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作 者:宋芸[1] 林岫芳[1] 王东伟[1] 董丹丹[1]
机构地区:[1]中山大学附属第五医院心内1科,广东珠海519000
出 处:《第四军医大学学报》2007年第22期2075-2078,共4页Journal of the Fourth Military Medical University
基 金:珠海市科技局资助(PC20061071)
摘 要:目的:探讨E-选择素(E-selectin)+G98T,+A561C基因多态性与原发性高血压及左室重构的关系.方法:对105例原发性高血压患者(高血压组)及94健康正常人(对照组)进行E-selectin+G98T,+A561C基因多态性检测及超声心动图、血脂水平检测.结果:①E-selectin+A561C各基因型在原发性高血压组和对照组间的分布差异存在统计学意义(P<0.05);②E-selectin+G98T基因型在原发性高血压组和对照组间的分布差异无统计学意义(P>0.05);等位基因频率在两组中分布差异亦无统计学意义(P>0.05);③原发性高血压组内,AC-CC基因型更倾向于发生左室肥厚(P<0.05);④原发性高血压组和对照组E-selectin+G98T位点及+A561C位点各基因型组间血脂水平比较差异均无统计学意义(P>0.05).结论:E-selectin+A561C位点单核苷酸多态性与原发性高血压具有相关关系,C等位基因可能是原发性高血压发病的遗传易感基因.C等位基因原发性高血压患者更倾向于出现左室重构.AM: To study the relationship between E-selectin gene polymorphisms and left ventricle reeonstitution in patients with essential hypertension. METHODS: Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method was used to determine + G98T and + A561C locus mutation polymorphisms in E-seletin gene in patients with essential hypertension and controls. Automated Biochemical Analyzer was used to measure the serum lipids. RESULTS. (1) There was significant difference in frequencies of genotype in E-selectin + A561C polymorphism between the essential hypertension group and the control group ( P 〈 0.05 ). (2) There was no significant difference in distribution of the E-selectin gene + G98T genotype between the essential hypertension group and the control group (P 〉 0. 05 ). (3) In essential hypertension group, AC-CC genotype was prone to suffer the left ventricle reeonstitution ( P 〈 0. 05 ). (4) There was no significant difference in the levels of serum lipids for different genotypes of + G98T or + A561C locus between the essential hypertension group and the control group. CONCLUSION: E-selectin gene + A561C polymorphism is associated with essential hypertension. C allele may be a risk factor for essential hypertension, and essential hypertension patients with C allelt are prone to suffer left ventricle reeonstitution.
分 类 号:R544.1[医药卫生—心血管疾病]
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