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T102C GENETIC POLYMORPHISM OF THE 5-HT2A RECEPTOR IN CHINESE HYPERTENSIVE PATIENTS AND HEALTHY CONTROLS.
- Source :
-
Clinical & Experimental Pharmacology & Physiology . Dec2004, Vol. 31 Issue 12, p847-849. 3p. - Publication Year :
- 2004
-
Abstract
- 1. The 5-HT2A receptor belongs to the G-protein superfamily. It plays an important role in vascular regulation. 2. Previous reports in the UK have indicated that there is an association of the T102C genetic polymorphism of the 5-HT2A receptor with hypertension, but no studies have been made on the T102C genetic polymorphism in Chinese hypertensive patients. In the present study, we investigated the T102C genetic polymorphism of 5-HT2A receptors in Chinese hypertensive patients to determine whether there is an association of this polymorphism with hypertension in Chinese. 3. The present study was conducted on 198 hypertensive patients and 164 healthy controls. Polymerase chain reaction-restriction fragment length polymorphism was used to identify the T102C genetic polymorphism of the 5-HT2A receptor. 4. In the present study, the C allele frequency of the 5-HT2A receptor genetic polymorphism was 0.343 in hypertensive patients, which was not significantly different to that in healthy controls (0.393; χ² = 1.922; P = 0.166; odds ratio = 0.807, 95% confidence interval 0.596-1.093). In addition, no gender differences were observed. 5. In conclusion, to our knowledge, this is the first report on the T102C genetic polymorphism of the 5-HT2A receptor in Chinese hypertensive patients. We find that no correlation exists between the T102C genetic polymorphism and hypertension, which affords useful information on the pathogenesis of hypertension in the Chinese population. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 03051870
- Volume :
- 31
- Issue :
- 12
- Database :
- Academic Search Index
- Journal :
- Clinical & Experimental Pharmacology & Physiology
- Publication Type :
- Academic Journal
- Accession number :
- 15636964
- Full Text :
- https://doi.org/10.1111/j.1440-1681.2004.04124.x