Mitochondrial DNA G13708A variation and multiple sclerosis: Is there an association?

S. Andalib, M. Talebi, E. Sakhinia, M. Farhoudi, H. Sadeghi-Bazargani, M. R. Emamhadi, N. Masoodian, M. Balaghi-Inalou, M. S. Vafaee, A. Gjedde

Research output: Contribution to journalArticlepeer-review

Abstract

Background Multiple sclerosis (MS) is considered a pathogenetic enigma. Recently, efforts to implicate genetics in human susceptibility to MS have identified an important role of mitochondrial DNA (mtDNA). G13708A is a common mtDNA variation associated with MS in specific populations. This study tested the hypothesis that the mtDNA G13708A variation is associated with MS in an Iranian population. Materials and methods Blood samples were collected from 100 MS patients and 100 unrelated healthy controls. DNA was extracted using a salting-out method, followed by polymerase chain reaction (PCR) amplification. For assessment of restriction fragment length polymorphism (RFLP), PCR products were restricted by restriction enzyme Mva I. Thereafter, the restriction products were assessed by means of an ultraviolet (UV) transilluminator following electrophoresis with 3% agarose gel. Accuracy of the genotyping procedure was assessed by direct sequencing. Results The mtDNA G13708A variation was found in 17 cases (17%) and 19 controls (19%) (P = 0.7, OR: 0.8, 95% CI: 0.3–1.9). Conclusion The findings of the present study fail to support the hypothesis that the G13708A mtDNA variation is associated with MS in the selected Iranian population.

Original languageEnglish (US)
Pages (from-to)164-168
Number of pages5
JournalRevue Neurologique
Volume173
Issue number3
DOIs
StatePublished - Mar 2017

Keywords

  • G13708A
  • Iranian population
  • Mitochondrial DNA
  • Multiple sclerosis
  • mtDNA variation

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

Fingerprint Dive into the research topics of 'Mitochondrial DNA G13708A variation and multiple sclerosis: Is there an association?'. Together they form a unique fingerprint.

Cite this