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X- vs. Y-chromosome influences on human behavior: a deep phenotypic comparison of psychopathology in XXY and XYY syndromes.
Schaffer, Lukas; Rau, Srishti; Larsen, Isabella G; Clasen, Liv; Warling, Allysa; Whitman, Ethan T; Nadig, Ajay; McDermott, Cassidy; Xenophontos, Anastasia; Wilson, Kathleen; Blumenthal, Jonathan; Torres, Erin; Raznahan, Armin.
Afiliación
  • Schaffer L; Section On Developmental Neurogenomics, Human Genetics Branch, National Institute of Mental Health Intramural Research Program, Magnuson Clinical Center, Room 4N242, MSC 1367, Bethesda, MD, 20814, USA.
  • Rau S; Center for Autism Spectrum Disorders and Division of Neuropsychology, Children's National Hospital, Washington, DC, USA.
  • Larsen IG; Section On Developmental Neurogenomics, Human Genetics Branch, National Institute of Mental Health Intramural Research Program, Magnuson Clinical Center, Room 4N242, MSC 1367, Bethesda, MD, 20814, USA.
  • Clasen L; Section On Developmental Neurogenomics, Human Genetics Branch, National Institute of Mental Health Intramural Research Program, Magnuson Clinical Center, Room 4N242, MSC 1367, Bethesda, MD, 20814, USA.
  • Warling A; Section On Developmental Neurogenomics, Human Genetics Branch, National Institute of Mental Health Intramural Research Program, Magnuson Clinical Center, Room 4N242, MSC 1367, Bethesda, MD, 20814, USA.
  • Whitman ET; Section On Developmental Neurogenomics, Human Genetics Branch, National Institute of Mental Health Intramural Research Program, Magnuson Clinical Center, Room 4N242, MSC 1367, Bethesda, MD, 20814, USA.
  • Nadig A; Section On Developmental Neurogenomics, Human Genetics Branch, National Institute of Mental Health Intramural Research Program, Magnuson Clinical Center, Room 4N242, MSC 1367, Bethesda, MD, 20814, USA.
  • McDermott C; Section On Developmental Neurogenomics, Human Genetics Branch, National Institute of Mental Health Intramural Research Program, Magnuson Clinical Center, Room 4N242, MSC 1367, Bethesda, MD, 20814, USA.
  • Xenophontos A; Section On Developmental Neurogenomics, Human Genetics Branch, National Institute of Mental Health Intramural Research Program, Magnuson Clinical Center, Room 4N242, MSC 1367, Bethesda, MD, 20814, USA.
  • Wilson K; Section On Developmental Neurogenomics, Human Genetics Branch, National Institute of Mental Health Intramural Research Program, Magnuson Clinical Center, Room 4N242, MSC 1367, Bethesda, MD, 20814, USA.
  • Blumenthal J; Section On Developmental Neurogenomics, Human Genetics Branch, National Institute of Mental Health Intramural Research Program, Magnuson Clinical Center, Room 4N242, MSC 1367, Bethesda, MD, 20814, USA.
  • Torres E; Section On Developmental Neurogenomics, Human Genetics Branch, National Institute of Mental Health Intramural Research Program, Magnuson Clinical Center, Room 4N242, MSC 1367, Bethesda, MD, 20814, USA.
  • Raznahan A; Section On Developmental Neurogenomics, Human Genetics Branch, National Institute of Mental Health Intramural Research Program, Magnuson Clinical Center, Room 4N242, MSC 1367, Bethesda, MD, 20814, USA. raznahana@mail.nih.gov.
J Neurodev Disord ; 16(1): 56, 2024 Oct 03.
Article en En | MEDLINE | ID: mdl-39363182
ABSTRACT

BACKGROUND:

Do different genetic disorders impart different psychiatric risk profiles? This question has major implications for biological and translational aspects of psychiatry, but has been difficult to tackle given limited access to shared batteries of fine-grained clinical data across genetic disorders.

METHODS:

Using a new suite of generalizable analytic approaches, we examine gold-standard diagnostic ratings, scores on 66 dimensional measures of psychopathology, and measures of cognition and functioning in two different sex chromosome aneuploidies (SCAs)-Klinefelter (XXY/KS) and XYY syndrome (n = 102 and 64 vs. n = 74 and 60 matched XY controls, total n = 300). We focus on SCAs for their high collective prevalence, informativeness regarding differential X- vs. Y-chromosome effects, and potential relevance for normative sex differences.

RESULTS:

We show that XXY/KS elevates rates for most psychiatric diagnoses as previously reported for XYY, but disproportionately so for anxiety disorders. Fine-mapping across all 66 traits provides a detailed profile of psychopathology in XXY/KS which is strongly correlated with that of XYY (r = .75 across traits) and robust to ascertainment biases, but reveals (i) a greater penetrance of XYY than KS/XXY for most traits except mood/anxiety problems, and (ii) a disproportionate impact of XYY vs. XXY/KS on social problems. XXY/KS and XYY showed a similar coupling of psychopathology with adaptive function and caregiver strain, but not IQ.

CONCLUSIONS:

This work provides new tools for deep-phenotypic comparisons of genetic disorders in psychiatry and uses these to detail unique and shared effects of the X- and Y-chromosome on human behavior.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Síndrome de Klinefelter Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurodev Disord Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Síndrome de Klinefelter Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurodev Disord Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido