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凝血因子Ⅱ、Ⅴ基因多态性与脑梗死的关联研究 被引量:3

Relationship between gene polymorphisms of blood coagulation factors( Ⅱ and Ⅴ) and cerebral infarction
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摘要 目的探讨中国湖南长沙地区汉族人群中凝血因子Ⅱ(FⅡ)、凝血因子Ⅴ(FⅤ)基因单核苷酸多态性与脑梗死之间的关联。方法采用PCR及飞行时间质谱技术对351例确诊为脑梗死的汉族患者(病例组)及417例对照组FⅡ基因rs1799963位点、FⅤ基因rs6025位点进行基因分型。结果病例组FⅡ基因rs1799963位点基因型均为G/G,对照组中基因型为G/G和A/G。病例组与对照组中FⅤ基因rs6025位点基因型均为G/G。对基因型及等位基因频率进行χ2检验示,病例组FⅡ基因rs1799963位点的基因型分布与对照组相比较差异无统计学意义(P>0.05);病例组等位基因频率与对照组相比较差异无统计学意义(P>0.05)。Logistic回归分析示,FⅡ基因rs1799963位点多态性与脑梗死不相关(P>0.05)。结论 FⅡ基因rs1799963位点多态性和FⅤ基因rs6025位点多态性均可能与中国长沙汉族人群脑梗死之间不存在关联。 Objective To study the relationship between gene polymorphisms of blood coagulation factors( factor Ⅱ,FⅡ; factor Ⅴ,FⅤ) and cerebral infarction in the Han Chinese population from Changsha,Hunan Province,China. Methods Polymerase chain reaction and matrix-assisted laser desorption / ionization time-of-flight mass spectrometry were used for genotyping of FⅡ rs1799963 and FⅤ rs6025 in 351 patients diagnosed with cerebral infarction( patient group) and 417 healthy individuals undergoing physical examination( control group). All participants were Han Chinese selected from the Department of Neurology,Third Xiangya Hospital of Central South University,from June 2011 to July 2012. The distribution of genotypes and allele frequency were analyzed by the χ2test. The relationship between selected gene polymorphisms and cerebral infarction was examined by logistic regression analysis. Results The genotypes of FⅡ rs1799963 were G / G in the patient group and G / G plus G / A in the control group. The genotype of FⅤ rs6025 was G / G in all participants. The distribution of genotypes and allele frequency at FⅡ rs1799963 showed no significant difference between the patient and control groups( P 0. 05). The gene polymorphisms of FⅡ rs1799963 had no association with cerebral infarction( P 0. 05). Conclusions There may exist no associati. Conclusions on between the gene polymorphisms of blood coagulation factors( FⅡ rs1799963 and FⅤ rs6025) and cerebral infarction in the Han Chinese population from Changsha.
出处 《国际神经病学神经外科学杂志》 2014年第5期407-411,共5页 Journal of International Neurology and Neurosurgery
基金 中南大学青年教师助推项目(2012QNZT159)
关键词 脑梗死 单核苷酸多态性 凝血因子Ⅱ 凝血因子Ⅴ 基因 cerebral infarction single nucleotide polymorphism blood coagulation factor Ⅱ blood coagulation factor Ⅴ gene
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参考文献10

  • 1Kisialiou A,.Grella R,. Carrizzo A, et al. Risk factors and acute ischemic stroke subtypes. J Neurol Sci, 2014,339(1-2):41-46.
  • 2Sartori M, Favaretto E, Legnani C, et al. G20210A prothrombin mutation and critical limb ischaemia in patients with peripheral arterial disease. Eur J Vasc Endovasc Surg, 2009, 38(1): 113-117.
  • 3Weischer M, Juul K, Zacho J, et al. Prothrombin and risk of venous thromboembolism, ischemic heart disease and ischemic cerebrovascular disease in the general population. Atherosclerosis, 2010, 208(2): 480-483.
  • 4They-They TP, Battas O,Slassi I, et al. Prothrombin G20210A and factor V Leiden polymorphisms in stroke. J Mol Neurosci, 2012, 46(1): 210-216.
  • 5Favaretto E, Sartori M, Conti E, et al. G1691A factor V and G20210A FII mutations, acute ischemic stroke of unknown cause, and patent foramen ovale. Thromb Res, 2012, 130(5): 720-724.
  • 6孟强,蒲传强.青年脑梗死与凝血酶原G20210A突变关系的研究[J].临床神经病学杂志,2003,16(3):131-133. 被引量:1
  • 7Aznar J, Mira Y, Vaya A, et al. Factor V Leiden and prothrombin G20210A mutations in young adults with cryptogenic ischemic stroke. Thromb Haemost, 2004, 91(5): 1031-1034.
  • 8Shaheen K, Alraies MC, Alraiyes AH, et al. Factor V Leiden: how great is the risk of venous thromboembolism? Cleve Clin J Med, 2012, 79(4): 265-272.
  • 9Kita T, Banno F, Yanamoto H, et al. Large infarct and high mortality by cerebral ischemia in mice carrying the factor V Leiden mutation. J Thromb Haemost, 2012, 10(7): 1453-1455.
  • 10Herak DC. Inherited coagulation disorders in children with arterial ischemic stroke and transient ischemic attack. Clin Biochem, 2011, 44(7): 512-513.

二级参考文献9

  • 1Poort SR, Rosendaal FR, Reitsma PH, et al. A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis.Blood, 1996,88:3698.
  • 2Rosendaal FR, Siscovick DS, Schwarta SM, et al. A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women. Blood, 1997,90:1747.
  • 3Moerloose Ph, Wutschert R, Heinzmann M, et al. Superficial vein thrombosis of lower limbs: influence of factor V Leiden, Factor Ⅱ G20210A and overweight. Thromb Haemost, 1998,80:239.
  • 4Reuner KH, Bur A, Grau A, et al. Prothrombin gene G20210→ A transition is a risk foctor for cerebral venous thrombosis. Stroke, 1998,29:1765.
  • 5Stefano VD, Chiusolo P, Paciaroni K, et al. Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients. Blood, 1998,91:3562.
  • 6Bentolila S, Ripoll L, Drouet L, et al. Thrombophilia due to 20210GA pmthrombin polymorphism and cerebral ischenda in the young. Stroke,1997,28:1846.
  • 7Zenz W, Bondó Z, Plotho J, et al. Factor V Leiden and prothrombin gene G 20210 A variant in children with ischemic stroke. Thromb Haemost,1998,80:763.
  • 8Lu Y, Zhao Y, Liu G, et al. Factor V gene G1691A mutation,prothromhin gene G20210A mutation, and MTHFR gene C677T mutation are not risk factors for pulmonary thromboemholism in Chinese population.Thromb Res,2002,106:7.
  • 9常建华,张广森.缺血性脑卒中患者凝血酶原基因3′-UT G20210A变异频度的研究[J].湖南医科大学学报,2000,25(1):36-38. 被引量:4

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