| Literature DB >> 30663853 |
Gong-Jun Ji1,2,3, Xingui Chen2,3,4, Tongjian Bai2,3,4, Lu Wang2,3,4, Qiang Wei2,3,4, Yaxiang Gao2,3, Longxiang Tao5, Kongliang He6,7, Dandan Li2,3,4, Yi Dong6,8, Panpan Hu2,3,4, Fengqiong Yu1,2,3, Chunyan Zhu1,2,3, Yanghua Tian2,3,4, Yongqiang Yu5, Kai Wang2,3,4.
Abstract
Functional connectomes have been suggested as fingerprinting for individual identification. Accordingly, we hypothesized that subjects in the same phenotypic group have similar functional connectome features, which could help to discriminate schizophrenia (SCH) patients from healthy controls (HCs) and from depression patients. To this end, we included resting-state functional magnetic resonance imaging data of SCH, depression patients, and HCs from three centers. We first investigated the characteristics of connectome similarity between individuals, and found higher similarity between subjects belonging to the same group (i.e., SCH-SCH) than different groups (i.e., HC-SCH). These findings suggest that the average connectome within group (termed as group-specific functional connectome [GFC]) may help in individual classification. Consistently, significant accuracy (75-77%) and area under curve (81-86%) were found in discriminating SCH from HC or depression patients by GFC-based leave-one-out cross-validation. Cross-center classification further suggests a good generalizability of the GFC classification. We additionally included normal aging data (255 young and 242 old subjects with different scanning sequences) to show factors could be improved for better classification performance, and the findings emphasized the importance of increasing sample size but not temporal resolution during scanning. In conclusion, our findings suggest that the average functional connectome across subjects contained group-specific biological features and may be helpful in clinical diagnosis for schizophrenia.Entities:
Keywords: classification; functional connectome; functional magnetic resonance imaging; multicenter; resting state; schizophrenia
Mesh:
Year: 2019 PMID: 30663853 PMCID: PMC6865403 DOI: 10.1002/hbm.24527
Source DB: PubMed Journal: Hum Brain Mapp ISSN: 1065-9471 Impact factor: 5.038