Genetic architecture study of rheumatoid arthritis and juvenile idiopathic arthritis

Author:

Jia Jun1,Li Junyi2,Yao Xueming2,Zhang YuHang3,Yang Xiaohao3,Wang Ping2,Xia Qianghua2,Hakonarson Hakon456,Li Jin2

Affiliation:

1. Department of Surgery of Foot and Ankle, Tianjin Hospital, Tianjin, China

2. Department of Cell Biology, 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, Tianjin Medical University, Tianjin, China

3. Tianjin University of Traditional Chinese Medicine, Tianjin, China

4. Center for Applied Genomics, Children’s Hospital of Philadelphia, Philadelphia, PA, United States of America

5. Division of Human Genetics, Children’s Hospital of Philadelphia, Philadelphia, PA, United States of America

6. Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States of America

Abstract

Background Rheumatoid arthritis and juvenile idiopathic arthritis are two types of autoimmune diseases with inflammation at the joints, occurring to adults and children respectively. There are phenotypic overlaps between these two types of diseases, despite the age difference in patient groups. Methods To systematically compare the genetic architecture of them, we conducted analyses at gene and pathway levels and constructed protein-protein-interaction network based on summary statistics of genome-wide association studies of these two diseases. We examined their difference and similarity at each level. Results We observed extensive overlap in significant SNPs and genes at the human leukocyte antigen region. In addition, several SNPs in other regions of the human genome were also significantly associated with both diseases. We found significantly associated genes enriched in 32 pathways shared by both diseases. Excluding genes in the human leukocyte antigen region, significant enrichment is present for pathways like interleukin-27 pathway and NO2-dependent interleukin-12 pathway in natural killer cells. Discussion The identification of commonly associated genes and pathways may help in finding population at risk for both diseases, as well as shed light on repositioning and designing drugs for both diseases.

Funder

National Natural Science Foundation of China

Tianjin Natural Science Foundation

Tianjin Medical University

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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