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载脂蛋白E基因变异与冠心病风险:一项荟萃分析。

Apolipoprotein E Gene Variants and Risk of Coronary Heart Disease: A Meta-Analysis.

作者信息

Xu Min, Zhao Jun, Zhang Yu, Ma Xu, Dai Qiaoyun, Zhi Hong, Wang Bei, Wang Lina

机构信息

Key Laboratory of Environmental Medicine Engineering, Ministry of Education, Department of Epidemiology and Biostatistics, School of Public Health, Southeast University, Nanjing, China.

Graduate School of Peking Union Medical College, Beijing, China; National Research Institute for Family Planning, Beijing, China.

出版信息

Biomed Res Int. 2016;2016:3912175. doi: 10.1155/2016/3912175. Epub 2016 Oct 27.

Abstract

. genes involved in lipoprotein synthesis and metabolism are considered one of the candidates to CHD. However, the results remain conflicting. . We performed this meta-analysis based on 30 published studies including 11,804 CHD patients and 17,713 controls. . Compared with the wild genotype E3/3, the variant genotypes E3/4 and E4/4 were associated with 22% and 45% increased risk of CHD, respectively (E3/4 versus E3/3: OR = 1.22, 95% CI = 1.15-1.29; E4/4 versus E3/3: OR = 1.45, 95% CI = 1.23-1.71). Besides, compared with 3 allele, carriers with the 4 allele had a 46% increased risk of CHD (OR = 1.46, 95% CI = 1.28-1.66), while the 2 had no significantly decreased risk of CHD. In the subgroup analysis by ethnicity, 4 had a 25% increased risk of CHD in Caucasians (OR = 1.25, 95% CI = 1.11-1.41), and the effects were more evident in Mongolians (OR = 2.29, 95% CI = 1.89-2.77). The 2 allele had a decreased risk of CHD in Caucasians (OR = 0.84, 95% CI = 0.74-0.96), but not in Mongolians. . The analysis suggested that 4 mutation was associated with the increased risk of CHD, while 2 allele had a decreased risk of CHD just in Caucasians.

摘要

参与脂蛋白合成与代谢的基因被认为是冠心病的候选基因之一。然而,结果仍存在矛盾。我们基于30项已发表的研究进行了这项荟萃分析,其中包括11804例冠心病患者和17713例对照。与野生基因型E3/3相比,变异基因型E3/4和E4/4分别使冠心病风险增加22%和45%(E3/4与E3/3相比:比值比=1.22,95%置信区间=1.15 - 1.29;E4/4与E3/3相比:比值比=1.45,95%置信区间=1.23 - 1.71)。此外,与3等位基因相比,携带4等位基因的个体患冠心病的风险增加46%(比值比=1.46,95%置信区间=1.28 - 1.66),而2等位基因并未使冠心病风险显著降低。在按种族进行的亚组分析中,4等位基因在白种人中使冠心病风险增加25%(比值比=1.25,95%置信区间=1.11 - 1.41),在蒙古人中影响更明显(比值比=2.29,95%置信区间=1.89 - 2.77)。2等位基因在白种人中使冠心病风险降低(比值比=0.84,95%置信区间=0.74 - 0.96),但在蒙古人中并非如此。该分析表明,4突变与冠心病风险增加相关,而2等位基因仅在白种人中使冠心病风险降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf7e/5102878/1dbd772df85d/BMRI2016-3912175.001.jpg

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