Tong Xiang, Ma Yao, Niu Xundong, Yan Zhipeng, Liu Sitong, Peng Bo, Peng Shifeng, Fan Hong
Department of Respiratory and Critical Care Medicine, West China Hospital/West China School of Medicine, Sichuan University, Chengdu, Sichuan Department of Endocrinology, The Second Affiliated Hospital of Ningxia Medical University, Yinchuan, Ningxia Department of Internal Medicine, Leshan Traditional Chinese Medicine Hospital, Leshan, Sichuan, China.
Medicine (Baltimore). 2016 Jul;95(30):e4325. doi: 10.1097/MD.0000000000004325.
The butyrophilin-like 2 (BTNL2) G16071A gene polymorphism has been implicated in the susceptibility to granulomatous diseases, but the results were inconclusive. The objective of the current study was to precisely explore the relationship between BTNL2 G16071A gene polymorphism and granulomatous disease susceptibility by the meta-analysis including false-positive report probability (FPRP) test.
A systematic literature search in the PubMed, Embase, and Wanfang databases, China National Knowledge Internet, and commercial Internet search engines was conducted to identify studies published up to April 1, 2016. The odds ratio (OR) with 95% confidence interval (CI) was used to assess the effect size. Statistical analysis was conducted using the STATA 12.0 software and FPRP test sheet.
In total, all 4324 cases and 4386 controls from 14 eligible studies were included in the current meta-analysis. By the overall meta-analysis, we found a significant association between BTNL2 G16071A gene polymorphism and granulomatous disease susceptibility (A vs G: OR = 1.25, 95% CI = 1.07-1.45, P = 0.005). The meta-regression analyses showed that a large proportion of the between-study heterogeneity was significantly attributed to the ethnicity (A vs G, P = 0.013) and the types of granulomatous diseases (A vs G, P = 0.002). By the subgroup meta-analysis, the BTNL2 G16071A gene polymorphism was associated with granulomatous disease susceptibility in Caucasians (A vs G: OR = 1.37, 95% CI = 1.18-1.58, P < 0.001). Moreover, a significant relationship between the BTNL2 G16071A gene polymorphism and sarcoidosis susceptibility (A vs G: OR = 1.52, 95% CI = 1.39-1.66, P < 0.001) was found. However, to avoid the "false-positive report," we further investigated the significant associations observed in the present meta-analysis by the FPRP test. Interestingly, the results of FPRP test indicated that the BTNL2 G16071A gene polymorphism was truly associated with sarcoidosis susceptibility (A vs G, FPRP < 0.001). Additionally, the FPRP test confirmed that the BTNL2 G16071A gene polymorphism was associated only with granulomatous disease susceptibility among Caucasians (A vs G, FPRP < 0.001) at the level of a prior probability, which was 0.001.
The meta-analysis indicated that BTNL2 G16071A gene polymorphism may as a likelihood factor contributed to granulomatous disease susceptibility, especially increasing the sarcoidosis susceptibility. In addition, the polymorphism may be greatly associated with likelihood of granulomatous diseases among Caucasians.
嗜乳脂蛋白样2(BTNL2)基因G16071A多态性与肉芽肿性疾病易感性有关,但结果尚无定论。本研究旨在通过包括假阳性报告概率(FPRP)检验的荟萃分析,精确探讨BTNL2基因G16071A多态性与肉芽肿性疾病易感性之间的关系。
在PubMed、Embase、万方数据库、中国知网以及商业互联网搜索引擎中进行系统文献检索,以识别截至2016年4月1日发表的研究。采用比值比(OR)及其95%置信区间(CI)评估效应量。使用STATA 12.0软件和FPRP检验表进行统计分析。
本荟萃分析共纳入了14项合格研究中的4324例病例和4386例对照。通过总体荟萃分析,我们发现BTNL2基因G16071A多态性与肉芽肿性疾病易感性之间存在显著关联(A与G比较:OR = 1.25,95%CI = 1.07 - 1.45,P = 0.005)。荟萃回归分析表明,研究间的大部分异质性显著归因于种族(A与G比较,P = 0.013)和肉芽肿性疾病类型(A与G比较,P = 0.002)。通过亚组荟萃分析,BTNL2基因G16071A多态性与白种人中的肉芽肿性疾病易感性相关(A与G比较:OR = 1.37,95%CI = 1.18 - 1.58,P < 0.001)。此外,还发现BTNL2基因G16071A多态性与结节病易感性之间存在显著关系(A与G比较:OR = 1.52,95%CI = 1.39 - 1.66,P < 0.001)。然而,为避免“假阳性报告”,我们通过FPRP检验进一步研究了本荟萃分析中观察到的显著关联。有趣的是,FPRP检验结果表明,BTNL2基因G16071A多态性与结节病易感性真正相关(A与G比较,FPRP < 0.001)。此外,FPRP检验证实,在0.001的先验概率水平上,BTNL2基因G16071A多态性仅与白种人中的肉芽肿性疾病易感性相关(A与G比较,FPRP < 0.001)。
荟萃分析表明,BTNL2基因G16071A多态性可能是导致肉芽肿性疾病易感性的一个潜在因素,尤其是增加了结节病易感性。此外,该多态性可能与白种人中肉芽肿性疾病的易感性密切相关。