Both ECG and echo LVH are markers of increased risk, but there is much less information on interdrug differences in ECG LVH regression. Therefore, changes in ECG LVH prevalence were examined after 3 mos titration phase and a 1 yr maintenance phase of randomized double-blind treatment with atenolol (AT), captopril (CP), clonidine (CL), diltiazem (DT), hydrochlorothiazide (HZ), prazosin (PZ) or placebo (PL) in 570 men with mild-moderate hypertension. The prevalence of Sokolow-Lyon (SL) and Minnesota code (MC) criteria were evaluated, as well as precordial voltage (Svl+ Rv5). Percent changes from baseline were:Empty Cell% of patients with LVHPrecordial Voltage (mV*10)Empty CellSL+MCEmpty CellEmpty CellEmpty CellRXBase3 mos1 yrBase3 mos1 yrBase3 mas1 yrAT12+9*+917+7#+1527.1+0.6-0.1CP23-8*-433-7-428.10+0.2CL16+3022+5+228.4+0.3-0.4DT18+5+829+6+16@30.0-0.9-0.5HZ26-5-941-8#-9@29.4-0.5-1.5PZ23+1-433-1+328.4-0.1+0.7PL16+5-25+7-28.3+0.4+1.1*AT v CP 3 mos#HZ v AT 3 mos@HZ v DZ 1 yr (p < 0.05) AT v CP 3 mos HZ v AT 3 mos HZ v DZ 1 yr (p < 0.05) Thus, HZ caused a decrease in LVH prevalence, while AT and DT caused an increase. These changes are concordant with echo observations, where HZ was the only drug to significantly reduce LV mass for equal levels of systolic BP reduction.
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