Jc. Daubresse et al., USEFULNESS OF FLUOXETINE IN OBESE NON-INSULIN-DEPENDENT DIABETICS - AMULTICENTER STUDY, Obesity research, 4(4), 1996, pp. 391-396
Weight reduction is essential in the management of most noninsulin-dep
endent diabetics, but this therapeutical goal is difficult to obtain.
In this double-blind parallel study, 82 noninsulin-dependent diabetics
, moderately obese (BMI = 30 - 39 kg/m(2)), were given for an 8-week p
eriod either placebo (P) or fluoxetine (F), a specific serotonin reupt
ake inhibitor, in addition to their usual antidiabetic treatment. Thir
ty-nine of them received 60 mg fluoxetine a day and 43 were given the
placebo. At admission, both groups had similar weight excess, metaboli
c control and serum lipid values. In comparison with the P-treated sub
jects, those treated with fluoxetine (F) lost more weight after 3 week
s (-1.9 vs. -0.7 kg, p<0.0009) and after 8 weeks (-3.1 vs. -0.9 kg, p<
0.0007). Easting blood glucose decreased in group F after 3 weeks (-1.
5 vs. -0.4 mmol/L, p<0.003) and after 8 weeks (-1.7 vs. -0.02 mmol/L,
p<0.0004). HbAlc decreased from 8.5% to 7.7% in group F and from 8.6%
to 8.3% in group P (p=0.057). Mean triglyceride level was also reduced
in group F after 8 weeks (p=0.042). Easting C-peptide did not change
in either group, but fasting insulin values decreased in group F after
3 weeks (p<0.02) and after 8 weeks (p<0.05). The insulin/C-peptide mo
lar ratio decreased significantly in group F after 3 weeks (p<0.04) an
d after 8 weeks (p<0.05) in comparison with group P. The drug was gene
rally well tolerated and no major side effects were reported. In concl
usion, the addition of fluoxetine to the usual oral hypoglycemic agent
therapy might be beneficial in obese non-insulin-dependent diabetics,
at least on a short-term basis.