4.5 Article

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

期刊

BMC INFECTIOUS DISEASES
卷 7, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/1471-2334-7-145

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资金

  1. Intramural NIH HHS Funding Source: Medline
  2. NCI NIH HHS [N02-CP-91027] Funding Source: Medline
  3. NCRR NIH HHS [M01 RR000079, M01-RR-00079, M01-RR-00071, M01-RR-00083, M01 RR000071, M01 RR000083] Funding Source: Medline
  4. NIAID NIH HHS [UO1-AI-31834, R01 AI055085, U01 AI042590, U01-AI-35004, U01 AI034994, K23 AI066943-05, UO1-AI-42590, R01 AI069952-01, R01 AI55085, UO1-AI-34993, U01 AI031834, K23 AI066943, R01 AI069952, U01 AI034989, UO1-AI-34994, U01 AI034993, U01 AI035004, UO1-AI-34989] Funding Source: Medline
  5. NICHD NIH HHS [UO1-HD-32632, U01 HD032632] Funding Source: Medline
  6. NIDA NIH HHS [R01 DA013245, R01 DA016159, R01-DA16159, R01 DA012109, R01-DA13245] Funding Source: Medline
  7. CSAT SAMHSA HHS [H79-TI12103] Funding Source: Medline

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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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