FREQUENCY OF RENIN GENE RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM IN HYPERTENSIVES WITH A GENETIC PREDISPOSITION TO HYPERTENSION

Citation
T. Morise et al., FREQUENCY OF RENIN GENE RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM IN HYPERTENSIVES WITH A GENETIC PREDISPOSITION TO HYPERTENSION, Hormone research, 41(5-6), 1994, pp. 218-221
Citations number
23
Categorie Soggetti
Endocrynology & Metabolism
Journal title
ISSN journal
03010163
Volume
41
Issue
5-6
Year of publication
1994
Pages
218 - 221
Database
ISI
SICI code
0301-0163(1994)41:5-6<218:FORGRI>2.0.ZU;2-1
Abstract
The genetic basis of essential hypertension is still uncertain. Becaus e renin is thought to be a candidate gene for essential hypertension, a prospective study was conducted to compare the frequency of renin ge ne HindIII restriction fragment length polymorphism (RFLP) in normoten sive and hypertensive subjects without (HTG-) and with a genetic predi sposition to essential hypertension (HTG+). The frequency of the 9.0-k b fragment was significantly (p < 0.05) higher in the HTG+ group than in the normotensive and HTG- groups. An association between renin RFLP and hypertension in man was shown for the first time. It is suggested that a gene for blood pressure regulation has been localized to a par t of the genome close to, or identical to, the renin locus.