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CRP 基因多态性预测汉族人群脑卒中后功能结局。

CRP gene polymorphism predicts post-stroke functional outcome in Han Chinese.

机构信息

Department of Neurology, West China Hospital of Sichuan University, Chengdu, China.

出版信息

Acta Neurol Scand. 2014 Apr;129(4):263-8. doi: 10.1111/ane.12180. Epub 2013 Aug 23.

Abstract

OBJECTIVES

Stroke is a major cause of long-term disability and morbidity worldwide. C-reactive protein (CRP), an inflammatory marker, has been reported to be an independent predictor of functional outcome after ischemic stroke (IS). Because several single nucleotide polymorphisms (SNPs) at the CRP locus have been linked with elevated CRP levels, we hypothesized that CRP genetic variation might be associated with functional disability in patients after first-ever IS.

METHODS

A total of 1716 patients from western China with first-ever IS were genotyped for the CRP SNPs rs1130864 and rs1800947 using the ligation detection reaction method. Functional outcome was assessed 3 months after IS using the modified Rankin Scale. Then, we tested the association of CRP SNP genotypes with stroke outcome after adjusting for non-genetic factors.

RESULTS

Our data showed a significant association between the T allele of rs1130864 and poor functional outcome in IS patients. In addition, the presence of TT+CT genotypes of rs1130864 strongly predicted functional disability within the first 3 months, even after adjusting for potential confounders.

CONCLUSIONS

Our study indicates that SNP rs1130864 in the CRP gene is an independent predictor of 3-month functional outcome in patients with first-onset IS in a Han Chinese population. Further studies in different ethnic groups are needed to validate our findings.

摘要

目的

卒中是全世界导致长期残疾和发病的主要原因。C 反应蛋白(CRP),一种炎症标志物,据报道是缺血性卒中(IS)后功能结局的独立预测因子。由于 CRP 基因座的几个单核苷酸多态性(SNP)与 CRP 水平升高有关,我们假设 CRP 遗传变异可能与首次 IS 后患者的功能障碍有关。

方法

采用连接酶检测反应法,对来自中国西部的 1716 例首次 IS 患者进行 CRP SNP rs1130864 和 rs1800947 的基因分型。IS 后 3 个月采用改良 Rankin 量表评估功能结局。然后,我们在调整非遗传因素后,检验 CRP SNP 基因型与卒中结局的相关性。

结果

我们的数据显示,rs1130864 的 T 等位基因与 IS 患者的不良功能结局显著相关。此外,rs1130864 的 TT+CT 基因型的存在强烈预测了卒中后 3 个月内的功能障碍,即使在调整了潜在的混杂因素后也是如此。

结论

本研究表明,CRP 基因中的 SNP rs1130864 是汉族人群首发 IS 患者 3 个月功能结局的独立预测因子。需要在不同种族群体中进行进一步的研究来验证我们的发现。

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