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. 2011 Feb 5;13(6):404–412. doi: 10.1111/j.1751-7176.2011.00437.x

Table I.

 Demographics and Baseline Characteristics

Characteristics Total Cohort (N=999) ABPM Cohorta (N=243)
Age, mean (SD), y      55.6 (11.4)       56.6 (10.1)
 ≥65 y, No. (%) 228 (22.8) 54 (22.2)
Women, No. (%) 491 (49.1) 113 (46.5)
Weight, mean (SD), kg 88.2 (21.5) 89.7 (20.8)
BMI, mean (SD), kg/m2 31.0 (6.4) 31.4 (6.5)
Race, No. (%)
 Caucasian 630 (63.1) 169 (69.5)
 Black 234 (23.4) 47 (19.3)
 Asian 129 (12.9) 26 (10.7)
 American Indian/Alaskan Native 6 (0.6) 1 (0.4)
Ethnicity, No. (%)
 Hispanic or Latino 105 (10.5) 33 (13.6)
Type 2 diabetes, No. (%) 192 (19.2) 32 (13.2)
Metabolic syndrome, No. (%) 462 (46.2) 107 (44.0)
Prior monotherapy, No. (%)
 ACE inhibitor 289 (28.9)
 ARB 237 (23.8)
 Diuretic 167 (16.7)
 DHP‐CCB 118 (11.8)
 β‐Blocker 115 (11.5)
 Non–DHP‐CCB 20 (2.0)
 Other 20 (2.0)
 Noneb 33 (3.3)
SeSBP, mean (SD), mm Hg 153.7 (9.2) 153.5 (8.8)
SeDBP, mean (SD), mm Hg 91.9 (8.6) 91.3 (7.7)
Ambulatory SBP, mean (SD), mm Hg NA 135.8 (11.7)
Ambulatory DBP, mean (SD), mm Hg NA 81.3 (9.0)

Abbreviations: ABPM, ambulatory blood pressure (BP) monitoring; ACE, angiotensin‐converting enzyme; ARB, angiotensin II receptor blocker; BMI, body mass index; DBP, diastolic BP; DHP‐CCB, dihydropyridine–calcium channel blocker; NA, not available; SBP, systolic BP; SD, standard deviation; Se, seated. aABPM cohort was monitored for 24 hours at baseline, week 12, and week 20. bDid not take antihypertensive therapy within 1 day prior to the first amlodipine/olmesartan medoxomil dose. Note that 11 patients received triamterene/hydrochlorothiazide combination therapy prior to study entry. This was the only combination allowed per protocol due to triamterene’s weak activity and potassium‐sparing effects.