中华病理学杂志
中華病理學雜誌
중화병이학잡지
Chinese Journal of Pathology
2014年
3期
158-162
,共5页
万国兴%李锋%李文琴%孙建平%曹玉文
萬國興%李鋒%李文琴%孫建平%曹玉文
만국흥%리봉%리문금%손건평%조옥문
乳腺肿瘤%谷胱甘肽转移酶%Meta分析%中国
乳腺腫瘤%穀胱甘肽轉移酶%Meta分析%中國
유선종류%곡광감태전이매%Meta분석%중국
Breast neoplasms%Glutathione transferase%Meta-analysis%China
目的 对已发表的文献采用meta分析方法系统评估谷胱甘肽-S-转移酶(GST) M1基因多态性与中国人群乳腺癌的易感性.方法 计算机检索Pubmed、Embase、Cochrane library、中国知网(CNKI)、维普(VIP)、万方数据及中国生物医学文献数据库(CBD),收集关于GSTM1基因多态性与中国人群乳腺癌易感性的相关研究,按纳入与排除标准筛选文献、提取资料并评价纳入研究的质量后,采用RevMan 5.2、Stata 12.0软件进行meta分析,计算合并OR值及其95% CI,并进行发表偏倚评估及敏感性分析.结果 共纳入15项研究,累积病例5 176例,对照5 890例.meta分析结果显示,中国人群中GSTM1基因缺失型个体较正常型个体乳腺癌发病风险明显增高(OR=1.34,95% CI=1.12 ~1.60,P=0.002);按地区进行亚组分析结果显示,中国南方及北方人群GSTM1基因缺失型个体乳腺癌发病风险均较正常型高(南方人群:OR=1.14,95%CI=1.01~1.28,P=0.03;北方人群:OR =2.65,95% CI =2.04 ~3.34,P<0.01).结论 GSTM1基因多态性与中国人群乳腺癌易感性相关,GSTM1基因缺失可能增加乳腺癌的发病风险.
目的 對已髮錶的文獻採用meta分析方法繫統評估穀胱甘肽-S-轉移酶(GST) M1基因多態性與中國人群乳腺癌的易感性.方法 計算機檢索Pubmed、Embase、Cochrane library、中國知網(CNKI)、維普(VIP)、萬方數據及中國生物醫學文獻數據庫(CBD),收集關于GSTM1基因多態性與中國人群乳腺癌易感性的相關研究,按納入與排除標準篩選文獻、提取資料併評價納入研究的質量後,採用RevMan 5.2、Stata 12.0軟件進行meta分析,計算閤併OR值及其95% CI,併進行髮錶偏倚評估及敏感性分析.結果 共納入15項研究,纍積病例5 176例,對照5 890例.meta分析結果顯示,中國人群中GSTM1基因缺失型箇體較正常型箇體乳腺癌髮病風險明顯增高(OR=1.34,95% CI=1.12 ~1.60,P=0.002);按地區進行亞組分析結果顯示,中國南方及北方人群GSTM1基因缺失型箇體乳腺癌髮病風險均較正常型高(南方人群:OR=1.14,95%CI=1.01~1.28,P=0.03;北方人群:OR =2.65,95% CI =2.04 ~3.34,P<0.01).結論 GSTM1基因多態性與中國人群乳腺癌易感性相關,GSTM1基因缺失可能增加乳腺癌的髮病風險.
목적 대이발표적문헌채용meta분석방법계통평고곡광감태-S-전이매(GST) M1기인다태성여중국인군유선암적역감성.방법 계산궤검색Pubmed、Embase、Cochrane library、중국지망(CNKI)、유보(VIP)、만방수거급중국생물의학문헌수거고(CBD),수집관우GSTM1기인다태성여중국인군유선암역감성적상관연구,안납입여배제표준사선문헌、제취자료병평개납입연구적질량후,채용RevMan 5.2、Stata 12.0연건진행meta분석,계산합병OR치급기95% CI,병진행발표편의평고급민감성분석.결과 공납입15항연구,루적병례5 176례,대조5 890례.meta분석결과현시,중국인군중GSTM1기인결실형개체교정상형개체유선암발병풍험명현증고(OR=1.34,95% CI=1.12 ~1.60,P=0.002);안지구진행아조분석결과현시,중국남방급북방인군GSTM1기인결실형개체유선암발병풍험균교정상형고(남방인군:OR=1.14,95%CI=1.01~1.28,P=0.03;북방인군:OR =2.65,95% CI =2.04 ~3.34,P<0.01).결론 GSTM1기인다태성여중국인군유선암역감성상관,GSTM1기인결실가능증가유선암적발병풍험.
Objective To evaluate the published data on association between present/null polymorphism of glutathione S-transferase M1 (GSTM1) and breast cancer risk in Chinese population in order to abttain a more precise and comprehensive estimation of the relationship.Methods A meta-analysis was performed to investigate the association between GSTM1 polymorphism and susceptibility to breast cancer in Chinese population by searching Pubmed,Embase,Cochrane library,CNKI,VIP,Wanfang and CBD database.The data were screened according to the inclusion and exclusion criteria,and extracted,and the quality of included studies was evaluated.The pooled odds ratios (OR) with 95% confidence intervals (95%CI) were calculated using RevMan 5.2 and Stata 12.0 software.Publication bias and sensitivity analysis were also assessed.Results A total of 15 case-control studies involving 5 176 cases and 5 890 controls were included in the meta-analysis.The results showed that individuals with GSTM1 null genotype harbored a significantly increased risk of breast cancer compared to that with GSTM1 non-null genotype in Chinese population (OR =1.34,95% CI =1.12-1.60,P =0.002).The subgroup analysis by region revealed that the individuals with GSTM1 null genotype were significantly associated with an increased risk of breast cancer in southern and northern China populations (southern:OR =1.14,95% CI =1.01-1.28,P =0.03; northern:OR=2.65,95%CI=2.04-3.34,P<0.01).Conclusion The current meta-analysis demonstrates that the GSTM1 polymorphism is significantly associated with susceptibility to breast cancer in Chinese population,and the GSTM1-deficit may increase the risk of breast cancer.