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Apolipoprotein E polymorphism and renal function in German type 1 and type 2 diabetic patients
E Werle1, W Fiehn, C Hasslacher
1Central Laboratory, University of Heidelberg, Germany. egon_werle@krzmail.krz.uni-heidelberg.de
Diabetes Care
|June 6, 1998
Summary
Apolipoprotein E (Apo E) polymorphism impacts kidney function in diabetic patients. The epsilon 2 allele is linked to reduced kidney filtration and increased protein excretion in type 1 diabetes.
Area of Science:
- Nephrology
- Endocrinology
- Genetics
Background:
- Diabetic nephropathy is a major complication of diabetes mellitus.
- Apolipoprotein E (Apo E) polymorphism is associated with lipid metabolism and cardiovascular disease.
- The role of Apo E polymorphism in diabetic kidney disease requires further investigation.
Purpose of the Study:
- To investigate the association between Apo E genotypes and renal function in patients with type 1 (IDDM) and type 2 (NIDDM) diabetes.
- To determine if Apo E polymorphism is an independent risk factor for renal dysfunction in diabetic patients.
Main Methods:
- Apolipoprotein E genotyping, lipid profiles, creatinine clearance (CCr), and urinary marker protein excretion were assessed in 162 IDDM and 124 NIDDM patients.
- Marker proteins (albumin, IgG, alpha 1-microglobulin) were used to evaluate glomerular filtration and tubular reabsorption.
- Statistical analyses included ANOVA and multiple linear regression.
Main Results:
- NIDDM patients exhibited higher lipid levels and lower CCr compared to IDDM patients.
- In IDDM patients, Apo E genotypes were associated with CCr, with a decreasing glomerular filtration rate observed in the order: epsilon 4/epsilon 4 > epsilon 4/epsilon 3 > epsilon 3/epsilon 3 > epsilon 2/epsilon 2 > epsilon 2/epsilon 3.
- The epsilon 2 allele in IDDM patients independently predicted lower CCr and increased urinary excretion of albumin, IgG, and alpha 1-microglobulin.
Conclusions:
- Apo E polymorphism influences serum lipoprotein levels in both IDDM and NIDDM patients.
- Apo E polymorphism represents a clinically relevant renal risk factor, particularly in normolipidemic IDDM patients.