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1.
Blood Press ; 23(3): 174-80, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24066715

ABSTRACT

BACKGROUND: Compared with Caucasians, African Americans have lower heart rate variability (HRV) in the high-frequency domain, but there are no studies in blacks born and living in Africa. METHODS: In the Newer versus Older Antihypertensive agents in African Hypertensive patients trial (NCT01030458), patients (30-69 years) with uncomplicated hypertension (140-179/90-109 mmHg) were randomized to single-pill combinations of bisoprolol/hydrochlorothiazide (R) or amlodipine/valsartan (E). 72 R and 84 E patients underwent 5-min ECG recordings at randomization and 8, 16 and 24 weeks. HRV was determined by fast Fourier transform and autoregressive modelling. RESULTS: Heart rate decreased by 9.5 beats/min in R patients with no change in E patients (- 2.2 beats/min). R patients had reduced total (- 0.13 ms²; p = 0.0038) and low-frequency power (- 3.6 nu; p = 0.057), higher high-frequency (+ 3.3 nu; p = 0.050) and a reduced low- to high-frequency ratio (- 0.08; p = 0.040). With adjustment for heart rate, these differences disappeared, except for the reduced low-frequency power in the R group (- 4.67 nu; p = 0.02). Analyses confined to 39 R and 47 E patients with HRV measurements at all visits or based on autoregressive modelling were confirmatory. CONCLUSION: In native black African patients, antihypertensive drugs modulate HRV, an index of autonomous nervous tone. However, these effects were mediated by changes in heart rate except for low-frequency variability, which was reduced on beta blockade independent of heart rate.


Subject(s)
Antihypertensive Agents/therapeutic use , Heart Rate/drug effects , Hypertension/drug therapy , Hypertension/physiopathology , Africa South of the Sahara , Cohort Studies , Female , Humans , Male , Middle Aged
2.
Trials ; 13: 59, 2012 May 17.
Article in English | MEDLINE | ID: mdl-22594907

ABSTRACT

BACKGROUND: The epidemic surge in hypertension in sub-Saharan Africa is not matched by clinical trials of antihypertensive agents in Black patients recruited in this area of the world. We mounted the Newer versus Older Antihypertensive agents in African Hypertensive patients (NOAAH) trial to compare, in native African patients, a single-pill combination of newer drugs, not involving a diuretic, with a combination of older drugs including a diuretic. METHODS: Patients aged 30 to 69 years with uncomplicated hypertension (140 to 179/90 to 109 mmHg) and ≤2 associated risk factors are eligible. After a four week run-in period off treatment, 180 patients have to be randomized to once daily bisoprolol/hydrochlorothiazide 5/6.25 mg (R) or amlodipine/valsartan 5/160 mg (E). To attain blood pressure <140/<90 mmHg during six months, the doses of bisoprolol and amlodipine should be increased to 10 mg/day with the possible addition of up to 2 g/day α-methyldopa. RESULTS: At the time of writing of this progress report, of 206 patients enrolled in the run-in period, 140 had been randomized. At randomization, the R and E groups were similar (P ≥ 0.11) with respect to mean age (50.7 years), body mass index (28.2 kg/m(2)), blood pressure (153.9/91.5 mmHg) and the proportions of women (53.6%) and treatment naïve patients (72.7%). After randomization, in the R and E groups combined, blood pressure dropped by 18.2/10.1 mmHg, 19.4/11.2 mmHg, 22.4/12.2 mmHg and 25.8/15.2 mmHg at weeks two (n = 122), four (n = 109), eight (n = 57), and 12 (n = 49), respectively. The control rate was >65% already at two weeks. At 12 weeks, 12 patients (24.5%) had progressed to the higher dose of R or E and/or had α-methyldopa added. Cohort analyses of 49 patients up to 12 weeks were confirmatory. Only two patients dropped out of the study. CONCLUSIONS: NOAAH (NCT01030458) demonstrated that blood pressure control can be achieved fast in Black patients born and living in Africa with a simple regimen consisting of a single-pill combination of two antihypertensive agents. NOAAH proves that randomized clinical trials of cardiovascular drugs in the indigenous populations of sub-Saharan Africa are feasible.


