Folic acid supplementation before and during pregnancy in the Newborn Epigenetics STudy (NEST).

dc.contributor.author

Hoyo, Cathrine

dc.contributor.author

Murtha, Amy P

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Schildkraut, Joellen M

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Forman, Michele R

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Calingaert, Brian

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Demark-Wahnefried, Wendy

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Kurtzberg, Joanne

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Jirtle, Randy L

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Murphy, Susan K

dc.date.accessioned

2022-03-23T19:08:29Z

dc.date.available

2022-03-23T19:08:29Z

dc.date.issued

2011-01-21

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2022-03-23T19:08:28Z

dc.description.abstract

Background

Folic acid (FA) added to foods during fortification is 70-85% bioavailable compared to 50% of folate occurring naturally in foods. Thus, if FA supplements also are taken during pregnancy, both mother and fetus can be exposed to FA exceeding the Institute of Medicine's recommended tolerable upper limit (TUL) of 1,000 micrograms per day (μg/d) for adult pregnant women. The primary objective is to estimate the proportion of women taking folic acid (FA) doses exceeding the TUL before and during pregnancy, and to identify correlates of high FA use.

Methods

During 2005-2008, pre-pregnancy and pregnancy-related data on dietary supplementation were obtained by interviewing 539 pregnant women enrolled at two obstetrics-care facilities in Durham County, North Carolina.

Results

Before pregnancy, 51% of women reported FA supplementation and 66% reported this supplementation during pregnancy. Before pregnancy, 11.9% (95% CI = 9.2%-14.6%) of women reported supplementation with FA doses above the TUL of 1,000 μg/day, and a similar proportion reported this intake prenatally. Before pregnancy, Caucasian women were more likely to take FA doses above the TUL (OR = 2.99; 95% = 1.28-7.00), compared to African American women, while women with chronic conditions were less likely to take FA doses above the TUL (OR = 0.48; 95%CI = 0.21-0.97). Compared to African American women, Caucasian women were also more likely to report FA intake in doses exceeding the TUL during pregnancy (OR = 5.09; 95%CI = 2.07-12.49).

Conclusions

Fifty-one percent of women reported some FA intake before and 66% during pregnancy, respectively, and more than one in ten women took FA supplements in doses that exceeded the TUL. Caucasian women were more likely to report high FA intake. A study is ongoing to identify possible genetic and non-genotoxic effects of these high doses.
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1471-2458-11-46

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1471-2458

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1471-2458

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https://hdl.handle.net/10161/24636

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eng

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Springer Science and Business Media LLC

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BMC public health

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10.1186/1471-2458-11-46

dc.subject

Humans

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Pregnancy Complications

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Chronic Disease

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Folic Acid

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Body Size

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Prenatal Care

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Prospective Studies

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Health Knowledge, Attitudes, Practice

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Smoking

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Marital Status

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Epigenesis, Genetic

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Gestational Age

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Pregnancy

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Socioeconomic Factors

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Dietary Supplements

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Adult

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Infant, Newborn

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African Americans

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Asian Americans

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European Continental Ancestry Group

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Hispanic Americans

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North Carolina

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Female

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Surveys and Questionnaires

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Catchment Area, Health

dc.title

Folic acid supplementation before and during pregnancy in the Newborn Epigenetics STudy (NEST).

dc.type

Journal article

duke.contributor.orcid

Kurtzberg, Joanne|0000-0002-3370-0703

duke.contributor.orcid

Murphy, Susan K|0000-0001-8298-7272

pubs.begin-page

46

pubs.issue

1

pubs.organisational-group

Duke

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Nicholas School of the Environment

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School of Medicine

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Faculty

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Clinical Science Departments

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Institutes and Centers

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Family Medicine and Community Health

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Pathology

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Pediatrics

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Family Medicine and Community Health, Prevention Research

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Duke Cancer Institute

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Environmental Sciences and Policy

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Institutes and Provost's Academic Units

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Initiatives

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Duke Innovation & Entrepreneurship

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Pediatrics, Transplant and Cellular Therapy

pubs.publication-status

Published

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11

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