IL28B gene polymorphism rs12979860, but not rs8099917, contributes to the occurrence of chronic HCV infection in uruguayan patients
Resumen:
Background: Host single-nucleotide polymorphisms (SNPs) near the interleukin 28B (IL28B) locus are associated with sustained virological response to antiviral therapy and with spontaneous Hepatitis C Virus (HCV) clearance. Prevalence of these SNPs varies depending on ethnicity. The impact of IL28B SNPs in HCV-infected patients is currently unknown in Uruguay. Therefore, the aim of this study was to evaluate and compare the distribution of polymorphisms in the IL28B gene (rs12979860 and rs8099917) among HCV-infected patients and healthy individuals in Uruguay and thus assess their possible association with the establishment of HCV infection. Methods: DNA was recovered from 92 non-infected individuals and 78 HCV-infected patients and SNPs were determined by RFLP and allelic discrimination by real-time PCR. Results: The distribution of rs12979860 genotypes for the infected population was 29.5%-CC, 47.4%-CT and 23.1%-TT and for the control group 45.7,% 42.4% and 11.9,% respectively. Prevalence in both infected and uninfected individuals is similar to that reported in other countries with admixed populations. The distribution of rs8099917 genotypes for the infected population was 57.7%-TT, 27.2%-TG and 14.1%-GG and for the control group 60.9,% 33.7% and 5.4,% respectively. The comparison of rs12979860 genotype distribution between the two populations evidenced a higher prevalence of the favourable genotype (CC) in the uninfected control group (p < 0.05). Additionally, results generated using logistic regression analysis show that individuals carrying rs12979860-TT or CT genotypes have a higher likelihood of developing chronic hepatitis upon infection with HCV, when compared to CC carriers, considering rs8099917 genotype as constant. Conclusion: Patients with HCV infection have a statistically significant lower prevalence of the favourable rs12979860 genotype when compared to uninfected individuals; therefore we can establish that only IL28B rs12979860-CT and TT genotypes seem to contribute to the occurrence of chronic HCV infection in the cohort of Uruguayan population studied. Considering that a trend towards a higher frequency of "good" response genotypes was observed in responder patients, we believe that IL28B rs12979860 genotyping could be a useful tool for predicting different therapies outcome, including in the DAA era.
2018 | |
Genotypic distribution Hepatitis C rs12979860 rs8099917 |
|
Inglés | |
Universidad de la República | |
COLIBRI | |
https://hdl.handle.net/20.500.12008/22081 | |
Acceso abierto | |
Licencia Creative Commons Atribución (CC –BY 4.0) |
_version_ | 1807522781219258368 |
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author | Echeverría Chagas, Natalia |
author2 | Chiodi, Daniela López, Pablo Sánchez Cicerón, Adriana Angulo, J. López-Lastra, M. Silvera, Paola Canavesi, Adrián Bianchi, C. Colistro, Valentina Cristina, Juan Hernández, Nelia Moreno Karlen, María del Pilar |
author2_role | author author author author author author author author author author author author |
author_facet | Echeverría Chagas, Natalia Chiodi, Daniela López, Pablo Sánchez Cicerón, Adriana Angulo, J. López-Lastra, M. Silvera, Paola Canavesi, Adrián Bianchi, C. Colistro, Valentina Cristina, Juan Hernández, Nelia Moreno Karlen, María del Pilar |
author_role | author |
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collection | COLIBRI |
dc.contributor.filiacion.es.fl_str_mv | Echeverría Chagas, Natalia. Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Investigaciones Nucleares Chiodi, Daniela. Universidad de la República (Uruguay). Facultad de Medicina López, Pablo. Universidad de la República (Uruguay). Facultad de Medicina Sanchez Ciceron, Adriana. Universidad de la República (Uruguay). Facultad de Medicina Silvera, Paola. Universidad de la República (Uruguay). Facultad de Medicina Canavesi, Adrián. Universidad de la República (Uruguay). Facultad de Medicina Colistro, Valentina. Universidad de la República (Uruguay). Facultad de Medicina Cristina, Juan. Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Investigaciones Nucleares Hernández, Nelia. Universidad de la República (Uruguay). Facultad de Medicina Moreno Karlen, María del Pilar. Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Investigaciones Nucleares |
dc.creator.none.fl_str_mv | Echeverría Chagas, Natalia Chiodi, Daniela López, Pablo Sánchez Cicerón, Adriana Angulo, J. López-Lastra, M. Silvera, Paola Canavesi, Adrián Bianchi, C. Colistro, Valentina Cristina, Juan Hernández, Nelia Moreno Karlen, María del Pilar |
