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

被引:19
作者
Bacchetti, Peter [1 ]
Tien, Phyllis C. [2 ]
Seaberg, Eric C. [3 ]
O'Brien, Thomas R. [4 ]
Augenbraun, Michael H. [5 ]
Kral, Alex H. [6 ]
Busch, Michael P. [7 ]
Edlin, Brian R. [8 ,9 ]
机构
[1] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Vet Affairs Med Ctr, Dept Med, Infect Dis Sect, San Francisco, CA 94121 USA
[3] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
[4] Natl Canc Inst, Div Canc Epidemiol & Genet, Bethesda, MD USA
[5] Suny Downstate Med Ctr, Div Infect Dis, Brooklyn, NY 11203 USA
[6] Univ Calif San Francisco, Dept Family & Community Med, RTI Int, San Francisco, CA 94143 USA
[7] Univ Calif San Francisco, Blood Syst Res Inst, Dept Lab Med, San Francisco, CA 94143 USA
[8] Cornell Univ, Weill Med Coll, Ctr Study Hepatitis C, New York, NY 10021 USA
[9] Univ Calif San Francisco, Dept Family & Community Med, San Francisco, CA 94143 USA
关键词
D O I
10.1186/1471-2334-7-145
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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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页数:11
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共 47 条
  • [1] The prevalence of hepatitis C virus infection in the United States, 1988 through 1994
    Alter, MJ
    Kruszon-Moran, D
    Nainan, OV
    McQuillan, GM
    Gao, FX
    Moyer, LA
    Kaslow, RA
    Margolis, HS
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (08) : 556 - 562
  • [2] Incident hepatitis C virus in women with human immunodeficiency virus infection
    Augenbraun, M
    Goedert, JJ
    Thomas, D
    Feldman, J
    Seaberg, EC
    French, AL
    Robison, E
    Nowicki, M
    Terrault, N
    [J]. CLINICAL INFECTIOUS DISEASES, 2003, 37 (10) : 1357 - 1364
  • [3] Age and variant Creutzfeldt-Jakob disease
    Bacchetti, P
    [J]. EMERGING INFECTIOUS DISEASES, 2003, 9 (12) : 1611 - 1612
  • [4] The Women's Interagency HIV Study: an observational cohort brings clinical sciences to the bench
    Bacon, MC
    von Wyl, V
    Alden, C
    Sharp, G
    Robison, E
    Hessol, N
    Gange, S
    Barranday, Y
    Holman, S
    Weber, K
    Young, MA
    [J]. CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2005, 12 (09) : 1013 - 1019
  • [5] The Women's Interagency HIV Study
    Barkan, SE
    Melnick, SL
    Preston-Martin, S
    Weber, K
    Kalish, LA
    Miotti, P
    Young, M
    Greenblatt, R
    Sacks, H
    Feldman, J
    [J]. EPIDEMIOLOGY, 1998, 9 (02) : 117 - 125
  • [6] An algorithm for the grading of activity in chronic hepatitis C
    Bedossa, P
    Poynard, T
    [J]. HEPATOLOGY, 1996, 24 (02) : 289 - 293
  • [7] HEPATITIS-C VIRUS IN INTRAVENOUS-DRUG-USERS
    BELL, J
    BATEY, RG
    FARRELL, GC
    CREWE, EB
    CUNNINGHAM, AL
    BYTH, K
    [J]. MEDICAL JOURNAL OF AUSTRALIA, 1990, 153 (05) : 274 - 276
  • [8] Factors affecting liver fibrosis in human immunodeficiency virus- and hepatitis C virus-coinfected patients: Impact of protease inhibitor therapy
    Benhamou, Y
    Di Martino, V
    Bochet, M
    Colombet, G
    Thibault, V
    Liou, A
    Katlama, C
    Poynard, T
    [J]. HEPATOLOGY, 2001, 34 (02) : 283 - 287
  • [9] Boyer JL, 2003, HIV CLIN TRIALS, V4, P55
  • [10] Correlates of hepatitis C virus (HCV) RNA negativity among HCV-seropositive blood donors
    Busch, MP
    Glynn, SA
    Stramer, SL
    Orland, J
    Murphy, EL
    Wright, DJ
    Kleinman, S
    [J]. TRANSFUSION, 2006, 46 (03) : 469 - 475