Li Xiao-ting, Yuan Yan-li, Xia Yin-yin, Yu Bao-zhu, Zhang Tie-juan, Liu Ou, Lv Xiao-zhen, Zhan Si-yan
Department of Epidemiology and Bio-statistics, School of Public Health, Peking University, Beijing 100191, China.
Zhonghua Liu Xing Bing Xue Za Zhi. 2009 May;30(5):502-6.
To investigate the distribution of glutathione-S-transferase M1 (GSTM1) and T1 (GSTT1) genes polymorphisms in Chinese population and smear-positive pulmonary tuberculosis cases of Jilin province.
Articles about GSTM1 and GSTT1 genes polymorphisms published before 2009 in China were searched. The study population was obtained from fourteen counties (or districts) of Jilin province, which included all cases from November, 2007 to May, 2008, totally 1120. The genotypes of GSTM1 and GSTT1 were detected by multiplex PCR technique.
The frequencies of GSTM1 and GSTT1 'null' genotypes and combination M1-T1 'null' genotype acquired from systematic review were 54.2%, 46.8% and 26.2%, respectively, in Chinese Hans they were 53.4%, 44.9% and 25.5%, and in our research they are 57.2%, 20.4% and 13.7%, respectively. No significant differences between the frequencies of males and females as well as among that of different age groups were observed (P > 0.05). The frequency of GSTM1 'null' genotype in our research is slightly higher than that in systematic review (P = 0.016) , and the frequencies of GSTT1 'null' genotype and combination M1-T1 'null' genotype and are significantly lower than those in systematic review (both P < 0.001).
The frequencies of GSTM1 and GSTT1 'null' genotypes were different among ethnic. The statistical difference between systematic review and our research may due to our large sample size and mostly Southern people in previous studies.
研究谷胱甘肽 - S - 转移酶M1(GSTM1)和T1(GSTT1)基因多态性在中国人群及吉林省涂阳肺结核病例中的分布情况。
检索2009年以前国内发表的关于GSTM1和GSTT1基因多态性的文章。研究人群来自吉林省14个县(区),包括2007年11月至2008年5月的所有病例,共1120例。采用多重PCR技术检测GSTM1和GSTT1的基因型。
系统评价得出的GSTM1和GSTT1“缺失”基因型以及M1 - T1“缺失”基因型组合的频率分别为54.2%、46.8%和26.2%,在中国汉族人群中分别为53.4%、44.9%和25.5%,而在本研究中分别为57.2%、20.4%和13.7%。未观察到男性和女性以及不同年龄组之间频率的显著差异(P>0.05)。本研究中GSTM1“缺失”基因型的频率略高于系统评价(P = 0.016),而GSTT1“缺失”基因型以及M1 - T1“缺失”基因型组合的频率均显著低于系统评价(均P<0.001)。
GSTM1和GSTT1“缺失”基因型的频率在不同种族间存在差异。系统评价与本研究之间的统计学差异可能归因于本研究样本量较大且以往研究中大多为南方人群。