Yin Yan-Wei, Wang Qi, Sun Qian-Qian, Hu Ai-Min, Liu Hong-Li
Department of Emergency, Chinese PLA Air Force General Hospital, 30 Fucheng Road, Haidian District, Beijing 100142, China.
Department of Emergency, Chinese PLA Air Force General Hospital, 30 Fucheng Road, Haidian District, Beijing 100142, China.
Thromb Res. 2015 Jan;135(1):130-6. doi: 10.1016/j.thromres.2014.10.022. Epub 2014 Nov 4.
ATP-binding cassette transporter 1 (ABCA1), a member of the ATP-binding cassette family, plays a critical role in the development of atherosclerosis (AS). This meta-analysis was performed to assess the associations of ABCA1 C69T and V825I polymorphisms with AS susceptibility.
A comprehensive search was conducted to identify all eligible studies from PubMed, Embase, Web of Science, Cochrane database, CBMdisc, CNKI and Google Scholar. Additionally, hand searching of the references of identified articles was performed. All statistical analyses were done with Review Manager 5.1.4 and Stata 11.0.
Eleven articles involving 14 studies were included in the final meta-analysis. For the ABCA1 C69T polymorphism, six studies involving 1854 AS cases and 5744 controls were combined showing significant association between this variant and AS risk (for T allele vs. C allele: OR =1.44, 95% CI =1.04-1.24, p =0.005; for T/T vs. C/C: OR =1.39, 95% CI =1.12-1.73, p =0.003; for T/T vs. C/T+C/C: OR =1.34, 95% CI =1.09-1.65, p =0.006; for T/T+C/T vs. C/C: OR =1.13, 95% CI =1.01-1.27, p =0.040). For the ABCA1 V825I polymorphism, eight studies involving 2026 AS cases and 8696 controls were combined. There was no significant association between the variant and AS risk (for I allele vs. V allele: OR =1.18, 95% CI =0.90-1.53, p =0.230; for I/I vs. V/V: OR =1.29, 95% CI =0.75-2.23, p =0.360; for I/I vs. V/I+V/V: OR =1.40, 95% CI =0.87-2.26, p =0.160; for I/I+V/I vs. V/V: OR =1.15, 95% CI =1.00-1.33, p =0.060).
This meta-analysis suggested that the ABCA1 C69T polymorphism was associated with an increased AS risk. Furthermore, there was no significant association between the ABCA1 V825I polymorphism and AS risk.
ATP结合盒转运蛋白1(ABCA1)是ATP结合盒家族的成员之一,在动脉粥样硬化(AS)的发展过程中起着关键作用。本荟萃分析旨在评估ABCA1基因C69T和V825I多态性与AS易感性之间的关联。
通过全面检索PubMed、Embase、Web of Science、Cochrane数据库、CBMdisc、CNKI和谷歌学术等数据库,以识别所有符合条件的研究。此外,还对已识别文章的参考文献进行了手工检索。所有统计分析均使用Review Manager 5.1.4和Stata 11.0软件完成。
最终的荟萃分析纳入了11篇文章,涉及14项研究。对于ABCA1基因C69T多态性,合并了6项研究,共1854例AS病例和5744例对照,结果显示该变异与AS风险之间存在显著关联(T等位基因与C等位基因相比:OR =1.44,95%CI =1.04 - 1.24,p =0.005;T/T与C/C相比:OR =1.39,95%CI =1.12 - 1.73,p =0.003;T/T与C/T + C/C相比:OR =1.34,95%CI =1.09 - 1.65,p =0.006;T/T + C/T与C/C相比:OR =1.13,95%CI =1.01 - 1.27,p =0.040)。对于ABCA1基因V825I多态性,合并了8项研究,共2026例AS病例和8696例对照。该变异与AS风险之间无显著关联(I等位基因与V等位基因相比:OR =1.18,95%CI =0.90 - 1.53,p =0.230;I/I与V/V相比:OR =1.29,95%CI =0.75 - 2.23,p =0.360;I/I与V/I + V/V相比:OR =1.40,95%CI =0.87 - 2.26,p =0.160;I/I + V/I与V/V相比:OR =1.15,95%CI =1.00 - 1.33,p =0.060)。
本荟萃分析表明,ABCA1基因C69T多态性与AS风险增加相关。此外,ABCA1基因V825I多态性与AS风险之间无显著关联。