Zhang Jixiang, Zhang Jihui, Wu Dandan, Wang Jun, Dong Weiguo
Department of Gastroenterology, Renmin Hospital of Wuhan University , Wuhan, Hubei Province , China and.
Autoimmunity. 2014 Dec;47(8):512-8. doi: 10.3109/08916934.2014.930735. Epub 2014 Jul 16.
Several polymorphisms have been identified in TNFSF15, while their roles in the incidence of ulcerative colitis (UC) and Crohn's disease (CD) are conflicting. This meta-analysis was aimed to clarify the impact of these polymorphisms on UC and CD risk.
Databases were searched until 31 January 2014 for eligible studies on TNFSF15 polymorphisms. Data were extracted, and pooled odd ratios (ORs) as well as 95% confidence intervals (95% CIs) were calculated.
Fifteen studies with 8903 CD patients, 4687 UC patients and 12 606 controls were included. Except for rs4263839 polymorphism, significant associations were found between the rest six TNFSF15 polymorphisms and CD risk (rs3810936: OR = 2.10, 95% CI, 1.47-3.00; rs6478108: OR = 2.19, 95% CI, 1.53-3.13; rs4979462: OR = 1.89, 95% CI, 1.42-2.52; rs6478109: OR = 2.00, 95% CI, 1.39-2.88; rs7848647: OR = 1.54, 95% CI, 1.15-2.06; rs7869487: OR = 1.51, 95% CI, 1.06-2.17). And we found rs3810936, rs6478108 and rs6478109 polymorphism were significantly associated with UC risk (rs3810936: OR = 1.19, 95% CI, 1.06-1.34; rs6478108: OR = 1.16, 95% CI, 1.06-1.26; rs6478109: OR = 1.16, 95% CI, 1.03-1.32). According to the subgroup analysis by ethnicity, except for rs4263839 in Caucasian and rs4979462 in Asian, all the rest investigated TNFSF15 polymorphisms were associated with CD risk and rs3810936 and rs7848647 polymorphism in Asian as well as rs6478108 polymorphism in Caucasian were associated with UC risk.
This meta-analysis indicated that most of the seven TNFSF15 polymorphisms (except for rs4263839) were risk factors contributed to CD and UC susceptibility. The differences in ethnicity did not influence the risk obviously.
已在肿瘤坏死因子超家族成员15(TNFSF15)中鉴定出多种多态性,但其在溃疡性结肠炎(UC)和克罗恩病(CD)发病中的作用存在争议。本荟萃分析旨在阐明这些多态性对UC和CD风险的影响。
检索数据库至2014年1月31日,查找有关TNFSF15多态性的符合条件的研究。提取数据,并计算合并比值比(OR)以及95%置信区间(95%CI)。
纳入了15项研究,包括8903例CD患者、4687例UC患者和12606例对照。除rs4263839多态性外,其余6种TNFSF15多态性与CD风险之间存在显著关联(rs3810936:OR = 2.10,95%CI,1.47 - 3.00;rs6478108:OR = 2.19,95%CI,1.53 - 3.13;rs4979462:OR = 1.89,95%CI,1.42 - 2.52;rs6478109:OR = 2.00,95%CI,1.39 - 2.88;rs7848647:OR = 1.54,95%CI,1.15 - 2.06;rs7869487:OR = 1.51,95%CI,1.06 - 2.17)。并且发现rs3810936、rs6478108和rs6478109多态性与UC风险显著相关(rs3810936:OR = 1.19,95%CI,1.06 - 1.34;rs6478108:OR = 1.16,95%CI,1.06 - 1.26;rs6478109:OR = 1.16,95%CI,1.03 - 1.32)。根据种族进行的亚组分析显示,除白种人中的rs4263839和亚洲人中的rs4979462外,其余所有研究的TNFSF15多态性均与CD风险相关,亚洲人中的rs3810936和rs7848647多态性以及白种人中的rs6478108多态性与UC风险相关。
本荟萃分析表明,七种TNFSF15多态性中的大多数(除rs4263839外)是导致CD和UC易感性的危险因素。种族差异对风险的影响不明显。