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
Main Authors: Núñez-Torres, Rocío, Macías, Juan, Mancebo, María, Frías, Mario, Dolci, Giovanni, Téllez, Francisco, Merino, Dolores, Merchante, Nicolás, Gómez-Mateos, Jesús, Guaraldi, Giovanni, Rivero-Juárez, Antonio, Pineda, Juan A, Real, Luis M
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Published: United States Public Library of Science 14-12-2016
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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.
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
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/27973562$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright COPYRIGHT 2016 Public Library of Science
2016 Núñez-Torres et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2016 Núñez-Torres et al 2016 Núñez-Torres et al
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CorporateAuthor HEPAVIR-esteatosis Study Group
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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.
OpenAccessLink https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5156377/
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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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StartPage e0168265
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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