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Diabetes, Vol 46, Issue 10 1601-1606, Copyright © 1997 by American Diabetes Association
Insulin and sulfonylurea therapy in NIDDM patients. Are the effects on lipoprotein metabolism different even with similar blood glucose control?
G Romano, L Patti, F Innelli, L Di Marino, G Annuzzi, M Iavicoli, GA Coronel, G Riccardi and AA Rivellese
Department of Clinical and Experimental Medicine, Federico II University Medical School, Naples, Italy.
This study evaluates the effects of insulin versus glibenclamide on
lipoprotein metabolism at comparable levels of blood glucose control, in
particular on the concentration and distribution of VLDL subfractions and
lipolytic enzyme activities in nine NIDDM men (aged 56 +/- 3 years, BMI
26.5 +/- 0.9 kg/m2) (means +/- SE) participating in a crossover study.
After a 3-week washout period, patients were randomly assigned to 2-month
treatment periods (insulin or glibenclamide); thereafter, each patient
crossed to the other treatment. At the end of each period, mean daily blood
glucose (MDBG), HbA1e, plasma lipids, lipoproteins (VLDL, LDL, HDL),
lipoprotein subfractions (VLDL1, 2, 3; HDL2, HDL3), and post-heparin lipase
activities (lipoprotein lipase [LPL], hepatic lipase [HL]) were evaluated.
Although glucose control was similar at the end of both periods (MDBG 8.3
+/- 0.3 vs. 7.9 +/- 0.3 mmol/l; HbA1c 7.4 +/- 0.3 vs. 7.0 +/- 0.2%, insulin
versus glibenclamide), insulin compared with glibenclamide induced a
significant reduction in plasma triglycerides (0.9 +/- 0.1 vs. 1.1 +/- 0.1
mmol/l, P < 0.05), VLDL triglycerides (50.1 +/- 12.2 vs. 63.6 +/- 12.3
mg/dl, P < 0.02), VLDL1 lipid concentration (24.9 +/- 7.5 vs. 39.9 +/-
9.5 mg/dl, P < 0.006), and increased HDL2 cholesterol (25.2 +/- 1.6 vs.
20.3 +/- 1.3 mg/dl, P < 0.03). In terms of VLDL percentage subfraction
distribution, with insulin, there was a decrease in the larger subfractions
(VLDL1 26.5 +/- 3.0 vs. 37.8 +/- 3.4%, P < 0.02) and an increase in the
smallest (VLDL3 47.3 +/- 3.8 vs. 37.3 +/- 3.3%, P < 0.05). Moreover, HL
activity was significantly lower after insulin than after glibenclamide (HL
247.2 +/- 22.3 vs. 263.5 +/- 22.6 mU/ml, P < 0.05). In conclusion,
compared with glibenclamide, insulin treatment (independent of variations
in glucose control) is able to decrease significantly plasma triglycerides,
to increase HDL2 cholesterol, and to reduce only the concentration of the
larger VLDL subfractions, with a consequent redistribution of their
profile.

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Copyright © 1997 by the American Diabetes Association.
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