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A Twin Study of Altered White Matter Heritability in Youth With Autism Spectrum Disorder.
Hegarty, John P; Monterrey, Julio C; Tian, Qiyuan; Cleveland, Sue C; Gong, Xinyi; Phillips, Jennifer M; Wolke, Olga N; McNab, Jennifer A; Hallmayer, Joachim F; Reiss, Allan L; Hardan, Antonio Y; Lazzeroni, Laura C.
Afiliación
  • Hegarty JP; Stanford University School of Medicine, Stanford, California. Electronic address: hegartyj@stanford.edu.
  • Monterrey JC; Stanford University School of Medicine, Stanford, California.
  • Tian Q; Tsinghua University School of Medicine, Beijing, China.
  • Cleveland SC; Stanford University School of Medicine, Stanford, California.
  • Gong X; Stanford University School of Medicine, Stanford, California.
  • Phillips JM; Stanford University School of Medicine, Stanford, California.
  • Wolke ON; Stanford University School of Medicine, Stanford, California.
  • McNab JA; Stanford University School of Medicine, Stanford, California.
  • Hallmayer JF; Stanford University School of Medicine, Stanford, California.
  • Reiss AL; Stanford University School of Medicine, Stanford, California.
  • Hardan AY; Stanford University School of Medicine, Stanford, California.
  • Lazzeroni LC; Stanford University School of Medicine, Stanford, California.
J Am Acad Child Adolesc Psychiatry ; 63(1): 65-79, 2024 Jan.
Article en En | MEDLINE | ID: mdl-37406770
OBJECTIVE: White matter alterations are frequently reported in autism spectrum disorder (ASD), yet the etiology is currently unknown. The objective of this investigation was to examine, for the first time, the impact of genetic and environmental factors on white matter microstructure in twins with ASD compared to control twins without ASD. METHOD: Diffusion-weighted MRIs were obtained from same-sex twin pairs (6-15 years of age) in which at least 1 twin was diagnosed with ASD or neither twin exhibited a history of neurological or psychiatric disorders. Fractional anisotropy (FA) and mean diffusivity (MD) were examined across different white matter tracts in the brain, and statistical and twin modeling were completed to assess the proportion of variation associated with additive genetic (A) and common/shared (C) or unique (E) environmental factors. We also developed a novel Twin-Pair Difference Score analysis method that produces quantitative estimates of the genetic and environmental contributions to shared covariance between different brain and behavioral traits. RESULTS: Good-quality data were available from 84 twin pairs, 50 ASD pairs (32 concordant for ASD [16 monozygotic; 16 dizygotic], 16 discordant for ASD [3 monozygotic; 13 dizygotic], and 2 pairs in which 1 twin had ASD and the other exhibited some subthreshold symptoms [1 monozygotic; 1 dizygotic]) and 34 control pairs (20 monozygotic; 14 dizygotic). Average FA and MD across the brain, respectively, were primarily genetically mediated in both control twins (A = 0.80, 95% CI [0.57, 1.02]; A = 0.80 [0.55, 1.04]) and twins concordant for having ASD (A = 0.71 [0.33, 1.09]; A = 0.84 [0.32,1.36]). However, there were also significant tract-specific differences between groups. For instance, genetic effects on commissural fibers were primarily associated with differences in general cognitive abilities and perhaps some diagnostic differences for ASD because Twin-Pair Difference-Score analysis indicated that genetic factors may have contributed to ∼40% to 50% of the covariation between IQ scores and FA of the corpus callosum. Conversely, the increased impact of environmental factors on some projection and association fibers were primarily associated with differences in symptom severity in twins with ASD; for example, our analyses suggested that unique environmental factors may have contributed to ∼10% to 20% of the covariation between autism-related symptom severity and FA of the cerebellar peduncles and external capsule. CONCLUSION: White matter alterations in youth with ASD are associated with both genetic contributions and potentially increased vulnerability or responsivity to environmental influences. DIVERSITY & INCLUSION STATEMENT: We worked to ensure sex and gender balance in the recruitment of human participants. We worked to ensure race, ethnic, and/or other types of diversity in the recruitment of human participants. We worked to ensure that the study questionnaires were prepared in an inclusive way. One or more of the authors of this paper self-identifies as a member of one or more historically underrepresented racial and/or ethnic groups in science. One or more of the authors of this paper self-identifies as a member of one or more historically underrepresented sexual and/or gender groups in science. One or more of the authors of this paper self-identifies as living with a disability. The author list of this paper includes contributors from the location and/or community where the research was conducted and they participated in the data collection, design, analysis, and/or interpretation of the work.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastorno Autístico / Sustancia Blanca / Trastorno del Espectro Autista Tipo de estudio: Prognostic_studies Límite: Adolescent / Female / Humans / Male Idioma: En Revista: J Am Acad Child Adolesc Psychiatry Asunto de la revista: PEDIATRIA / PSIQUIATRIA Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastorno Autístico / Sustancia Blanca / Trastorno del Espectro Autista Tipo de estudio: Prognostic_studies Límite: Adolescent / Female / Humans / Male Idioma: En Revista: J Am Acad Child Adolesc Psychiatry Asunto de la revista: PEDIATRIA / PSIQUIATRIA Año: 2024 Tipo del documento: Article
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