HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Urinary L-FABP and anaemia: distinct roles of urinary markers in type 2 diabetes.

AbstractBACKGROUND:
Urinary liver-type fatty acid binding protein (L-FABP) and kidney injury molecule (KIM)-1, novel urinary biomarkers of renal tubulointerstitial function, have previously been associated with acute ischaemic kidney injury. We studied the clinical significance of urinary L-FABP, KIM-1 and N-acetyl-beta-glucosaminidase (NAG) as potential markers of renal function and chronic ischaemic injury in patients with diabetic nephropathy.
MATERIAL AND METHODS:
A total of 130 type 2 diabetes patients with early diabetic nephropathy and 40 healthy controls were studied. Urinary L-FABP, KIM-1, NAG, albumin excretion rate (AER) and creatinine clearance were obtained from 24-h urine samples, and correlated with measures of red blood cell count, renal function and metabolic control.
RESULTS:
Urinary L-FABP was significantly increased in diabetes patients compared with healthy controls [8.1 (interquartile 0.6-11.6) vs. 2.4 (0.5-3.6) microg/g creatinine, P < 0.001] and correlated with AER (r = 0.276, P = 0.002), creatinine clearance (r = -0.189, P = 0.033) and haemoglobin levels (r = -0.190, P = 0.030). In multivariable linear regression analysis, haemoglobin (beta = -0.247, P = 0.015) and AER (beta = 0.198, P = 0.046) were significant predictors of urinary L-FABP. Prevalent anaemia was independently associated with a 6-fold risk for increased tubulointerstitial kidney damage (upper vs. lower two L-FABP tertiles: OR, 6.06; 95% CI: 1.65-22.23; P = 0.007). Urinary KIM-1 was not significantly associated with kidney function, AER, or measures of red blood cell count while urinary NAG was associated with parameters of glucose control and renal function.
CONCLUSIONS:
Different urinary biomarkers may reflect distinct pathophysiological mechanisms of tubulointerstitial damage in early diabetic nephropathy: Urinary L-FABP could be a novel biomarker for chronic intrarenal ischaemia.
AuthorsM von Eynatten, M Baumann, U Heemann, D Zdunek, G Hess, P P Nawroth, A Bierhaus, P M Humpert
JournalEuropean journal of clinical investigation (Eur J Clin Invest) Vol. 40 Issue 2 Pg. 95-102 (Feb 2010) ISSN: 1365-2362 [Electronic] England
PMID19912308 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Albumins
  • Biomarkers
  • Fatty Acid-Binding Proteins
  • HAVCR1 protein, human
  • Hemoglobins
  • Hepatitis A Virus Cellular Receptor 1
  • Membrane Glycoproteins
  • NBAS protein, human
  • Neoplasm Proteins
  • Receptors, Virus
  • Creatinine
  • Glucose
Topics
  • Aged
  • Albumins (analysis)
  • Anemia (diagnosis, epidemiology, urine)
  • Biomarkers (urine)
  • Creatinine (urine)
  • Diabetes Mellitus, Type 2 (complications, urine)
  • Diabetic Nephropathies (urine)
  • Erythrocyte Count
  • Fatty Acid-Binding Proteins (urine)
  • Female
  • Glucose (metabolism)
  • Hemoglobins (analysis)
  • Hepatitis A Virus Cellular Receptor 1
  • Humans
  • Kidney Failure, Chronic (epidemiology, urine)
  • Kidney Function Tests
  • Male
  • Membrane Glycoproteins (urine)
  • Middle Aged
  • Multivariate Analysis
  • Neoplasm Proteins (urine)
  • Receptors, Virus

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: