Evidence map›Paper›PMID 30977899›Full record

ArticleAlcoholism, clinical and experimental research2019

Are Low-to-Moderate Average Alcohol Consumption and Isolated Episodes of Binge Drinking in Early Pregnancy Associated with Facial Features Related to Fetal Alcohol Syndrome in 5-Year-Old Children?

Ulrik Schiøler Kesmodel, Siv Steffen Nygaard, Erik Lykke Mortensen, Jacquelyn Bertrand, Clark H Denny, Alex Glidewell, Susan Astley Hemingway

Open access · greenAbstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
4.7field-weighted citation impact, top 6% 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

7 citing papers in PubMed, 21 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Ulrik Schiøler KesmodelDepartment of Obstetrics and Gynecology, (USK, SSN), Herlev University Hospital, Herlev, Denmark.ORCID 0000-0003-3868-106X
Siv Steffen NygaardDepartment of Obstetrics and Gynecology, (USK, SSN), Herlev University Hospital, Herlev, Denmark.
Erik Lykke MortensenCenter for Healthy Aging, (ELM), Institute of Public Health, University of Copenhagen, Copenhagen, Denmark.
Jacquelyn BertrandCenters for Disease Control and Prevention (CDC), (JB, CHD), Atlanta, Georgia.
Clark H DennyCenters for Disease Control and Prevention (CDC), (JB, CHD), Atlanta, Georgia.
Alex GlidewellUniversity of Washington, (AG), Seattle, Washington.
Susan Astley HemingwayDepartments of Epidemiology and Pediatrics, (SAH), University of Washington, Seattle, Washington.
Centers for Disease Control and Prevention · USUniversity of Copenhagen · DKUniversity of Washington · USHerlev Hospital · DK

Funding

Intramural CDC HHS CC999999
6 · The paper itself

Abstract

backgroundFetal alcohol syndrome (FAS) typically is observed among individuals with high prenatal alcohol exposures (PAE), but exposure histories obtained in clinical diagnostic settings are often inaccurate. The present analysis used the Lifestyle During Pregnancy Study (LDPS) to assess the potential effects of low-to-moderate average weekly alcohol consumption and binge drinking in early pregnancy on facial features associated with FAS among children 5 years of age.

methodsThe analysis is a prospective follow-up study of 670 women and their children sampled from the LDPS cohort based on maternal alcohol consumption during pregnancy. The 4-Digit Code FAS Facial Photographic Analysis Software was used to measure the magnitude of expression of the 3 diagnostic facial features of FAS from standardized digital photographs. Logistic regression was used to estimate the odds of presenting with the FAS/partial fetal alcohol syndrome (PFAS) facial phenotypes relative to different patterns of prenatal alcohol exposure.

resultsTen children presented with the FAS/PFAS facial phenotypes. None of the children sampled met the central nervous system (CNS) criteria for FAS or PFAS at age 5 years. All remained at risk for PFAS since some types of CNS dysfunction associated with this diagnosis may only be assessed at older ages. The FAS/PFAS facial phenotypes were 8.5-fold more likely among children exposed to an average of 1 to 4 drinks/wk and 2.5-fold more likely among children with a single binge exposure in gestational weeks 3 to 4 compared to children with no such exposures. The magnitude of expression of the FAS facial phenotype was significantly correlated with all other diagnostic features of FAS: growth deficiency, microcephaly, and measures of CNS dysfunction.

conclusionsThese findings suggest that low-to-moderate levels of PAE or isolated binge exposures may place some fetuses at risk for FAS/PFAS. Thus, conservative advice is still for women to abstain from alcohol consumption during pregnancy.

Indexed as

Binge DrinkingAdultChild, PreschoolFaceFemaleFetal Alcohol Spectrum DisordersFollow-Up StudiesHumansMalePhenotypePregnancyPrenatal Exposure Delayed EffectsProspective StudiesAlcoholAlcohol Binge DrinkingFetal Alcohol Spectrum DisordersFetal Alcohol SyndromePregnancy

Identifiers

PMID30977899
PMCPMC6691727
OpenAlexW2937388521

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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.