dc.date.accessioned.none.fl_str_mv | 2019-10-02T22:14:47Z |
dc.date.available.none.fl_str_mv | 2019-10-02T22:14:47Z |
dc.date.issued.es.fl_str_mv | 2018 |
dc.date.submitted.es.fl_str_mv | 20191001 |
dc.description.abstract.none.fl_txt_mv | Background: Host single-nucleotide polymorphisms (SNPs) near the interleukin 28B (IL28B) locus are associated with sustained virological response to antiviral therapy and with spontaneous Hepatitis C Virus (HCV) clearance. Prevalence of these SNPs varies depending on ethnicity. The impact of IL28B SNPs in HCV-infected patients is currently unknown in Uruguay. Therefore, the aim of this study was to evaluate and compare the distribution of polymorphisms in the IL28B gene (rs12979860 and rs8099917) among HCV-infected patients and healthy individuals in Uruguay and thus assess their possible association with the establishment of HCV infection. Methods: DNA was recovered from 92 non-infected individuals and 78 HCV-infected patients and SNPs were determined by RFLP and allelic discrimination by real-time PCR. Results: The distribution of rs12979860 genotypes for the infected population was 29.5%-CC, 47.4%-CT and 23.1%-TT and for the control group 45.7,% 42.4% and 11.9,% respectively. Prevalence in both infected and uninfected individuals is similar to that reported in other countries with admixed populations. The distribution of rs8099917 genotypes for the infected population was 57.7%-TT, 27.2%-TG and 14.1%-GG and for the control group 60.9,% 33.7% and 5.4,% respectively. The comparison of rs12979860 genotype distribution between the two populations evidenced a higher prevalence of the favourable genotype (CC) in the uninfected control group (p < 0.05). Additionally, results generated using logistic regression analysis show that individuals carrying rs12979860-TT or CT genotypes have a higher likelihood of developing chronic hepatitis upon infection with HCV, when compared to CC carriers, considering rs8099917 genotype as constant. Conclusion: Patients with HCV infection have a statistically significant lower prevalence of the favourable rs12979860 genotype when compared to uninfected individuals; therefore we can establish that only IL28B rs12979860-CT and TT genotypes seem to contribute to the occurrence of chronic HCV infection in the cohort of Uruguayan population studied. Considering that a trend towards a higher frequency of "good" response genotypes was observed in responder patients, we believe that IL28B rs12979860 genotyping could be a useful tool for predicting different therapies outcome, including in the DAA era. |
dc.format.mimetype.es.fl_str_mv | application/pdf |
dc.identifier.citation.es.fl_str_mv | Echeverría, N. y otros. "IL28B gene polymorphism rs12979860, but not rs8099917, contributes to the occurrence of chronic HCV infection in uruguayan patients". Virology Journal, 2018, 15 (1), art. no. 40. doi: 10.1186/s12985-018-0946-2 |
dc.identifier.doi.es.fl_str_mv | 10.1186/s12985-018-0946-2 |
dc.identifier.issn.es.fl_str_mv | 1743-422X |
dc.identifier.uri.none.fl_str_mv | https://hdl.handle.net/20.500.12008/22081 |
dc.language.iso.none.fl_str_mv | en eng |
dc.publisher.es.fl_str_mv | BioMed Central Ltd. |
dc.relation.ispartof.es.fl_str_mv | Virology Journal, 2018, 15 (1), art. no. 40 |
dc.rights.license.none.fl_str_mv | Licencia Creative Commons Atribución (CC –BY 4.0) |
dc.rights.none.fl_str_mv | info:eu-repo/semantics/openAccess |
dc.source.none.fl_str_mv | reponame:COLIBRI instname:Universidad de la República instacron:Universidad de la República |
dc.subject.es.fl_str_mv | Genotypic distribution Hepatitis C rs12979860 rs8099917 |
dc.title.none.fl_str_mv | IL28B gene polymorphism rs12979860, but not rs8099917, contributes to the occurrence of chronic HCV infection in uruguayan patients |
dc.type.es.fl_str_mv | Artículo |
dc.type.none.fl_str_mv | info:eu-repo/semantics/article |
dc.type.version.none.fl_str_mv | info:eu-repo/semantics/publishedVersion |
