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CD40 基因 5' 非翻译区单核苷酸多态性与缺血性脑卒中相关。

Single nucleotide polymorphism of CD40 in the 5'-untranslated region is associated with ischemic stroke.

机构信息

Department of Neurology, Affiliated Hospital of North Sichuan Medical College, Nanchong 637000, PR China.

出版信息

Gene. 2013 Oct 25;529(2):257-61. doi: 10.1016/j.gene.2013.07.086. Epub 2013 Aug 14.

Abstract

OBJECTIVES

Ischemic stroke is influenced by both environmental and genetic factors. The CD40/CD40L system is related to proinflammatory and prothrombogenic responses, which are involved in the pathophysiology of ischemic stroke. The aim of this study was to evaluate association between the CD40 -1C/T single nucleotide polymorphism (SNP) and ischemic stroke in a Chinese population.

METHODS

We conducted a case-control study including 286 ischemic stroke patients and 336 controls. CD40 -1C/T SNP was genotyped using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and DNA sequencing methods, and evaluated its relevance to ischemic stroke susceptibility.

RESULTS

Significantly increased ischemic stroke risk was found to be associated with the T allele of CD40 -1C/T (OR=1.273, 95% CI=1.016-1.594). The frequencies of CT and TT/CT genotypes of CD40 -1C/T in ischemic stroke patients were significantly higher than those of controls, respectively (for CT: OR=2.350, 95% CI=1.601-3.449; for TT/CT: OR=2.148, 95% CI=1.479-3.119). And, similar results were obtained after adjusting non-matched variables. We found that the frequency of carried T genotypes (TT and TT/CT) was significantly increased in patients with history of stroke compared with patients without (for TT: OR=6.538, 95%CI=1.655-25.833; for TT/CT: OR=3.469, 95%CI=1.031-11.670), respectively.

CONCLUSIONS

The findings suggested that the CD40 -1C/T polymorphism might contribute to the susceptibility to ischemic stroke in the Chinese population, and might be associated with history of previous stroke.

摘要

目的

缺血性脑卒中受环境和遗传因素的影响。CD40/CD40L 系统与促炎和促血栓形成反应有关,这些反应涉及缺血性脑卒中的病理生理学。本研究旨在评估 CD40-1C/T 单核苷酸多态性(SNP)与中国人群缺血性脑卒中之间的关系。

方法

我们进行了一项病例对照研究,纳入了 286 例缺血性脑卒中患者和 336 例对照。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)和 DNA 测序方法检测 CD40-1C/T SNP,并评估其与缺血性脑卒中易感性的相关性。

结果

发现 CD40-1C/T 的 T 等位基因与缺血性脑卒中风险显著增加相关(OR=1.273,95%CI=1.016-1.594)。与对照组相比,缺血性脑卒中患者 CD40-1C/T 的 CT 和 TT/CT 基因型的频率明显更高(对于 CT:OR=2.350,95%CI=1.601-3.449;对于 TT/CT:OR=2.148,95%CI=1.479-3.119)。并且,在调整非匹配变量后,得到了相似的结果。我们发现,与无脑卒中病史的患者相比,有脑卒中病史的患者携带 T 基因型(TT 和 TT/CT)的频率明显增加(对于 TT:OR=6.538,95%CI=1.655-25.833;对于 TT/CT:OR=3.469,95%CI=1.031-11.670)。

结论

研究结果表明,CD40-1C/T 多态性可能导致中国人群缺血性脑卒中易感性增加,并可能与既往脑卒中病史有关。

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