The PNPLA3 Genetic Variant rs738409 Influences the Progression to Cirrhosis in HIV/Hepatitis C Virus Coinfected Patients
Contradictory data about the impact of the rs738409 steatosis-related polymorphism within PNPLA3 gene on liver fibrosis progression in HIV/hepatitis C virus (HIV/HCV)-coinfected patients have been reported. Our objective was to test whether this, and other polymorphisms previously related to fatty l...
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Published in: | PloS one Vol. 11; no. 12; p. e0168265 |
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Abstract | Contradictory data about the impact of the rs738409 steatosis-related polymorphism within PNPLA3 gene on liver fibrosis progression in HIV/hepatitis C virus (HIV/HCV)-coinfected patients have been reported. Our objective was to test whether this, and other polymorphisms previously related to fatty liver disease in HIV infection linked to SAMM50 or LPPR4 genes, influence liver fibrosis progression in HIV/HCV-coinfected individuals. Three hundred and thirty two HIV/HCV-coinfected patients who consecutively attended four Spanish university hospitals from November 2011 to July 2013 were included. A liver stiffness cut-off of 14.6 kPa, as determined by transient elastography, was used to diagnose cirrhosis. Liver stiffness progression was studied in 171 individuals who had two available LS determinations without anti-HCV treatment between them. Moreover, 28 HIV/HCV-coinfected patients who underwent liver transplant, as well as 19 non-cirrhotic coinfected individuals used as controls, were included in an additional study. Only rs738409 was associated with cirrhosis: 45 (29.6%) of 152 G allele carriers versus 36 (20.0%) of 180 CC carriers showed cirrhosis (multivariate p = 0.018; adjusted odds ratio = 1.98; 95% confidence interval = 1.12-3.50). Also, 21 (30.4%) of 69 G allele carriers versus 16 (15.7%) of 102 CC patients showed significant liver stiffness progression (adjusted p-value = 0.015; adjusted odds ratio = 2.89; 95% confidence interval = 1.23-6.83). Finally, the proportion of rs738409 G allele carriers was significantly higher in transplanted individuals than in controls (p = 0.044, odds ratio = 3.43; 95% confidence interval = 1.01-11.70). Our results strongly suggest that the rs738409 polymorphism is associated with liver fibrosis progression in HIV/HCV-coinfected patients. |
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AbstractList | Contradictory data about the impact of the rs738409 steatosis-related polymorphism within PNPLA3 gene on liver fibrosis progression in HIV/hepatitis C virus (HIV/HCV)-coinfected patients have been reported. Our objective was to test whether this, and other polymorphisms previously related to fatty liver disease in HIV infection linked to SAMM50 or LPPR4 genes, influence liver fibrosis progression in HIV/HCV-coinfected individuals. Three hundred and thirty two HIV/HCV-coinfected patients who consecutively attended four Spanish university hospitals from November 2011 to July 2013 were included. A liver stiffness cut-off of 14.6 kPa, as determined by transient elastography, was used to diagnose cirrhosis. Liver stiffness progression was studied in 171 individuals who had two available LS determinations without anti-HCV treatment between them. Moreover, 28 HIV/HCV-coinfected patients who underwent liver transplant, as well as 19 non-cirrhotic coinfected individuals used as controls, were included in an additional study. Only rs738409 was associated with cirrhosis: 45 (29.6%) of 152 G allele carriers versus 36 (20.0%) of 180 CC carriers showed cirrhosis (multivariate p = 0.018; adjusted odds ratio = 1.98; 95% confidence interval = 1.12-3.50). Also, 21 (30.4%) of 69 G allele carriers versus 16 (15.7%) of 102 CC patients showed significant liver stiffness progression (adjusted p-value = 0.015; adjusted odds ratio = 2.89; 95% confidence interval = 1.23-6.83). Finally, the proportion of rs738409 G allele carriers was significantly higher in transplanted individuals than in controls (p = 0.044, odds ratio = 3.43; 95% confidence interval = 1.01-11.70). Our results strongly suggest that the rs738409 polymorphism is associated with liver fibrosis progression in HIV/HCV-coinfected patients. Contradictory data about the impact of the rs738409 steatosis-related polymorphism within PNPLA3 gene on liver fibrosis progression in HIV/hepatitis C virus (HIV/HCV)-coinfected patients have been reported. Our objective was to test whether this, and other polymorphisms previously related to fatty liver disease in HIV infection linked to SAMM50 or LPPR4 genes, influence liver fibrosis progression in HIV/HCV-coinfected individuals. Three hundred and thirty two HIV/HCV-coinfected patients who consecutively attended four Spanish university hospitals from November 2011 to July 2013 were included. A liver stiffness cut-off of 14.6 kPa, as determined by transient elastography, was used to diagnose cirrhosis. Liver stiffness progression was studied in 171 individuals who had two available LS determinations without anti-HCV treatment between them. Moreover, 28 HIV/HCV-coinfected patients who underwent liver transplant, as well as 19 non-cirrhotic coinfected individuals used as controls, were included in an additional study. Only rs738409 was associated with cirrhosis: 45 (29.6%) of 152 G allele carriers versus 36 (20.0%) of 180 CC carriers showed cirrhosis (multivariate p = 0.018; adjusted odds ratio = 1.98; 95% confidence interval = 1.12–3.50). Also, 21 (30.4%) of 69 G allele carriers versus 16 (15.7%) of 102 CC patients showed significant liver stiffness progression (adjusted p-value = 0.015; adjusted odds ratio = 2.89; 95% confidence interval = 1.23–6.83). Finally, the proportion of rs738409 G allele carriers was significantly higher in transplanted individuals than in controls (p = 0.044, odds ratio = 3.43; 95% confidence interval = 1.01–11.70). Our results strongly suggest that the rs738409 polymorphism is associated with liver fibrosis progression in HIV/HCV-coinfected patients. |
