Multiple sclerosis and cognitive decline: is ApoE-4 a surrogate marker?

Acta Neurol Scand. 2011 Oct;124(4):258-63. doi: 10.1111/j.1600-0404.2010.01473.x. Epub 2011 Jan 6.

Abstract

BACKGROUND - The role of the apolipoprotein E (ApoE) polymorphism has been well demonstrated in neurodegenerative disorders such as Alzheimer. However, its role in multiple sclerosis (MS) remains unclear. AIMS - The aims of our study were as follows: (i) to assess whether ApoE-4 might be a surrogate marker of cognitive decline in MS; (ii) to confirm the presence of cognitive impairment in mildly disabled patients treated with interferon-beta; and (iii) to analyse the correlation between cognitive disturbances and clinical variables. MATERIAL AND METHODS - Fifty relapsing-remitting MS patients underwent a battery of neuropsychological tests and were genotyped for ApoE. Their scores were compared with those of 35 controls. RESULTS - No association was found between ApoE-4 and cognitive impairment. Significant differences in most domains were observed between MS and the control group. Cognitive decline was not related to disability progression. CONCLUSION - No association between cognitive impairment and ApoE-4 or clinical markers was detected in our MS patients.

MeSH terms

  • Adult
  • Aged
  • Apolipoprotein E4 / genetics*
  • Apolipoprotein E4 / metabolism
  • Biomarkers
  • Case-Control Studies
  • Cognition Disorders / diagnosis
  • Cognition Disorders / drug therapy
  • Cognition Disorders / genetics*
  • Cognition Disorders / psychology
  • Disability Evaluation
  • Female
  • Genotype
  • Humans
  • Immunologic Factors / administration & dosage
  • Interferon-beta / administration & dosage
  • Logistic Models
  • Male
  • Middle Aged
  • Multiple Sclerosis, Relapsing-Remitting / complications
  • Multiple Sclerosis, Relapsing-Remitting / genetics*
  • Multiple Sclerosis, Relapsing-Remitting / psychology*
  • Neuropsychological Tests
  • Polymorphism, Genetic
  • Risk Factors

Substances

  • Apolipoprotein E4
  • Biomarkers
  • Immunologic Factors
  • Interferon-beta