Multisite schizophrenia classification by integrating structural magnetic resonance imaging data with polygenic risk score

•Schizophrenia classification was studied using a large sample data from eight sites.•Both brain images and genetic factors were used as features for classification.•Machine learning methods and leave-one-site-out cross-validation were performed. Previous brain structural magnetic resonance imaging...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:NeuroImage clinical 2021-01, Vol.32, p.102860-102860, Article 102860
Hauptverfasser: Hu, Ke, Wang, Meng, Liu, Yong, Yan, Hao, Song, Ming, Chen, Jun, Chen, Yunchun, Wang, Huaning, Guo, Hua, Wan, Ping, Lv, Luxian, Yang, Yongfeng, Li, Peng, Lu, Lin, Yan, Jun, Wang, Huiling, Zhang, Hongxing, Zhang, Dai, Wu, Huawang, Ning, Yuping, Jiang, Tianzi, Liu, Bing
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:•Schizophrenia classification was studied using a large sample data from eight sites.•Both brain images and genetic factors were used as features for classification.•Machine learning methods and leave-one-site-out cross-validation were performed. Previous brain structural magnetic resonance imaging studies reported that patients with schizophrenia have brain structural abnormalities, which have been used to discriminate schizophrenia patients from normal controls. However, most existing studies identified schizophrenia patients at a single site, and the genetic features closely associated with highly heritable schizophrenia were not considered. In this study, we performed standardized feature extraction on brain structural magnetic resonance images and on genetic data to separate schizophrenia patients from normal controls. A total of 1010 participants, 508 schizophrenia patients and 502 normal controls, were recruited from 8 independent sites across China. Classification experiments were carried out using different machine learning methods and input features. We tested a support vector machine, logistic regression, and an ensemble learning strategy using 3 feature sets of interest: (1) imaging features: gray matter volume, (2) genetic features: polygenic risk scores, and (3) a fusion of imaging features and genetic features. The performance was assessed by leave-one-site-out cross-validation. Finally, some important brain and genetic features were identified. We found that the models with both imaging and genetic features as input performed better than models with either alone. The average accuracy of the classification models with the best performance in the cross-validation was 71.6%. The genetic feature that measured the cumulative risk of the genetic variants most associated with schizophrenia contributed the most to the classification. Our work took the first step toward considering both structural brain alterations and genome-wide genetic factors in a large-scale multisite schizophrenia classification. Our findings may provide insight into the underlying pathophysiology and risk mechanisms of schizophrenia.
ISSN:2213-1582
2213-1582
DOI:10.1016/j.nicl.2021.102860