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   association between interleukin-8 -251t/a polymorphism and endometriosis in iranian women  
   
نویسنده rabbanizadeh farnoosh ,kohan leila ,najib fatemesadat
منبع research in molecular medicine - 2015 - دوره : 3 - شماره : 2 - صفحه:45 -49
چکیده    Background: endometriosis is a disease of female genital system, which is defined by the presence of ectopic endometrial tissue outside the uterine cavity. il-8 is an autocrine growth factor in the endometrium that contributes to the pathogenesis of endometriosis. the aim of this study was to investigate the association between -251t/a polymorphism in the il-8 gene and risk of developing endometriosis in iranian population. materials and methods: this case-control study was performed in 100 endometriosis patients and 100 healthy individuals. the il-8 -251t/a genotypes were determined using pcr-rflp method. the association between genotypes of the -251t/a polymorphism and the risk of developing endometriosis was examined by odds ratios (or) and 95% of confidence intervals (cis). results: no statistically significant associations were observed between il-8 -251 variants and the risk of developing endometriosis (χ2: 1.02, p: 0.63). in addition, subgroup analysis (according to severity of disease) were unable to identify any association between il-8 -251t/a polymorphism and endometriosis (p>0.05). conclusions: to our knowledge this is the first study investigating the association between -251t/a polymorphism and risk of developing endometriosis. our results indicate that the presence of the -251t/a polymorphism in il-8 gene is not associated with the risk of endometriosis.
کلیدواژه endometriosis; interleukin-8; iranian population; polymorphism
آدرس islamic azad university, arsanjan branch, college of sciences, department of biology, iran, islamic azad university, arsanjan branch, college of sciences, department of biology, yong researchers and elite club, iran, shiraz university of medical sciences, department of obstetrics and gynecology, iran
پست الکترونیکی najibf@sums.ac.ir
 
     
   
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