Xu Zhi-Wei, Wang Guan-Nan, Dong Zhou-Zhou, Li Tao-Hong, Cao Chao, Jin Yu-Hong
Department of Critical Care Medicine, Ningbo Medical Center, Lihuili Hospital, Ningbo University, Ningbo, China E-mail :
Asian Pac J Cancer Prev. 2015;16(15):6685-90. doi: 10.7314/apjcp.2015.16.15.6685.
Genetic studies have shown a possible relationship between the rs16969968 polymorphism in CHRNA5 and the risk of lung cancer. However, the results have been conflicting. Thus we rigorously conducted a meta-analysis to clarify any association.
A total of 10 case-control studies involving 17,962 lung cancer cases and 77,216 control subjects were analysed. Odds ratios (ORs) with 95% confidence intervals (CIs) were used to measure the strength of the association.
We found the CHRNA5 rs16969968 polymorphism to be associated with the risk of lung cancer (AA vs GG: OR=1.60, 95%CI=1.51-1.71). On stratified analysis by smoking status, a statistically significant increased risk was observed in the smoking group (AA vs GG: OR=1.80, 95%CI=1.61-2.01). However, this polymorphism was not associated with lung cancer risk in Asians (AA vs GG: OR=0.95, 95%CI=0.35-2.59), whereas it was linked to increased risk of lung cancer among Caucasians (AA vs GG: OR=1.65, 95%CI=1.55-1.76).
Our meta-analysis provided statistical evidence for a strong association between rs16969968 polymorphism and the risk of lung cancer, especially in smokers and Caucasians. Application of this relationship may contribute to identification of individuals at high risk of lung cancer and indicate a chemoprevention target.
基因研究表明,CHRNA5基因中的rs16969968多态性与肺癌风险之间可能存在关联。然而,研究结果一直存在争议。因此,我们进行了一项严格的荟萃分析以阐明其中的关联。
共分析了10项病例对照研究,涉及17962例肺癌患者和77216例对照受试者。采用比值比(OR)及95%置信区间(CI)来衡量关联强度。
我们发现CHRNA5基因的rs16969968多态性与肺癌风险相关(AA与GG相比:OR = 1.60,95%CI = 1.51 - 1.71)。按吸烟状况进行分层分析时,吸烟组中观察到风险显著增加(AA与GG相比:OR = 1.80,95%CI = 1.61 - 2.01)。然而,该多态性在亚洲人中与肺癌风险无关(AA与GG相比:OR = 0.95,95%CI = 0.35 - 2.59),而在白种人中与肺癌风险增加相关(AA与GG相比:OR = 1.65,95%CI = 1.55 - 1.76)。
我们的荟萃分析为rs16969968多态性与肺癌风险之间的强关联提供了统计学证据,尤其是在吸烟者和白种人中。应用这种关联可能有助于识别肺癌高危个体并指明化学预防靶点。