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dc.creatorDardiotis E., Karampinis E., Siokas V., Aloizou A.-M., Rikos D., Ralli S., Papadimitriou D., Bogdanos D.P., Hadjigeorgiou G.M.en
dc.date.accessioned2023-01-31T07:50:47Z
dc.date.available2023-01-31T07:50:47Z
dc.date.issued2019
dc.identifier10.1007/s10072-019-03825-3
dc.identifier.issn15901874
dc.identifier.urihttp://hdl.handle.net/11615/73084
dc.description.abstractBackground: Α number of genetic variants have been associated with amyotrophic lateral sclerosis (ALS). A recent study supports that rs591486 across the ERCC6L2 gene and exposure to pesticides seem to have a joint effect on the development of Parkinson’s disease, a disease which shares a few common characteristics with ALS. Objective: To detect a possible contribution of rs591486 ERCC6L2 to ALS. Methods: A total of 155 patients with ALS and 155 healthy controls were included in the study and genotyped for rs591486. Using logistic regression analyses (crude and adjusted for age and sex), rs591486 was tested for association with ALS risk. Subgroup analysis based on ALS site of onset was also performed. Cox regression analysis was applied in order for the effect of ERCC6L2 rs591486 on ALS age of onset to be tested. Results: Adjusted analysis showed that ERCC6L2 rs591486 was associated with an increased risk of ALS development, in dominant [odds ratio, OR (95% confidence interval, CI) 2.15 (1.04–4.46), p = 0.037] and over-dominant [OR (95%CI) = 1.91 (1.01–3.60), p = 0.043], modes. Subgroup analysis based on ALS site of onset revealed an association between ERCC6L2 rs591486 and ALS with limb onset. Results for Cox regression analysis indicated that G/A carriers had a lower age of ALS limb onset when compared to G/G carriers. Conclusions: The current study provides preliminary indication for an implication of ERCC6L2 rs591486 in ALS development, as a possible genetic risk factor. These results possibly suggest that oxidative stress may be the main contributor in the pathophysiology of ALS. © 2019, Fondazione Società Italiana di Neurologia.en
dc.language.isoenen
dc.sourceNeurological Sciencesen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85063103811&doi=10.1007%2fs10072-019-03825-3&partnerID=40&md5=e382935f148a0ede1eb897f125effcb9
dc.subjectDNA helicaseen
dc.subjectERCC6L2 protein, humanen
dc.subjectageden
dc.subjectamyotrophic lateral sclerosisen
dc.subjectCaucasianen
dc.subjectfemaleen
dc.subjectgenetic association studyen
dc.subjectgenetic predispositionen
dc.subjectgeneticsen
dc.subjectgenotypeen
dc.subjectGreeceen
dc.subjecthumanen
dc.subjectmaleen
dc.subjectmiddle ageden
dc.subjectsingle nucleotide polymorphismen
dc.subjectAgeden
dc.subjectAmyotrophic Lateral Sclerosisen
dc.subjectDNA Helicasesen
dc.subjectEuropean Continental Ancestry Groupen
dc.subjectFemaleen
dc.subjectGenetic Association Studiesen
dc.subjectGenetic Predisposition to Diseaseen
dc.subjectGenotypeen
dc.subjectGreeceen
dc.subjectHumansen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectPolymorphism, Single Nucleotideen
dc.subjectSpringer-Verlag Italia s.r.l.en
dc.titleERCC6L2 rs591486 polymorphism and risk for amyotrophic lateral sclerosis in Greek populationen
dc.typejournalArticleen


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