跳至主要内容
临床试验/NCT00448162
NCT00448162暂停不适用

The Chinese Mutation Hotspot of ENaC Causing Liddle's Syndrome and the Association of ENaC Variations and Hypertension

Peking Union Medical College1 个研究点 分布在 1 个国家目标入组 2,000 人开始时间: 2005年5月最近更新:
适应症

试验速览

阶段
不适用
状态
暂停
发起方
入组人数
2,000
试验地点
1

研究概览

简要总结

The variations of ENaC have an impact on the degradation of epithelial sodium channels and sodium reabsorption, and thus are associated with hypertension and hypokalemia.

Liddle's syndrome is a rare monogenic form of autosomal-dominant hypertension caused by truncating or missense mutations in the C-termini of epithelial sodium channel β- or γ-subunit encoded by SCNN1B or SCNN1G. Our purpose is to determine the hotspot of mutation causing Chinese Liddle's syndrome.

The second purpose is to determine wether the polymorphisms of ENaC are associated with hypertension in Chinese. Some polymorphisms of ENaC associated with hypertension may be genetic risk factors for Chinese hypertension.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
8 Years 至 70 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Clinical diagnosis of hypertension and Liddle's syndrome
  • Clinical diagnosis of normal controls with no cardiovascular disease

排除标准

  • Hypertension caused by other single gene mutation

研究者

发起方
Peking Union Medical College
申办方类型
Other

研究点 (1)

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