Estimating the future health burden of chronic hepatitis C and human immunodeficiency virus infections in the United States

被引:125
作者
Deuffic-Burban, S.
Poynard, T.
Sulkowski, M. S.
Wong, J. B.
机构
[1] Inst Catholique Lille, CRESGE, LEM, CNRS,UMR 8179, F-59016 Lille, France
[2] Grp Hosp Pitie Salpetriere, Serv Hepatogastroenterol, F-75634 Paris, France
[3] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[4] Tufts Univ, Sch Med, Tufts New England Med Ctr, Boston, MA 02111 USA
关键词
back-calculation; chronic hepatitis C; human immunodeficiency virus; Markov model; mortality predictions; HEPATOCELLULAR-CARCINOMA; HIV-INFECTION; AIDS INCIDENCE; PREVALENCE; EPIDEMIC; COMPLETENESS; MORTALITY; TRENDS; TIME; MORBIDITY;
D O I
10.1111/j.1365-2893.2006.00785.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The aim of this work was to estimate the future disease burden of hepatitis C virus (HCV) and human immunodeficiency virus (HIV) infections in the United States until the year 2030. Two back-calculation models of the HIV and the HCV epidemic were developed. They were based on US epidemiological data regarding prevalence, age and gender of incident cases, AIDS, hepatocellular carcinoma (HCC) mortality and general population mortality from the Centers for Disease Control and WHO. Based on the HCV back-calculation model, HCV incidence peaked in 1984 at 350 000 new infections and then fell to about 77 000 in 1998. Based on the HIV back-calculation model, HIV incidence reached its maximum in 1989 at 142 000 new infections and then declined to 79 000 in 1998. Mortality related to HCV (death from liver failure or HCC) rose from about 3700 in 1998 and is expected to peak at about 13 000 in 2030. Predicted HCV mortality would fall only if increased access to or more effective antiviral therapy occurs. For comparison, observed HIV-related mortality was 14 400 in 1998 and projected to be 4200 for 2030. With the availability of effective highly active antiretroviral therapy for HIV infection, mortality from HIV appears to have declined substantially, whereas HCV-related deaths as a result of pre-1999 infections will likely continue to increase over the next 25 years.
引用
收藏
页码:107 / 115
页数:9
相关论文
共 42 条
[1]   Hepatitis C in asymptomatic blood donors [J].
Alter, HJ ;
ConryCantilena, C ;
Melpolder, J ;
Tan, D ;
VanRaden, M ;
Herion, D ;
Lau, D ;
Hoofnagle, JH .
HEPATOLOGY, 1997, 26 (03) :S29-S33
[2]   The prevalence of hepatitis C virus infection in the United States, 1988 through 1994 [J].
Alter, MJ ;
Kruszon-Moran, D ;
Nainan, OV ;
McQuillan, GM ;
Gao, FX ;
Moyer, LA ;
Kaslow, RA ;
Margolis, HS .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (08) :556-562
[3]   RISK-FACTORS FOR ACUTE NON-A, NON-B HEPATITIS IN THE UNITED-STATES AND ASSOCIATION WITH HEPATITIS-C VIRUS-INFECTION [J].
ALTER, MJ ;
HADLER, SC ;
JUDSON, FN ;
MARES, A ;
ALEXANDER, WJ ;
HU, PY ;
MILLER, JK ;
MOYER, LA ;
FIELDS, HA ;
BRADLEY, DW ;
MARGOLIS, HS .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1990, 264 (17) :2231-2235
[4]  
[Anonymous], 1997, WEEKLY EPIDEMIOLOGIC, V72, P65
[5]   The past incidence of hepatitis C virus infection: Implications for the future burden of chronic liver disease in the United States [J].
Armstrong, GL ;
Alter, MJ ;
McQuillan, GM ;
Margolis, HS .
HEPATOLOGY, 2000, 31 (03) :777-782
[6]   DIFFERENT AIDS INCUBATION PERIODS AND THEIR IMPACTS ON RECONSTRUCTING HUMAN-IMMUNODEFICIENCY-VIRUS EPIDEMICS AND PROJECTING AIDS INCIDENCE [J].
BACCHETTI, P ;
SEGAL, MR ;
HESSOL, NA ;
JEWELL, NP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (06) :2194-2196
[7]   A METHOD FOR ESTIMATING THE AGE-SPECIFIC RELATIVE RISK OF HIV-INFECTION FROM AIDS INCIDENCE DATA [J].
BECKER, NG ;
MARSCHNER, IC .
BIOMETRIKA, 1993, 80 (01) :165-178
[8]   RECONSTRUCTION AND FUTURE-TRENDS OF THE AIDS EPIDEMIC IN THE UNITED-STATES [J].
BROOKMEYER, R .
SCIENCE, 1991, 253 (5015) :37-42
[9]  
BROOKMEYER R, 1986, LANCET, V2, P1320
[10]  
BUEHLER JW, 1992, J ACQ IMMUN DEF SYND, V5, P257