Hyperviscosity and microproteinuria in central obesity: relevance to cardiovascular risk

Int J Obes Relat Metab Disord. 1997 Jun;21(6):417-23. doi: 10.1038/sj.ijo.0800421.

Abstract

Objectives: To investigate the role of blood rheology changes in the occurrence of glomerular proteinuria in obese patients with central fat distribution.

Subjects: Fifty-nine obese out-patients (31 with central and 28 with peripheral body fat distribution) and 24 healthy subjects.

Measurements: Blood and plasma viscosity (Rotational viscometer CV100 HAAKE), erythrocyte deformability (whole-blood filtration time), fibrinogen (nephelometry), urinary excretion rates of albumin, IgG, transferrin and IgA (nephelometry).

Results: Higher blood viscosity (at low and high shear-rates), plasma viscosity, fibrinogen, erythrocyte aggregability and lower erythrocyte deformability were found in patients with central obesity than in patients with peripheral obesity (P < 0.01) and in healthy subjects (P < 0.001). Furthermore an increased urinary excretion rate of albumin (P < 0.001), IgG (P < 0.001), transferrin (P < 0.01) and IgA (P < 0.05) was found in patients with central obesity than in the other two groups. Blood hyperviscosity (at shear-rate 1 s-1 and 1/200 ratio) significantly correlated with the amount of urinary excretion of proteins independently of the other clinical and metabolic variables.

Conclusions: The data demonstrated haemorheologic disorders related to pathologic proteinuria in patients with central obesity. The interaction between these two components may increase the risk of widespread cardiovascular disease.

MeSH terms

  • Adult
  • Albuminuria
  • Blood Viscosity*
  • Body Constitution
  • Body Mass Index
  • Cardiovascular Diseases / etiology*
  • Erythrocyte Deformability
  • Female
  • Glucose Tolerance Test
  • Humans
  • Immunoglobulin A / urine
  • Immunoglobulin G / urine
  • Male
  • Middle Aged
  • Obesity / complications*
  • Proteinuria*
  • Rheology
  • Risk Factors
  • Transferrin / urine

Substances

  • Immunoglobulin A
  • Immunoglobulin G
  • Transferrin