description | Background: Host single-nucleotide polymorphisms (SNPs) near the interleukin 28B (IL28B) locus are associated with sustained virological response to antiviral therapy and with spontaneous Hepatitis C Virus (HCV) clearance. Prevalence of these SNPs varies depending on ethnicity. The impact of IL28B SNPs in HCV-infected patients is currently unknown in Uruguay. Therefore, the aim of this study was to evaluate and compare the distribution of polymorphisms in the IL28B gene (rs12979860 and rs8099917) among HCV-infected patients and healthy individuals in Uruguay and thus assess their possible association with the establishment of HCV infection. Methods: DNA was recovered from 92 non-infected individuals and 78 HCV-infected patients and SNPs were determined by RFLP and allelic discrimination by real-time PCR. Results: The distribution of rs12979860 genotypes for the infected population was 29.5%-CC, 47.4%-CT and 23.1%-TT and for the control group 45.7,% 42.4% and 11.9,% respectively. Prevalence in both infected and uninfected individuals is similar to that reported in other countries with admixed populations. The distribution of rs8099917 genotypes for the infected population was 57.7%-TT, 27.2%-TG and 14.1%-GG and for the control group 60.9,% 33.7% and 5.4,% respectively. The comparison of rs12979860 genotype distribution between the two populations evidenced a higher prevalence of the favourable genotype (CC) in the uninfected control group (p < 0.05). Additionally, results generated using logistic regression analysis show that individuals carrying rs12979860-TT or CT genotypes have a higher likelihood of developing chronic hepatitis upon infection with HCV, when compared to CC carriers, considering rs8099917 genotype as constant. Conclusion: Patients with HCV infection have a statistically significant lower prevalence of the favourable rs12979860 genotype when compared to uninfected individuals; therefore we can establish that only IL28B rs12979860-CT and TT genotypes seem to contribute to the occurrence of chronic HCV infection in the cohort of Uruguayan population studied. Considering that a trend towards a higher frequency of "good" response genotypes was observed in responder patients, we believe that IL28B rs12979860 genotyping could be a useful tool for predicting different therapies outcome, including in the DAA era. |
eu_rights_str_mv | openAccess |
format | article |
id | COLIBRI_f3cce3e02b02845b575588a928a25228 |
identifier_str_mv | Echeverría, N. y otros. "IL28B gene polymorphism rs12979860, but not rs8099917, contributes to the occurrence of chronic HCV infection in uruguayan patients". Virology Journal, 2018, 15 (1), art. no. 40. doi: 10.1186/s12985-018-0946-2 1743-422X 10.1186/s12985-018-0946-2 |
instacron_str | Universidad de la República |
institution | Universidad de la República |
instname_str | Universidad de la República |
language | eng |
language_invalid_str_mv | en |
network_acronym_str | COLIBRI |
network_name_str | COLIBRI |
oai_identifier_str | oai:colibri.udelar.edu.uy:20.500.12008/22081 |
publishDate | 2018 |
reponame_str | COLIBRI |
repository.mail.fl_str_mv | mabel.seroubian@seciu.edu.uy |
repository.name.fl_str_mv | COLIBRI - Universidad de la República |
repository_id_str | 4771 |
rights_invalid_str_mv | Licencia Creative Commons Atribución (CC –BY 4.0) |
spelling | Echeverría Chagas, Natalia. Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Investigaciones NuclearesChiodi, Daniela. Universidad de la República (Uruguay). Facultad de MedicinaLópez, Pablo. Universidad de la República (Uruguay). Facultad de MedicinaSanchez Ciceron, Adriana. Universidad de la República (Uruguay). Facultad de MedicinaSilvera, Paola. Universidad de la República (Uruguay). Facultad de MedicinaCanavesi, Adrián. Universidad de la República (Uruguay). Facultad de MedicinaColistro, Valentina. Universidad de la República (Uruguay). Facultad de MedicinaCristina, Juan. Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Investigaciones NuclearesHernández, Nelia. Universidad de la República (Uruguay). Facultad de MedicinaMoreno Karlen, María del Pilar. Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Investigaciones Nucleares2019-10-02T22:14:47Z2019-10-02T22:14:47Z201820191001Echeverría, N. y otros. "IL28B gene polymorphism rs12979860, but not rs8099917, contributes to the occurrence of chronic HCV infection in uruguayan patients". Virology Journal, 2018, 15 (1), art. no. 40. doi: 10.1186/s12985-018-0946-21743-422Xhttps://hdl.handle.net/20.500.12008/2208110.1186/s12985-018-0946-2Background: Host single-nucleotide polymorphisms (SNPs) near the interleukin 28B (IL28B) locus are associated with sustained virological response to antiviral therapy and with spontaneous Hepatitis C Virus (HCV) clearance. Prevalence of these SNPs varies depending on ethnicity. The impact of IL28B SNPs in HCV-infected patients is currently unknown in Uruguay. Therefore, the aim of this study was to evaluate and compare the distribution of polymorphisms in the IL28B gene (rs12979860 and rs8099917) among HCV-infected patients and healthy individuals in Uruguay and thus assess their possible association with the