Disparities in accelerated brain aging in recent-onset and chronic schizophrenia

Sung Woo Joo, Junhyeok Lee, Juhyuk Han, Minjae Kim, Yeonwoo Kim, Howook Lee, Young Tak Jo, Jaewook Shin, Jungsun Lee, Won Hee Lee

Research output: Contribution to journalArticlepeer-review

Abstract

Background Patients with schizophrenia experience accelerated aging, accompanied by abnormalities in biomarkers such as shorter telomere length. Brain age prediction using neuroimaging data has gained attention in schizophrenia research, with consistently reported increases in brain-predicted age difference (brain-PAD). However, its associations with clinical symptoms and illness duration remain unclear. Methods We developed brain age prediction models using structural magnetic resonance imaging (MRI) data from 10,938 healthy individuals. The models were validated on an independent test dataset comprising 79 healthy controls, 57 patients with recent-onset schizophrenia, and 71 patients with chronic schizophrenia. Group comparisons and the clinical associations of brain-PAD were analyzed using multiple linear regression. SHapley Additive exPlanations (SHAP) values estimated feature contributions to the model, and between-group differences in SHAP values and group-by-SHAP value interactions were also examined. Results Patients with recent-onset schizophrenia and chronic schizophrenia exhibited increased brain-PAD values of 1.2 and 0.9 years, respectively. Between-group differences in SHAP values were identified in the right lateral prefrontal area (false discovery rate [FDR] p = 0.022), with group-by-SHAP value interactions observed in the left prefrontal area (FDR p = 0.049). A negative association between brain-PAD and Full-scale Intelligence Quotient scores in chronic schizophrenia was noted, which did not remain significant after correction for multiple comparisons. Conclusions Brain-PAD increases were pronounced in the early phase of schizophrenia. Regional brain abnormalities contributing to brain-PAD likely vary with illness duration. Future longitudinal studies are required to overcome limitations related to sample size, heterogeneity, and the cross-sectional design of this study.

Original languageEnglish
Article numbere60
JournalPsychological Medicine
Volume55
DOIs
Publication statusPublished - 24 Feb 2025

Bibliographical note

Publisher Copyright:
© The Author(s), 2025.

Keywords

  • brain aging
  • chronic
  • recent-onset
  • schizophrenia

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