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Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

期刊

AMERICAN JOURNAL OF PSYCHIATRY
卷 171, 期 6, 页码 627-639

出版社

AMER PSYCHIATRIC PUBLISHING, INC
DOI: 10.1176/appi.ajp.2013.13070864

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资金

  1. NIMH International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome
  2. Swiss National Fund [PP00B_102864, 32473B_121996]
  3. National Center of Competence in Research program Synapsy
  4. Swiss National Science Foundation [51AU40_125759]
  5. Canadian Institutes of Health Research [MOP-97800, MOP-89066, MOP-74631]
  6. Ontario Mental Health Foundation
  7. Baily Thomas Charitable Trust [2315/1]
  8. Waterloo Foundation [9121234]
  9. Wellcome Trust Institutional Strategic Support Fund
  10. Wellcome Trust [GR067869MF]
  11. Ireland's Health Research Board [RP/2004/30, RP/2008/169]
  12. Health Foundation [1206/188]
  13. NIMH [MH-064824, MH-087626, MH-087636, MH-78015, MH-09131, RO1 MH-085953]
  14. National Institute of Child Health and Human Development [HD-070454, P50 HD-055784, R01 HD-042974]
  15. Brain and Behavior Research Foundation
  16. State University of New York Hendricks Fund
  17. Basil O'Connor Starter Scholar Research Award [5-FY06-590]
  18. Binational Science Foundation [2011378]
  19. Gazit-Globe Award
  20. Dutch Brain Foundation
  21. Robert W. Woodruff Fund
  22. Simons Foundation
  23. Hunter Medical Research Institute Post-Doctoral Fellowship
  24. Australian Training Fellowship awarded by the National Health and Medical Research Council of Australia [455614]
  25. Health Research Board (HRB) [RP-2008-169] Funding Source: Health Research Board (HRB)
  26. Medical Research Council [MR/L010305/1] Funding Source: researchfish
  27. Swiss National Science Foundation (SNF) [32473B_121996] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

Objective: Chromosome 22q11.2 deletion syndrome is a neurogenetic disorder associated with high rates of schizophrenia and other psychiatric conditions. The authors report what is to their knowledge the first large-scale collaborative study of rates and sex distributions of psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome. The associations among psychopathology, intellect, and functioning were examined in a subgroup of participants. Method: The 1,402 participants With 22q11.2 deletion syndrome, ages 6-68 years, were assessed for psychiatric disorders with validated diagnostic instruments. Data on intelligence and adaptive functioning were available for 183 participants ages 6 to 24 years. Results: Attention deficit hyperactivity disorder (ADHD) was the most frequent disorder in children (37.10%) and was overrepresented in males. Anxiety disorders were more prevalent than mood disorders at all ages, but especially in children and adolescents. Anxiety and unipolar mood disorders were overrepresented in females. Psychotic disorders were present in 41% of adults over age 25. Males did not predominate in psychotic or autism spectrum disorders. Hierarchical regressions in the subgroup revealed that daily living skills were predicted by the presence of anxiety disorders. Psychopathology was not associated with communication or socialization skills. Conclusions: To the authors' knowledge, this is the largest study of psychiatric morbidity in 22q11.2 deletion syndrome. It validates previous findings that this condition is one of the strongest risk factors for psychosis. Anxiety and developmental disorders were also prevalent. These results highlight the need to monitor and reduce the long-term burden of psychopathology in 22q11.2 deletion syndrome.

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