RELATIONS BETWEEN FASTING SERUM-INSULIN, GLUCOSE, AND DIHYDROEPIANDROSTERONE-SULFATE CONCENTRATIONS IN OBESE PATIENTS WITH HYPERTENSION - SHORT-TERM EFFECTS OF ANTIHYPERTENSIVE DRUGS
Nt. Fuenmayor et al., RELATIONS BETWEEN FASTING SERUM-INSULIN, GLUCOSE, AND DIHYDROEPIANDROSTERONE-SULFATE CONCENTRATIONS IN OBESE PATIENTS WITH HYPERTENSION - SHORT-TERM EFFECTS OF ANTIHYPERTENSIVE DRUGS, Journal of cardiovascular pharmacology, 30(4), 1997, pp. 523-527
A randomized, single-blind, placebo-controlled study was conducted in
82 obese patients with mild to moderate essential hypertension, to det
ermine the incidence of hyperinsulinemia, the relations between fastin
g insulin and dihydroepiandrosterone-sulfate (DHEA-S) levels, and the
short-term effects of antihypertensives on DHEA-S and insulin serum co
ncentrations. Increased insulin/glucose ratios (IGR) suggestive of ins
ulin resistance were found in half of our patients. Hyperinsulinemic a
nd normoinsulinemic obese patients with hypertension had comparable fa
sting glucose and DHEA-S concentrations and comparable blood pressure
(BP) levels. Thus no relations were found between fasting insulin and
DHEA-S levels. Fasting hyperinsulinemia was found in only half of the
obese subjects with hypertension, suggesting that not all obese patien
ts with hypertension are at the same high cardiovascular risk. Short-t
erm treatment with captopril, prazosin, verapamil, atenolol, or hydroc
hlorothiazide (HCTZ) reduced BP; greater BP reduction was observed wit
h drugs with vasodilatory effects. Captopril, prazosin, and verapamil
reduced fasting insulin levels, whereas atenolol and hydrochlorothiazi
de did not. The former drugs reduced fasting insulin levels that were
either within normal limits or in the hyperinsulinemic range. None of
the drug treatments produced significant increases in serum DHEA-S con
centrations, although some of them considerably reduced fasting insuli
n levels. No relations between insulin and DHEA-S levels were observed
either at baseline or at the end of the antihypertensive treatment. T
he BP reduction resulting from the peripheral vasodilation may explain
the insulin-reducing action of captopril, verapamil, and prazosin. Th
ese results further emphasize the large heterogeneity present in the p
athophysiologic mechanisms operating in obesity and hypertension.