| Autor: |
Sandin, Sven, Yip, Benjamin H. K., Yin, Weiyao, Weiss, Lauren A., Dougherty, Joseph D., Fass, Stuart, Constantino, John N., Hailin, Zhu, Turner, Tychele N., Marrus, Natasha, Gutmann, David H., Sanders, Stephan J., Christoffersson, Benjamin |
| Předmět: |
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| Zdroj: |
JAMA Psychiatry; Jul2024, Vol. 81 Issue 7, p673-680, 8p |
| Abstrakt: |
This cohort study analyzes sex-specific differences in heritability of autism spectrum disorder among individuals in Sweden. Key Points: Question: What are the sex-specific etiological origins of autism spectrum disorder? Findings: In this cohort study including 1 047 649 Swedish children, 12 226 (1.17%) received a diagnosis of autism spectrum disorder; heritability was estimated at 87.0% for males and 75.7% for females, a statistically significant difference. Meaning: These findings suggest that variation in the occurrence of autism spectrum disorder in the population differs between males and females, indicating that some of the underlying causes and prevalence of the condition may differ between the 2 sexes. Importance: Autism spectrum disorder (ASD) is a neurodevelopmental disorder more prevalent in males than in females. The cause of ASD is largely genetic, but the association of genetics with the skewed sex ratio is not yet understood. To our knowledge, no large population-based study has provided estimates of heritability by sex. Objective: To estimate the sex-specific heritability of ASD. Design, Setting, and Participants: This was a population-based, retrospective analysis using national health registers of nontwin siblings and cousins from Sweden born between January 1, 1985, and December 31, 1998, with follow-up to 19 years of age. Data analysis occurred from August 2022 to November 2023. Main Outcomes and Measures: Models were fitted to estimate the relative variance in risk for ASD occurrence owing to sex-specific additive genetics, shared environmental effects, and a common residual term. The residual term conceptually captured other factors that promote individual behavioral variation (eg, maternal effects, de novo variants, rare genetic variants not additively inherited, or gene-environment interactions). Estimates were adjusted for differences in prevalence due to birth year and maternal and paternal age by sex. Results: The sample included 1 047 649 individuals in 456 832 families (538 283 males [51.38%]; 509 366 females [48.62%]). Within the entire sample, 12 226 (1.17%) received a diagnosis of ASD, comprising 8128 (1.51%) males and 4098 (0.80%) females. ASD heritability was estimated at 87.0% (95% CI, 81.4%-92.6%) for males and 75.7% (95% CI, 68.4%-83.1%) for females with a difference in heritability estimated at 11.3% (95% CI, 1.0%-21.6%). There was no support for shared environmental contributions. Conclusions and Relevance: These findings suggest that the degree of phenotypic variation attributable to genetic differences (heritability) differs between males and females, indicating that some of the underlying causes of the condition may differ between the 2 sexes. The skewed sex ratio in ASD may be partly explained by differences in genetic variance between the sexes. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Supplemental Index |
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