Ding He-Guo, Yin Yan-Wei, Liu Sun-Lin
Department of Respiration, Huzhou 3rd Hospital, 2088 Tiaoxi Road, Huzhou, Zhejiang 313000, China.
Department of Emergency, Chinese PLA Air Force General Hospital, Beijing, China.
Open Med (Wars). 2020 May 15;15(1):376-383. doi: 10.1515/med-2020-0407. eCollection 2020.
The association between () gene -572 G^C polymorphism and myocardial infarction (MI) risk has not been established. We adopted this meta-analysis for further insight into the case-control studies.
To investigate the genetic association, we searched multiple databases, including Web of Science, EMbase, CBM disc, PubMed and CNKI. Also, we manually identified the searched references. All the statistical analyses were conducted using Stata 11.0.
A total of five studies were identified, involving 2,526 MI cases and 3,027 controls. The results revealed a significant association between gene -572 G^C polymorphism and MI, implying that the gene -572 C allele may be a protective factor for MI (for C allele vs K allele: OR = 0.85, 95% CI = 0.73-0.99, = 0.041; for C/C vs G/G: OR = 0.55, 95% CI = 0.31-0.98, = 0.044; for C/C vs G/C + G/G: OR = 0.60, 95% CI = 0.41-0.89, = 0.011). However, in the subgroup analysis with regard to ethnicity, no significant correlation was identified between gene -572 G^C polymorphism and MI among Europeans.
The gene -572 C allele may be a protective factor for MI. Future studies involving larger sample bases are still recommended.
()基因-572G^C多态性与心肌梗死(MI)风险之间的关联尚未明确。我们采用此项荟萃分析以进一步深入了解病例对照研究。
为研究基因关联,我们检索了多个数据库,包括科学网、EMbase、中国生物医学文献数据库、PubMed和中国知网。此外,我们还手动筛选了检索到的参考文献。所有统计分析均使用Stata 11.0进行。
共纳入五项研究,涉及2526例MI病例和3027例对照。结果显示()基因-572G^C多态性与MI之间存在显著关联,这意味着()基因-572C等位基因可能是MI的一个保护因素(C等位基因与K等位基因相比:OR = 0.85,95%CI = 0.73 - 0.99,P = 0.041;C/C与G/G相比:OR = 约0.55,95%CI = 0.31 - 0.98,P = 0.044;C/C与G/C + G/G相比:OR = 0.60,95%CI = 0.41 - 0.89,P = 0.011)。然而,在按种族进行的亚组分析中,未发现欧洲人中()基因-572G^C多态性与MI之间存在显著相关性。
()基因-572C等位基因可能是MI的一个保护因素。仍建议未来开展涉及更大样本量的研究。