60. Department of Health. Dietary reference values for food, energy and nutrients in the United Kingdom. Report on health and social subjects, no. 41. London, UK: HSMO; 1991.
  61. EFSA NDA Panel (EFSA Panel on Dietetic Products, Nutrition and Allergies), 2015. Scientific opinion on dietary reference values for iron. EFSA J 2015; 13:4254.
  62. Institute of Medicine. Iron deficiency anemia: Recommended guidelines for the prevention, detection, and management among U.S. children and women of childbearing age. National Academy Press; Washington, DC 1993.
  63. Stoffel NU, Cercamondi CI, Brittenham G, et al. Iron absorption from oral iron supplements given on consecutive versus alternate days and as single morning doses versus twice-daily split dosing in iron-depleted women: two open-label, randomised controlled trials. Lancet Haematol 2017; 4:e524.
  64. Peña-Rosas JP, De-Regil LM, Dowswell T, Viteri FE. Intermittent oral iron supplementation during pregnancy. Cochrane Database Syst Rev 2012; :CD009997.
  65. Dietary Reference Intakes for Vitamin A, Vitamin K, Arsenic, Boron, Chromium, Copper, Iodine, Iron, Manganese, Molybdenum, Nickel, Silicon, Vanadium, and Zinc, Institute of Medicine (US) Panel on Micronutrients. (Ed), National Academies Press (US), Washington (DC) 2001.
  66. Schümann K, Ettle T, Szegner B, et al. On risks and benefits of iron supplementation recommendations for iron intake revisited. J Trace Elem Med Biol 2007; 21:147.
  67. Delaney KM, Cao C, Guillet R, et al. Fetal iron uptake from recent maternal diet and the maternal RBC iron pool. Am J Clin Nutr 2022; 115:1069.
  68. Barrett JF, Whittaker PG, Williams JG, Lind T. Absorption of non-haem iron from food during normal pregnancy. BMJ 1994; 309:79.
  69. Stoffel NU, Zimmermann MB, Cepeda-Lopez AC, et al. Maternal iron kinetics and maternal-fetal iron transfer in normal-weight and overweight pregnancy. Am J Clin Nutr 2022; 115:1166.
  70. Wong L, Smith S, Gilstrop M, et al. Safety and efficacy of rapid (1,000 mg in 1 hr) intravenous iron dextran for treatment of maternal iron deficient anemia of pregnancy. Am J Hematol 2016; 91:590.
  71. Avni T, Bieber A, Grossman A, et al. The safety of intravenous iron preparations: systematic review and meta-analysis. Mayo Clin Proc 2015; 90:12.
  72. Froessler B, Collingwood J, Hodyl NA, Dekker G. Intravenous ferric carboxymaltose for anaemia in pregnancy. BMC Pregnancy Childbirth 2014; 14:115.
  73. Hurrell R, Egli I. Iron bioavailability and dietary reference values. Am J Clin Nutr 2010; 91:1461S.
  74. Hacker AN, Fung EB, King JC. Role of calcium during pregnancy: maternal and fetal needs. Nutr Rev 2012; 70:397.
  75. Hofmeyr GJ, Lawrie TA, Atallah ÁN, Torloni MR. Calcium supplementation during pregnancy for preventing hypertensive disorders and related problems. Cochrane Database Syst Rev 2018; 10:CD001059.
  76. Buppasiri P, Lumbiganon P, Thinkhamrop J, et al. Calcium supplementation (other than for preventing or treating hypertension) for improving pregnancy and infant outcomes. Cochrane Database Syst Rev 2015; :CD007079.
  77. Calcium. Fact Sheet for Health Professionals. National Institutes of Health. Available at: https://ods.od.nih.gov/factsheets/Calcium-HealthProfessional/ (Accessed on August 10, 2021).
  78. Cannell JJ. Vitamin D and autism, what's new? Rev Endocr Metab Disord 2017; 18:183.
  79. Litonjua AA, Carey VJ, Laranjo N, et al. Effect of Prenatal Supplementation With Vitamin D on Asthma or Recurrent Wheezing in Offspring by Age 3 Years: The VDAART Randomized Clinical Trial. JAMA 2016; 315:362.
