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Autor(en) / Beteiligte
Titel
Cognitive and functional deficits are associated with white matter abnormalities in two independent cohorts of patients with schizophrenia
Ist Teil von
  • European archives of psychiatry and clinical neuroscience, 2022-09, Vol.272 (6), p.957-969
Ort / Verlag
Berlin/Heidelberg: Springer Berlin Heidelberg
Erscheinungsjahr
2022
Link zum Volltext
Quelle
Psychology & Behavioral Sciences Collection
Beschreibungen/Notizen
  • Background Significant evidence links white matter (WM) microstructural abnormalities to cognitive impairment in schizophrenia (SZ), but the relationship of these abnormalities with functional outcome remains unclear. Methods In two independent cohorts (C1, C2), patients with SZ were divided into two subgroups: patients with higher cognitive performance (SZ-HCP-C1, n  = 25; SZ-HCP-C2, n  = 24) and patients with lower cognitive performance (SZ-LCP-C1, n  = 25; SZ-LCP-C2, n  = 24). Healthy controls (HC) were included in both cohorts (HC-C1, n  = 52; HC-C2, n  = 27). We compared fractional anisotropy (FA) of the whole-brain WM skeleton between the three groups (SZ-LCP, SZ-HCP, HC) by a whole-brain exploratory approach and an atlas-defined WM regions-of-interest approach via tract-based spatial statistics. In addition, we explored whether FA values were associated with Global Assessment of Functioning (GAF) scores in the SZ groups. Results In both cohorts, mean FA values of whole-brain WM skeleton were significantly lower in the SCZ-LCP group than in the SCZ-HCP group. Whereas in C1 the FA of the frontal part of the left inferior fronto-occipital fasciculus (IFOF) was positively correlated with GAF score, in C2 the FA of the temporal part of the left IFOF was positively correlated with GAF score. Conclusions We provide robust evidence for WM microstructural abnormalities in SZ. These abnormalities are more prominent in patients with low cognitive performance and are associated with the level of functioning.
Sprache
Englisch
Identifikatoren
ISSN: 0940-1334
eISSN: 1433-8491
DOI: 10.1007/s00406-021-01363-8
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9388472

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