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- Publisher Website: 10.1007/s00406-021-01300-9
- Scopus: eid_2-s2.0-85118447541
- PMID: 34467451
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Article: Investigation of structural brain correlates of neurological soft signs in individuals at ultra-high risk for psychosis
| Title | Investigation of structural brain correlates of neurological soft signs in individuals at ultra-high risk for psychosis |
|---|---|
| Authors | |
| Keywords | Grey matter volume Neurological soft signs Transition Ultra-high risk Voxel-based morphometry |
| Issue Date | 2021 |
| Citation | European Archives of Psychiatry and Clinical Neuroscience, 2021, v. 271, n. 8, p. 1475-1485 How to Cite? |
| Abstract | Increased severity of neurological soft signs (NSS) in schizophrenia have been associated with abnormal brain morphology in cerebello-thalamo-cortical structures, but it is unclear whether similar structures underlie NSS prior to the onset of psychosis. The present study investigated the relationship between severity of NSS and grey matter volume (GMV) in individuals at ultra-high risk for psychosis (UHR) stratified for later conversion to psychosis. Structural T1-weighted MRI scans were obtained from 56 antipsychotic-naïve UHR individuals and 35 healthy controls (HC). The UHR individuals had follow-up data (mean follow-up: 5.2 years) to ascertain clinical outcome. Using whole-brain voxel-based morphometry, the relationship between NSS and GMV at baseline was assessed in UHR, HC, as well as individuals who later transitioned (UHR-P, n = 25) and did not transition (UHR-NP, n = 31) to psychosis. NSS total and subscale scores except motor coordination were significantly higher in UHR compared to HC. Higher signs were also found in UHR-P, but not UHR-NP. Total NSS was not associated with GMV in the whole sample or in each group. However, in UHR-P individuals, greater deficits in sensory integration was associated with lower GMV in the left cerebellum, right insula, and right middle frontal gyrus. In conclusion, NSS are present in UHR individuals, particularly those who later transitioned to a psychotic disorder. While these signs show little overall variation with GMV, the association of sensory integration deficits with lower GMV in UHR-P suggests that certain brain areas may be implicated in the development of specific neurological abnormalities in the psychosis prodrome. |
| Persistent Identifier | http://hdl.handle.net/10722/367843 |
| ISSN | 2023 Impact Factor: 3.5 2023 SCImago Journal Rankings: 1.381 |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Wang, Ya | - |
| dc.contributor.author | Braam, Esmee E. | - |
| dc.contributor.author | Wannan, Cassandra M.J. | - |
| dc.contributor.author | Van Rheenen, Tamsyn E. | - |
| dc.contributor.author | Chan, Raymond C.K. | - |
| dc.contributor.author | Nelson, Barnaby | - |
| dc.contributor.author | McGorry, Patrick D. | - |
| dc.contributor.author | Yung, Alison R. | - |
| dc.contributor.author | Lin, Ashleigh | - |
| dc.contributor.author | Brewer, Warrick J. | - |
| dc.contributor.author | Koutsogiannis, John | - |
| dc.contributor.author | Wood, Stephen J. | - |
| dc.contributor.author | Velakoulis, Dennis | - |
| dc.contributor.author | Pantelis, Christos | - |
| dc.contributor.author | Cropley, Vanessa L. | - |
| dc.date.accessioned | 2025-12-19T07:59:49Z | - |
| dc.date.available | 2025-12-19T07:59:49Z | - |
| dc.date.issued | 2021 | - |
| dc.identifier.citation | European Archives of Psychiatry and Clinical Neuroscience, 2021, v. 271, n. 8, p. 1475-1485 | - |
| dc.identifier.issn | 0940-1334 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/367843 | - |
| dc.description.abstract | Increased severity of neurological soft signs (NSS) in schizophrenia have been associated with abnormal brain morphology in cerebello-thalamo-cortical structures, but it is unclear whether similar structures underlie NSS prior to the onset of psychosis. The present study investigated the relationship between severity of NSS and grey matter volume (GMV) in individuals at ultra-high risk for psychosis (UHR) stratified for later conversion to psychosis. Structural T1-weighted MRI scans were obtained from 56 antipsychotic-naïve UHR individuals and 35 healthy controls (HC). The UHR individuals had follow-up data (mean follow-up: 5.2 years) to ascertain clinical outcome. Using whole-brain voxel-based morphometry, the relationship between NSS and GMV at baseline was assessed in UHR, HC, as well as individuals who later transitioned (UHR-P, n = 25) and did not transition (UHR-NP, n = 31) to psychosis. NSS total and subscale scores except motor coordination were significantly higher in UHR compared to HC. Higher signs were also found in UHR-P, but not UHR-NP. Total NSS was not associated with GMV in the whole sample or in each group. However, in UHR-P individuals, greater deficits in sensory integration was associated with lower GMV in the left cerebellum, right insula, and right middle frontal gyrus. In conclusion, NSS are present in UHR individuals, particularly those who later transitioned to a psychotic disorder. While these signs show little overall variation with GMV, the association of sensory integration deficits with lower GMV in UHR-P suggests that certain brain areas may be implicated in the development of specific neurological abnormalities in the psychosis prodrome. | - |
| dc.language | eng | - |
| dc.relation.ispartof | European Archives of Psychiatry and Clinical Neuroscience | - |
| dc.subject | Grey matter volume | - |
| dc.subject | Neurological soft signs | - |
| dc.subject | Transition | - |
| dc.subject | Ultra-high risk | - |
| dc.subject | Voxel-based morphometry | - |
| dc.title | Investigation of structural brain correlates of neurological soft signs in individuals at ultra-high risk for psychosis | - |
| dc.type | Article | - |
| dc.description.nature | link_to_subscribed_fulltext | - |
| dc.identifier.doi | 10.1007/s00406-021-01300-9 | - |
| dc.identifier.pmid | 34467451 | - |
| dc.identifier.scopus | eid_2-s2.0-85118447541 | - |
| dc.identifier.volume | 271 | - |
| dc.identifier.issue | 8 | - |
| dc.identifier.spage | 1475 | - |
| dc.identifier.epage | 1485 | - |
| dc.identifier.eissn | 1433-8491 | - |
