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

Publikation: Forskning - peer reviewTidsskriftartikel

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

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.
OriginalsprogEngelsk
TidsskriftRevue Neurologique
Vol/bind173
Tidsskriftsnummer3
Sider (fra-til)164-168
ISSN0035-3787
DOI
StatusUdgivet - 2017

ID: 182544921