NOCTURNAL REDUCTION OF BLOOD-PRESSURE AND THE ANTIHYPERTENSIVE RESPONSE TO A DIURETIC OR ANGIOTENSIN-CONVERTING ENZYME-INHIBITOR IN OBESE HYPERTENSIVE PATIENTS
Mr. Weir et al., NOCTURNAL REDUCTION OF BLOOD-PRESSURE AND THE ANTIHYPERTENSIVE RESPONSE TO A DIURETIC OR ANGIOTENSIN-CONVERTING ENZYME-INHIBITOR IN OBESE HYPERTENSIVE PATIENTS, American journal of hypertension, 11(8), 1998, pp. 914-920
During a 12-week, multicenter study to evaluate the efficacy and safet
y of lisinopril and hydrochlorothiazide (HCTZ) for the treatment of ob
esity-related hypertension, ambulatory blood pressure (ABP) monitoring
was performed both at baseline and at study completion in 124 patient
s. Patients were randomized to three groups: placebo, lisinopril (10,
20, or 40 mg/day), or HCTZ (12.5, 25, or 50 mg/day). All groups were m
atched with regard to sex, race, age, body mass index, and waist/hip r
atio. The primary analysis of ABP data revealed that both lisinopril a
nd HCTZ effectively lowered mean 24-h systolic (SBP) and diastolic (DB
P) blood pressure compared with placebo, (mean change from baseline SB
P/DBP: -12.0/-8.2, -10.6/-5.5, and -0.3/-0.5 mm Hg, respectively); how
ever, lisinopril lowered DBP better than HCTZ (P <.05). Secondary anal
yses of groups revealed that men responded better to lisinopril than H
CTZ (-11.9/-7.3 v -6.6/-3.5 mm Hg, respectively), whereas women respon
ded well to both drugs. White patients responded better to lisinopril
than HCTZ, whereas black patients showed a significant response to HCT
Z only. Response to treatment was also influenced by patient classific
ation of 24-h blood pressure profiles, ie, ''dipper'' or ''nondipper.'
' Overall, the majority of obese hypertensives were nondippers. Nondip
pers (n = 82) responded well to both drugs (-10.4/-6.9 v -12.5/-5.7 mm
Hg, P <.05 v placebo), whereas dippers (n 42) responded to lisinopril
(-11.7/-9.4 mm Hg, P <.05 v placebo and HCTZ), but not HCTZ (-5.6/-4.1
mn Hg, P = NS v placebo). Results of 24-h ABP data show that both lis
inopril and HCTZ are effective therapies for obesity-related hypertens
ion and that response to treatment is influenced by sex, race, and dip
per/nondipper status. Am J Hypertens 1998; 11:914-920. (C) 1998 Americ
an Journal of Hypertension, Ltd.