Subject(s)
Amlodipine/therapeutic use , Antihypertensive Agents/therapeutic use , Bisoprolol/therapeutic use , Black People , Blood Pressure/drug effects , Hydrochlorothiazide/therapeutic use , Hypertension/drug therapy , Tetrazoles/therapeutic use , Administration, Oral , Adult , Africa South of the Sahara/epidemiology , Aged , Amlodipine/administration & dosage , Amlodipine, Valsartan Drug Combination , Antihypertensive Agents/administration & dosage , Bisoprolol/administration & dosage , Diuretics/therapeutic use , Drug Combinations , Female , Humans , Hydrochlorothiazide/administration & dosage , Hypertension/ethnology , Hypertension/physiopathology , Male , Middle Aged , Patient Dropouts , Patient Selection , Risk Factors , Tablets , Tetrazoles/administration & dosage , Time Factors , Treatment Outcome
3.
Blood Press ; 20(5): 256-66, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21495829

ABSTRACT

BACKGROUND: Sub-Saharan Africa experiences an epidemic surge in hypertension. Studies in African Americans led to the recommendation to initiate antihypertensive treatment in Blacks with a diuretic or a low-dose fixed combination including a diuretic. We mounted the Newer versus Older Antihypertensive Agents in African Hypertensive Patients (NOAAH) trial to compare in native African patients a fixed combination of newer drugs, not involving a diuretic, with a combination of older drugs including a diuretic. METHODS: Patients aged 30-69 years with uncomplicated hypertension (140-179/90-109 mmHg) and two or fewer associated risk factors are eligible. After a 4-week run-in period off treatment, 180 patients will be randomized to once daily bisoprolol/hydrochlorothiazide 5/6.25 mg or amlodipine/valsartan 5/160 mg. To attain and maintain blood pressure below 140/90 mmHg during 6 months of follow-up, the doses of bisoprolol and amlodipine in the combination tablets will be increased to 10 mg/day with the possible addition of α-methyldopa or hydralazine. NOAAH is powered to demonstrate a 5-mmHg between-group difference in sitting systolic pressure with a two-sided p-value of 0.01 and 90% power. NOAAH is investigator-led and complies with the Helsinki declaration. RESULTS: Six centers in four sub-Saharan countries started patient recruitment on September 1, 2010. On December 1, 195 patients were screened, 171 were enrolled, and 51 were randomized and followed up. The trial will be completed in the third quarter of 2011. CONCLUSIONS: NOAAH (NCT01030458) is the first randomized multicenter trial of antihypertensive medications in hypertensive patients born and living in sub-Saharan Africa.


Subject(s)
Antihypertensive Agents/administration & dosage , Black People , Blood Pressure/drug effects , Hypertension/drug therapy , Research Design , Adult , Africa South of the Sahara/epidemiology , Aged , Amlodipine/administration & dosage , Amlodipine/therapeutic use , Antihypertensive Agents/therapeutic use , Bisoprolol/administration & dosage , Bisoprolol/therapeutic use , Blood Pressure Monitoring, Ambulatory , Diuretics/administration & dosage , Diuretics/therapeutic use , Drug Combinations , Female , Humans , Hydralazine/administration & dosage , Hydralazine/therapeutic use , Hydrochlorothiazide/administration & dosage , Hydrochlorothiazide/therapeutic use , Hypertension/epidemiology , Hypertension/physiopathology , Male , Methyldopa/administration & dosage , Methyldopa/therapeutic use , Middle Aged , Risk Factors , Tetrazoles/administration & dosage , Tetrazoles/therapeutic use , Valine/administration & dosage , Valine/analogs & derivatives , Valine/therapeutic use , Valsartan
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