ApoE4-positive multiple sclerosis patients are more likely to have cognitive impairment: a cross-sectional study

Farshid Mashayekhi1, Saeed Sadigh-Eteghad1, Amirreza Naseri2

  • 1Neurosciences Research Center (NSRC), Tabriz University of Medical Sciences, 5166614756, Tabriz, Iran.

Abstract

Insights

The apolipoprotein E4 (ApoE4) allele may increase the risk of cognitive dysfunction in multiple sclerosis (MS) patients. ApoE4-positive MS patients showed higher rates of impaired cognitive tests, suggesting a potential link.

Area of Science:

  • Neurology
  • Genetics
  • Neuropsychology

Background:

  • Multiple sclerosis (MS) is characterized by diverse symptoms, including cognitive dysfunction.
  • Previous research on the association between the apolipoprotein E4 (ApoE4) allele and cognitive impairment in MS patients yielded conflicting results.
  • This study investigated the role of the ApoE4 allele as a risk factor for cognitive dysfunction in MS.

Purpose of the Study:

  • To determine if the ApoE4 allele is associated with cognitive dysfunction in patients with relapsing-remitting multiple sclerosis (RRMS).

Main Methods:

  • Recruited mildly disabled RRMS patients.
  • Administered the Minimal Assessment of Cognitive Function in MS (MACFIMS) for neurocognitive assessment.
  • Genotyped patients for ApoE alleles and compared cognitive performance between ApoE4-positive and ApoE4-negative groups.

Main Results:

  • ApoE4-positive patients (n=17) had a higher rate of at least one impaired cognitive test (64.70%) compared to ApoE4-negative patients (n=54) (29.62%, p < 0.01).
  • No statistically significant difference in overall cognitive impairment (≥2 failed tests) was observed between the groups (p=0.75).
  • Significant differences were found in performance on the Paced Auditory Serial Addition Test (PASAT) (p=0.01) and the Brief Visuospatial Memory Test-Revised (BVMT-R) (p=0.02).

Conclusions:

  • MS patients carrying the ApoE4 allele are more prone to exhibiting at least one cognitive test impairment.
  • Further research with larger cohorts and MS-specific cognitive assessments is warranted to validate these findings.