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Association between the catechol-o-methyltransferase val158met polymorphism with susceptibility and severity of carpal tunnel syndrome.
Erkol Inal, E; Eroglu, P; Görükmez, O; Özemri Sag, S; Yakut, T.
Afiliação
  • Erkol Inal E; Department of Physical Medicine and Rehabilitation, Süleyman Demirel University, Faculty of Medicine, Çünür, Isparta, Turkey.
  • Eroglu P; Department of Physical Medicine and Rehabilitation, Ankara Occupational Disease Hospital, Ankara, Turkey.
  • Görükmez O; Department of Medical Genetics, Bursa Sevket Yilmaz Education and Research Hospital, Bursa, Turkey.
  • Özemri Sag S; Department of Medical Genetics, Uludag University, Faculty of Medicine, Bursa, Turkey.
  • Yakut T; Department of Medical Genetics, Uludag University, Faculty of Medicine, Bursa, Turkey.
Balkan J Med Genet ; 18(2): 43-48, 2015 Dec 01.
Article em En | MEDLINE | ID: mdl-27785396
ABSTRACT
Carpal 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. Ninety-five 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 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.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2015 Tipo de documento: Article