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American journal of human genetics · 2023

Assortative mating and parental genetic relatedness contribute to the pathogenicity of variably expressive variants.

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Smolen Corrine, Jensen Matthew, Dyer Lisa, Pizzo Lucilla, Tyryshkina Anastasia, Banerjee Deepro, Rohan Laura, Huber Emily, El Khattabi Laila, Prontera Paolo, Caberg Jean-Hubert, Van Dijck Anke, Schwartz Charles, Faivre Laurence, Callier Patrick, Mosca-Boidron Anne-Laure, Lefebvre Mathilde, Pope Kate, Snell Penny, Lockhart Paul J, Castiglia Lucia, Galesi Ornella, Avola Emanuela, Mattina Teresa, Fichera Marco, Luana Mandarà Giuseppa Maria, Bruccheri Maria Grazia, Pichon Olivier, Le Caignec Cedric, Stoeva Radka, Cuinat Silvestre, Mercier Sandra, Bénéteau Claire, Blesson Sophie, Nordsletten Ashley, Martin-Coignard Dominique, Sistermans Erik, Kooy R Frank, Amor David J, Romano Corrado, Isidor Bertrand, Juusola Jane, Girirajan Santhosh

Аннотация

We examined more than 97,000 families from four neurodevelopmental disease cohorts and the UK Biobank to identify phenotypic and genetic patterns in parents contributing to neurodevelopmental disease risk in children. We identified within- and cross-disorder correlations between six phenotypes in parents and children, such as obsessive-compulsive disorder (R = 0.32-0.38, p < 10-126). We also found that measures of sub-clinical autism features in parents are associated with several autism severity measures in children, including biparental mean Social Responsiveness Scale scores and proband Repetitive Behaviors Scale scores (regression coefficient = 0.14, p = 3.38 × 10-4). We further describe patterns of phenotypic similarity between spouses, where spouses show correlations for six neurological and psychiatric phenotypes, including a within-disorder correlation for depression (R = 0.24-0.68, p < 0.001) and a cross-disorder correlation between anxiety and bipolar disorder (R = 0.09-0.22, p < 10-92). Using a simulated population, we also found that assortative mating can lead to increases in disease liability over generations and the appearance of "genetic anticipation" in families carrying rare variants. We identified several families in a neurodevelopmental disease cohort where the proband inherited multiple rare variants in disease-associated genes from each of their affected parents. We further identified parental relatedness as a risk factor for neurodevelopmental disorders through its inverse relationship with variant pathogenicity and propose that parental relatedness modulates disease risk by increasing genome-wide homozygosity in children (R = 0.05-0.26, p < 0.05). Our results highlight the utility of assessing parent phenotypes and genotypes toward predicting features in children who carry rare variably expressive variants and implicate assortative mating as a risk factor for increased disease severity in these families.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты