Insulin resistance contributes to obesity-related proteinuria

Intern Med. 2005 Jun;44(6):548-53. doi: 10.2169/internalmedicine.44.548.

Abstract

Objective: Proteinuria is a recognized complication of obesity, but the pathogenesis remains unclear. We undertook the present study to clarify the factors contributing to proteinuria associated with obesity.

Methods: We studied 12 obese patients with proteinuria. Twenty-seven age-matched obese subjects without proteinuria served as controls. A glucose tolerance test and renal biopsy were performed in all patients. Fasting serum insulin and homeostasis model assessment-insulin resistance (HOMA-IR) were regarded as reflecting insulin resistance. To delineate the relation between insulin resistance and proteinuria, troglitazone, which acts an insulin sensitizer was given to 6 of 12 patients with a regular diet for 8 weeks. The 6 others were observed without receiving troglitazone.

Results: The 12 patients showed the presence of a cluster of insulin resistance factors: higher blood pressure, higher body mass index, higher fasting plasma glucose, higher fasting serum insulin, and higher HOMA-IR than controls. The renal biopsy specimens exhibited no histological abnormalities in 7, focal segmental glomerulosclerosis in 3 and benign nephrosclerosis in 2. Troglitazone attenuated HOMA-IR and ameliorated proteinuria, but did not affect body weight, creatinine clearance, or blood pressure. In contrast, the parameters in the patients not given troglitazone did not change.

Conclusion: Insulin resistance is a factor contributing to obesity-related proteinuria. The role of insulin resistance as a factor reducing proteinuria remains to be clarified.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Biopsy
  • Blood Glucose / metabolism*
  • Blood Pressure / physiology
  • Body Mass Index
  • Chromans
  • Creatinine / blood
  • Female
  • Follow-Up Studies
  • Glucose Tolerance Test / methods
  • Humans
  • Hypoglycemic Agents
  • Insulin Resistance*
  • Kidney / pathology
  • Male
  • Models, Biological
  • Obesity / complications*
  • Obesity / metabolism
  • Obesity / physiopathology
  • Proteinuria / etiology*
  • Proteinuria / metabolism
  • Proteinuria / pathology
  • Risk Factors
  • Thiazolidinediones
  • Troglitazone

Substances

  • Blood Glucose
  • Chromans
  • Hypoglycemic Agents
  • Thiazolidinediones
  • Creatinine
  • Troglitazone