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Significant Role for Maternal Genetic Nurture in the Risk Architecture of Attention Deficit Hyperactivity Disorder
Behrang Mahjani1, Adrianna P Kępińska1, Shelby Smout1
1Seaver Autism Center for Research and Treatment (Mahjani, Kępińska, Smout, Cohen, Caballero, Buxbaum, Grice), Department of Psychiatry (Mahjani, Kępińska, Smout, Cohen, Caballero, Buxbaum, Grice), Department of Genetics and Genomic Sciences (Mahjani, Kępińska, Buxbaum), Department of Artificial Intelligence and Human Health (Mahjani), Mindich Child Health and Development Institute (Mahjani, Buxbaum, Grice), Friedman Brain Institute (Buxbaum), Department of Neuroscience (Buxbaum), and Division of Tics, OCD, and Related Disorders (Grice), Icahn School of Medicine at Mount Sinai, New York; Department of Molecular Medicine and Surgery and Department of Medical Epidemiology and Biostatistics (Mahjani), Karolinska Institutet, Stockholm.
Objective:
Previous studies have shown that parental factors are associated with an increased risk for attention deficit hyperactivity disorder (ADHD). However, the pathways by which parental factors are associated with risk of ADHD in offspring are not well understood. These associations can arise directly from parental genotypes inherited by offspring, and/or via environmental effects, some of which may themselves be influenced by the parental genotype (i.e., parental genetic nurture). This study specifically examined the impact of the maternal phenotype on offspring ADHD risk, above and beyond the direct genetic effect of maternally inherited genes.
Methods:
The study population consisted of 982,544 individuals from the Swedish Medical Birth Register. The authors partitioned the liability of ADHD into direct additive genetic effect, maternal genetic nurture effect, and maternal common environment effect.
Results:
A total of 66,707 (7%) individuals with an ADHD diagnosis were identified in the birth cohort. Maternal half-siblings were associated with a higher ADHD risk compared to paternal half-siblings, suggesting maternal effect. Estimates indicated 66.1% direct additive genetic effect (95% credible interval=0.647, 0.676) and 14.3% maternal genetic nurture effect (95% credible interval=0.136, 0.151). Additionally, evidence for substantial assortative mating among individuals with ADHD was observed.
Conclusions:
The findings indicate that maternal genotypes influence offspring's risk of ADHD through environmental pathways beyond the effects of direct genetic transmission. Exploring the impact of the genetics of the mother beyond the maternally inherited genes can lead to new insights into ADHD risk. Future studies should also investigate paternal effects to provide a more comprehensive understanding of the ADHD risk architecture.
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