Association between Fas/FasL gene polymorphism and musculoskeletal degenerative diseases: a meta-analysis

被引:13
|
作者
Huang, Donghua [1 ]
Xiao, Jinrong [2 ]
Deng, Xiangyu [1 ]
Ma, Kaige [1 ]
Liang, Hang [1 ]
Shi, Deyao [1 ]
Wu, Fashuai [1 ]
Shao, Zengwu [1 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Orthopaed, 1277 JieFang Ave, Wuhan 430022, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Sch Publ Hlth, Dept Epidemiol & Biostat,Minist Educ,Key Lab Envi, Wuhan 430030, Hubei, Peoples R China
来源
BMC MUSCULOSKELETAL DISORDERS | 2018年 / 19卷
基金
中国国家自然科学基金;
关键词
Fas/FasL polymorphism; Musculoskeletal degenerative diseases; Intervertebral disc degeneration; Osteoarthritis; Rheumatoid arthritis; SYSTEMIC-LUPUS-ERYTHEMATOSUS; LUMBAR DISC HERNIATION; CELL-SURFACE ANTIGEN; RHEUMATOID-ARTHRITIS; PROMOTER POLYMORPHISM; KNEE OSTEOARTHRITIS; ARTICULAR-CARTILAGE; CHINESE PATIENTS; FAS LIGAND; APOPTOSIS;
D O I
10.1186/s12891-018-2057-z
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: It was reported that Fas (rs1800682, rs2234767) and FasL (rs5030772, rs763110) gene polymorphism might be related to the risk of musculoskeletal degenerative diseases (MSDD), such as osteoarthritis (OA), intervertebral disc degeneration (IVDD) and rheumatoid arthritis (RA). However, data from different studies was inconsistent. Here we aim to elaborately summarize and explore the association between the Fas (rs1800682, rs2234767) and FasL (rs5030772, rs763110) and MSDD. Methods: Literatures were selected from PubMed, Web of Science, Embase, Scopus and Medline in English and VIP, SinoMed, Wanfang and the China National Knowledge Infrastructure (CNKI) in Chinese up to August 21, 2017. All the researches included are case-control studies about human. We calculated the pooled odds ratios (ORs) with 95% confidence intervals (95% CI) to evaluate the strengths of the associations of Fas (rs1800682, rs2234767) and FasL (rs5030772, rs763110) polymorphisms with MSDD risk. Results: Eleven eligible studies for rs1800682 with 1930 cases and 1720 controls, 6 eligible studies for rs2234767 with 1794 cases and 1909 controls, 3 eligible studies for rs5030772 with 367 cases and 313 controls and 8 eligible studies for rs763110 with 2010 cases and 2105 controls were included in this analysis. The results showed that the G allele of Fas (rs1800682) is associated with an increased risk of IVDD in homozygote and recessive models. The G allele of Fas (rs2234767) is linked to a decreased risk of RA but an enhanced risk of OA in allele and recessive models. In addition, the T allele of FasL (rs763110) is correlated with a reduced risk of IVDD in all of models. However, no relationship was found between FasL (rs5030772) and these three types of MSDD in any models. Conclusions: Fas (rs1800682) and FasL (rs763110) polymorphism were associated with the risk of IVDD and Fas (rs2234767) was correlated to the susceptibility of OA and RA. Fas (rs1800682) and Fas (rs2234767) are more likely to be associated with MSDD for Chinese people. FasL (rs763110) is related to the progression of MSDD for both Caucasoid and Chinese race groups. But FasL (rs5030772) might not be associated with any types of MSDD or any race groups statistically.
引用
收藏
页数:15
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