A dose–response analysis of the effects of prenatal alcohol exposure on cognitive development

Author:

Jacobson Joseph L.1ORCID,Akkaya‐Hocagil Tugba2,Jacobson Sandra W.1ORCID,Coles Claire D.3ORCID,Richardson Gale A.4,Olson Heather Carmichael5ORCID,Day Nancy L.4,Carter R. Colin678ORCID,Dodge Neil C.1,Dang Khue‐Dung9,Cook Richard J.2,Ryan Louise M.1011

Affiliation:

1. Department of Psychiatry and Behavioral Neurosciences Wayne State University School of Medicine Detroit Michigan USA

2. Department of Statistics and Actuarial Science University of Waterloo Waterloo Ontario Canada

3. Department of Psychiatry and Behavioral Sciences Emory University School of Medicine Atlanta Georgia USA

4. Department of Psychiatry University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA

5. Department of Psychiatry and Behavioral Sciences University of Washington School of Medicine Seattle Washington USA

6. Department of Emergency Medicine Columbia University Vagelos College of Physicians and Surgeons New York City New York USA

7. Department of Pediatrics Columbia University Vagelos College of Physicians and Surgeons New York City New York USA

8. Institute of Human Nutrition Columbia University Vagelos College of Physicians and Surgeons New York City New York USA

9. School of Mathematics and Statistics University of Melbourne Parkville Victoria Australia

10. School of Mathematical and Physical Sciences University of Technology Sydney Sydney New South Wales Australia

11. ARC Centre of Excellence for Mathematical and Statistical Frontiers University of Melbourne Parkville Victoria Australia

Abstract

AbstractBackgroundMost studies of the effects of prenatal alcohol exposure (PAE) on cognitive function have assumed that the dose–response curve is linear. However, data from a few animal and human studies suggest that there may be an inflection point in the dose–response curve above which PAE effects are markedly stronger and that there may be differences associated with pattern of exposure, assessed in terms of alcohol dose per drinking occasion and drinking frequency.MethodsWe performed second‐order confirmatory factor analysis on data obtained at school age, adolescence, and early adulthood from 2227 participants in six US longitudinal cohorts to derive a composite measure of cognitive function. Regression models were constructed to examine effects of PAE on cognitive function, adjusted for propensity scores. Analyses based on a single predictor (absolute alcohol (AA)/day) were compared with analyses based on two predictors (dose/occasion and drinking frequency), using (1) linear models and (2) nonparametric general additive models (GAM) that allow for both linear and nonlinear effects.ResultsThe single‐predictor GAM model showed virtually no nonlinearity in the effect of AA/day on cognitive function. However, the two‐predictor GAM model revealed differential effects of maternal drinking pattern. Among offspring of infrequent drinkers, PAE effects on cognitive function were markedly stronger in those whose mothers drank more than ~3 drinks/occasion, and the effect of dose/occasion was strongest among the very frequent drinkers. Frequency of drinking did not appear to alter the PAE effect on cognitive function among participants born to mothers who limited their drinking to ~1 drink/occasion or less.ConclusionsThese findings suggest that linear models based on total AA/day are appropriate for assessing whether PAE affects a given cognitive outcome. However, examination of alcohol dose/occasion and drinking frequency is needed to fully characterize the impact of different levels of alcohol intake on cognitive impairment.

Funder

National Institute on Alcohol Abuse and Alcoholism

Natural Sciences and Engineering Research Council of Canada

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Australian Research Council Centre of Excellence for Mathematical and Statistical Frontiers

Publisher

Wiley

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