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Relationship between plasminogen activator inhibitor type-1 (PAI-1) gene polymorphisms and osteoporosis in Turkish women

OBJECTIVE: The development of osteoporosis is associated with several risk factors, such as genetic structures that affect bone turnover and bone mass. The impact of genetic structures on osteoporosis is not known. Plasminogen activator inhibitor type-1 regulates the bone matrix and bone balance. Th...

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Autores principales: Ozgen, Merih, Cosan, Didem Turgut, Doganer, Fulya, Soyocak, Ahu, Armagan, Onur, Gunes, Hasan Veysi, Degirmenci, Irfan, Ozkara, Gulsah Ogutler, Mutlu, Fezan Sahin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488989/
https://www.ncbi.nlm.nih.gov/pubmed/23184207
http://dx.doi.org/10.6061/clinics/2012(11)13
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author Ozgen, Merih
Cosan, Didem Turgut
Doganer, Fulya
Soyocak, Ahu
Armagan, Onur
Gunes, Hasan Veysi
Degirmenci, Irfan
Ozkara, Gulsah Ogutler
Mutlu, Fezan Sahin
author_facet Ozgen, Merih
Cosan, Didem Turgut
Doganer, Fulya
Soyocak, Ahu
Armagan, Onur
Gunes, Hasan Veysi
Degirmenci, Irfan
Ozkara, Gulsah Ogutler
Mutlu, Fezan Sahin
author_sort Ozgen, Merih
collection PubMed
description OBJECTIVE: The development of osteoporosis is associated with several risk factors, such as genetic structures that affect bone turnover and bone mass. The impact of genetic structures on osteoporosis is not known. Plasminogen activator inhibitor type-1 regulates the bone matrix and bone balance. This study assessed the correlation between plasminogen activator inhibitor type-1 gene 4G/5G polymorphisms and osteoporosis in a population of Turkish women. METHODS: A total of 195 postmenopausal female patients who were diagnosed with osteoporosis (Group I) based on bone mineral density measurements via dual-energy x-ray absorptiometry and 90 females with no osteoporosis (Group II) were included in this study. Correlations between PAI-1 gene 4G/5G polymorphisms and osteoporosis were investigated through the identification of PAI-1 gene 4G/5G polymorphism genotypes using the polymerase chain reaction. RESULTS: No significant differences in the genotype and allele frequency of 4G/5G plasminogen activator inhibitor type-1 polymorphisms were observed between the two groups, and both groups exhibited the most frequently observed 4G5G genotype. CONCLUSION: No correlation between the development of osteoporosis in the female Turkish population and 4G/5G plasminogen activator inhibitor type-1 gene polymorphisms was observed.
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spelling pubmed-34889892012-11-06 Relationship between plasminogen activator inhibitor type-1 (PAI-1) gene polymorphisms and osteoporosis in Turkish women Ozgen, Merih Cosan, Didem Turgut Doganer, Fulya Soyocak, Ahu Armagan, Onur Gunes, Hasan Veysi Degirmenci, Irfan Ozkara, Gulsah Ogutler Mutlu, Fezan Sahin Clinics (Sao Paulo) Clinical Science OBJECTIVE: The development of osteoporosis is associated with several risk factors, such as genetic structures that affect bone turnover and bone mass. The impact of genetic structures on osteoporosis is not known. Plasminogen activator inhibitor type-1 regulates the bone matrix and bone balance. This study assessed the correlation between plasminogen activator inhibitor type-1 gene 4G/5G polymorphisms and osteoporosis in a population of Turkish women. METHODS: A total of 195 postmenopausal female patients who were diagnosed with osteoporosis (Group I) based on bone mineral density measurements via dual-energy x-ray absorptiometry and 90 females with no osteoporosis (Group II) were included in this study. Correlations between PAI-1 gene 4G/5G polymorphisms and osteoporosis were investigated through the identification of PAI-1 gene 4G/5G polymorphism genotypes using the polymerase chain reaction. RESULTS: No significant differences in the genotype and allele frequency of 4G/5G plasminogen activator inhibitor type-1 polymorphisms were observed between the two groups, and both groups exhibited the most frequently observed 4G5G genotype. CONCLUSION: No correlation between the development of osteoporosis in the female Turkish population and 4G/5G plasminogen activator inhibitor type-1 gene polymorphisms was observed. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2012-11 /pmc/articles/PMC3488989/ /pubmed/23184207 http://dx.doi.org/10.6061/clinics/2012(11)13 Text en Copyright © 2012 Hospital das Clínicas da FMUSP http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Science
Ozgen, Merih
Cosan, Didem Turgut
Doganer, Fulya
Soyocak, Ahu
Armagan, Onur
Gunes, Hasan Veysi
Degirmenci, Irfan
Ozkara, Gulsah Ogutler
Mutlu, Fezan Sahin
Relationship between plasminogen activator inhibitor type-1 (PAI-1) gene polymorphisms and osteoporosis in Turkish women
title Relationship between plasminogen activator inhibitor type-1 (PAI-1) gene polymorphisms and osteoporosis in Turkish women
title_full Relationship between plasminogen activator inhibitor type-1 (PAI-1) gene polymorphisms and osteoporosis in Turkish women
title_fullStr Relationship between plasminogen activator inhibitor type-1 (PAI-1) gene polymorphisms and osteoporosis in Turkish women
title_full_unstemmed Relationship between plasminogen activator inhibitor type-1 (PAI-1) gene polymorphisms and osteoporosis in Turkish women
title_short Relationship between plasminogen activator inhibitor type-1 (PAI-1) gene polymorphisms and osteoporosis in Turkish women
title_sort relationship between plasminogen activator inhibitor type-1 (pai-1) gene polymorphisms and osteoporosis in turkish women
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488989/
https://www.ncbi.nlm.nih.gov/pubmed/23184207
http://dx.doi.org/10.6061/clinics/2012(11)13
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