PDCD-1基因rs 2227982多态性与强直性脊柱炎易感性的Meta分析
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湖北省自然科学基金(2016CFB255)


PDCD-1 rs 2227982 polymorphism and susceptibility to ankylosing spondylitis: A Metaanalysis
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    【摘要】 目的 采用Meta分析的方法评价程序性细胞死亡因子1(PDCD1)基因rs 2227982多态性与强直性脊柱炎(AS)易感性的相关性。方法 计算机检索PubMed、Embase、CBM、CNKI、VIP和WanFang Data,查找关于PDCD1基因rs 2227982多态性与AS相关性的病例对照研究,检索时限均为从建库至2015年12月。由2位评价者独立筛选文献、提取资料和质量评价后,共纳入5个病例对照研究,共计968例AS患者和985例非AS对照,采用Stata 120软件进行Meta分析。结果 Meta分析结果显示,T等位基因人群AS发病风险高于C等位基因人群(OR=174,95%CI 148~206,P<0001);TT基因型人群AS发病风险高于CC基因型人群(OR=188,95%CI 130~273,P=0001);TT+CT基因型人群AS发病风险高于CC基因型人群(OR=229,95%CI 165~318,P<0001);但TT基因型人群AS发病风险与CT基因型人群(OR=081,95%CI 055~119,P=0283)和CT+CC基因型人群(OR=133,95%CI 094~189,P=0118)的差异无统计学意义。结论 当前的证据表明,PDCD1基因rs 2227982多态性可能会增加AS的发病风险。由于纳入研究数量的限制,该结论尚需进一步开展研究加以验证。

    Abstract:

    【Abstract】 Objective To evaluate the association between programmed cell death factor1 (PDCD1) gene rs 2227982 polymorphism and the ankylosing spondylitis (AS) susceptibility by metaanalysis. Methods PubMed, Embase, CNKI, VIP and WanFang Data were systematically searched to collect casecontrol studies with the association between PDCD1 rs 2227982 polymorphism and AS susceptibility published from setting up to December, 2015. Two valuators independently screened literature, extracted data, and assessed the quality of included studies.A total of 5 casecontrol studies were included, involving 968 AS cases and 985 controls. Then metaanalysis was performed by using Stata 120 software. Results The results of metaanalysis showed that T allele carriers presented higher risk of AS than C allele carriers(OR=174, 95%CI 148 to 206, P<0001), TT genotype carriers presented higher risk than CC genotype carriers (OR=188, 95%CI 130 to 273, P=0001), and TT+CT genotype carriers presented higher risk than CC genotype carriers (OR=229, 95%CI 165 to 318, P<0001). Compared with TT genotype carriers, no significant difference was observed in the CT genotype carriers (OR=081, 95%CI 055 to 119, P=0283) and CT+CC genotype carriers (OR=133, 95%CI 094 to 189, P=0118). Conclusion Current evidence suggested that PDCD1 rs 2227982 polymorphism might increase the susceptibility of AS. Due to limited quantity of included studies, the conclusion was needed to be confirmed with further studies.

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  • 在线发布日期: 2017-08-03
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