Ao. Marcus, ANTIHYPERTENSIVE THERAPY WITH THE CALCIUM-CHANNEL BLOCKER ISRADIPINE - AN APPROPRIATE CHOICE FOR THE DIABETIC PATIENT WITH HYPERTENSION - AREVIEW, Current therapeutic research, 54(6), 1993, pp. 763-778
Citations number
76
Categorie Soggetti
Pharmacology & Pharmacy","Medicine, Research & Experimental
Treatment of hypertension in diabetic patients or patients with impair
ed glucose tolerance requires a specialized approach. Such hypertensiv
e, glucose-impaired patients often have multiple medical problems, pos
sibly from common causes, such as renal impairment, atherosclerosis, e
lectrolyte disturbance, neuropathy, or cardiac dysfunction. Antihypert
ensive therapy in these high-risk, medically compromised patients must
reduce blood pressure while having a beneficial or neutral effect on
the diabetic state and other coexisting diseases with possible catastr
ophic end points. Isradipine is a second-generation, dihydropyridine-t
ype calcium channel blocker shown to be efficacious, safe, and well to
lerated in the treatment of diabetic patients with hypertension. In cl
inical trials of patients with insulin-dependent or non-insulin-depend
ent diabetes mellitus, monotherapy with isradipine normalized blood pr
essure in a majority of patients with minimal adverse reactions and no
clinically significant alteration of heart rate. More importantly, is
radipine had either a neutral or a beneficial effect on glucose homeos
tasis and lipid metabolism. In studies of nondiabetic patients with hy
pertension, isradipine has been shown to facilitate renal function by
decreasing renal vascular resistance, increasing renal plasma flow, an
d maintaining or improving glomerular filtration rate and filtration f
raction. These physiological effects may benefit patients with coexist
ing diabetes and hypertension, in whom end-stage renal disease is a co
mmon consequence. Studies to evaluate the effects of isradipine on a n
umber of parameters or conditions important to the diabetic patient, i
ncluding serum lipids, atherosclerosis, and proteinuria, are currently
in progress.