Low density lipoprotein (
LDL-) particles can be subfractionated in large-buoyant (lb), intermediate-dense (id) and small-dense (sd)
LDL-subtypes.
Fibrates improve the
LDL-subtype profile by reducing proatherogenic sd-
LDL which are prominent in diabetic
dyslipoproteinemia. We evaluated the effect of
etofibrate on the
LDL-subtype distribution in patients with
type 2 diabetes mellitus (n = 13, 55 +/- 18 years, BMI 27.9 +/- 5.5 kg/m2, HbA1c 10.1 +/- 3.9 %) and diabetic
dyslipoproteinemia (
triglycerides 343 +/- 253 mg/dl,
HDL-cholesterol 36 +/- 7 mg/dl,
LDL-cholesterol 110 +/- 37 mg/dl). Plasma
lipids (enzymatic methods) and
LDL-subtypes (7
LDL-subfractions, density gradient ultracentrifugation) were measured before and during
etofibrate therapy (500 mg/d, 7 - 16 weeks).
Etofibrate significantly (p < 0.05, Wilcoxon-test) reduced
triglycerides (- 31 +/- 60 %) and increased
HDL-cholesterol (+ 24 +/- 22 %), whereas total
cholesterol and
LDL-cholesterol did not change.
Cholesterol concentration decreased in sd-
LDL by 12 % (p < 0.05), while it increased in id- and lb-
LDL (+ 26 %,+ 39 %, respectively). Thus, the
LDL-subtype profile showed a relative increase of the fraction of lb- (+ 13 +/- 32 %, n.s.) and id-
LDL (+ 23 +/- 33 %, p < 0.05) and a relative decrease of the fraction of sd-
LDL (- 19 +/- 18 %, p < 0.05). We conclude that
etofibrate not only decreases
triglycerides and increases
HDL-cholesterol but also improves the
LDL-subtype profile and thus may reduce the cardiovascular risk in patients with an abundance of sd-
LDL such as diabetic patients.