Evidence map›Paper›PMID 24263126›Full record

ArticleNeurotoxicology and teratology

Protective effects of the alcohol dehydrogenase-ADH1B*3 allele on attention and behavior problems in adolescents exposed to alcohol during pregnancy.

Neil C Dodge, Joseph L Jacobson, Sandra W Jacobson

Open access · greenAbstract read
In one paragraph

Article in Neurotoxicology and teratology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
3.9field-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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Zebrafish models of fetal alcohol spectrum disorders.Genesis (New York, N.Y. : 2000) · 2021
    Review
  11. Infant Cardiac Orienting Responses Predict Later FASD in the Preschool Period.Alcoholism, clinical and experimental research · 2021
    Article
  12. Article
  13. Review
  14. Article
  15. Effects of Fetal Substance Exposure on Offspring Substance Use.Pediatric clinics of North America · 2019
    Review
  16. Review
  17. ADH1B: From alcoholism, natural selection, and cancer to the human phenome.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2018
    Review
  18. Article
  19. Article
  20. Article
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

3 authors at 2 institutions in 2 countries.

Neil C DodgeDepartment of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit, MI, USA.
Joseph L JacobsonDepartment of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit, MI, USA; Department of Human Biology, University of Cape Town Faculty of Health Sciences, Cape Town, South Africa; Department of Psychiatry and Mental Health, University of Cape Town Faculty of Health Sciences, Cape Town, South Africa.
Sandra W JacobsonDepartment of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit, MI, USA; Department of Human Biology, University of Cape Town Faculty of Health Sciences, Cape Town, South Africa; Department of Psychiatry and Mental Health, University of Cape Town Faculty of Health Sciences, Cape Town, South Africa. Electronic address: sandra.jacobson@wayne.edu.
Wayne State University · USUniversity of Cape Town · ZA

Funding

FETAL ALCOHOL EXPOSURE AND SCHOOL-AGE COGNITIVE FUNCTIONR01AA009524 · NIAAA · WAYNE STATE UNIVERSITY · PI JACOBSON, SANDRA W. · 1993 to 2003
$1.5M
PROTECTING THE NEXT PREGNANCYP50AA007606 · NIAAA · WAYNE STATE UNIVERSITY · PI MAY, GAIL · 1987 to 1998
–
PRENATAL ALCOHOL EXPOSURE AND INFANT COGNITIONR01AA006966 · NIAAA · WAYNE STATE UNIVERSITY · PI SOKOL, ROBERT · 1986 to 1989
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NIAAA NIH HHS P50 AA007606NIAAA NIH HHS P50-AA07606NIAAA NIH HHS R01 AA006966NIAAA NIH HHS R01 AA009524NIAAA NIH HHS R01-AA09524
6 · The paper itself

Abstract

Alcohol dehydrogenase is a critical enzyme in the metabolism of alcohol. Expression of three alleles at the ADH1B locus results in enzymes that differ in turnover rate and affinity for alcohol. The ADH1B*3 allele, which appears to be unique to individuals of African descent, is associated with more rapid alcohol metabolism than the more prevalent ADH1B*1 allele. It has been previously demonstrated that the presence of at least one maternal ADH1B*3 allele confers a protective effect against alcohol teratogenicity in infants and children. This study was conducted to determine whether the presence of the ADH1B*3 allele in the mother or child continues to be protective in alcohol-exposed individuals during adolescence. 186 adolescents and 167 mothers participating in a 14-year follow-up of the Detroit Longitudinal Cohort were genotyped for ADH1B alleles. Behavioral reports were obtained from classroom teachers. Frequencies of the ADH1B*3 allele were 17.6% in the mothers and 21.0% in the adolescents, which are consistent with the 15-20% expected for African Americans. Prenatal alcohol exposure was associated with increased attention problems and externalizing behaviors in adolescents born to mothers with two ADH1B*1 alleles but not in those whose mothers had at least one ADH1B*3 allele. A similar pattern was seen in relation to the presence or absence of an ADH1B*3 allele in the adolescent, which may have reflected the presence/absence of the maternal variant. This study is the first to demonstrate that the protective effects of the maternal ADH1B*3 allele continue to be evident during adolescence. These persistent individual differences in vulnerability of offspring to the behavioral effects of fetal alcohol exposure are likely attributable to more rapid metabolism of alcohol that the ADH1B*3 variant confers on the mother, leading to a reduction of the peak blood alcohol concentration to which the fetus is exposed during each drinking episode.

Indexed as

AdolescentAlcohol DehydrogenaseAllelesAttention Deficit Disorder with HyperactivityBlack or African AmericanChild Behavior DisordersFemaleGenotypeHumansLongitudinal StudiesMalePregnancyPrenatal Exposure Delayed EffectsADH1B protein, humanAlcohol DehydrogenaseADH1B*3 alleleAdolescent externalizing behaviorAlcohol dehydrogenaseFetal alcohol spectrum disordersPrenatal alcohol exposure

Identifiers

PMID24263126
PMCPMC3943945
OpenAlexW2057253223

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

None linked

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.