Ontology highlight
ABSTRACT: Background
Several lines of research have suggested that the 472G > A (Val158Met) polymorphism at Catechol-O-methyltranferase (COMT) gene is implicated in the pathophysiology of FMS. Here, we have evaluated the association of COMT 472G > A polymorphism with risk of FMS.Methods
In this study 250 patients with FMS and 250 healthy controls were evaluated for COMT 472G > A polymorphism by RFLP-PCR assay.Results
There were no significant differences in the allele and genotype frequencies of COMT 472G > A polymorphism between FMS cases and healthy controls.Conclusions
Our results suggested that the COMT 472G > A polymorphism may not be risk factor for development of FMS.
SUBMITTER: Hatami M
PROVIDER: S-EPMC7042409 | biostudies-literature | 2020 Jul-Aug
REPOSITORIES: biostudies-literature
Hatami Maryam M Sobhan Mohammad Reza MR Dastgheib Seyed Alireza SA Jarahzadeh Mohammad Hossein MH Jafari Mohammadali M Yadegari Amirhossein A Sadeghizadeh-Yazdi Jalal J Neamatzadeh Hossein H
Journal of orthopaedics 20200113
<h4>Background</h4>Several lines of research have suggested that the 472G > A (Val158Met) polymorphism at Catechol-O-methyltranferase (COMT) gene is implicated in the pathophysiology of FMS. Here, we have evaluated the association of COMT 472G > A polymorphism with risk of FMS.<h4>Methods</h4>In this study 250 patients with FMS and 250 healthy controls were evaluated for COMT 472G > A polymorphism by RFLP-PCR assay.<h4>Results</h4>There were no significant differences in the allele and genotype ...[more]