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Interleukin-10 and Transforming Growth Factor Beta1 Gene Polymorphisms in Chronic Heart Failure
BACKGROUND: As cytokines, including interleukin-10 (IL-10) and transforming growth factor beta 1(TGF-β1) seem to contribute towards the pathogenesis of chronic heart failure (CHF), this study was performed to assess the associations of certain single nucleotide polymorphisms (SNPs) of these genes in...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mattioli 1885
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776215/ https://www.ncbi.nlm.nih.gov/pubmed/31124999 http://dx.doi.org/10.23750/abm.v90i2.6681 |
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author | Mohammad, Jafar Mahmoudi Mona, Hedayat Mohammad, Taghvaei Sara, Harsini Ebrahim, Nematipour Elham, Farhadi Maryam, Mahmoudi Maryam, Sadr Nilufar, Esfahanian Keramat, Nourijelyani Ali, Akbar Amirzargar Nima, Rezaei |
author_facet | Mohammad, Jafar Mahmoudi Mona, Hedayat Mohammad, Taghvaei Sara, Harsini Ebrahim, Nematipour Elham, Farhadi Maryam, Mahmoudi Maryam, Sadr Nilufar, Esfahanian Keramat, Nourijelyani Ali, Akbar Amirzargar Nima, Rezaei |
author_sort | Mohammad, Jafar Mahmoudi |
collection | PubMed |
description | BACKGROUND: As cytokines, including interleukin-10 (IL-10) and transforming growth factor beta 1(TGF-β1) seem to contribute towards the pathogenesis of chronic heart failure (CHF), this study was performed to assess the associations of certain single nucleotide polymorphisms (SNPs) of these genes in a case control study. METHODS: This investigation was carried out to determine the frequency of alleles, genotypes and haplotypes of TGF-β1 and IL-10 single-nucleotide polymorphisms (SNPs) in 57 Iranian patients with CHF compared with 140 healthy subjects using polymerase chain reaction with sequence-specific primers method. Results: Results of the analyzed data divulged a negative association for both TGF-β1 GC genotype at codon 25 (P=0.047) and CT genotype at codon 10 (P=0.018) and CHF proneness. Although, TGF-β1 CC genotype at codon 10 was found to be positively associated with CHF (P=0.011). Moreover, the frequency of IL-10 (−1082, -819, -592) ATA haplotype and TGF-β1 (codon 10, codon 25) TG haplotype were significantly lower in the patients group (P=0.004 and P=0.040, respectively), while TGF-β1 (codon 10, codon 25) CG haplotype was overrepresented in patients with CHF (P=0.007). CONCLUSIONS: Cytokine gene polymorphisms might affect vulnerability to CHF. Particular genotypes and haplotypes in IL-10 and TGF-β1 genes could render individuals more susceptible to CHF. (www.actabiomedica.it) |
format | Online Article Text |
id | pubmed-6776215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Mattioli 1885 |
record_format | MEDLINE/PubMed |
spelling | pubmed-67762152019-11-25 Interleukin-10 and Transforming Growth Factor Beta1 Gene Polymorphisms in Chronic Heart Failure Mohammad, Jafar Mahmoudi Mona, Hedayat Mohammad, Taghvaei Sara, Harsini Ebrahim, Nematipour Elham, Farhadi Maryam, Mahmoudi Maryam, Sadr Nilufar, Esfahanian Keramat, Nourijelyani Ali, Akbar Amirzargar Nima, Rezaei Acta Biomed Original Article BACKGROUND: As cytokines, including interleukin-10 (IL-10) and transforming growth factor beta 1(TGF-β1) seem to contribute towards the pathogenesis of chronic heart failure (CHF), this study was performed to assess the associations of certain single nucleotide polymorphisms (SNPs) of these genes in a case control study. METHODS: This investigation was carried out to determine the frequency of alleles, genotypes and haplotypes of TGF-β1 and IL-10 single-nucleotide polymorphisms (SNPs) in 57 Iranian patients with CHF compared with 140 healthy subjects using polymerase chain reaction with sequence-specific primers method. Results: Results of the analyzed data divulged a negative association for both TGF-β1 GC genotype at codon 25 (P=0.047) and CT genotype at codon 10 (P=0.018) and CHF proneness. Although, TGF-β1 CC genotype at codon 10 was found to be positively associated with CHF (P=0.011). Moreover, the frequency of IL-10 (−1082, -819, -592) ATA haplotype and TGF-β1 (codon 10, codon 25) TG haplotype were significantly lower in the patients group (P=0.004 and P=0.040, respectively), while TGF-β1 (codon 10, codon 25) CG haplotype was overrepresented in patients with CHF (P=0.007). CONCLUSIONS: Cytokine gene polymorphisms might affect vulnerability to CHF. Particular genotypes and haplotypes in IL-10 and TGF-β1 genes could render individuals more susceptible to CHF. (www.actabiomedica.it) Mattioli 1885 2019 2019-12-09 /pmc/articles/PMC6776215/ /pubmed/31124999 http://dx.doi.org/10.23750/abm.v90i2.6681 Text en Copyright: © 2019 ACTA BIO MEDICA SOCIETY OF MEDICINE AND NATURAL SCIENCES OF PARMA http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution 4.0 International License |
spellingShingle | Original Article Mohammad, Jafar Mahmoudi Mona, Hedayat Mohammad, Taghvaei Sara, Harsini Ebrahim, Nematipour Elham, Farhadi Maryam, Mahmoudi Maryam, Sadr Nilufar, Esfahanian Keramat, Nourijelyani Ali, Akbar Amirzargar Nima, Rezaei Interleukin-10 and Transforming Growth Factor Beta1 Gene Polymorphisms in Chronic Heart Failure |
title | Interleukin-10 and Transforming Growth Factor Beta1 Gene Polymorphisms in Chronic Heart Failure |
title_full | Interleukin-10 and Transforming Growth Factor Beta1 Gene Polymorphisms in Chronic Heart Failure |
title_fullStr | Interleukin-10 and Transforming Growth Factor Beta1 Gene Polymorphisms in Chronic Heart Failure |
title_full_unstemmed | Interleukin-10 and Transforming Growth Factor Beta1 Gene Polymorphisms in Chronic Heart Failure |
title_short | Interleukin-10 and Transforming Growth Factor Beta1 Gene Polymorphisms in Chronic Heart Failure |
title_sort | interleukin-10 and transforming growth factor beta1 gene polymorphisms in chronic heart failure |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776215/ https://www.ncbi.nlm.nih.gov/pubmed/31124999 http://dx.doi.org/10.23750/abm.v90i2.6681 |
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