Hypertension Clinical Trial
Verified date | May 2009 |
Source | Peking Union Medical College |
Contact | n/a |
Is FDA regulated | No |
Health authority | China: Ministry of Health |
Study type | Observational |
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.
Status | Suspended |
Enrollment | 2000 |
Est. completion date | December 2009 |
Est. primary completion date | |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 8 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Clinical diagnosis of hypertension and Liddle's syndrome - Clinical diagnosis of normal controls with no cardiovascular disease Exclusion Criteria: - Hypertension caused by other single gene mutation |
Observational Model: Cohort, Time Perspective: Cross-Sectional
Country | Name | City | State |
---|---|---|---|
China | FuWai Hospital | Beijing | Beijing |
Lead Sponsor | Collaborator |
---|---|
Peking Union Medical College |
China,
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