Why the study?
Does aggressive inhibition of the renin-angiotensin system with maximal doses of benazepril plus losartan improve microalbuminuria and surrogate markers of atherosclerosis compared to low-dose benazepril in type 2 diabetic patients?
Does aggressive inhibition of the renin-angiotensin system with maximal doses of benazepril plus losartan improve microalbuminuria and surrogate markers of atherosclerosis compared to low-dose benazepril in type 2 diabetic patients?
Aggressive dual renin-angiotensin system inhibition with benazepril and losartan does not improve microalbuminuria or surrogate markers of atherosclerosis compared to low-dose benazepril alone in type 2 diabetics.
Offers no benefit over low-dose monotherapy for microalbuminuria or atherosclerosis markers in T2DM; challenges routine intensification of RAS inhibition.
Objective. This study compares low dose versus aggressive inhibition of the renin angiotensin system (RAS) to treat microalbuminuria (MA). Methods. Patients with MA after a run-in period to control BP to <130/80 mm Hg with 10 mg benazepril plus other drugs and HbA1c levels to <8.0% were randomized to either continue 10 mg benazepril (N = 12) or to take maximal doses of benazepril plus losartan in monthly stepwise increases to achieve normoalbuminuria (N = 11). Because MA is associated with CVD and inflammation, carotid intima medial thickness (CIMT) and endothelial function by peripheral arterial tonometry (PAT) as surrogate indices of atherosclerosis and highly sensitive C-reactive protein (hs-CRP) to assess inflammation were measured every six months. Results. BP, HbA1c levels, albumin : creatinine ratios, CIMT, PAT, and hs-CRP did not differ over a mean of 12 months between the two groups. Conclusions. Aggressive inhibition of the RAS is unnecessary to treat MA.
No takes yet. Share an insight, caveat, or question.
Davidson et al. (2011) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
More from ISRN Endocrinology