Compared with other angiotensin-converting enzyme (ACE) inhibitors, the eli
mination of temocapril is less dependent on renal function. To investigate
the metabolic and antihypertensive effects of temocapril in diabetic hypert
ensives, 30 patients with diabetes mellitus type 2 and mild to moderate hyp
ertension [diastolic blood pressure (BP) 90-115 mm Hg] and without azotemia
(plasma creatinine <180 mu M) were evaluated in a prospective randomized d
ouble-blind placebo-controlled study. After a 4-week placebo run-in, they r
eceived temocapril, 20 mg daily (n = 19), or placebo (n = 11) for 6 weeks.
Insulin sensitivity index (SI), determined by the Minimal Model method of B
ergman, serum lipoproteins, plasma renin activity, fibrinogen, and microalb
uminuria were assessed at the end of the placebo run-in phase and the doubl
e-blind treatment phases. Temocapril but not placebo administration produce
d a significant decrease in supine BP (152/92 +/- 5/3 vs. 162/98 +/- 5/2 mm
Hg; p < 0.01) and increase in plasma renin (p < 0.05). Variation of SI dur
ing temocapril treatment did not reach statistical significance (0.95 +/- 0
.2 before vs. 1.44 +/- 0.4 x 10(-4)/min/mU/L after treatment). During admin
istration of temocapril or placebo, no significant changes in fasting plasm
a glucose, insulin, and serum levels of total triglycerides, cholesterol, l
ipoprotein cholesterol fractions, or fibrinogen were observed. Microalbumin
uria decreased significantly on temocapril treatment (49 +/- 10 vs. 79 +/-
17 mg/24 h; p < 0.01) but not on placebo. These findings demonstrate that i
n hypertensive patients with diabetes mellitus type 2, short-term treatment
with temocapril is neutral to insulin sensitivity, lipoprotein metabolism,
and fibrinogen, and significantly reduces microalbuminuria.