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Association of IGF-1 CA(n) and IGFBP3 rs2854746 Polymorphisms with Endometrial Polyp Risk

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....

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Autores principales: Doria, Pedro Leopoldo Silva, Moscovitz, Thomas, Tcherniakovsky, Marcos, Fernandes, Cesar Eduardo, Pompei, Luciano Melo, Wajman, Milton, Nimwegen, Angela Van, Haimovich, Sergio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6311315/
https://www.ncbi.nlm.nih.gov/pubmed/30643822
http://dx.doi.org/10.1155/2018/8704346
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author Doria, Pedro Leopoldo Silva
Moscovitz, Thomas
Tcherniakovsky, Marcos
Fernandes, Cesar Eduardo
Pompei, Luciano Melo
Wajman, Milton
Nimwegen, Angela Van
Haimovich, Sergio
author_facet Doria, Pedro Leopoldo Silva
Moscovitz, Thomas
Tcherniakovsky, Marcos
Fernandes, Cesar Eduardo
Pompei, Luciano Melo
Wajman, Milton
Nimwegen, Angela Van
Haimovich, Sergio
author_sort Doria, Pedro Leopoldo Silva
collection PubMed
description 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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spelling pubmed-63113152019-01-14 Association of IGF-1 CA(n) and IGFBP3 rs2854746 Polymorphisms with Endometrial Polyp Risk Doria, Pedro Leopoldo Silva Moscovitz, Thomas Tcherniakovsky, Marcos Fernandes, Cesar Eduardo Pompei, Luciano Melo Wajman, Milton Nimwegen, Angela Van Haimovich, Sergio Biomed Res Int Research Article 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. Hindawi 2018-12-13 /pmc/articles/PMC6311315/ /pubmed/30643822 http://dx.doi.org/10.1155/2018/8704346 Text en Copyright © 2018 Pedro Leopoldo Silva Doria et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Doria, Pedro Leopoldo Silva
Moscovitz, Thomas
Tcherniakovsky, Marcos
Fernandes, Cesar Eduardo
Pompei, Luciano Melo
Wajman, Milton
Nimwegen, Angela Van
Haimovich, Sergio
Association of IGF-1 CA(n) and IGFBP3 rs2854746 Polymorphisms with Endometrial Polyp Risk
title Association of IGF-1 CA(n) and IGFBP3 rs2854746 Polymorphisms with Endometrial Polyp Risk
title_full Association of IGF-1 CA(n) and IGFBP3 rs2854746 Polymorphisms with Endometrial Polyp Risk
title_fullStr Association of IGF-1 CA(n) and IGFBP3 rs2854746 Polymorphisms with Endometrial Polyp Risk
title_full_unstemmed Association of IGF-1 CA(n) and IGFBP3 rs2854746 Polymorphisms with Endometrial Polyp Risk
title_short Association of IGF-1 CA(n) and IGFBP3 rs2854746 Polymorphisms with Endometrial Polyp Risk
title_sort association of igf-1 ca(n) and igfbp3 rs2854746 polymorphisms with endometrial polyp risk
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6311315/
https://www.ncbi.nlm.nih.gov/pubmed/30643822
http://dx.doi.org/10.1155/2018/8704346
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