The American Academy of Pediatrics endorses the US Public Health Service (USPHS) recommendation that all women capable of becoming pregnant consume 400 μg of folic acid daily to prevent neural tube defects (NTDs). Studies have demonstrated that periconceptional folic acid supplementation can prevent 50% or more of NTDs such as spina bifida and anencephaly. For women who have previously had an NTD-affected pregnancy, the Centers for Disease Control and Prevention (CDC) recommends increasing the intake of folic acid to 4000 μg per day beginning at least 1 month before conception and continuing through the first trimester. Implementation of these recommendations is essential for the primary prevention of these serious and disabling birth defects. Because fewer than 1 in 3 women consume the amount of folic acid recommended by the USPHS, the Academy notes that the prevention of NTDs depends on an urgent and effective campaign to close this prevention gap.

Neural tube defects (NTDs) are among the most common birth defects contributing to infant mortality and serious disability. NTDs, which include anencephaly, spina bifida, and encephalocele, occur in approximately 1 of 1000 births in the United States.1  An estimated 4000 pregnancies are affected with NTDs each year. More than one third of these pregnancies are spontaneously lost or electively terminated; thus, about 2500 infants per year are born with an NTD. The results of 2 randomized controlled trials and several observational studies showed that 50% or more of NTDs can be prevented if women consume a folic acid–containing supplement before and during the early weeks of pregnancy2 ,3  in addition to the folate in their diet. Based on a synthesis of these data, the US Public Health Service (USPHS) and Centers for Disease Control and Prevention (CDC) recommendations were developed.4 ,5  Because the evidence for folic acid prevention evolved over time, there are two separate recommendations: one for women who have no history of a previous NTD-affected pregnancy and one for women who have had a previous NTD-affected pregnancy.

Of children with an NTD, 95% are born to couples with no family history of these defects. Evidence to date suggests that supplementation with a multivitamin containing 400 (0.4 mg) μg of folic acid prevents the occurrence of >50% of NTDs when it is taken before conception and continued throughout the first trimester of pregnancy.5  The USPHS recommends that all women of childbearing age who are capable of becoming pregnant take 400 μg of folic acid daily.5  Implementing this recommendation may provide the opportunity for primary prevention of 50% or more of these serious disabling birth defects. Regular and ongoing ingestion of folic acid by women of childbearing age is necessary because approximately half of the pregnancies in the United States are unplanned,6  and neural tube closure occurs during the first 4 weeks of gestation.7  Despite the publication of the USPHS recommendation in September 1992, a 1998 poll showed that 70% of women aged 18 to 45 years still are not following the USPHS recommendation.8 

Among US couples who have had a child with an NTD, the recurrence risk is 2% to 3% in subsequent pregnancies.9  In 1991, the Medical Research Council (MRC) Vitamin Study Group reported the results of a well-designed, prospective, randomized trial of folic acid supplementation for the prevention of NTDs in pregnancies of women who had a previous child with an NTD, and the CDC published its recommendations for consumption of 4000 (4 mg) μg of folic acid.4  The results of the MRC study conclusively demonstrated that a daily dosage of 4000 μg of folic acid, in addition to folate in the diet, before and during early pregnancy resulted in a 71% reduction of recurrence of NTDs. The addition of other vitamins to the dosage of folic acid did not reduce the risk further. Use of multivitamins without folic acid did not result in a reduced risk for NTDs. The MRC study did not explore the possible benefit of a dosage lower than 4000 μg of folic acid. However, an earlier nonrandomized study conducted in the United Kingdom suggested that a lower dosage, 360 μg daily, resulted in a comparable reduction of recurrence of NTDs.10  Although adverse maternal or fetal effects of a daily 4000 μg dosage of folic acid were not detected by the MRC study, the small size of the study groups precluded detection of uncommon adverse effects.

Folic acid, also known as pteroylmonoglutamic acid, is a synthetic compound used in dietary supplements and fortified foods. The term folate includes all compounds that have the vitamin properties of folic acid—including folic acid and naturally occurring compounds in food.11  The average diet in the United States contains 200 μg of naturally occurring food folate, which is less bioavailable than folic acid.12  Additional intake of foods rich in folate could raise the average intake, but it has not been demonstrated that increased consumption of food folate would prevent NTDs as effectively as a daily vitamin supplement containing 400 μg of folic acid. A small comparison study suggests that blood folate concentrations are increased much more by folic acid supplementation than by naturally occurring food folate in the diet.13 Economic and social circumstances may make an adequate increase in dietary folate difficult or unlikely, and the behavioral change required among a large fraction of women may take years to achieve.

Folic acid is a water-soluble vitamin that has no known toxicity. However, higher doses of folic acid can correct the anemia of vitamin B12 deficiency (pernicious anemia), which might be an important clue to the presence of vitamin B12 deficiency in some instances. Folic acid does not prevent the neurologic consequences of vitamin B12 deficiency, and, for this reason, the USPHS recommendation cautioned that intake of folate should be not >1000 μg per day. However, the Institute of Medicine (IOM) Food and Nutrition Board recently set the tolerable upper intake limit of synthetic folic acid at 1000 μg, thus eliminating food folate from the calculation.14  Because pernicious anemia rarely occurs before the age of 50 years, it is likely to be rare among women consuming folic acid during the reproductive years. Folic acid has been consumed by about a quarter of all women for many years and extensively during later pregnancy without apparent adverse effects; however, studies that definitively address the question of maternal and fetal safety of folic acid are not available.

