Repetitive element hypermethylation in multiple sclerosis patients

K. Y. Neven, M. Piola, L. Angelici, F. Cortini, C. Fenoglio, D. Galimberti, A. C. Pesatori, E. Scarpini, V. Bollati

Research output: Contribution to journalArticle

Abstract

Background: Multiple sclerosis (MS) is a complex disorder of the central nervous system whose cause is currently unknown. Evidence is increasing that DNA methylation alterations could be involved in inflammatory and neurodegenerative diseases and could contribute to MS pathogenesis. Repetitive elements Alu, LINE-1 and SAT-α, are widely known as estimators of global DNA methylation. We investigated Alu, LINE-1 and SAT-α methylation levels to evaluate their difference in a case-control setup and their role as a marker of disability. Results: We obtained blood samples from 51 MS patients and 137 healthy volunteers matched by gender, age and smoking. Methylation was assessed using bisulfite-PCR-pyrosequencing. For all participants, medical history, physical and neurological examinations and screening laboratory tests were collected. All repetitive elements were hypermethylated in MS patients compared to healthy controls. A lower Expanded Disability Status Scale (EDSS) score was associated with a lower levels of LINE-1 methylation for 'EDSS = 1.0' and '1.5 ≤ EDSS ≤ 2.5' compared to an EDSS higher than 3, while Alu was associated with a higher level of methylation in these groups: 'EDSS = 1.0' and '1.5 ≤ EDSS ≤ 2.5'. Conclusions: MS patients exhibit an hypermethylation in repetitive elements compared to healthy controls. Alu and LINE-1 were associated with degree of EDSS score. Forthcoming studies focusing on epigenetics and the multifactorial pathogenetic mechanism of MS could elucidate these links further.

Original languageEnglish
Article number84
JournalBMC Genetics
Volume17
Issue number1
DOIs
Publication statusPublished - Jun 18 2016

Keywords

  • DNA methylation
  • Epigenetics
  • Expanded disability status scale
  • Hypermethylation
  • Multiple sclerosis
  • Repetitive elements

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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