4.7 Article

Translating ENIGMA schizophrenia findings using the regional vulnerability index: Association with cognition, symptoms, and disease trajectory

Journal

HUMAN BRAIN MAPPING
Volume 43, Issue 1, Pages 566-575

Publisher

WILEY
DOI: 10.1002/hbm.25045

Keywords

ENIGMA; gray matter; regional vulnerability index; schizophrenia; white matter

Funding

  1. National Key R & D Program of China [2016YFC1307000]
  2. National Natural Science Foundation of China [81071086, 81461130016]
  3. National Institutes of Health [R01MH112180, R01MH116948, S10OD023696, R01EB015611, U01MH108148]

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Patients with schizophrenia exhibit brain deficits including reduced cortical thickness, subcortical gray matter volumes, and cerebral white matter integrity. The regional vulnerability index (RVI) can be used to measure these deficits at the individual level. In this study, RVIs were elevated in patients compared to controls, with the multimodal RVI showing the largest effect size. The multimodal and white matter RVIs were elevated in intermediate and chronic patients, suggesting ongoing progression, while cortical RVIs remained stable, indicating neurodevelopmental origins.
Patients with schizophrenia have patterns of brain deficits including reduced cortical thickness, subcortical gray matter volumes, and cerebral white matter integrity. We proposed the regional vulnerability index (RVI) to translate the results of Enhancing Neuro Imaging Genetics Meta-Analysis studies to the individual level. We calculated RVIs for cortical, subcortical, and white matter measurements and a multimodality RVI. We evaluated RVI as a measure sensitive to schizophrenia-specific neuroanatomical deficits and symptoms and studied the timeline of deficit formations in: early (<= 5 years since diagnosis, N = 45, age = 28.8 +/- 8.5); intermediate (6-20 years, N = 30, age 43.3 +/- 8.6); and chronic (21+ years, N = 44, age = 52.5 +/- 5.2) patients and healthy controls (N = 76, age = 38.6 +/- 12.4). All RVIs were significantly elevated in patients compared to controls, with the multimodal RVI showing the largest effect size, followed by cortical, white matter and subcortical RVIs (d = 1.57, 1.23, 1.09, and 0.61, all p < 10(-6)). Multimodal RVI was significantly correlated with multiple cognitive variables including measures of visual learning, working memory and the total score of the MATRICS consensus cognitive battery, and with negative symptoms. The multimodality and white matter RVIs were significantly elevated in the intermediate and chronic versus early diagnosis group, consistent with ongoing progression. Cortical RVI was stable in the three disease-duration groups, suggesting neurodevelopmental origins of cortical deficits. In summary, neuroanatomical deficits in schizophrenia affect the entire brain; the heterochronicity of their appearance indicates both the neurodevelopmental and progressive nature of this illness. These deficit patterns may be useful for early diagnosis and as quantitative targets for more effective treatment strategies aiming to alter these neuroanatomical deficit patterns.

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