Can We Use Plasma Fibronectin Levels as a Marker for Early Diabetic Nephropathy

Although increased plasma fibronectin (PF) levels have been found in diabetic patients with microalbuminuria, there is still controversy about its clinical implication for detecting early diabetic nephropathy. To evaluate the PF concentration as a possible marker for early diabetic nephropathy, thre...

Full description

Saved in:
Bibliographic Details
Published in:ENDOCRINE JOURNAL Vol. 42; no. 2; pp. 301 - 305
Main Authors: OZATA, METIN, KURT, ISMAIL, AZAL, OMER, BOLU, EROL, CORAKCI, AHMET, BEYHAN, ZEYNEL, KARACA, LEVENT, GÜNDOGAN, MEHMET ALI
Format: Journal Article
Language:English
Published: Japan The Japan Endocrine Society 1995
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Although increased plasma fibronectin (PF) levels have been found in diabetic patients with microalbuminuria, there is still controversy about its clinical implication for detecting early diabetic nephropathy. To evaluate the PF concentration as a possible marker for early diabetic nephropathy, three groups of sex-and age-matched patients were studied I) 22 insulin dependent diabetic (IDDM) patients with microalbuminuria (mean age±SEM: 23.3±3.6 years, mean urinary albumin excretion rate (AER)±SEM: 47.1±39.5μg/min); II) 17 IDDM patients with normoalbuminuria (mean age: 23.4±4.4 years, mean AER: 7.8±2.1μg/min) and III) 20 healthy control subjects (mean age: 22.6±4.1 years, mean AER: 6.7±2.1μg/min). PF and urinary excretion of albumin were measured by an immunoturbidimetric method using commercially available kits (Boehringer Mannheim GMBH FRG, and Miles Lab., UK). The mean PF was significantly higher in the group with microalbuminuria (406.5±122.9μg/ml) than in the group with normoalbuminuria (295.6±96.9μg/ml, P<0.01) or in the control group (299.54±105.5 μg/ml, P<0.01). A weak positive correlation was found between PF and urinary albumin values (r=0.35, P<0.05). There were no significant correlations between PF and the other variables such as age, duration of diabetes, body mass index, arterial blood pressure, fasting blood glucose, fructosamine and HbA1 in the diabetic patients or in the control group. Our results suggest that the PF concentration could be a weak marker for early diabetic nephropathy. We cannot therefore use PF instead of microalbuminuria because there is only a weak correlation between PF and microalbuminuria.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0918-8959
1348-4540
DOI:10.1507/endocrj.42.301