  80. Hollis BW, Wagner CL. Vitamin D supplementation during pregnancy: Improvements in birth outcomes and complications through direct genomic alteration. Mol Cell Endocrinol 2017; 453:113.
  81. Venter C, Agostoni C, Arshad SH, et al. Dietary factors during pregnancy and atopic outcomes in childhood: A systematic review from the European Academy of Allergy and Clinical Immunology. Pediatr Allergy Immunol 2020; 31:889.
  82. Mustapa Kamal Basha MA, Majid HA, Razali N, Yahya A. Risk of eczema, wheezing and respiratory tract infections in the first year of life: A systematic review of vitamin D concentrations during pregnancy and at birth. PLoS One 2020; 15:e0233890.
  83. van Schoor NM, Lips P. Worldwide vitamin D status. Best Pract Res Clin Endocrinol Metab 2011; 25:671.
  84. Dietary Reference Intakes for Calcium and Vitamin D, Institute of Medicine (US) Committee to Review Dietary Reference Intakes for Vitamin D and Calcium. (Ed), National Academies Press (US), Washington (DC) 2011.
  85. US Preventive Services Task Force, Bibbins-Domingo K, Grossman DC, et al. Folic Acid Supplementation for the Prevention of Neural Tube Defects: US Preventive Services Task Force Recommendation Statement. JAMA 2017; 317:183.
  86. Viswanathan M, Treiman KA, Kish-Doto J, et al. Folic Acid Supplementation for the Prevention of Neural Tube Defects: An Updated Evidence Report and Systematic Review for the US Preventive Services Task Force. JAMA 2017; 317:190.
  87. McNulty B, McNulty H, Marshall B, et al. Impact of continuing folic acid after the first trimester of pregnancy: findings of a randomized trial of Folic Acid Supplementation in the Second and Third Trimesters. Am J Clin Nutr 2013; 98:92.
  88. Derbyshire E, Obeid R. Choline, Neurological Development and Brain Function: A Systematic Review Focusing on the First 1000 Days. Nutrients 2020; 12.
  89. NIH. Choline. Fact sheet for health progessionals https://ods.od.nih.gov/factsheets/Choline-HealthProfessional/ (Accessed on August 10, 2021).
  90. Wallace TC, Fulgoni VL. Usual Choline Intakes Are Associated with Egg and Protein Food Consumption in the United States. Nutrients 2017; 9.
  91. Carducci B, Keats EC, Bhutta ZA. Zinc supplementation for improving pregnancy and infant outcome. Cochrane Database Syst Rev 2021; 3:CD000230.
  92. Zinc. Fact sheet for health professionals. National Institutes of Health. Available at: https://ods.od.nih.gov/factsheets/Zinc-HealthProfessional/ (Accessed on August 10, 2021).
  93. Hennigar SR, Lieberman HR, Fulgoni VL 3rd, McClung JP. Serum Zinc Concentrations in the US Population Are Related to Sex, Age, and Time of Blood Draw but Not Dietary or Supplemental Zinc. J Nutr 2018; 148:1341.
  94. FoodData Central. U.S. Department of Agriculture, Agricultural Research Service. Available at: https://fdc.nal.usda.gov/ (Accessed on July 22, 2021).
  95. Harding KB, Peña-Rosas JP, Webster AC, et al. Iodine supplementation for women during the preconception, pregnancy and postpartum period. Cochrane Database Syst Rev 2017; 3:CD011761.
  96. Dineva M, Fishpool H, Rayman MP, et al. Systematic review and meta-analysis of the effects of iodine supplementation on thyroid function and child neurodevelopment in mildly-to-moderately iodine-deficient pregnant women. Am J Clin Nutr 2020; 112:389.
  97. World Health Organization, United Nations Children’s Fund, International Council for Control of Iodine Deficiency Disorders. Assessment of iodine deficiency disorders and monitoring theirelimination. A guide for programme managers. Geneva: WHO; 2007.
  98. Iodine. Centers for Disease Control and Prevention. Available at: https://www.cdc.gov/breastfeeding/breastfeeding-special-circumstances/diet-and-micronutrients/iodine.html (Accessed on August 10, 2021).
