The ε4 allele of the APOE gene is associated with more severe peripheral neuropathy in type 2 diabetic patients

Angiology. 2013 Aug;64(6):451-5. doi: 10.1177/0003319712453645. Epub 2012 Jul 23.

Abstract

We examined the association between the ε4 allele of the apolipoprotein E gene and severity of peripheral neuropathy in 234 patients with type 2 diabetes mellitus (T2DM). Based on the Neuropathy Disability Score (NDS), patients were divided into group A (NDS ≤ 6: mild or no neuropathy) and group B (NDS > 6: severe neuropathy). In each group, patients were further divided into ε4 carriers and non-ε4 carriers. In multivariate analysis, a more than 5-fold increased risk of severe neuropathy was associated with ε4 carrier status (adjusted odds ratio [aOR]: 5.26, 95% confidence interval [CI]: 2.24-12.31, P = .0001). The other significant risk factors for severe neuropathy included male gender (aOR: 2.08, 95% CI: 1.05-4.14, P = .036), diabetes duration (aOR: 1.05, 95% CI: 1.00-1.09, P = .039), and hemoglobin A1c (aOR: 1.32, 95% CI: 1.05-1.66, P = .020). In conclusion, the ε4 carrier status appears to be associated with severe peripheral neuropathy in T2DM.

Keywords: apolipoprotein E; diabetes mellitus; diabetic neuropathy; genes; polymorphisms.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Apolipoproteins E / genetics*
  • Biomarkers / blood
  • Chi-Square Distribution
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / diagnosis
  • Diabetes Mellitus, Type 2 / genetics*
  • Diabetic Neuropathies / diagnosis
  • Diabetic Neuropathies / genetics*
  • Disability Evaluation
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Glycated Hemoglobin / analysis
  • Humans
  • Logistic Models
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Odds Ratio
  • Phenotype
  • Predictive Value of Tests
  • Risk Assessment
  • Risk Factors
  • Severity of Illness Index
  • Sex Factors

Substances

  • Apolipoproteins E
  • Biomarkers
  • Glycated Hemoglobin A
  • hemoglobin A1c protein, human