Genetic architecture study of rheumatoid arthritis and juvenile idiopathic arthritis

被引:5
作者
Jia, Jun [1 ]
Li, Junyi [2 ]
Yao, Xueming [2 ]
Zhang, YuHang [3 ]
Yang, Xiaohao [3 ]
Wang, Ping [2 ]
Xia, Qianghua [2 ]
Hakonarson, Hakon [4 ,5 ,6 ]
Li, Jin [2 ]
机构
[1] Tianjin Hosp, Dept Surg Foot & Ankle, Tianjin, Peoples R China
[2] Tianjin Med Univ, Tianjin Key Lab Med Epigenet, Dept Cell Biol, 2011 Collaborat Innovat Ctr Tianjin Med Epigenet, Tianjin, Peoples R China
[3] Tianjin Univ Tradit Chinese Med, Tianjin, Peoples R China
[4] Childrens Hosp Philadelphia, Ctr Appl Genom, Philadelphia, PA 19104 USA
[5] Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
[6] Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USA
基金
中国国家自然科学基金;
关键词
Juvenile idiopathic arthritis; Rheumatoid arthritis; Genome-wide association studies; Genetic architecture comparison; Pathway enrichment; SUSCEPTIBILITY LOCUS; ASSOCIATION; DATABASE; SET; CLASSIFICATION; HERITABILITY; POPULATION; PREVALENCE; DISEASES; KEGG;
D O I
10.7717/peerj.8234
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:18
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