M. Maccario et al., EFFECTS OF 3-MONTH NIFEDIPINE TREATMENT ON ENDOCRINE-METABOLIC PARAMETERS IN PATIENTS WITH ABDOMINAL OBESITY AND MILD HYPERTENSION, Journal of endocrinological investigation, 21(1), 1998, pp. 56-63
It is widely accepted that abdominal obesity presents with exaggerated
insulin secretion, insulin resistance and a trend toward glucose into
lerance. Hypertension is frequently associated to abdominal obesity, a
nd hyperinsulinism could play a role in its pathogenesis. Some studies
reported that Ca-antagonists positively influence insulin sensitivity
and glucose tolerance in obese patients with normal or elevated brood
pressure. However, other studies reported worsening of metabolic bala
nce during treatment with Ca-antagonists in hypertensive non-insulin-d
ependent diabetes mellitus (NIDDM) patients and in normal subjects. We
studied 19 patients with abdominal obesity, mild hypertension and ins
ulin resistance on balanced, mild hypocaloric diet (1400 Kcal), to ver
ify the effects of the Ca-antagonist nifedipine on both basal and oral
glucose tolerance test (OGTT)-induced glucose and insulin levels as w
ell as on IGF-I basal and DHEA-S levels and fat mass (FM). To achieve
this goal, 10 hypertensive obese subjects (HOB-NIFE, 3 mates, 7 female
s, mean age+/-SD 44.6+/-1.7 yr; body mass index (BMI) 37.1+/-2.5 Kg/m(
2), WHR 0.95+/-0.02) received 3-month treatment with nifedipine (Adala
t Crono 30 Bayer, ? tab daily) while other 9 hypertensive obese (HOB,
3 males, 6 females, 42+/-2.4 yr, BMI 35.8+/-1.8 Kg/m(2), WHR 0.91+/-0.
03) were studied during diet only. The same parameters were studied al
so in 8 normotensive obese patients (OB: 3 males, 5 females, 48.1+/-2.
1 yr, BMI 35.8+/-2.4 Kg/m(2), WHR 0.90+/-0.03) on the same balanced hy
pocaloric diet. Basal systolic (SEP) and diastolic (DBP) blood pressur
e levels in HOB-NIFE and HOB were similar. At baseline, ail groups had
similar basal and OGTT-induced glucose, insulin and glucose insulin r
atio (GIR) levels as well as IGF-I and DHEA-S levels. After 3 months B
MI fell to the same extent in all groups (p<0.05 vs baseline) while WH
R and FFM/FM ratio did not change. SEP and DBP decreased HOB-NIFE (p<0
.02) but also during diet alone in both HOB and OB, though to a lesser
extent (p<0.05). Both basal and OGTT-stimulated glucose and insulin l
evers as well as IGF-I and DHEA-S levels were not modified in HOB-NIFE
as well as in HOB and OB. In conclusion, our data indicate that nifed
ipine treatment does not modify glucose tolerance as well as insulin s
ecretion and sensitivity, IGF-I and DHEA-S levels in hypertensive abdo
minal obese patients. Thus, nifedipine treatment has no detrimental ef
fects on endocrine-metabolic balance in hypertensive obese patients. (
C) 1998, Editrice Kurtis.