Classification of four distinct osteoarthritis subtypes with a knee joint tissue transcriptome atlas

被引:15
作者
Chunhui Yuan [1 ,2 ]
Zongyou Pan [1 ,2 ,3 ]
Kun Zhao [1 ,2 ,3 ]
Jun Li [1 ,2 ]
Zixuan Sheng [1 ,2 ]
Xudong Yao [1 ,2 ]
Hua Liu [1 ,2 ]
Xiaolei Zhang [1 ,3 ,4 ,5 ]
Yang Yang [4 ]
Dongsheng Yu [1 ,2 ,3 ,6 ]
Yu Zhang [4 ]
Yuzi Xu [1 ,2 ]
ZhiYong Zhang [5 ,7 ]
Tianlong Huang [8 ]
Wanlu Liu [1 ,2 ]
Hongwei Ouyang [1 ,2 ,3 ,5 ]
机构
[1] DrLi Dak Sum & Yip Yio Chin Center for Stem Cells and Regenerative Medicine,and Department of Orthopedic Surgery of the Second Affiliated Hospital,Zhejiang University School of Medicine
[2] Zhejiang University-University of Edinburgh Institute,Zhejiang University School of Medicine,and Key Laboratory of Tissue Engineering and Regenerative Medicine of Zhejiang Province,Zhejiang University School of Medicine
[3] Department of Sports Medicine,Zhejiang University School of Medicine
[4] Department of Orthopedics,The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University
[5] China Orthopedic Regenerative Medicine Group (CORMed)
[6] Department of Orthopedics,Zhejiang Provincial People's Hospital,Hangzhou Medical College
[7] Translational Research Centre of Regenerative Medicine and D Printing Technologies of Guangzhou Medical University,State Key Laboratory of Respiratory Disease,The Third Affiliated Hospital of Guangzhou Medical University
[8] The Second Xiangya Hospital of Central South University
关键词
D O I
暂无
中图分类号
R684.3 [关节炎];
学科分类号
100220 [骨科学];
摘要
The limited molecular classifications and disease signatures of osteoarthritis(OA) impede the development of prediagnosis and targeted therapeutics for OA patients. To classify and understand the subtypes of OA, we collected three types of tissue including cartilage, subchondral bone, and synovium from multiple clinical centers and constructed an extensive transcriptome atlas of OA patients. By applying unsupervised clustering analysis to the cartilage transcriptome, OA patients were classified into four subtypes with distinct molecular signatures: a glycosaminoglycan metabolic disorder subtype(C1), a collagen metabolic disorder subtype(C2), an activated sensory neuron subtype(C3), and an inflammation subtype(C4). Through ligand-receptor crosstalk analysis of the three knee tissue types, we linked molecular functions with the clinical symptoms of different OA subtypes. For example, the Gene Ontology functional term of vasculature development was enriched in the subchondral bone-cartilage crosstalk of C2 and the cartilage-subchondral bone crosstalk of C4, which might lead to severe osteophytes in C2 patients and apparent joint space narrowing in C4 patients. Based on the marker genes of the four OA subtypes identified in this study, we modeled OA subtypes with two independent published RNA-seq datasets through random forest classification. The findings of this work contradicted traditional OA diagnosis by medical imaging and revealed distinct molecular subtypes in knee OA patients, which may allow for precise diagnosis and treatment of OA.
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收藏
页码:406 / 415
页数:10
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