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An rs13293512 polymorphism in the promoter of let-7 is associated with a reduced risk of ischemic stroke.
Zhang, Li; Yang, Junsu; Xue, Qiang; Yang, Dong; Lu, Yibing; Guang, Xuefeng; Zhang, Weihua; Ba, Ruiqiong; Zhu, Hongwen; Ma, Xiang.
Afiliación
  • Zhang L; Department of Neurology, The First People's Hospital of Qujing City, Qingjing, 655000, Yunnan, China.
  • Yang J; Department of Neurology, The First People's Hospital of Qujing City, Qingjing, 655000, Yunnan, China.
  • Xue Q; Department of Cardiology, Yanan Hospital of Kunming, Kunming, 650051, Yunnan, China. xueqiang3513@126.com.
  • Yang D; Department of Cardiology, Yanan Hospital of Kunming, Kunming, 650051, Yunnan, China. yd707@163.com.
  • Lu Y; Department of Cardiology, Yanan Hospital of Kunming, Kunming, 650051, Yunnan, China.
  • Guang X; Department of Cardiology, Yanan Hospital of Kunming, Kunming, 650051, Yunnan, China.
  • Zhang W; Department of Cardiology, Yanan Hospital of Kunming, Kunming, 650051, Yunnan, China.
  • Ba R; Department of Neurology, The First People's Hospital of Qujing City, Qingjing, 655000, Yunnan, China.
  • Zhu H; Department of Neurology, The First People's Hospital of Qujing City, Qingjing, 655000, Yunnan, China.
  • Ma X; Department of Neurology, The First People's Hospital of Qujing City, Qingjing, 655000, Yunnan, China.
J Thromb Thrombolysis ; 42(4): 610-5, 2016 Nov.
Article en En | MEDLINE | ID: mdl-27530126
The expression of let-7 family members was differentiated in ischemic stroke (IS), functioning as an important regulating molecular in the pathophysiology of stroke. We hypothesized that genetic polymorphism in the promoters of let-7 family may be associated with the risk of IS. To test this hypothesis, we investigated the association of the rs10877887 and rs13293512 in the promoters of let-7 family with the susceptibility to IS. A hospital-based case-control study was performed. The rs10877887 genotype was determined by using a polymerase chain reaction-restriction fragment length polymorphism assay, and the rs13293512 genotype was determined by using a TaqMan assay. We found that the rs13293512CC genotype was associated with a reduced risk of IS (CC vs. TT: adjusted OR = 0.43, 95 % CI 0.26-0.71; dominant model: adjusted OR = 0.70, 95 % CI 0.49-0.98; recessive model: adjusted OR = 0.45, 95 % CI, 0.28-0.73). Stratification analysis showed that the rs10877887TT carriers had a higher level of total cholesterol compared to rs10877887TC/CC carriers (P = 0.03). Combined analysis showed that the rs10877887TC/CC and rs13293512TC/CC genotypes had a reduced risk of IS risk (adjusted OR = 0.58, 95 % CI 0.36-0.95). Our findings suggest that the rs13293512 polymorphism may be a protective factor for the development of IS.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Isquemia Encefálica / Regiones Promotoras Genéticas / Accidente Cerebrovascular / MicroARNs Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Thromb Thrombolysis Asunto de la revista: ANGIOLOGIA Año: 2016 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Isquemia Encefálica / Regiones Promotoras Genéticas / Accidente Cerebrovascular / MicroARNs Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Thromb Thrombolysis Asunto de la revista: ANGIOLOGIA Año: 2016 Tipo del documento: Article País de afiliación: China