  99. Iodine supplementation in pregnant and lactating women. World Health Organization. Available at: https://www.who.int/elena/titles/guidance_summaries/iodine_pregnancy/en/ (Accessed on August 10, 2021).
  100. Stagnaro-Green A, Abalovich M, Alexander E, et al. Guidelines of the American Thyroid Association for the diagnosis and management of thyroid disease during pregnancy and postpartum. Thyroid 2011; 21:1081.
  101. Leung AM, Pearce EN, Braverman LE. Iodine content of prenatal multivitamins in the United States. N Engl J Med 2009; 360:939.
  102. Caldwell KL, Pan Y, Mortensen ME, et al. Iodine status in pregnant women in the National Children's Study and in U.S. women (15-44 years), National Health and Nutrition Examination Survey 2005-2010. Thyroid 2013; 23:927.
  103. Kerver JM, Pearce EN, Ma T, et al. Prevalence of inadequate and excessive iodine intake in a US pregnancy cohort. Am J Obstet Gynecol 2021; 224:82.e1.
  104. Bath SC, Steer CD, Golding J, et al. Effect of inadequate iodine status in UK pregnant women on cognitive outcomes in their children: results from the Avon Longitudinal Study of Parents and Children (ALSPAC). Lancet 2013; 382:331.
  105. Rogne T, Tielemans MJ, Chong MF, et al. Associations of Maternal Vitamin B12 Concentration in Pregnancy With the Risks of Preterm Birth and Low Birth Weight: A Systematic Review and Meta-Analysis of Individual Participant Data. Am J Epidemiol 2017; 185:212.
  106. Vitamin B12. Fact sheet for health professionals. National Institutes of Health. Available at: https://ods.od.nih.gov/factsheets/VitaminB12-HealthProfessional/ (Accessed on August 10, 2021).
  107. Piccoli GB, Clari R, Vigotti FN, et al. Vegan-vegetarian diets in pregnancy: danger or panacea? A systematic narrative review. BJOG 2015; 122:623.
  108. World Health Organization guideline: Vitamin A supplementation in pregnant women (2011). Available at: http://www.who.int/nutrition/publications/micronutrients/guidelines/vas_pregnant/en/ (Accessed on April 07, 2015).
  109. Bastos Maia S, Rolland Souza AS, Costa Caminha MF, et al. Vitamin A and Pregnancy: A Narrative Review. Nutrients 2019; 11.
  110. Quadro L, Hamberger L, Gottesman ME, et al. Pathways of vitamin A delivery to the embryo: insights from a new tunable model of embryonic vitamin A deficiency. Endocrinology 2005; 146:4479.
  111. Global prevalence of vitamin A deficiency in populations at risk 1995 to 2005: WHO global database on vitamin A deficiency, 2009. World Health Organization. Available at: http://apps.who.int/iris/bitstream/10665/44110/1/9789241598019_eng.pdf (Accessed on June 23, 2020).
  112. Vitamin A. Fact sheet for health professionals. National Institutes of Health. Available at: https://ods.od.nih.gov/factsheets/VitaminA-HealthProfessional/ (Accessed on August 10, 2021).
  113. Safe vitamin A dosage during pregnancy and lactation: recommendations and report of a consultation, 1998. World Health Organization. Available at: http://whqlibdoc.who.int/hq/1998/WHO_NUT_98.4_eng.pdf (Accessed on June 22, 2015).
  114. Checkley W, West KP Jr, Wise RA, et al. Maternal vitamin A supplementation and lung function in offspring. N Engl J Med 2010; 362:1784.
  115. McCauley ME, van den Broek N, Dou L, Othman M. Vitamin A supplementation during pregnancy for maternal and newborn outcomes. Cochrane Database Syst Rev 2015; :CD008666.
  116. Rothman KJ, Moore LL, Singer MR, et al. Teratogenicity of high vitamin A intake. N Engl J Med 1995; 333:1369.
  117. Mathews-Roth MM. Lack of genotoxicity with beta-carotene. Toxicol Lett 1988; 41:185.
  118. Nelson M. Vitamin A, liver consumption, and risk of birth defects. BMJ 1990; 301:1176.
  119. Kolb E. [The problem of a high content of vitamin A in the liver of calves, cattle, sheep and swine for the consumer. Amount of accumulation and mechanism of teratogenic effect (review article)]. Berl Munch Tierarztl Wochenschr 1994; 107:342.
