Urinary prostaglandin D synthase (beta-trace) excretion increases in the early stage of diabetes mellitus

Nephron. 2001 Apr;87(4):321-7. doi: 10.1159/000045937.

Abstract

Objective: Circulating levels of lipocalin-type prostaglandin D synthase (L-PGDS)/beta-trace reportedly increase in renal failure as well as in cardiovascular injuries. We investigated the alterations of L-PGDS in urine and plasma in the early stage of type-2 diabetic patients.

Method: Thirty-six type-2 diabetic patients and 29 normal subjects were studied. Overnight spot urine and plasma samples were obtained in the morning. L-PGDS was measured by ELISA method using anti-L-PGDS antibody. Variables indicating renal function were determined.

Results: Plasma L-PGDS concentration was slightly higher in the patients with diabetes mellitus than in the control subjects, whereas the urinary L-PGDS excretion almost doubled in the diabetic patients as compared with that in the control subjects. Plasma L-PGDS was determined by plasma creatinine (Cr) concentration while urinary L-PGDS excretion was correlated solely with urinary protein excretion. There was no relationship between plasma L-PGDS concentration and urinary L-PGDS excretion. The averaged plasma concentration of L-PGDS in the diabetics with a normal Cr level in plasma, corresponding to that in the controls, was determined by the plasma Cr concentration. On the other hand, the urinary L-PGDS excretion was determined by the amount of proteinuria and greater in the diabetics with a normal Cr level in plasma than in the controls even when the patients exhibited urinary protein excretion equal to that in the control subjects.

Conclusions: Urinary L-PGDS excretion increased in the early stage of kidney injury in patients with type-2 diabetes mellitus. The urinary excretion was correlated independently with urinary protein excretion even when there was no difference in urinary protein or albumin excretions, thereby suggesting that urinary L-PGDS excretion is possibly a more sensitive indicator of renal injuries than proteinuria. Urinary L-PGDS may thus predict the progression of renal injuries in diabetic patients.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Biomarkers / urine
  • Blood Glucose / metabolism
  • Cholesterol / blood
  • Creatinine / blood
  • Diabetes Mellitus, Type 2 / enzymology
  • Diabetes Mellitus, Type 2 / physiopathology
  • Diabetes Mellitus, Type 2 / urine*
  • Diabetic Nephropathies / diagnosis
  • Diabetic Nephropathies / physiopathology
  • Diabetic Nephropathies / urine*
  • Enzyme-Linked Immunosorbent Assay
  • Glycated Hemoglobin / analysis
  • Humans
  • Intramolecular Oxidoreductases / blood
  • Intramolecular Oxidoreductases / urine*
  • Kidney Function Tests
  • Lipocalins
  • Middle Aged
  • Reference Values
  • Regression Analysis
  • Sensitivity and Specificity
  • Triglycerides / blood

Substances

  • Biomarkers
  • Blood Glucose
  • Glycated Hemoglobin A
  • Lipocalins
  • Triglycerides
  • Cholesterol
  • Creatinine
  • Intramolecular Oxidoreductases
  • prostaglandin R2 D-isomerase