Maternal and paternal risk factors for fetal alcohol spectrum disorders: Alcohol and other drug use as proximal influences

Author:

May Philip A.123ORCID,Hasken Julie M.1,de Vries Marlene M.2,Marais Anna‐Susan2,Abdul‐Rahman Omar4,Robinson Luther K.5,Adam Margaret P.6,Manning Melanie A.7,Kalberg Wendy O.3,Buckley David3,Seedat Soraya2,Parry Charles D. H.28ORCID,Hoyme H. Eugene29

Affiliation:

1. Nutrition Research Institute The University of North Carolina at Chapel Hill Kannapolis North Carolina USA

2. Department of Psychiatry, Faculty of Medicine and Health Sciences Stellenbosch University Cape Town South Africa

3. Center on Alcoholism, Substance Abuse and Addictions The University of New Mexico Albuquerque New Mexico USA

4. Department of Pediatrics, New York‐ Presbyterian Weill Cornell Medicine Columbia University New York New York USA

5. Department of Pediatrics State University of New York Buffalo New York USA

6. Department of Pediatrics University of Washington Seattle Washington USA

7. Department of Pathology and Pediatrics Stanford University School of Medicine Stanford California USA

8. Alcohol, Tobacco and Other Drug Research Unit, South African Medical Research Council Francie van Zijl Drive Cape Town South Africa

9. Sanford Children's Genomic Medicine Consortium, Sanford Health Sioux Falls South Dakota USA

Abstract

AbstractObjectiveTo explore and analyze the significance of proximal influences of maternal and paternal traits associated with bearing a child with a fetal alcohol spectrum disorder (FASD).MethodsAggregated, maternal interview‐collected data (N = 2515) concerning alcohol, tobacco, and other drug use were examined to determine risk for FASD from seven cross‐sectional samples of mothers of first‐grade students who were evaluated for a possible diagnosis of FASD.ResultsMothers of children with fetal alcohol syndrome (FAS) reported the highest alcohol use throughout pregnancy, proportion of binge drinking, drinks per drinking day (DDD), drinking days per week, and total drinks per week. Mothers of children with FAS also consumed significantly more alcohol than mothers of children with partial FAS (PFAS), alcohol‐related neurodevelopmental disorder (ARND), or typically developing controls. Mothers of children with PFAS and ARND reported similar drinking patterns, which exposed fetuses to 3–4 times more alcohol than mothers of controls, but the PFAS group was more likely than the ARND group to abstain in latter trimesters. Fathers of all children were predominantly drinkers (70%–85%), but more fathers of children with FASD binged heavily on more days than fathers of controls. Compared to the few mothers of controls who used alcohol during pregnancy, the ARND group binge drank more (3+ DDD) throughout pregnancy and drank more DDD before pregnancy and first trimester. Regression analysis, controlling for tobacco use, indicated that mothers who reported drinking <1 DDD were significantly more likely than abstainers to bear a child with FASD (OR = 2.75) as were those reporting higher levels such as 5–5.9 DDD (OR = 32.99). Exclusive, first‐trimester maternal drinking increased risk for FASD five times over that of abstinence (p < 0.001, OR = 5.05, 95% CI: 3.88–6.58), first‐ and second‐trimester drinking by 12.4 times, and drinking all trimesters by 16 times (p < 0.001, OR = 15.69, 95% CI: 11.92–20.64). Paternal drinking during and prior to pregnancy, without adjustment, increased the likelihood of FASD significantly (OR = 1.06 and 1.11, respectively), but the significance of both relationships disappeared when maternal alcohol and tobacco use were controlled.ConclusionsDifferences in FASD risk emerged from the examination of multiple proximal variables of maternal alcohol and tobacco use, reflecting increased FASD risk at greater levels of maternal alcohol consumption.

Funder

National Institute on Alcohol Abuse and Alcoholism

Publisher

Wiley

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Maternal risk factors for fetal alcohol spectrum disorders: Distal variables;Alcohol: Clinical and Experimental Research;2024-01-08

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