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载脂蛋白关联磷脂酶 A2 基因 V279F 多态性与冠心病的关系:荟萃分析。

Lipoprotein-associated phospholipase A2 gene V279F polymorphisms and coronary heart disease: a meta-analysis.

机构信息

The Centre of Evidence Based Medicine, Academy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, No 1 Huatuo road, Shangjie University Town, Fuzhou, China.

出版信息

Mol Biol Rep. 2011 Aug;38(6):4089-99. doi: 10.1007/s11033-010-0529-9. Epub 2010 Nov 24.

Abstract

Lipoprotein-associated phospholipase A2 (LP-PLA2) may play an important role in the pathophysiology of coronary heart disease (CHD). The polymorphism of LP-PLA2 gene caused LP-PLA2 enzyme activity depressing or lost. But there is not a definite conclusion for the association of between the LP-PLA2 gene polymorphism and CHD risk. To assess the relationship between LP-PLA2 gene V279F polymorphism and CHD, a comprehensive Meta-analysis was performed. All the case-control studies evaluating the association of between the LP-PLA2 gene V279F polymorphism and CHD risk were identified. Seven case-control studies involving 3,614 patients with CHD and 4,334 controls were included. The crude odds ratios (ORs) of meta-analysis under the different gene model were not significant. But in the stratified analysis by study size, ethnicity, cases definition, and source of controls under the additive model, the association was evident in ethnicity for Japanese group (OR=1.38, 95%CI=1.22-1.56), cases definition for MI (OR=1.22, 95%CI=1.01-1.49), source of controls for the based-hospital (OR=1.42, 95%CI=1.24-1.59). These data suggested that the V279F polymorphism in LP-PLA2 gene may contribute to CHD development. But there is necessary that more well-designed large studies are required for the validation of this association.

摘要

脂蛋白相关磷脂酶 A2(LP-PLA2)可能在冠心病(CHD)的病理生理学中起重要作用。LP-PLA2 基因的多态性导致 LP-PLA2 酶活性降低或丧失。但是,LP-PLA2 基因多态性与 CHD 风险之间的关联尚无明确结论。为了评估 LP-PLA2 基因 V279F 多态性与 CHD 之间的关系,进行了一项综合的荟萃分析。确定了所有评估 LP-PLA2 基因 V279F 多态性与 CHD 风险之间关联的病例对照研究。纳入了 7 项病例对照研究,涉及 3614 例 CHD 患者和 4334 例对照。在不同基因模型下,荟萃分析的粗比值比(ORs)没有显著差异。但是,在按研究规模、种族、病例定义和对照来源进行分层分析时,在加性模型下,日本人群的种族关联明显(OR=1.38,95%CI=1.22-1.56),MI 的病例定义(OR=1.22,95%CI=1.01-1.49),基于医院的对照来源(OR=1.42,95%CI=1.24-1.59)。这些数据表明,LP-PLA2 基因中的 V279F 多态性可能导致 CHD 发展。但是,需要更多设计良好的大型研究来验证这种关联。

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