Angiotensinogen and angiotensin-converting enzyme genotypes, and day and night blood pressures in elderly Japanese hypertensives

There are inconsistent reports that the angiotensinogen (ATG) variant Met(2 35)-->Thr (T235) allele and angiotensin converting enzyme (ACE) insertion/d eletion (I/D) variants are associated with hypertension and related target organ damage. Both high blood pressure (BP) and abnormal diurnal BP variati on patterns are related to target organ damage, but it is not known whether the above genetic variants of the renin-angiotensin system are related to 24 h BP and the diurnal BP pattern in Japanese. We studied the association of the ATG T235 allele and ACE D allele with 24 h BP and diurnal BP variati on in 235 of 262 consecutive untreated (or off medication) elderly Japanese hypertensives who underwent 24 h ambulatory BP monitoring. There was no si gnificant association between the T235 or ACE D allele with office BP, but the T235 allele was significantly associated with 24 h BP and day BP, and t he D allele was significantly associated with increased 24 h BP, day BP, an d night BP, There were no effects of the T235 or D alleles on any BP parame ters. Those with white-coat hypertension had a significantly lower T235 all ele frequency (0.68) than those with sustained hypertension (0.79, p = 0.01 0), but the difference in D allele frequency was marginal (0.30 vs. 0.38, p = 0.057). In conclusion, in elderly Japanese hypertensive individuals, bot h the ATG T 235 and ACE D alleles are associated with increased 24 h BP and day BP, while only the ACE D allele is associated with increased night BP.