Key result
The IGF-1 CA(19)/CA(19) genotype increased endometrial polyp risk (OR 2.57; 95% CI 1.09-6.01), while the IGFBP3 rs2854746 CG genotype was protective (OR 0.37; 95% CI 0.19-0.73).
Why the study?
Genetic variations influence levels of IGF-1 and IGFBP3, but their association with the risk of endometrial polyps had not been examined.
Are IGF-1 CA(n) and IGFBP3 rs2854746 polymorphisms associated with the risk of endometrial polyps in women?
Case-Control (n=185)
Are IGF-1 CA(n) and IGFBP3 rs2854746 polymorphisms associated with the risk of endometrial polyps in women?
Odds Ratio: 2.57 (95% CI 1.09–6.01)
Specific genetic variations in IGF-1 and IGFBP3 are associated with altered risk of developing endometrial polyps.
May link IGF-1/IGFBP3 variants to polyp risk; hypothesis-generating and requires validation before clinical use.
Introduction . Insulin-like growth factor 1 (IGF-1) is a peptide growth factor that promotes cell proliferation and inhibits apoptosis. The bioavailability of IGF-1 is regulated by the insulin-like growth factor binding protein 3 (IGFBP3). Genetic variations influence the levels of IGF-1 and IGFBP3 . The purpose of this study was to examine the association of polymorphisms IGF-1 CA(n) and IGFBP3 rs2854746 with risk of endometrial polyps. Materials and Methods . Case control observational study, composed of 104 women with antecedent of endometrial polyp (case group) and 81 postmenopausal women without antecedent of endometrial diseases (control group). Genotyping of IGF-1 CA(n) was performed by PCR and fragment analysis by capillary electrophoresis, and genotyping of IGFBP3 rs2854746 was performed by PCR-HRM. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated by logistic regression. Results . The genotype IGF-1 CA(19)/CA(19) was associated with an increased endometrial polyp risk (OR=2,57; IC 95%= 1,09 - 6,01); this was also found when combining it with CA(>19)/CA(n) genotypes (OR=2,18; IC 95%= 1,06-4,47). The IGFBP3 rs2854746 analyses showed the CG genotype having a protective effect for endometrial polyp (OR=0,37; IC 95%= 0,19-0,73), fact also observed when grouping CG and GG carriers (OR=0,51; IC 95%= 0,28-0,93). Conclusion . The genotypes CA(19)/CA(19) and CA(19)/CA(19) + CA(>19)/CA(n) of the IGF-1 CA(n) may be considered a risk for endometrial polyp, whereas the genotypes CG and CG + GG of IGFBP3 rs2854746 polymorphism have an inverse effect of endometrial polyp risk.
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Doria et al. (2018) conducted a case-control in Endometrial polyps (n=185). IGF-1 CA(n) and IGFBP3 rs2854746 polymorphisms vs. Other genotypes was evaluated on Endometrial polyp risk (OR 2.57, 95% CI 1.09-6.01). The IGF-1 CA(19)/CA(19) genotype increased endometrial polyp risk (OR 2.57; 95% CI 1.09-6.01), while the IGFBP3 rs2854746 CG genotype was protective (OR 0.37; 95% CI 0.19-0.73).
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