H. Shionoiri et al., EFFECT OF CILAZAPRIL THERAPY ON GLUCOSE AND LIPID-METABOLISM IN PATIENTS WITH HYPERTENSION, Clinical therapeutics, 17(6), 1995, pp. 1126-1135
The effects of long-term monotherapy with cilazapril, an angiotensin-c
onverting enzyme inhibitor, on blood pressure, glucose tolerance, and
serum lipid profiles were prospectively investigated in 66 patients wi
th hypertension: 23 with normal glucose tolerance and 43 with glucose
intolerance (including 9 patients with non-insulin-dependent diabetes
mellitus). The levels of plasma glucose, serum insulin, serum lipids,
glycated hemoglobin A(1c) (Hb A(1c)), and fructosamine were determined
before and during long-term (mean +/- SD, 26.2 +/- 1.2 weeks) therapy
with cilazapril. A 75-g oral glucose tolerance test was performed bef
ore and during treatment. Significant reductions in both systolic and
diastolic blood pressures in both patient groups were maintained durin
g the study. Neither fasting nor post-glucose load venous plasma gluco
se levels were altered in either group of patients, and no patient wit
h normal glucose tolerance developed diabetes mellitus during the stud
y. There was no significant change in the insulinogenic index (Delta s
erum insulin/Delta venous plasma glucose at 30 minutes post-glucose lo
ad) in either group, and glucose intolerance was slightly improved wit
h significant reductions (P < 0.01) in Hb A(1c) and fruc tosamine in t
he patient group with impaired glucose tolerance. Serum total choleste
rol (TC), low-density lipoprotein cholesterol, and triglyceride levels
were significantly (P < 0.01) decreased and high-density lipoprotein
cholesterol levels increased in patients with hypercholesterolemia (TC
levels greater than or equal to 5.69 mmol/L). These results suggest t
hat long-term cilazapril therapy may improve glucose and lipid metabol
ism in hypertensive patients with impaired glucose tolerance. Cilazapr
il also appears to be useful as an antihypertensive agent for hyperten
sive patients with either impaired glucose tolerance or hypercholester
olemia.