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白细胞介素-10基因多态性与鼻咽癌风险:一项荟萃分析。

Interleukin-10 polymorphisms and nasopharyngeal carcinoma risk: a meta-analysis.

作者信息

Yu Y-F, Han Z-G, Guo W-B, Zhang G-J, Yang J-K, Wu F-L, Ou Q-Y, Li Y-H, Cai X-Y, Zhan Z-N, Chen J-H, Xie W-L, Tang L, Liu C-D

机构信息

Department of Radiology, The First People's Hospital of Shunde, Foshan, Guangdong, China.

Ear Nose and Throat Diagnosis and Treatment Center, Xinjiang Uygur Autonomous Region People's Hospital, Urumqi, Xinjiang, China.

出版信息

Genet Mol Res. 2015 Dec 29;14(4):18945-57. doi: 10.4238/2015.December.29.1.

Abstract

It has been reported that interleukin-10 (IL-10) promoter genes (1082 A/G, 819 T/C, 592 A/C) are associated with nasopharyngeal carcinoma (NPC). However, the results remain controversial and ambiguous. To resolve inconsistencies in published data, we performed a meta-analysis to ascertain the association between IL-10 polymorphisms and NPC risk. Two case-control studies and two cohort studies were quantitatively analyzed to evaluate IL-10 promoter gene polymorphisms and NPC risk. Odds ratios (ORs) and their 95% confidence intervals (CIs) were calculated for each genetic model and allelic comparison. A random-effect model or a fixed-effect model was used to calculate the overall combined risk estimates. Overall, the variant genotypes (AA and AG) of the IL-10-1082 A/G polymorphism were associated with elevated risk of NPC compared with the GG homozygote (AG vs GG: OR = 1.77; 95%CI = 1.39-2.26; AG + GG vs AA: OR = 1.78; 95%CI = 1.42-2.22); no significant associations were observed in allelic contrast and the recessive model. Strong positive association was seen in the cohort studies but not in the case-control studies. No statistically significant association was detected between IL-10-819 T/C and IL-10-592 A/C polymorphisms and NPC. Additionally, publication bias was not found. Based on the current evidence, this meta-analysis suggests that IL-1082 A/G polymorphism may increase the risk of NPC, but IL-10-819 T/C and IL-10-592 A/C polymorphisms do not. Further multicenter studies that are better controlled are required to confirm these findings.

摘要

据报道,白细胞介素-10(IL-10)启动子基因(1082 A/G、819 T/C、592 A/C)与鼻咽癌(NPC)相关。然而,结果仍存在争议且不明确。为解决已发表数据中的不一致性,我们进行了一项荟萃分析,以确定IL-10基因多态性与NPC风险之间的关联。对两项病例对照研究和两项队列研究进行了定量分析,以评估IL-10启动子基因多态性与NPC风险。针对每个遗传模型和等位基因比较计算比值比(OR)及其95%置信区间(CI)。采用随机效应模型或固定效应模型计算总体合并风险估计值。总体而言,与GG纯合子相比,IL-10 - 1082 A/G多态性的变异基因型(AA和AG)与NPC风险升高相关(AG与GG:OR = 1.77;95%CI = 1.39 - 2.26;AG + GG与AA:OR = 1.78;95%CI = 1.42 - 2.22);在等位基因对比和隐性模型中未观察到显著关联。在队列研究中发现了强正相关,但在病例对照研究中未发现。未检测到IL-10 - 819 T/C和IL-10 - 592 A/C多态性与NPC之间存在统计学显著关联。此外,未发现发表偏倚。基于当前证据,这项荟萃分析表明IL-1082 A/G多态性可能增加NPC风险,但IL-10 - 819 T/C和IL-10 - 592 A/C多态性不会。需要进一步开展控制更好的多中心研究来证实这些发现。

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