Repaglinide is a novel, rapid-acting prandial glucose regulator. To investi
gate the effect of repaglinide, 1 mg before each meal, in maintaining glyca
emic control in Type 2 diabetic patients who either miss a meal or have an
extra meal, 25 patients were randomized to either a fixed-meal regimen of t
hree meals/day or one of two mixed-meal regimens consisting of repeating pa
tterns of two, three or four meals/day over a 20-day period. On the 21st da
y each patient received three meals. Overall glycaemic control was assessed
by weekly serum fructosamine concentrations and 13-point and 37-point seru
m glucose profiles. Mean fructosamine concentrations decreased significantl
y to normal values during the treatment period (from 3.10 to 2.68 mg/dl on
the fu;ed-meal regimen and from 3.37 to 2.85 mg/dl on the mixed-meal regime
ns; P < 0.05), with no statistically significant difference in glucose cont
rol between the fixed-meal and mixed-meal regimen groups. Fasting serum glu
cose levels decreased slightly in both groups, but were not altered by the
number of meals consumed. Similarly, serum glucose profiles were not altere
d significantly by the number of meals consumed. Repaglinide was well toler
ated, and no hypoglycaemic events were reported. Serum cholesterol levels w
ere significantly reduced (P < 0.05) in both the fixed-meal and mixed-meal
groups, as were triglyceride levels in the mixed-meal group (P < 0.05). It
was concluded that meal-associated treatment with repaglinide was well tole
rated irrespective of the number of meals consumed/day. Thus, since missing
or postponing a meal is a realistic scenario for many individuals, repagli
nide offers an oral anti-diabetic treatment which can be adjusted to suit e
ach individual's lifestyle. (C) 1999 Elsevier Science Ireland Ltd. All righ
ts reserved.