Patterns of co‐altered brain structure and function underlying neurological soft signs in schizophrenia spectrum disorders

Neurological soft signs (NSS) comprise a broad range of subtle neurological deficits and are considered to represent external markers of sensorimotor dysfunction frequently found in mental disorders of presumed neurodevelopmental origin. Although NSS frequently occur in schizophrenia spectrum disord...

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Veröffentlicht in:Human brain mapping 2019-12, Vol.40 (17), p.5029-5041
Hauptverfasser: Hirjak, Dusan, Rashidi, Mahmoud, Fritze, Stefan, Bertolino, Alina L., Geiger, Lena S., Zang, Zhenxiang, Kubera, Katharina M., Schmitgen, Mike M., Sambataro, Fabio, Calhoun, Vince D., Weisbrod, Matthias, Tost, Heike, Wolf, Robert C.
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Sprache:eng
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Zusammenfassung:Neurological soft signs (NSS) comprise a broad range of subtle neurological deficits and are considered to represent external markers of sensorimotor dysfunction frequently found in mental disorders of presumed neurodevelopmental origin. Although NSS frequently occur in schizophrenia spectrum disorders (SSD), specific patterns of co‐altered brain structure and function underlying NSS in SSD have not been investigated so far. It is unclear whether gray matter volume (GMV) alterations or aberrant brain activity or a combination of both, are associated with NSS in SSD. Here, 37 right‐handed SSD patients and 37 matched healthy controls underwent motor assessment and magnetic resonance imaging (MRI) at 3 T. NSS were examined on the Heidelberg NSS scale. We used a multivariate data fusion technique for multimodal MRI data—multiset canonical correlation and joint independent component analysis (mCCA + jICA)—to investigate co‐altered patterns of GMV and intrinsic neural fluctuations (INF) in SSD patients exhibiting NSS. The mCCA + jICA model indicated two joint group‐discriminating components (temporoparietal/cortical sensorimotor and frontocerebellar/frontoparietal networks) and one modality‐specific group‐discriminating component (p
ISSN:1065-9471
1097-0193
DOI:10.1002/hbm.24755