establishment of HCV infection. Methods: DNA was recovered from 92 non-infected individuals and 78 HCV-infected patients and SNPs were determined by RFLP and allelic discrimination by real-time PCR. Results: The distribution of rs12979860 genotypes for the infected population was 29.5%-CC, 47.4%-CT and 23.1%-TT and for the control group 45.7,% 42.4% and 11.9,% respectively. Prevalence in both infected and uninfected individuals is similar to that reported in other countries with admixed populations. The distribution of rs8099917 genotypes for the infected population was 57.7%-TT, 27.2%-TG and 14.1%-GG and for the control group 60.9,% 33.7% and 5.4,% respectively. The comparison of rs12979860 genotype distribution between the two populations evidenced a higher prevalence of the favourable genotype (CC) in the uninfected control group (p < 0.05). Additionally, results generated using logistic regression analysis show that individuals carrying rs12979860-TT or CT genotypes have a higher likelihood of developing chronic hepatitis upon infection with HCV, when compared to CC carriers, considering rs8099917 genotype as constant. Conclusion: Patients with HCV infection have a statistically significant lower prevalence of the favourable rs12979860 genotype when compared to uninfected individuals; therefore we can establish that only IL28B rs12979860-CT and TT genotypes seem to contribute to the occurrence of chronic HCV infection in the cohort of Uruguayan population studied. Considering that a trend towards a higher frequency of "good" response genotypes was observed in responder patients, we believe that IL28B rs12979860 genotyping could be a useful tool for predicting different therapies outcome, including in the DAA era.Made available in DSpace on 2019-10-02T22:14:47Z (GMT). No. of bitstreams: 5 101186s1298501809462.pdf: 562270 bytes, checksum: e83774393fe84f2e633a4f21c068839d (MD5) license_text: 38297 bytes, checksum: 4fe6ac477f5a2df0424a5ff1a9bf000c (MD5) license_url: 44 bytes, checksum: a0ebbeafb9d2ec7cbb19d7137ebc392c (MD5) license_rdf: 8067 bytes, checksum: bc1bc9659a4a06e9516479a5adfd8b0e (MD5) license.txt: 4194 bytes, checksum: 7f2e2c17ef6585de66da58d1bfa8b5e1 (MD5) Previous issue date: 2018application/pdfenengBioMed Central Ltd.Virology Journal, 2018, 15 (1), art. no. 40Las obras depositadas en el Repositorio se rigen por la Ordenanza de los Derechos de la Propiedad Intelectual de la Universidad De La República. (Res. Nº 91 de C.D.C. de 8/III/1994 – D.O. 7/IV/1994) y por la Ordenanza del Repositorio Abierto de la Universidad de la República (Res. Nº 16 de C.D.C. de 07/10/2014)info:eu-repo/semantics/openAccessLicencia Creative Commons Atribución (CC –BY 4.0)Genotypic distributionHepatitis Crs12979860rs8099917IL28B gene polymorphism rs12979860, but not rs8099917, contributes to the occurrence of chronic HCV infection in uruguayan patientsArtículoinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionreponame:COLIBRIinstname:Universidad de la Repúblicainstacron:Universidad de la RepúblicaEcheverría Chagas, NataliaChiodi, DanielaLópez, PabloSánchez Cicerón, AdrianaAngulo, J.López-Lastra, M.Silvera, PaolaCanavesi, AdriánBianchi, C.Colistro, ValentinaCristina, JuanHernández, NeliaMoreno Karlen, María del 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- Universidad de la Repúblicafalse |
spellingShingle | IL28B gene polymorphism rs12979860, but not rs8099917, contributes to the occurrence of chronic HCV infection in uruguayan patients Echeverría Chagas, Natalia Genotypic distribution Hepatitis C rs12979860 rs8099917 |
status_str | publishedVersion |
title | IL28B gene polymorphism rs12979860, but not rs8099917, contributes to the occurrence of chronic HCV infection in uruguayan patients |
title_full | IL28B gene polymorphism rs12979860, but not rs8099917, contributes to the occurrence of chronic HCV infection in uruguayan patients |
title_fullStr | IL28B gene polymorphism rs12979860, but not rs8099917, contributes to the occurrence of chronic HCV infection in uruguayan patients |
title_full_unstemmed | IL28B gene polymorphism rs12979860, but not rs8099917, contributes to the occurrence of chronic HCV infection in uruguayan patients |
title_short | IL28B gene polymorphism rs12979860, but not rs8099917, contributes to the occurrence of chronic HCV infection in uruguayan patients |
title_sort | IL28B gene polymorphism rs12979860, but not rs8099917, contributes to the occurrence of chronic HCV infection in uruguayan patients |
topic | Genotypic distribution Hepatitis C rs12979860 rs8099917 |
url | https://hdl.handle.net/20.500.12008/22081 |