Publication:
Association between the catechol-o-methyltransferase val158met polymorphism with susceptibility and severity of carpal tunnel syndrome

dc.contributor.authorİnal, Erkol E.
dc.contributor.authorEroğlu, P.
dc.contributor.authorGörükmez, O.
dc.contributor.authorSağ, Özemri S.
dc.contributor.authorYakut, T.
dc.contributor.buuauthorÖZEMRİ SAĞ, ŞEBNEM
dc.contributor.buuauthorYakut, Tahsin
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı.
dc.contributor.researcheridGIS-1493-2022
dc.contributor.researcheridAAH-8355-2021
dc.date.accessioned2024-08-13T06:08:49Z
dc.date.available2024-08-13T06:08:49Z
dc.date.issued2015-01-01
dc.description.abstractCarpal tunnel syndrome (CTS) is the most common entrapment neuropathy of the upper extremity. In this study, we aimed to clarify the relationships between the catechol-O-methyltransferase (COMT) gene Val158Met (rs4680) polymorphism and development, functional and clinical status of CTS. Ninetyfive women with electro diagnostically confirmed CTS and 95 healthy controls were enrolled in the study. The functional and clinical status of the patients was measured by the Turkish version of the Boston Questionnaire and intensity of pain related to the past 2 weeks was evaluated on a visual analog scale (VAS). The Val158Met polymorphism was determined using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP), method. We divided patients according to the genotypes of the Val158Met polymorphism as Val/Val, Val/Met and Met/Met. There were not any significant differences in terms of Val158Met polymorphisms between patients and healthy controls (p >0.05). We also did not find any relationships between the Val158Met polymorphism and functional and clinical status of CTS (p >0.05). In conclusion, although we did not find any relationships between CTS and the Val158Met polymorphism, we could not generalize this result to the general population. Future studies are warranted to conclude precise associations.
dc.identifier.doi10.1515/bjmg-2015-0085
dc.identifier.endpage47
dc.identifier.issn1311-0160
dc.identifier.issue2
dc.identifier.startpage43
dc.identifier.urihttps://doi.org/10.1515/bjmg-2015-0085
dc.identifier.urihttps://sciendo.com/article/10.1515/bjmg-2015-0085
dc.identifier.urihttps://hdl.handle.net/11452/43951
dc.identifier.volume18
dc.identifier.wos000375181600006
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherSciendo
dc.relation.journalBalkan Journal of Medical Genetics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectLow-back-pain
dc.subjectComt
dc.subjectSensitivity
dc.subjectDisability
dc.subjectBoston questionnaire
dc.subjectCarpal tunnel syndrome (CTS)
dc.subjectCatechol-o-methyltransferase (COMT) gene
dc.subjectPain
dc.subjectVal158met (rs4680) polymorphism
dc.subjectGenetics & heredity
dc.titleAssociation between the catechol-o-methyltransferase val158met polymorphism with susceptibility and severity of carpal tunnel syndrome
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublicationdf8aeae7-a31e-454f-a84a-198138a42763
relation.isAuthorOfPublication.latestForDiscoverydf8aeae7-a31e-454f-a84a-198138a42763

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