Abstract
Background and Hypothesis: Abnormal thalamic nuclei volumes and their link to cognitive impairments have been observed in schizophrenia. However, whether and how this finding extends to the schizophrenia spectrum is unknown. We hypothesized a distinct pattern of aberrant thalamic nuclei volume across the spectrum and examined its potential associations with cognitive symptoms. Study Design: We performed a FreeSurfer-based volumetry of T1-weighted brain MRIs from 137 healthy controls, 66 at-risk mental state (ARMS) subjects, 89 first-episode psychosis (FEP) individuals, and 126 patients with schizophrenia to estimate thalamic nuclei volumes of six nuclei groups (anterior, lateral, ventral, intralaminar, medial, and pulvinar). We used linear regression models, controlling for sex, age, and estimated total intracranial volume, both to compare thalamic nuclei volumes across groups and to investigate their associations with positive, negative, and cognitive symptoms. Study Results: We observed significant volume alterations in medial and lateral thalamic nuclei. Medial nuclei displayed consistently reduced volumes across the spectrum compared to controls, while lower lateral nuclei volumes were only observed in schizophrenia. Whereas positive and negative symptoms were not associated with reduced nuclei volumes across all groups, higher cognitive scores were linked to lower volumes of medial nuclei in ARMS. In FEP, cognition was not linked to nuclei volumes. In schizophrenia, lower cognitive performance was associated with lower medial volumes. Conclusions: Results demonstrate distinct thalamic nuclei volume reductions across the schizophrenia spectrum, with lower medial nuclei volumes linked to cognitive deficits in ARMS and schizophrenia. Data suggest a distinctive trajectory of thalamic nuclei abnormalities along the course of schizophrenia.
| Originalsprache | Englisch |
|---|---|
| Zeitschrift | Schizophrenia Bulletin |
| Jahrgang | 50 |
| Ausgabenummer | 5 |
| Seiten (von - bis) | 1208-1222 |
| Seitenumfang | 15 |
| ISSN | 0586-7614 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 01.09.2024 |
Fördermittel
M.K. receives support from the National Bank Fellowship (McGill University) and the Swiss National Foundation (P2SKP3_178175). F.B. was supported by the Else Kröner Memorial Stipendium and the Hans und Klementia Langmatz Foundation. C.S. was supported by the German Federal Ministry of Education and Research (BMBF; 01ER0803) and the German Research Council (DFG; SO1336/7). M.T. holds a scholarship of the Studienstiftung des deutschen Volkes.
| Träger | Trägernummer |
|---|---|
| Hans und Klementia Langmatz Stiftung | |
| McGill University | |
| Studienstiftung des Deutschen Volkes | |
| Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung | P2SKP3_178175 |
| Bundesministerium für Bildung und Forschung | 01ER0803 |
| Deutsche Forschungsgemeinschaft | SO1336/7 |
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
-
SDG 3 – Gesundheit und Wohlergehen
DFG-Fachsystematik
- 2.23-10 Klinische Psychiatrie, Psychotherapie und Kinder- und Jugendpsychiatrie
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