Results
| PMID | 24943061 |
| Gene Name | PGR |
| Condition | Endometriosis |
| Association |
Associated |
| Mutation | PROGINS polymorphism |
| Population size | 3,321 |
| Population details | 3321 (1,323 cases, 1,998 controls) |
| Sex | Female |
| Other associated phenotypes |
Endometriosis |
|
Arch Gynecol Obstet. 2014 Nov;290(5):1015-22. doi: 10.1007/s00404-014-3308-3. Pabalan, Noel| Salvador, Alice| Jarjanazi, Hamdi| Christofolini, Denise Maria| Barbosa, Caio Parente| Bianco, Bianca School of Natural Sciences and Nursing, Saint Louis University, Baguio City, 2600, Philippines. BACKGROUND: Reported associations of progesterone receptor gene polymorphism (PROGINS) with endometriosis have been inconsistent. AIM OF THE STUDY: To evaluate the association between the PROGINS polymorphism and the risk of endometriosis. METHODOLOGY: A meta-analysis of 12 published case-control studies with a total sample size of 3,321 (1,323 cases/1,998 controls) was performed. We estimated the risk (odds ratio [OR] 95 % confidence intervals) of endometriosis association with the PROGINS polymorphism. RESULTS: An association between the presence of the variant allele and risk of endometriosis was found, more in the homozygous and recessive models (OR 1.41-1.43, p = 0.15-0.17), and less in the dominant and co-dominant models (OR 1.22, p = 0.11-0.15). Reanalysis without the studies whose controls deviated from the Hardy-Weinberg Equilibrium did not materially alter the dominant and co-dominant effects (OR 1.19-1.22, p = 0.19-0.32), but exacerbated the homozygous and recessive effects (OR 1.59, p = 0.09). The subgroups based on geography showed increased risk associations, consistently significant in the European (OR 1.52-2.72, p = 0.0008-0.03) but not in the Brazilian studies, where ORs ranged from reduced (OR 0.70-0.74, p = 0.54-0.61) to increased (OR 1.11, p = 0.75) risks. Heterogeneity was confined in all comparisons to the dominant and co-dominant models (I (2) = 38-70 %), except in the European subgroup, which had zero heterogeneity (I (2) = 0 %) in all genetic models, as did all homozygous and recessive effects. CONCLUSION: This meta-analysis provides a comprehensive profile of the role of the PROGINS polymorphism in endometriosis by exploring the magnitude of the summary effects with modifier analysis. This magnitude is expressed with modulation or exacerbation of the summary effects, as defined by the parameters of the analysis. Thus, the results showed trend towards an increased risk of the variant PROGINS allele and susceptibility for the endometriosis. Mesh Terms: Alleles| Confidence Intervals| Endometriosis/*genetics| Female| Genetic Predisposition to Disease/genetics| Humans| Odds Ratio| *Polymorphism, Genetic| Receptors, Progesterone/*genetics| Risk|DA 2015/02/11 06:00 |
|