  120. Julkunen P, Hasunen K, Idänpään-Heikkilä J. [Health risks related to high content of vitamin A in liver]. Nord Med 1990; 105:149.
  121. Blomhoff R, Alexander J. [Vitamin A and toxicity. Should pregnant women and small children reduce their intake of liver products and vitamin A?]. Tidsskr Nor Laegeforen 1993; 113:3037.
  122. Hartmann S, Brørs O, Bock J, et al. Exposure to retinoic acids in non-pregnant women following high vitamin A intake with a liver meal. Int J Vitam Nutr Res 2005; 75:187.
  123. van den Berg H, Hulshof KF, Deslypere JP. Evaluation of the effect of the use of vitamin supplements on vitamin A intake among (potentially) pregnant women in relation to the consumption of liver and liver products. Eur J Obstet Gynecol Reprod Biol 1996; 66:17.
  124. https://ndb.nal.usda.gov/ndb/ (Accessed on March 01, 2017).
  125. Connelly KJ, Boston BA, Pearce EN, et al. Congenital hypothyroidism caused by excess prenatal maternal iodine ingestion. J Pediatr 2012; 161:760.
  126. Thomas Jde V, Collett-Solberg PF. Perinatal goiter with increased iodine uptake and hypothyroidism due to excess maternal iodine ingestion. Horm Res 2009; 72:344.
  127. Nishiyama S, Mikeda T, Okada T, et al. Transient hypothyroidism or persistent hyperthyrotropinemia in neonates born to mothers with excessive iodine intake. Thyroid 2004; 14:1077.
  128. Innis SM. Trans fatty intakes during pregnancy, infancy and early childhood. Atheroscler Suppl 2006; 7:17.
  129. Trans Fat. Food and Drug Administration. Available at: https://www.fda.gov/food/food-additives-petitions/trans-fat (Accessed on July 16, 2021).
  130. Replace Trans Fat. World Health Organization. Available at: https://www.who.int/teams/nutrition-and-food-safety/replace-trans-fat (Accessed on July 16, 2021).
  131. Rumbold A, Ota E, Hori H, et al. Vitamin E supplementation in pregnancy. Cochrane Database Syst Rev 2015; :CD004069.
  132. Woods JR Jr, Plessinger MA, Miller RK. Vitamins C and E: missing links in preventing preterm premature rupture of membranes? Am J Obstet Gynecol 2001; 185:5.
  133. Rumbold A, Ota E, Nagata C, et al. Vitamin C supplementation in pregnancy. Cochrane Database Syst Rev 2015; :CD004072.
  134. Salam RA, Zuberi NF, Bhutta ZA. Pyridoxine (vitamin B6) supplementation during pregnancy or labour for maternal and neonatal outcomes. Cochrane Database Syst Rev 2015; :CD000179.
  135. VandeVusse L, Hanson L, Safdar N. Perinatal outcomes of prenatal probiotic and prebiotic administration: an integrative review. J Perinat Neonatal Nurs 2013; 27:288.
  136. Dallanora S, Medeiros de Souza Y, Deon RG, et al. Do probiotics effectively ameliorate glycemic control during gestational diabetes? A systematic review. Arch Gynecol Obstet 2018; 298:477.
  137. Okesene-Gafa KA, Moore AE, Jordan V, et al. Probiotic treatment for women with gestational diabetes to improve maternal and infant health and well-being. Cochrane Database Syst Rev 2020; 6:CD012970.
  138. Grev J, Berg M, Soll R. Maternal probiotic supplementation for prevention of morbidity and mortality in preterm infants. Cochrane Database Syst Rev 2018; 12:CD012519.
  139. Institute of Medicine. Dietary Reference Intakes: The Essential Guide to Nutrient Requirements. The National Academies Press, Washington, DC 2006. https://www.nal.usda.gov/sites/default/files/fnic_uploads//DRIEssentialGuideNutReq.pdf (Accessed on December 12, 2016).
Topic 453 Version 131.0

References