Evidence map›Paper›PMID 23822873›Full record

ArticleAlcoholism, clinical and experimental research2013

Commentary on Day and colleagues : the association between prenatal alcohol exposure and behavior at 22 years of age--adverse effects of risky patterns of drinking among low to moderate alcohol-using pregnant women.

Sandra W Jacobson, R Colin Carter, Joseph L Jacobson

Abstract readComment
In one paragraph

Article in Alcoholism, clinical and experimental research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Sandra W JacobsonDepartment of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit, MI 48201, USA. sandra.jacobson@wayne.edu
R Colin Carter
Joseph L Jacobson

Funding

Harvard Clinical and Translational Science Center (KL2)KL2RR025757 · NCRR · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2008 to 2011
$4.1M
Neural Bases of Eyeblink Conditioning in FASDR01AA016781 · NIAAA · WAYNE STATE UNIVERSITY · PI JACOBSON, SANDRA W. · 2008 to 2012
$2.5M
FETAL ALCOHOL EXPOSURE AND SCHOOL-AGE COGNITIVE FUNCTIONR01AA009524 · NIAAA · WAYNE STATE UNIVERSITY · PI JACOBSON, SANDRA W. · 1993 to 2003
$1.5M
Neural Bases of ADHD in Fetal Drug or Alcohol ExposureR21DA021034 · NIDA · VANDERBILT UNIVERSITY · PI AVISON, MALCOLM J · 2005 to 2007
$1.1M
The Role of Maternal Nutrition in the Teratogenesis of Alcohol in HumansK23AA020516 · NIAAA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CARTER, ROBERT COLIN · 2011 to 2015
$891k
PRENATAL ALCOHOL EXPOSURE AND INFANT COGNITIONR01AA006966 · NIAAA · WAYNE STATE UNIVERSITY · PI SOKOL, ROBERT · 1986 to 1989
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NCRR NIH HHS KL2 RR025757NIAAA NIH HHS K23 AA020516NIAAA NIH HHS R01 AA006966NIAAA NIH HHS R01 AA009524NIAAA NIH HHS R01 AA016781NIAAA NIH HHS R01 AA06966NIAAA NIH HHS R01 AA09524NIDA NIH HHS R21 DA021034
6 · The paper itself

Abstract

Day and colleagues have presented the first data showing that the behavioral effects of low to moderate prenatal alcohol exposure seen in childhood and adolescence persist into adulthood. Using the Achenbach Adult Self-Report, they found dose-dependent effects of prenatal exposure on internalizing, externalizing, and attention problems that persist in young adults and, thus, appear to be permanent. To date, few studies have attempted to identify thresholds at which prenatal alcohol exposure is harmful, although the animal literature suggests that even 1 to 2 binge episodes can result in adverse effects in the offspring. Four prospective longitudinal studies have reported adverse effects at what can be characterized as moderate exposure levels based on NIAAA criteria, but moderate drinking women often concentrate their alcohol use on 1 to 2 days per week, thereby engaging in binge drinking. In this study, binge drinking was not a strong predictor of adverse outcome when average daily dose was held constant, a conclusion that the authors note runs "counter to studies that have reported that binge drinking has a greater effect." This inconsistency may be due to the difficulty of allocating variance that is shared (overlapping) between average daily dose and binge drinking (i.e., dose/occasion). Data from laboratory animal studies, in which dosage can be manipulated experimentally, demonstrate that a higher dose per occasion, the key feature of binge drinking, leads to more severe adverse effects. Day and colleagues' findings of adverse effects at low levels of exposure provides clear evidence that there is no safe level of drinking during pregnancy and that, even at low levels, drinking results in irreversible behavioral impairment. On the other hand, given the evidence from the animal and most human studies, it is important for all women who drink during pregnancy, even at light to moderate levels, to recognize that minimizing their intake per occasion and refraining from binge drinking can reduce risk to the fetus.

Indexed as

Alcohol DrinkingFemaleHumansMaleMental DisordersPregnancyPrenatal Exposure Delayed EffectsAdult BehaviorAttentionBinge DrinkingFetal Alcohol Spectrum DisordersInternalizing and Externalizing BehaviorLight to Moderate Prenatal Alcohol ExposureProspective Longitudinal Studies

Identifiers

PMID23822873
PMCPMC3703854

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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.