Prenatal tobacco exposure on brain morphometry partially mediated poor cognitive performance in preadolescent children

Author:

Rodriguez Rivera Pedro J.1ORCID,Liang Huajun1,Isaiah Amal23,Cloak Christine C.1ORCID,Menken Miriam S.1,Ryan Meghann C.1,Ernst Thomas1,Chang Linda145

Affiliation:

1. Department of Diagnostic Radiology and Nuclear Medicine , University of Maryland School of Medicine , Baltimore , MD , USA

2. Department of Otorhinolaryngology-Head and Neck Surgery , University of Maryland School of Medicine , Baltimore , MD , USA

3. Department of Pediatrics , University of Maryland School of Medicine , Baltimore , MD , USA

4. Department of Neurology , Johns Hopkins University School of Medicine , Baltimore , MD , USA

5. Department of Neurology , University of Maryland School of Medicine , Baltimore , MD , USA

Abstract

Abstract Objectives To evaluate whether prenatal tobacco exposure (PTE) is related to poorer cognitive performance, abnormal brain morphometry, and whether poor cognitive performance is mediated by PTE-related structural brain differences. Methods The Adolescent Brain Cognitive Development study dataset was used to compare structural MRI data and neurocognitive (NIH Toolbox®) scores in 9-to-10-year-old children with (n=620) and without PTE (n=10,989). We also evaluated whether PTE effects on brain morphometry mediated PTE effects on neurocognitive scores. Group effects were evaluated using Linear Mixed Models, covaried for socio-demographics and prenatal exposures to alcohol and/or marijuana, and corrected for multiple comparisons using the false-discovery rate (FDR). Results Compared to unexposed children, those with PTE had poorer performance (all p-values <0.05) on executive function, working memory, episodic memory, reading decoding, crystallized intelligence, fluid intelligence and overall cognition. Exposed children also had thinner parahippocampal gyri, smaller surface areas in the posterior-cingulate and pericalcarine cortices; the lingual and inferior parietal gyri, and smaller thalamic volumes (all p-values <0.001). Furthermore, among children with PTE, girls had smaller surface areas in the superior-frontal (interaction-FDR-p=0.01), precuneus (interaction-FDR-p=0.03) and postcentral gyri (interaction-FDR-p=0.02), while boys had smaller putamen volumes (interaction-FDR-p=0.02). Smaller surface areas across regions of the frontal and parietal lobes, and lower thalamic volumes, partially mediated the associations between PTE and poorer neurocognitive scores (p-values <0.001). Conclusions Our findings suggest PTE may lead to poorer cognitive performance and abnormal brain morphometry, with sex-specific effects in some brain regions, in pre-adolescent children. The poor cognition in children with PTE may result from the smaller areas and subcortical brain volumes.

Funder

National Institute on Drug Abuse

Publisher

Walter de Gruyter GmbH

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