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作 者:孙志军[1] 李妍[2] 吕晶玉[2] 时景璞[3] 李岭[2] 赵彦艳[2]
机构地区:[1]中国医科大学附属盛京医院心内科,辽宁沈阳110004 [2]中国医科大学医学遗传学教研室,辽宁沈阳110001 [3]中国医科大学流行病学教研室,辽宁沈阳110001
出 处:《中国实用内科杂志:临床前沿版》2006年第12期1974-1976,共3页
基 金:国家自然科学基金资助(30300204)
摘 要:目的阐明WNK4基因G1816T多态性与原发性高血压的关系。方法2001年3~10月选择中国东北高血压病高发地区辽宁省彰武县采集的259例原发性高血压患者和235名健康对照组的血样应用聚合酶链反应-限制性长度片段长度多态性分析(PCR—RFLP)方法检测G1816T多态,结果经测序验证,同时检测所有人群的血糖、血脂等生化指标。结果原发性高血压组WNK4基因G1816T多态T等位基因频率显著高于对照组(25.9%对20.2%,P=0.035);AS和SS基因型与收缩压及舒张压升高密切相关(P分别为0.041和0.032)。结论WNK4基因G1816T多态与高血压密切相关。Objective To elucidate the association of WNK4 gene G1816T polymorphism with essential hypertension. Methods Genotyping was performed using polymerase chain reaction -restriction fragment length polymorphism ( PCR - RFLP) and confirmed by direct sequencing. 259 unrelated patients with essential hypertension and 235 unrelated normal controls were recruited. All the subjects had routine laboratory tests. Results The frequency of the T allele of exon8 G1816T polymorphism in hypertension group is significantly higher than that in controls (25. 9% versus 20. 2%, P = 0. 035 ). The AS and SS genotypes were closely associated with raised systolic and diastolic blood pressure ( P =0. 041, 0. 032 respectively). Conclusion The WNK4 gene G1816T polymorphism is associated with essential hypertension.
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