Audience | Academic |
Author | Merchante, Nicolás Pineda, Juan A Gómez-Mateos, Jesús Rivero-Juárez, Antonio Frías, Mario Téllez, Francisco Macías, Juan Guaraldi, Giovanni Dolci, Giovanni Real, Luis M Núñez-Torres, Rocío Merino, Dolores Mancebo, María |
AuthorAffiliation | 1 Unit of Infectious Diseases and Microbiology, Valme University Hospital, Seville, Spain 4 Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBC), University of Córdoba, Córdoba, Spain 5 Department of Medical and Surgical Science for Adults and Children, Clinic and Infectious Diseases, University of Modena and Reggio Emilia, Modena, Italy 7 Unit of Infectious Diseases, Huelva University Hospital, Huelva, Spain 2 Instituto de Biomedicina de Sevilla (IBIS), Seville, Spain 3 Unit of Infectious Diseases, Reina Sofía University Hospital, Córdoba, Spain 6 Unit of Infectious Diseases, La Línea de la Concepción Hospital, Cádiz, Spain CAEBI, SPAIN |
AuthorAffiliation_xml | – name: 4 Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBC), University of Córdoba, Córdoba, Spain – name: 6 Unit of Infectious Diseases, La Línea de la Concepción Hospital, Cádiz, Spain – name: 5 Department of Medical and Surgical Science for Adults and Children, Clinic and Infectious Diseases, University of Modena and Reggio Emilia, Modena, Italy – name: CAEBI, SPAIN – name: 1 Unit of Infectious Diseases and Microbiology, Valme University Hospital, Seville, Spain – name: 3 Unit of Infectious Diseases, Reina Sofía University Hospital, Córdoba, Spain – name: 2 Instituto de Biomedicina de Sevilla (IBIS), Seville, Spain – name: 7 Unit of Infectious Diseases, Huelva University Hospital, Huelva, Spain |
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CitedBy_id | crossref_primary_10_2174_0118746136280350240214064332 crossref_primary_10_1007_s11904_023_00669_7 crossref_primary_10_1038_s42255_020_0183_z crossref_primary_10_1016_j_cgh_2023_01_001 crossref_primary_10_3389_fphar_2022_905126 crossref_primary_10_1016_j_jcv_2018_04_008 crossref_primary_10_2217_pgs_2018_0046 crossref_primary_10_1371_journal_pone_0222609 crossref_primary_10_35761_reesme_2017_1_02 crossref_primary_10_1016_j_ajg_2020_09_002 crossref_primary_10_1007_s10620_018_5278_y crossref_primary_10_1080_23808993_2020_1764346 |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Conceptualization: LMR RN-T JAP GG.Data curation: MM JM.Formal analysis: LMR RN-T JM JAP NM.Funding acquisition: LMR JAP.Investigation: LMR RN-T MM MF GD.Methodology: LMR RN-T AR-J JAP JM.Project administration: LMR JAP JG-M.Resources: FT DM NM JG-M GG JM JAP AR-J.Supervision: LMR JAP JG-M JM.Validation: GD GG MF.Visualization: RN-T LMR AR-J JAP.Writing – original draft: RN-T LMR JM JAP.Writing – review & editing: MF GD GG AR-J FT DM. Competing Interests: The authors have declared that no competing interests exist. Complete membership of the author group can be found in the Acknowledgments. |
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Snippet | Contradictory data about the impact of the rs738409 steatosis-related polymorphism within PNPLA3 gene on liver fibrosis progression in HIV/hepatitis C virus... Contradictory data about the impact of the rs738409 steatosis-related polymorphism within PNPLA3 gene on liver fibrosis progression in HIV/hepatitis C virus... |
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SubjectTerms | Adult Alleles Biology and Life Sciences Carriers Cirrhosis Coinfection - virology Confidence intervals Cross-Sectional Studies Disease Progression Elasticity Imaging Techniques Fatty liver Fatty Liver - genetics Female Fibrosis Gene polymorphism Genetic aspects Genetic diversity Genetic Markers Genetic variance Genetic Variation Health aspects Hepatitis Hepatitis C Hepatitis C virus Hepatitis C, Chronic - genetics Hepatitis C, Chronic - physiopathology Hepatology HIV HIV Infections - genetics HIV Infections - physiopathology Hospitals Human immunodeficiency virus Humans Infections Infectious diseases Lentivirus Lipase - genetics Liver Liver cirrhosis Liver Cirrhosis - diagnosis Liver Cirrhosis - genetics Liver Cirrhosis - virology Liver diseases Liver Transplantation Liver transplants Longitudinal Studies Male Medicine and Health Sciences Membrane Proteins - genetics Metabolism Middle Aged Multivariate Analysis Odds Ratio Patients Polymorphism Polymorphism, Genetic Population Retrospective Studies Retroviridae Risk factors Steatosis Stiffness Transplants & implants Viruses |
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Title | The PNPLA3 Genetic Variant rs738409 Influences the Progression to Cirrhosis in HIV/Hepatitis C Virus Coinfected Patients |
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