SHORT CYCLES OF VERY-LOW-CALORIE DIET IN THE THERAPY OF OBESE TYPE-IIDIABETES-MELLITUS

Citation
Cm. Rotella et al., SHORT CYCLES OF VERY-LOW-CALORIE DIET IN THE THERAPY OF OBESE TYPE-IIDIABETES-MELLITUS, Journal of endocrinological investigation, 17(3), 1994, pp. 171-179
Citations number
30
Categorie Soggetti
Endocrynology & Metabolism
ISSN journal
03914097
Volume
17
Issue
3
Year of publication
1994
Pages
171 - 179
Database
ISI
SICI code
0391-4097(1994)17:3<171:SCOVDI>2.0.ZU;2-Z
Abstract
Very Low Calorie Diet (VLCD) is known to induce not only weight loss, but also an improvement of metabolic control, in obese type II diabeti cs. In order to evaluate the therapeutical efficacy of cycles of VLCD shorter than those previously described, 29 obese type II diabetics an d 31 obese nondiabetic subjects were entered as inpatients and prescri bed a 450 kcal/day diet for 15 days. Metabolic results obtained were s imilar to those achieved with longer cycles of VLCD, showing that 15 d ays are sufficient to induce a BMI decrease in diabetic (BMI from 35.3 +/-4.8 to 33.3+/-4.6 after VLCD) and nondiabetic patients (BMI from 40 .5+/-7.4 to 38.1+/-7.2 after VLCD), a desired fall of blood glucose le vels and the decrease of daily insulin needs in insulin-treated patien ts. Glucagon tests were performed before and after VLCD in order to st udy possible modifications of insulin secretion. Although we did not o bserve any significant increase of C-peptide basal or peak levels (nM/ ml) either in diabetic (basal levels before VLDC: 1.2+/-0.4 and peak l evels 2.4+/-0.7; basal after VLCD 1.23+/-0.6 and peak 2.6+/-0.7) and n ondiabetic patients (basal levels before VLDC 1.0+/-0.3 and peak level s 2.5+/-0.4; basal after VLCD 0.9+/-0.3 and peak 2.4+/-0.6). The rise of the C-peptide/glycemia ratio is an index of an improvement of insul in biological activity, which could be partly responsible for the ther apeutical effects of VLCD. In 5 diabetics and 5 obese nondiabetics, in sulin receptor number was determined on circulating lymphomonocytes at the beginning and at the end of VLCD. The improvement of insulin sens itivity in diabetic patients after VLCD, which was previously describe d, does not seem to depend upon an increase in the number or affinity of insulin receptors, and therefore should be mostly ascribed to possi ble modifications at a post-receptorial level.