Factors Associated With Rates of HBsAg Seroclearance in Adults With Chronic HBV Infection: A Systematic Review and Meta-analysis.


Journal

Gastroenterology
ISSN: 1528-0012
Titre abrégé: Gastroenterology
Pays: United States
ID NLM: 0374630

Informations de publication

Date de publication:
02 2019
Historique:
received: 18 07 2018
revised: 13 09 2018
accepted: 09 10 2018
pubmed: 21 10 2018
medline: 19 3 2019
entrez: 21 10 2018
Statut: ppublish

Résumé

Seroclearance of hepatitis B surface antigen (HBsAg) is a marker for clearance of chronic hepatitis B virus (HBV) infection, but reported annual incidence rates of HBsAg seroclearance vary. We performed a systematic review and meta-analysis to provide more precise estimates of HBsAg seroclearance rates among subgroups and populations. We searched PubMed, Embase, and the Cochrane library for cohort studies that reported HBsAg seroclearance in adults with chronic HBV infection with more than 1 year of follow-up and at least 1 repeat test for HBsAg. Annual and 5-, 10-, and 15-year cumulative incidence rates were pooled using a random effects model. We analyzed 34 published studies (with 42,588 patients, 303,754 person-years of follow-up, and 3194 HBsAg seroclearance events), including additional and updated aggregated data from 19 studies. The pooled annual rate of HBsAg seroclearance was 1.02% (95% CI, 0.79-1.27). Cumulative incidence rates were 4.03% at 5 years (95% CI, 2.49-5.93), 8.16% at 10 years (95% CI, 5.24-11.72), and 17.99% at 15 years (95% CI, 6.18-23.24). There were no significant differences between the sexes. A higher proportion of patients who tested negative for HBeAg at baseline had seroclearance (1.33%; 95% CI, 0.76-2.05) than those who tested positive for HBeAg (0.40%; 95% CI, 0.25-0.59) (P < .01). Having HBsAg seroclearance was also associated with a lower baseline HBV DNA level (6.61 log In a systematic review and meta-analysis, we found a low rate of HBsAg seroclearance in untreated and treated patients (pooled annual rate, approximately 1%). Seroclearance occurred mainly in patients with less active disease. Patients with chronic HBV infection should therefore be counseled on the need for lifelong treatment, and curative therapies are needed.

Sections du résumé

BACKGROUND & AIMS
Seroclearance of hepatitis B surface antigen (HBsAg) is a marker for clearance of chronic hepatitis B virus (HBV) infection, but reported annual incidence rates of HBsAg seroclearance vary. We performed a systematic review and meta-analysis to provide more precise estimates of HBsAg seroclearance rates among subgroups and populations.
METHODS
We searched PubMed, Embase, and the Cochrane library for cohort studies that reported HBsAg seroclearance in adults with chronic HBV infection with more than 1 year of follow-up and at least 1 repeat test for HBsAg. Annual and 5-, 10-, and 15-year cumulative incidence rates were pooled using a random effects model.
RESULTS
We analyzed 34 published studies (with 42,588 patients, 303,754 person-years of follow-up, and 3194 HBsAg seroclearance events), including additional and updated aggregated data from 19 studies. The pooled annual rate of HBsAg seroclearance was 1.02% (95% CI, 0.79-1.27). Cumulative incidence rates were 4.03% at 5 years (95% CI, 2.49-5.93), 8.16% at 10 years (95% CI, 5.24-11.72), and 17.99% at 15 years (95% CI, 6.18-23.24). There were no significant differences between the sexes. A higher proportion of patients who tested negative for HBeAg at baseline had seroclearance (1.33%; 95% CI, 0.76-2.05) than those who tested positive for HBeAg (0.40%; 95% CI, 0.25-0.59) (P < .01). Having HBsAg seroclearance was also associated with a lower baseline HBV DNA level (6.61 log
CONCLUSION
In a systematic review and meta-analysis, we found a low rate of HBsAg seroclearance in untreated and treated patients (pooled annual rate, approximately 1%). Seroclearance occurred mainly in patients with less active disease. Patients with chronic HBV infection should therefore be counseled on the need for lifelong treatment, and curative therapies are needed.

