Decreased release of lipoprotein lipase is associated with vascular endothelial damage in NIDDM patients with microalbuminuria

Diabetes Care. 1998 Nov;21(11):2016-20. doi: 10.2337/diacare.21.11.2016.

Abstract

Objective: To explore mechanisms for hypertriglyceridemia in diabetic patients with microalbuminuria, we examined an association between heparin-releasable lipoprotein lipase (LPL) and the von Willebrand factor (vWF), based on the hypothesis that LPL bound to endothelium is decreased by generalized endothelial damage.

Research design and methods: A total of 37 NIDDM patients with microalbuminuria and 69 patients with normoalbuminuria were studied. Plasma LPL mass in post-heparin plasma and plasma vWF antigen were quantified by sandwich-enzyme immunoassay and enzyme-linked immunosorbent assay, respectively.

Results: The NIDDM patients with microalbuminuria had higher plasma triglyceride (TG) and lower HDL cholesterol concentrations compared with the patients with normoalbuminuria. Heparin-releasable LPL mass was significantly lower in the microalbuminuric than in the normoalbuminuric subjects. Plasma level of vWF, a marker for endothelial damage, was significantly increased in microalbuminuric subjects compared with their normoalbuminuric counterparts. The LPL mass was inversely correlated with plasma vWF level at a high correlation coefficient value. The LPL mass was inversely related to TG and positively to HDL cholesterol concentrations.

Conclusions: These results suggest that widespread endothelial damage occurred in NIDDM patients with microalbuminuria, thereby LPL moiety bound to the endothelium is decreased, which results in an impaired catabolism of TG-rich lipoproteins.

MeSH terms

  • Albuminuria / complications*
  • Albuminuria / pathology
  • Cholesterol, HDL / blood
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / enzymology*
  • Diabetes Mellitus, Type 2 / pathology*
  • Endothelium, Vascular / pathology*
  • Female
  • Humans
  • Lipoprotein Lipase / blood*
  • Male
  • Middle Aged
  • Triglycerides / blood
  • von Willebrand Factor / analysis

Substances

  • Cholesterol, HDL
  • Triglycerides
  • von Willebrand Factor
  • Lipoprotein Lipase