The natural history and evaluation of standard treatment of chronic hepatitis B: A critical treatment criteria and end points

被引:151
作者
Lai, Ching-Lung [1 ]
Yuen, Man-Fung [1 ]
机构
[1] Queen Mary Hosp, Dept Med, Hong Kong, Hong Kong, Peoples R China
关键词
D O I
10.7326/0003-4819-147-1-200707030-00010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The definite indications for the treatment of chronic hepatitis B are serum hepatitis B virus (HBV) DNA levels greater than 10(5) copies/mL and alanine aminotransferase (ALT) levels more than 2 times the upper limit of normal. if cirrhosis is present, an HBV DNA level greater than 105 copies/mL is the sole criterion for treatment. Treatment end points include hepatitis B e antigen (HEeAg) seroconversion for HBeAg-positive patients, reduction of HEV DNA levels to less than 105 copies/mL, and normalization of ALT values. These guidelines may apply to patients who acquire the hepatitis B infection during adolescence or adulthood but are less suitable for most hepatitis B carriers, who are infected in early life. Cirrhosis complications, including hepatocellular carcinoma, often occur in this latter group despite HBeAg seroconversion, HBV DNA levels less than 10(4) copies/mL, or ALT levels between 0.5 and 2 times the upper limit of normal. Therefore, HBeAg seroconversion may not be an adequate end point for these patients; the ideal treatment end points are permanent suppression of HBV DNA to levels undetectable by polymerase chain reaction and reduction of ALT levels to less than 0.5 times the upper limit of normal.
引用
收藏
页码:58 / 61
页数:4
相关论文
共 26 条
  • [11] Asian-Pacific consensus statement on the management of chronic hepatitis B: a 2005 update
    Liaw, YF
    Leung, N
    Guan, R
    Lau, GKK
    Merican, I
    McCaughan, G
    Gane, E
    Kao, JH
    Omata, M
    [J]. LIVER INTERNATIONAL, 2005, 25 (03) : 472 - 489
  • [12] Lamivudine for patients with chronic hepatitis B and advanced liver disease
    Liaw, YF
    Sung, JJY
    Chow, WC
    Farrell, G
    Lee, CZ
    Yuen, H
    Tanwandee, T
    Tao, QM
    Shue, K
    Keene, ON
    Dixon, JS
    Gray, DF
    Sabbat, J
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (15) : 1521 - 1531
  • [13] Chronic hepatitis B
    Lok, Anna S. F.
    McMahon, Brian J.
    [J]. HEPATOLOGY, 2007, 45 (02) : 507 - 539
  • [14] Management of hepatitis B: 2000 - Summary of a workshop
    Lok, AS
    Heathcote, EJ
    Hoofnagle, JH
    [J]. GASTROENTEROLOGY, 2001, 120 (07) : 1828 - 1853
  • [15] Natural history of chronic HBV in northern Italy:: Morbidity and morality after 30 years
    Manno, M
    Cammá, C
    Schepis, F
    Bassi, F
    Gelmini, R
    Giannini, F
    Miselli, F
    Grottola, A
    Ferretti, I
    Vecchi, C
    De Palma, M
    Villa, E
    [J]. GASTROENTEROLOGY, 2004, 127 (03) : 756 - 763
  • [16] Carcinogenicity of lipid-lowering drugs
    Newman, TB
    Hulley, SB
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 275 (01): : 55 - 60
  • [17] Nguyen MH, 2005, HEPATOLOGY, V42, p593A
  • [18] Long-term follow-up of HBeAg-positive patients treated with interferon alfa for chronic hepatitis B
    Niederau, C
    Heintges, T
    Lange, S
    Goldmann, G
    Niederau, CM
    Mohr, L
    Haussinger, D
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (22) : 1422 - 1427
  • [19] Hepatitis B - Predicting survival in hepatitis B
    Sherman, M
    [J]. GUT, 2005, 54 (11) : 1521 - 1523
  • [20] *TAIW COMM BAS CAN, 2002, NEW ENGL J MED, V347, P168