Department of Thoracic Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, PR China.
PLoS One. 2014 Mar 18;9(3):e91100. doi: 10.1371/journal.pone.0091100. eCollection 2014.
Previous studies investigating the association between TGF-β1 polymorphisms and Radiation Pneumonia (RP) risk have provided inconsistent results. The aim of our study was to assess the association between the TGF-β1 genes C509T, G915C and T869C polymorphisms and risk of RP in lung cancer patients treated with definitive radiotherapy.
Two investigators independently searched the Medline, Embase, CNKI, and Chinese Biomedicine Databases for studies published before September 2013. Summary odds ratios (ORs) and 95% confidence intervals (CIs) for TGF-β1 polymorphisms and RP were calculated in a fixed-effects model or a random-effects model when appropriate.
Ultimately, each 7 studies were found to be eligible for meta-analyses of C509T, G915C and T869C, respectively. Our analysis suggested that the variant genotypes of T869C were associated with a significantly increased RP risk in dominant model (OR = 0.59, 95% CI = 0.45-0.79) and CT vs. TT model (OR = 0.47, 95% CI = 0.32-0.69). In the subgroup analyses by ethnicity/country, a significantly increased risk was observed among Caucasians. For C509T and G915C polymorphism, no obvious associations were found for all genetic models.
This meta-analysis suggests that T869C polymorphism of TGF-β1 may be associated with RP risk only in Caucasians, and there may be no association between C509T and G915C polymorphism and RP risk.
先前研究探讨了转化生长因子-β1(TGF-β1)多态性与放射性肺炎(RP)风险之间的关系,但结果并不一致。本研究旨在评估 TGF-β1 基因 C509T、G915C 和 T869C 多态性与接受根治性放疗的肺癌患者 RP 风险之间的相关性。
两位研究者独立检索 Medline、Embase、中国知网(CNKI)和中国生物医学文献数据库,查找截至 2013 年 9 月发表的研究。在适当的情况下,采用固定效应模型或随机效应模型计算 TGF-β1 多态性与 RP 之间的汇总比值比(OR)和 95%置信区间(CI)。
最终,有 7 项研究分别符合 TGF-β1 C509T、G915C 和 T869C 多态性的 meta 分析条件。我们的分析表明,T869C 变异基因型在显性模型(OR=0.59,95%CI=0.45-0.79)和 CT 与 TT 模型(OR=0.47,95%CI=0.32-0.69)中与 RP 风险显著增加相关。在按种族/国家进行的亚组分析中,白种人观察到风险显著增加。对于 C509T 和 G915C 多态性,所有遗传模型均未发现明显相关性。
这项 meta 分析提示,TGF-β1 的 T869C 多态性可能仅与白种人的 RP 风险相关,而 C509T 和 G915C 多态性与 RP 风险之间可能没有关联。