Evidence map›Paper›PMID 37083819›Full record

ArticleJMIR public health and surveillance2023

Racial/Ethnic Disparity in Association Between Fetal Alcohol Syndrome and Alcohol Intake During Pregnancy: Multisite Retrospective Cohort Study.

Sarah Soyeon Oh, Bada Kang, Jewel Park, SangMin Kim, Eun-Cheol Park, Seung Hee Lee, Ichiro Kawachi

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in JMIR public health and surveillance, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
4.1field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Sarah Soyeon OhDepartment of Social and Behavioral Sciences, Harvard TH Chan School of Public Health, Boston, MA, United States.ORCID 0000-0001-5709-2311
Bada KangMo-Im Kim Nursing Research Institute, Yonsei University College of Nursing, Seoul, Republic of Korea.ORCID 0000-0002-7002-2315
Jewel ParkDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.ORCID 0000-0003-1375-3565
SangMin KimHarvard Medical School, Boston, MA, United States.ORCID 0000-0003-2921-9738
Eun-Cheol ParkInstitute of Health Services Research, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0002-2306-5398
Seung Hee LeeCollege of Nursing and Brain Korea 21 Four Project, Yonsei University, Seoul, Republic of Korea.ORCID 0000-0003-1444-748X
Ichiro KawachiDepartment of Social and Behavioral Sciences, Harvard TH Chan School of Public Health, Boston, MA, United States.ORCID 0000-0003-3579-4456
Harvard University · USYonsei University · KRCincinnati Children's Hospital Medical Center · US

Funding

National Centralized Repository for Alzheimer's Disease and Related Dementias (NCRAD)U24AG021886 · NIA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI TATIANA M. FOROUD · 2002 to 2026
$119.8M
FASD in San Diego and Moscow (U01 Research Project)U01AA014834 · NIAAA · SAN DIEGO STATE UNIVERSITY · PI SARAH N MATTSON WELLER · 2003 to 2026
$12.4M
Image Analysis of Neurofacial Effects of Prenatal AlcoholExposureU01AA014809 · NIAAA · UNIVERSITY OF OXFORD · PI Michael Suttie · 2007 to 2026
$5.8M
FASD Diagnostic Telemedicine ResourceU24AA014815 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Lauren Gist, SARAH N MATTSON WELLER · 2003 to 2026
$5.6M
Dissecting the genetic contributions to fetal alcohol spectrum disordersU01AA026103 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI FOROUD, TATIANA M. · 2017 to 2021
$2.6M
NIAAA NIH HHS U01 AA014809NIAAA NIH HHS U01 AA014834NIAAA NIH HHS U01 AA026103NIAAA NIH HHS U24 AA014815NIA NIH HHS U24 AG021886
6 · The paper itself

Abstract

backgroundAlcohol consumption during pregnancy is associated with a range of adverse birth-related outcomes, including stillbirth, low birth weight, preterm birth, and fetal alcohol syndrome (FAS). With more than 10% of women consuming alcohol during pregnancy worldwide, it is increasingly important to understand how racial/ethnic variations affect FAS onset. However, whether race and ethnicity inform FAS risk assessment when daily ethanol intake is controlled for remains unknown.

objectiveThis study aimed to assess racial/ethnic disparities in FAS risk associated with alcohol consumption during pregnancy.

methodsWe used data from a longitudinal cohort study (the Collaborative Initiative on Fetal Alcohol Spectrum Disorders) at 5 hospital sites around the United States of 595 women who consumed alcohol during pregnancy from 2007 to 2017. Questionnaires, in-person interviews, and reviews of medical, legal, and social service records were used to gather data on average alcoholic content (AAC) during pregnancy. Self-reports of maternal race (American Indian/Alaska Native [AI/AN], Asian, Native Hawaiian or other Pacific Islander, Black or African American, White, more than one race, and other) and ethnicity (Hispanic/Latino or not Hispanic/Latino), as well as FAS diagnoses based on standardized dysmorphological criteria, were used for analysis. Log-binomial regression was used to examine the risk of FAS associated with each 1-gram increase in ethanol consumption during pregnancy, stratified by race/ethnicity.

resultsA total of 3.4% (20/595) of women who reported consuming alcohol during pregnancy gave birth to a baby with FAS. Women who gave birth to a baby with FAS had a mean AAC of 32.06 (SD 9.09) grams, which was higher than that of women who did not give birth to a baby with FAS (mean 12.07, SD 15.87 grams). AI/AN mothers with FAS babies had the highest AAC (mean 42.62, SD 8.35 grams), followed by White (mean 30.13, SD 4.88 grams) and Black mothers (mean 27.05, SD 12.78 grams). White (prevalence ratio [PR] 1.10, 95% CI 1.03-1.19), Black (PR 1.13, 95% CI 1.04-1.23), and AI/AN (PR 1.10, 95% CI 1.00-1.21) mothers had 10% to 13% increased odds of giving birth to a baby with FAS given the same exposure to alcohol during pregnancy. Regardless of race, a 1-gram increase in AAC resulted in a 4% increase (PR 1.04, 95% CI 1.02-1.07) in the chance of giving birth to a baby with ≥2 facial anomalies (ie, short palpebral fissures, thin vermilion border of the upper lip, and smooth philtrum) and a 4% increase (PR 1.04, 95% CI 1.01-1.07) in the chance of deficient brain growth.

conclusionsThe risk of delivering a baby with FAS was comparable among White, Black, and AI/AN women at similar levels of drinking during pregnancy. Regardless of race, a 1-gram increase in AAC resulted in increased odds of giving birth to a baby with facial anomalies or deficient brain growth.

Indexed as

Fetal Alcohol Spectrum DisordersPregnancy ComplicationsPremature BirthAlcohol DrinkingCohort StudiesEthanolFemaleHumansInfantInfant, NewbornLongitudinal StudiesPregnancyRetrospective StudiesUnited StatesWhiteEthanolalcohol intakeethnic disparityfetal alcohol syndromefetal healthhealth disparityminority populationpediatricspregnancypublic healthvulnerable populationwomen's health

Identifiers

PMID37083819
PMCPMC10147559
OpenAlexW4360776488

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.