4.6 Article

Kraepelin Was Right: A Latent Class Analysis of Symptom Dimensions in Patients and Controls

期刊

SCHIZOPHRENIA BULLETIN
卷 38, 期 3, 页码 495-505

出版社

OXFORD UNIV PRESS
DOI: 10.1093/schbul/sbq103

关键词

phenotypic heterogeneity; schizophrenia; bipolar; controls; factor analysis; latent class analysis

资金

  1. Dutch Health Research Council (ZON-MW) [10-000-1002]
  2. EU (EU-GEI)
  3. Academic Psychiatric Centre AMC, Amsterdam
  4. Ingeest, Amsterdam
  5. Arkin, Amsterdam
  6. Dijk en Duin, Amsterdam
  7. Rivierduinen, Amsterdam
  8. Erasmus MC, Amsterdam
  9. GGZ Noord Holland Noord, Amsterdam
  10. University Medical Centre Utrecht, Utrecht
  11. Altrecht, Utrecht
  12. Symfora, Utrecht
  13. Meerkanten, Utrecht
  14. Riagg Amersfoort, Utrecht
  15. Delta, Utrecht
  16. University Medical Center Groningen, Groningen
  17. Lentis, Groningen
  18. GGZ Friesland, Groningen
  19. GGZ Drenthe, Groningen
  20. Adhesie, Groningen
  21. Mediant, Groningen
  22. GGZ De Grote Rivieren and Parnassia psycho-medical centre, Groningen
  23. Maastricht University Medical Center, Maastricht
  24. GGZ Eindhoven, Maastricht
  25. GGZ Midden-Brabant, Maastricht
  26. GGZ Oost-Brabant, Maastricht
  27. GGZ Noord-Midden Limburg, Maastricht
  28. Mondriaan Zorggroep, Maastricht
  29. Prins Clauscentrum Sittard, Maastricht
  30. RIAGG Roermond, Maastricht
  31. Universitair Centrum Sint-Jozef Kortenberg, Maastricht
  32. CAPRI University of Antwerp, Maastricht
  33. PC Ziekeren Sint-Truiden, Maastricht
  34. PZ Sancta Maria Sint-Truiden, Maastricht
  35. GGZ Overpelt, Maastricht
  36. OPZ Rekem, Maastricht
  37. Netherlands Organisation for scientific research (NWO) [451-080-010]
  38. Eli Lilly
  39. BMS
  40. Lundbeck
  41. Organon
  42. Janssen-Cilag
  43. GSK
  44. AstraZeneca
  45. Pfizer
  46. Servier

向作者/读者索取更多资源

Phenotypic heterogeneity within patients and controls may explain why the genetic variants contributing to schizophrenia risk explain only a fraction of the heritability. The aim of this study is to investigate quantitative and qualitative differences in psychosis symptoms in a sample including psychosis patients, their relatives, and community controls. We combined factor analysis and latent class analysis to analyze variation in Comprehensive Assessment of Symptoms and History lifetime-rated symptoms in 4286 subjects. The Wechsler Adult Intelligence Scale-Intelligence Quotient (N = 2663) and the Camberwell Assessment of Need rating scale (N = 625) were assessed in a subsample. Variation in 5 continuous dimensions (disorganization, positive, negative, mania, and depression) was accounted for by the presence of 7 homogeneous classes (Kraepelinian schizophrenia, affective psychosis, manic-depression, deficit nonpsychosis, depression, healthy, and no symptoms). Eighty-five percent of the schizophrenia patients was assigned to the Kraepelinian schizophrenia class (characterized by high scores on the 5 dimensions, low IQ, and poor outcome) while 15% was assigned to the affective psychosis class (relatively low disorganization and negative scores, normal IQ, and good outcome). In bipolar patients (91% bipolar I), 41% was assigned to the Kraepelinian schizophrenia class, 44% to the affective psychosis class, and 10% to the manic-depression class. Latent class membership was associated with intelligence in psychosis patients and in their relatives but not in community controls. In conclusion, symptom heterogeneity is more pronounced in bipolar disorder compared with schizophrenia. Reducing phenotypic heterogeneity within psychosis patients and controls may facilitate etiological research.

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