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Hepatitis C Testing and Liver Fibrosis Predictors in the Birth Cohort of a Primary Care Practice

OBJECTIVE: To determine the prevalence of and risk factors for advanced fibrosis in patients born from 1945 through 1965 (birth cohort) who underwent testing for hepatitis C virus (HCV). PATIENTS AND METHODS: Data were extracted from the electronic health record of all patients receiving primary car...

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Autores principales: Bersoux, Sophie, Mi, Lanyu, Aqel, Bashar A., Dickson, Rolland C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7411155/
https://www.ncbi.nlm.nih.gov/pubmed/32793866
http://dx.doi.org/10.1016/j.mayocpiqo.2020.04.003
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author Bersoux, Sophie
Mi, Lanyu
Aqel, Bashar A.
Dickson, Rolland C.
author_facet Bersoux, Sophie
Mi, Lanyu
Aqel, Bashar A.
Dickson, Rolland C.
author_sort Bersoux, Sophie
collection PubMed
description OBJECTIVE: To determine the prevalence of and risk factors for advanced fibrosis in patients born from 1945 through 1965 (birth cohort) who underwent testing for hepatitis C virus (HCV). PATIENTS AND METHODS: Data were extracted from the electronic health record of all patients receiving primary care at a single academic institution who underwent HCV testing between September 8, 2010, and March 5, 2018. The birth cohort patients were the primary focus of the study. Fibrosis 4 (FIB-4) and aspartate aminotransferase to platelet ratio index (APRI) scores were calculated to screen for fibrosis. RESULTS: During the study period, 7097 birth cohort patients had HCV antibody testing, 3462 (48.8%) of whom were men, 6435 (91.0%) were white, 1028 (14.5%) had diabetes mellitus, 2,034 (36.5%) had an alanine aminotransferase (ALT) level greater than 30 U/L, and 2,396 (34.2%) had body mass index of 30 kg/m(2) or greater. Hepatitis C virus antibody was present in 124 (1.7%), 33 (26.6%) of whom had HCV viremia. Estimated prevalence of METAVIR [Meta-analysis of Histological Data in Viral Hepatitis] stage 4 fibrosis was 4.1% (180 of 4433) by a FIB-4 score of 3.25 or greater and 4.3% (204 of 4763) by an APRI score greater than 1.0. The odds ratio (OR) for fibrosis, determined by APRI, was significant for HCV RNA positivity (OR, 15.98; 95% CI, 7.23-35.32; P<.001), diabetes mellitus (OR, 1.98; 95% CI, 1.40-2.79; P<.001), and ALT value greater than 30 U/L (OR, 15.07 U/L; 95% CI, 9.27-24.52 U/L; P<.001) but not for body mass index of 30 kg/m(2) or greater (OR, 0.77; 95% CI, 0.56-1.06; P=.11). CONCLUSION: Hepatitis C virus viremia, diabetes mellitus, and elevated ALT levels were associated with increased odds for development of fibrosis. In addition to HCV testing, diabetes mellitus and elevated ALT level are potential parameters to use for recommending noninvasive testing for fibrosis.
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spelling pubmed-74111552020-08-12 Hepatitis C Testing and Liver Fibrosis Predictors in the Birth Cohort of a Primary Care Practice Bersoux, Sophie Mi, Lanyu Aqel, Bashar A. Dickson, Rolland C. Mayo Clin Proc Innov Qual Outcomes Original Article OBJECTIVE: To determine the prevalence of and risk factors for advanced fibrosis in patients born from 1945 through 1965 (birth cohort) who underwent testing for hepatitis C virus (HCV). PATIENTS AND METHODS: Data were extracted from the electronic health record of all patients receiving primary care at a single academic institution who underwent HCV testing between September 8, 2010, and March 5, 2018. The birth cohort patients were the primary focus of the study. Fibrosis 4 (FIB-4) and aspartate aminotransferase to platelet ratio index (APRI) scores were calculated to screen for fibrosis. RESULTS: During the study period, 7097 birth cohort patients had HCV antibody testing, 3462 (48.8%) of whom were men, 6435 (91.0%) were white, 1028 (14.5%) had diabetes mellitus, 2,034 (36.5%) had an alanine aminotransferase (ALT) level greater than 30 U/L, and 2,396 (34.2%) had body mass index of 30 kg/m(2) or greater. Hepatitis C virus antibody was present in 124 (1.7%), 33 (26.6%) of whom had HCV viremia. Estimated prevalence of METAVIR [Meta-analysis of Histological Data in Viral Hepatitis] stage 4 fibrosis was 4.1% (180 of 4433) by a FIB-4 score of 3.25 or greater and 4.3% (204 of 4763) by an APRI score greater than 1.0. The odds ratio (OR) for fibrosis, determined by APRI, was significant for HCV RNA positivity (OR, 15.98; 95% CI, 7.23-35.32; P<.001), diabetes mellitus (OR, 1.98; 95% CI, 1.40-2.79; P<.001), and ALT value greater than 30 U/L (OR, 15.07 U/L; 95% CI, 9.27-24.52 U/L; P<.001) but not for body mass index of 30 kg/m(2) or greater (OR, 0.77; 95% CI, 0.56-1.06; P=.11). CONCLUSION: Hepatitis C virus viremia, diabetes mellitus, and elevated ALT levels were associated with increased odds for development of fibrosis. In addition to HCV testing, diabetes mellitus and elevated ALT level are potential parameters to use for recommending noninvasive testing for fibrosis. Elsevier 2020-07-15 /pmc/articles/PMC7411155/ /pubmed/32793866 http://dx.doi.org/10.1016/j.mayocpiqo.2020.04.003 Text en © 2020 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Bersoux, Sophie
Mi, Lanyu
Aqel, Bashar A.
Dickson, Rolland C.
Hepatitis C Testing and Liver Fibrosis Predictors in the Birth Cohort of a Primary Care Practice
title Hepatitis C Testing and Liver Fibrosis Predictors in the Birth Cohort of a Primary Care Practice
title_full Hepatitis C Testing and Liver Fibrosis Predictors in the Birth Cohort of a Primary Care Practice
title_fullStr Hepatitis C Testing and Liver Fibrosis Predictors in the Birth Cohort of a Primary Care Practice
title_full_unstemmed Hepatitis C Testing and Liver Fibrosis Predictors in the Birth Cohort of a Primary Care Practice
title_short Hepatitis C Testing and Liver Fibrosis Predictors in the Birth Cohort of a Primary Care Practice
title_sort hepatitis c testing and liver fibrosis predictors in the birth cohort of a primary care practice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7411155/
https://www.ncbi.nlm.nih.gov/pubmed/32793866
http://dx.doi.org/10.1016/j.mayocpiqo.2020.04.003
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