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

Authors :
Smolen C
Jensen M
Dyer L
Pizzo L
Tyryshkina A
Banerjee D
Rohan L
Huber E
El Khattabi L
Prontera P
Caberg JH
Van Dijck A
Schwartz C
Faivre L
Callier P
Mosca-Boidron AL
Lefebvre M
Pope K
Snell P
Lockhart PJ
Castiglia L
Galesi O
Avola E
Mattina T
Fichera M
Luana Mandarà GM
Bruccheri MG
Pichon O
Le Caignec C
Stoeva R
Cuinat S
Mercier S
Bénéteau C
Blesson S
Nordsletten A
Martin-Coignard D
Sistermans E
Kooy RF
Amor DJ
Romano C
Isidor B
Juusola J
Girirajan S
Source :
American journal of human genetics [Am J Hum Genet] 2023 Dec 07; Vol. 110 (12), pp. 2015-2028. Date of Electronic Publication: 2023 Nov 17.
Publication Year :
2023

Abstract

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 <superscript>-126</superscript> ). 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 <superscript>-4</superscript> ). 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 <superscript>-92</superscript> ). 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.<br />Competing Interests: Declaration of interests L.D. and J.J. are employees of GeneDx, LLC.<br /> (Copyright © 2023 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1537-6605
Volume :
110
Issue :
12
Database :
MEDLINE
Journal :
American journal of human genetics
Publication Type :
Academic Journal
Accession number :
37979581
Full Text :
https://doi.org/10.1016/j.ajhg.2023.10.015