Identifiants

pubmed: 30342034
pii: S0016-5085(18)35158-8
doi: 10.1053/j.gastro.2018.10.027
pii:
doi:

Substances chimiques

Biomarkers 0
DNA, Viral 0
Hepatitis B Surface Antigens 0

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

635-646.e9

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2019 AGA Institute. Published by Elsevier Inc. All rights reserved.

Auteurs

Yee Hui Yeo (YH)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California.

Hsiu J Ho (HJ)

Division of Translational Research, Taipei Veterans General Hospital, Taipei City, Taiwan.

Hwai-I Yang (HI)

Genomics Research Center, Academia Sinica, Taipei, Taiwan.

Tai-Chung Tseng (TC)

Division of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.

Tetsuya Hosaka (T)

Department of Hepatology, Toranomon Hospital, Takatsu-ku, Kawasaki, Japan.

Huy N Trinh (HN)

San Jose Gastroenterology, San Jose, California.

Min-Sun Kwak (MS)

Department of Internal Medicine and Liver Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.

Young Min Park (YM)

Hepatology Center, Department of Internal Medicine and Biomedical Research Center, Bundang Jesaeng General Hospital, Seongnam-si, Gyeonggi-do, Republic of Korea.

James Yan Yue Fung (JYY)

Department of Medicine, The University of Hong Kong, Hong Kong, People's Republic of China.

Maria Buti (M)

Liver Unit, Hospital Universitari Vall d'Hebron and Ciberehd del Instituto Carlos III, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, Barcelona, Spain.

Manuel Rodríguez (M)

Liver Unit, Division of Gastroenterology and Hepatology, Hospital Universitario Central de Asturias, Oviedo, Asturias, Spain.

Sombat Treeprasertsuk (S)

Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Carmen Monica Preda (CM)

Department of Gastroenterology, Clinic Fundeni Institute, Bucharest, Romania.

Teerapat Ungtrakul (T)

Faculty of Medicine and Public Health, HRH Princess Chulabhorn College of Medical Science, Chulabhorn Royal Academy, Thailand.

Phunchai Charatcharoenwitthaya (P)

Department of Medicine, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.

Xiangyong Li (X)

Department of Infectious Diseases, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, People's Republic of China.

Jiayi Li (J)

Palo Alto Medical Foundation, Mountain View Division, Palo Alto, California.

Jian Zhang (J)

Chinese Hospital, San Francisco, California; School of Nursing, University of California, San Francisco, California.

Michael Huan Le (MH)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California.

Bin Wei (B)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California.

Biyao Zou (B)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California.

An Le (A)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California.

Donghak Jeong (D)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California.

Nicholas Chien (N)

Kaohsiung Medical University, Kaohsiung, Taiwan.

Leslie Kam (L)

Kaohsiung Medical University, Kaohsiung, Taiwan.

Chiao-Chin Lee (CC)

Department of Internal Medicine, Tri-Service General Hospital, Taipei, Taiwan.

Mar Riveiro-Barciela (M)

Liver Unit, Hospital Universitari Vall d'Hebron and Ciberehd del Instituto Carlos III, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, Barcelona, Spain.

Doina Istratescu (D)

Department of Gastroenterology, Clinic Fundeni Institute, Bucharest, Romania.

Tassanee Sriprayoon (T)

Department of Medicine, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.

Yutian Chong (Y)

Department of Infectious Diseases, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, People's Republic of China.

Tawesak Tanwandee (T)

Department of Medicine, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.

Mariko Kobayashi (M)

Research Institute for Hepatology, Toranomon Hospital, Takatsu-ku, Kawasaki, Japan.

Fumitaka Suzuki (F)

Department of Hepatology, Toranomon Hospital, Takatsu-ku, Kawasaki, Japan.

Man-Fung Yuen (MF)

Department of Medicine, The University of Hong Kong, Hong Kong, People's Republic of China.

Hyo-Suk Lee (HS)

Department of Internal Medicine and Liver Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.

Jia-Horng Kao (JH)

Division of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan; Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.

Anna S Lok (AS)

Division of Gastroenterology and Hepatology, University of Michigan, Ann Arbor, Michigan.

Chun-Ying Wu (CY)

Division of Translational Research, Taipei Veterans General Hospital, Taipei City, Taiwan; College of Public Health, China Medical University, Taichung, Taiwan. Electronic address: cywu22@vghtpe.gov.tw.

Mindie H Nguyen (MH)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California. Electronic address: mindiehn@stanford.edu.

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