The IOM Food and Nutrition Board's recommended dietary allowance (RDA) for folate is 400 μg for adults and 600 μg for pregnant women.14  To reduce the risk for NTDs, the IOM recommended that women capable of becoming pregnant consume 400 μg of folic acid daily from fortified foods, vitamin supplements, or a combination of the two. This is in addition to the naturally occurring folate obtained from a varied diet.14  The majority of multivitamin preparations contain 400 μg of folic acid. These preparations are available over the counter and are already being taken by about 30% of nonpregnant women aged 18 to 45 years in the United States.8  Tablets containing folic acid alone are available over the counter in dosages up to 800 μg but the availability is very limited when compared with multivitamin preparations. Folic acid tablets in a 1000 μg dose are available by prescription only. This preparation is most frequently utilized by women who are taking 4000 μg because of a previous NTD-affected pregnancy.

In March 1996, the Food and Drug Administration mandated that enriched cereal-grain products be fortified with 140 μg of folic acid per 100 g of flour.15  This measure increases the proportion of women who consume the USPHS-recommended daily dosage of 400 μg of folic acid only an additional 3%, because this fortification level will provide the average woman only an additional 100 μg of folic acid per day (unpublished data, 1992).

  1. Prevention for Women With No History of a Previous NTD-Affected Pregnancy. The American Academy of Pediatrics (AAP) endorses the USPHS recommendation that all women of childbearing age who are capable of becoming pregnant should consume 400 (0.4 mg) μg of folic acid daily. Because of the high rate of unplanned pregnancies in the United States, the AAP encourages efforts at devising a program of food fortification to provide all women a daily intake of 400 μg of folic acid. In the absence of optimal fortification, the AAP encourages women to consume 400 μg of folic acid daily in addition to eating a healthy diet. At present, the most convenient, inexpensive, and direct way to meet the recommended dosage is by taking a multivitamin containing 400 μg of folic acid, but efforts to increase the availability of folic acid-only supplements should be encouraged for women who prefer not to take multivitamins. Because the risk for NTDs is not totally eliminated by folic acid use, routine prenatal screening for NTDs is still advisable.

  2. Prevention for Women Who Have Had a Previous NTD-Affected Pregnancy. Women with a history of a previous pregnancy resulting in a fetus with an NTD should be advised of the results of the MRC study. During times in which a pregnancy is not planned, these high-risk women should consume 4000 (4 mg) μg of folic acid per day. However, they should be offered treatment with 4000 μg of folic acid per day starting 1 month before the time they plan to become pregnant and throughout the first 3 months of pregnancy, unless contraindicated. Women should be advised not to attempt to achieve the 4000 μg daily dosage of folic acid by taking over-the-counter or prescription multivitamins containing folic acid because of the possibility of ingesting harmful levels of other vitamins, for example, Vitamin A.17  It should be noted that 4000 μg of folic acid did not prevent all NTDs in the MRC study. Therefore, high-risk patients should be cautioned that folic acid supplementation does not preclude the need for counseling or consideration of prenatal testing for NTDs.

  3. Prevention for Other High-Risk Persons. No intervention or observational studies address prevention for other high-risk persons. Women with a close relative (eg, sibling, niece, or nephew) who has an NTD (risk is approximately 0.3% to 1.0%), women with type 1 diabetes mellitus (risk is approximately 1%), women with seizure disorders being treated with valproic acid or carbamazepine (risk is approximately 1%), and women or their partners who have an NTD (risk may be 2% to 3%)18  and are planning a pregnancy should discuss with their physician the risk for an affected child and the advantages and disadvantages of increasing their daily periconceptional folic acid intake to 4000 μg.

  4. Public Health Programs: Supplementation, Surveillance, and Food Fortification. The AAP recommends that the Department of Health and Human Services expeditiously devise and implement an educational program to prevent folic acid–preventable NTDs throughout the use of supplements, fortified foods, or a combination of both. The program should support surveillance of effectiveness and adverse outcomes to further refine the effective folate dose and mechanisms of actions. In light of the recent IOM recommendation, the AAP also encourages additional efforts at devising a program of food fortification with folic acid to provide all women capable of becoming pregnant a daily intake of 400 μg of folic acid.

    Committee on Genetics, 1998–1999
  • Franklin Desposito, MD, Chairperson

  • Christopher Cunniff, MD

  • Jaime L. Frias, MD

  • Susan R. Panny, MD

  • Tracy L. Trotter, MD

  • Rebecca S. Wappner, MD

    Liaison Representatives
  • James W. Hanson, MD

  •  American College of Medical Genetics

  • Sherman Elias, MD

  •  American College of Obstetricians and Gynecologists

  • Cynthia A. Moore, MD, PhD

  •  Centers for Disease Control and Prevention

  • Michele Lloyd-Puryear, MD, PhD

  •  Health Resources and Services Administration

  • Felix de la Cruz, MD, MPH

  •  National Institutes of Health

    Section Liaison
  • Beth A. Pletcher, MD

  •  Section on Genetics and Birth Defects

  • Sechin Cho, MD

The recommendations in this statement do not indicate an exclusive course of treatment or serve as a standard of medical care. Variations, taking into account individual circumstances, may be appropriate.


neural tube defects


US Public Health Service


Centers for Disease Control and Prevention


Medical Research Council


Institute of Medicine


American Academy of Pediatrics

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