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Estimating past hepatitis C infection risk from reported risk factor histories: implications for imputing age of infection and modeling fibrosis progression

BACKGROUND: Chronic hepatitis C virus infection is prevalent and often causes hepatic fibrosis, which can progress to cirrhosis and cause liver cancer or liver failure. Study of fibrosis progression often relies on imputing the time of infection, often as the reported age of first injection drug use...

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Autores principales: Bacchetti, Peter, Tien, Phyllis C, Seaberg, Eric C, O'Brien, Thomas R, Augenbraun, Michael H, Kral, Alex H, Busch, Michael P, Edlin, Brian R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2238758/
https://www.ncbi.nlm.nih.gov/pubmed/18070362
http://dx.doi.org/10.1186/1471-2334-7-145
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author Bacchetti, Peter
Tien, Phyllis C
Seaberg, Eric C
O'Brien, Thomas R
Augenbraun, Michael H
Kral, Alex H
Busch, Michael P
Edlin, Brian R
author_facet Bacchetti, Peter
Tien, Phyllis C
Seaberg, Eric C
O'Brien, Thomas R
Augenbraun, Michael H
Kral, Alex H
Busch, Michael P
Edlin, Brian R
author_sort Bacchetti, Peter
collection PubMed
description BACKGROUND: Chronic hepatitis C virus infection is prevalent and often causes hepatic fibrosis, which can progress to cirrhosis and cause liver cancer or liver failure. Study of fibrosis progression often relies on imputing the time of infection, often as the reported age of first injection drug use. We sought to examine the accuracy of such imputation and implications for modeling factors that influence progression rates. METHODS: We analyzed cross-sectional data on hepatitis C antibody status and reported risk factor histories from two large studies, the Women's Interagency HIV Study and the Urban Health Study, using modern survival analysis methods for current status data to model past infection risk year by year. We compared fitted distributions of past infection risk to reported age of first injection drug use. RESULTS: Although injection drug use appeared to be a very strong risk factor, models for both studies showed that many subjects had considerable probability of having been infected substantially before or after their reported age of first injection drug use. Persons reporting younger age of first injection drug use were more likely to have been infected after, and persons reporting older age of first injection drug use were more likely to have been infected before. CONCLUSION: In cross-sectional studies of fibrosis progression where date of HCV infection is estimated from risk factor histories, modern methods such as multiple imputation should be used to account for the substantial uncertainty about when infection occurred. The models presented here can provide the inputs needed by such methods. Using reported age of first injection drug use as the time of infection in studies of fibrosis progression is likely to produce a spuriously strong association of younger age of infection with slower rate of progression.
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spelling pubmed-22387582008-02-12 Estimating past hepatitis C infection risk from reported risk factor histories: implications for imputing age of infection and modeling fibrosis progression Bacchetti, Peter Tien, Phyllis C Seaberg, Eric C O'Brien, Thomas R Augenbraun, Michael H Kral, Alex H Busch, Michael P Edlin, Brian R BMC Infect Dis Research Article BACKGROUND: Chronic hepatitis C virus infection is prevalent and often causes hepatic fibrosis, which can progress to cirrhosis and cause liver cancer or liver failure. Study of fibrosis progression often relies on imputing the time of infection, often as the reported age of first injection drug use. We sought to examine the accuracy of such imputation and implications for modeling factors that influence progression rates. METHODS: We analyzed cross-sectional data on hepatitis C antibody status and reported risk factor histories from two large studies, the Women's Interagency HIV Study and the Urban Health Study, using modern survival analysis methods for current status data to model past infection risk year by year. We compared fitted distributions of past infection risk to reported age of first injection drug use. RESULTS: Although injection drug use appeared to be a very strong risk factor, models for both studies showed that many subjects had considerable probability of having been infected substantially before or after their reported age of first injection drug use. Persons reporting younger age of first injection drug use were more likely to have been infected after, and persons reporting older age of first injection drug use were more likely to have been infected before. CONCLUSION: In cross-sectional studies of fibrosis progression where date of HCV infection is estimated from risk factor histories, modern methods such as multiple imputation should be used to account for the substantial uncertainty about when infection occurred. The models presented here can provide the inputs needed by such methods. Using reported age of first injection drug use as the time of infection in studies of fibrosis progression is likely to produce a spuriously strong association of younger age of infection with slower rate of progression. BioMed Central 2007-12-10 /pmc/articles/PMC2238758/ /pubmed/18070362 http://dx.doi.org/10.1186/1471-2334-7-145 Text en Copyright © 2007 Bacchetti et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bacchetti, Peter
Tien, Phyllis C
Seaberg, Eric C
O'Brien, Thomas R
Augenbraun, Michael H
Kral, Alex H
Busch, Michael P
Edlin, Brian R
Estimating past hepatitis C infection risk from reported risk factor histories: implications for imputing age of infection and modeling fibrosis progression
title Estimating past hepatitis C infection risk from reported risk factor histories: implications for imputing age of infection and modeling fibrosis progression
title_full Estimating past hepatitis C infection risk from reported risk factor histories: implications for imputing age of infection and modeling fibrosis progression
title_fullStr Estimating past hepatitis C infection risk from reported risk factor histories: implications for imputing age of infection and modeling fibrosis progression
title_full_unstemmed Estimating past hepatitis C infection risk from reported risk factor histories: implications for imputing age of infection and modeling fibrosis progression
title_short Estimating past hepatitis C infection risk from reported risk factor histories: implications for imputing age of infection and modeling fibrosis progression
title_sort estimating past hepatitis c infection risk from reported risk factor histories: implications for imputing age of infection and modeling fibrosis progression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2238758/
https://www.ncbi.nlm.nih.gov/pubmed/18070362
http://dx.doi.org/10.1186/1471-2334-7-145
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