Incidence, Factors, and Patient-Level Data for Spontaneous HBsAg Seroclearance: A Cohort Study of 11,264 Patients.


Journal

Clinical and translational gastroenterology
ISSN: 2155-384X
Titre abrégé: Clin Transl Gastroenterol
Pays: United States
ID NLM: 101532142

Informations de publication

Date de publication:
09 2020
Historique:
entrez: 23 10 2020
pubmed: 24 10 2020
medline: 9 7 2021
Statut: ppublish

Résumé

Spontaneous hepatitis B surface antigen (HBsAg) seroclearance, the functional cure of hepatitis B infection, occurs rarely. Prior original studies are limited by insufficient sample size and/or follow-up, and recent meta-analyses are limited by inclusion of only study-level data and lack of adjustment for confounders to investigate HBsAg seroclearance rates in most relevant subgroups. Using a cohort with detailed individual patient data, we estimated spontaneous HBsAg seroclearance rates through patient and virologic characteristics. We analyzed 11,264 untreated patients with chronic hepatitis B with serial HBsAg data from 4 North American and 8 Asian Pacific centers, with 1,393 patients with HBsAg seroclearance (≥2 undetectable HBsAg ≥6 months apart) during 106,192 person-years. The annual seroclearance rate with detailed categorization by infection phase, further stratified by hepatitis B e antigen (HBeAg) status, sex, age, and quantitative HBsAg (qHBsAg), was performed. The annual seroclearance rate was 1.31% (95% confidence interval: 1.25-1.38) and over 7% in immune inactive patients aged ≥55 years and with qHBsAg <100 IU/mL. The 5-, 10-, 15-, and 20-year cumulative rates were 4.74%, 10.72%, 18.80%, and 24.79%, respectively. On multivariable analysis, male (adjusted hazard ratio [aHR] = 1.66), older age (41-55 years: aHR = 1.16; >55 years: aHR = 1.21), negative HBeAg (aHR = 6.34), and genotype C (aHR = 1.82) predicted higher seroclearance rates, as did lower hepatitis B virus DNA and lower qHBsAg (P < 0.05 for all), and inactive carrier state. The spontaneous annual HBsAg seroclearance rate was 1.31%, but varied from close to zero to about 5% among most chronic hepatitis B subgroups, with older, male, HBeAg-negative, and genotype C patients with lower alanine aminotransferase and hepatitis B virus DNA, and qHBsAg independently associated with higher rates (see Visual Abstract, Supplementary Digital Content 2, http://links.lww.com/CTG/A367).

Identifiants

pubmed: 33094953
doi: 10.14309/ctg.0000000000000196
pii: 01720094-202009000-00005
pmc: PMC7494149
doi:

Substances chimiques

Hepatitis B Surface Antigens 0
Hepatitis B e Antigens 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e00196

Références

Gastroenterology. 2008 Oct;135(4):1192-9
pubmed: 18722377
Gastroenterology. 2011 Aug;141(2):517-25, 525.e1-2
pubmed: 21672542
J Hepatol. 2013 May;58(5):853-60
pubmed: 23246508
Lifetime Data Anal. 1995;1(3):255-73
pubmed: 9385105
Gut. 2014 Oct;63(10):1648-57
pubmed: 24225939
Hepatology. 2012 Sep;56(3):812-9
pubmed: 22422518
Aliment Pharmacol Ther. 2015 May;41(10):949-60
pubmed: 25809540
Ann Intern Med. 2017 Aug 15;167(4):268-274
pubmed: 28693043
Gut. 2015 Jun;64(6):966-72
pubmed: 25006011
Aliment Pharmacol Ther. 2016 Jun;43(12):1253-61
pubmed: 27117732
Clin Infect Dis. 2004 May 1;38(9):1222-8
pubmed: 15127332
Lancet. 2018 Nov 24;392(10161):2313-2324
pubmed: 30496122
Gastroenterology. 2019 Feb;156(3):635-646.e9
pubmed: 30342034
Hepatology. 2004 Jun;39(6):1694-701
pubmed: 15185311
Hepatology. 2007 May;45(5):1187-92
pubmed: 17465003
J Hepatol. 2008 Feb;48(2):335-52
pubmed: 18096267
Hepatology. 2010 May;51(5):1531-7
pubmed: 20087968
Hepatology. 2018 Apr;67(4):1560-1599
pubmed: 29405329
Gastroenterology. 2010 Aug;139(2):474-82
pubmed: 20434450
Gastroenterology. 2003 Apr;124(4):925-32
pubmed: 12671889
Hepatology. 1991 Apr;13(4):627-31
pubmed: 2010157
Lancet Gastroenterol Hepatol. 2019 Mar;4(3):227-238
pubmed: 30679109

Auteurs

Yee Hui Yeo (YH)

Department of Medicine, Stanford University Medical Center, Palo Alto, California, USA.

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, Tokyo, Japan.

Chris Cunningham (C)

Research Centre for Maori Health and Development, Massey University, Wellington, New Zealand.
The Hepatitis Foundation of New Zealand, Whakatane, New Zealand.

James Yan Yue Fung (JYY)

Department of Medicine, The University of Hong Kong, Hong Kong, China.

Hsiu J Ho (HJ)

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

Min-Sun Kwak (MS)

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

Huy N Trinh (HN)

San Jose Gastroenterology, San Jose, California, USA.

Teerapat Ungtrakul (T)

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

Ming-Lung Yu (ML)

Hepatobiliary Section, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Center for Liver Research, School of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Center for Cancer Research, Kaohsiung Medical University, Kaohsiung, Taiwan.

Mariko Kobayashi (M)

Research Institute for Hepatology, Toranomon Hospital, Tokyo, Japan.

An K Le (AK)

Department of Medicine, Stanford University Medical Center, Palo Alto, California, USA.

Linda Henry (L)

Department of Medicine, Stanford University Medical Center, Palo Alto, California, USA.

Jiayi Li (J)

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

Jian Zhang (J)

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

Tassanee Sriprayoon (T)

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

Donghak Jeong (D)

Department of Medicine, Stanford University Medical Center, Palo Alto, California, USA.

Tawesak Tanwandee (T)

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

Ed Gane (E)

New Zealand Liver Transplant Unit, Auckland City Hospital, Auckland, New Zealand.
Department of Medicine, University of Auckland, Auckland, New Zealand.

Ramsey C Cheung (RC)

Department of Medicine, Stanford University Medical Center, Palo Alto, California, USA.
Division of Gastroenterology and Hepatology, Veterans Affairs Palo Alto Health Care System, Palo Alto, California, USA.

Chun-Ying Wu (CY)

Division of Translational Research, Taipei Veterans General Hospital, Taipei City, Taiwan.
College of Public Health, China Medical University, Taichung, Taiwan.

Anna S Lok (AS)

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

Hyo-Suk Lee (HS)

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

Fumitaka Suzuki (F)

Department of Hepatology, Toranomon Hospital, Tokyo, Japan.

Man-Fung Yuen (MF)

Department of Medicine, The University of Hong Kong, Hong Kong, China.

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.

Hwai-I Yang (HI)

Genomics Research Center, Academia Sinica, Taipei, Taiwan.
Institute of Clinical Medicine, National Yang-Ming University, Taipei, Taiwan.

Mindie H Nguyen (MH)

Department of Medicine, Stanford University Medical Center, Palo Alto, California, USA.

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