TY - JOUR
T1 - Low Incidence of Adverse Outcomes in Adults With Chronic Hepatitis B Virus Infection in the Era of Antiviral Therapy
AU - Hepatitis B Research Network (HBRN)
AU - Lok, Anna S.
AU - Perrillo, Robert
AU - Lalama, Christina M.
AU - Fried, Michael W.
AU - Belle, Steven H.
AU - Ghany, Marc G.
AU - Khalili, Mandana
AU - Fontana, Robert J.
AU - Sterling, Richard K.
AU - Terrault, Norah
AU - Feld, Jordan J.
AU - Di Bisceglie, Adrian M.
AU - Lau, Daryl T.Y.
AU - Hassan, Mohamed
AU - Janssen, Harry L.A.
AU - Niu, Jianghe
AU - Javaid, Asad
AU - Nasir, Bilal
AU - Susheela, Ammu
AU - Nasser, Imad
AU - Donovan, Arley
AU - Rusibamayila, Nifasha
AU - Foley, Cara
AU - Stahler, Alisha C.
AU - Stadheim, Linda
AU - Lake, John
AU - Lacher, Philip
AU - ShawN., Debra De Marco
AU - Kessels, Lisa
AU - Klebert, Michael K.
AU - Noureldin, Seham
AU - La, Danie
AU - Mooney, Jody
AU - Cardona-Gonzalez, Lupita
AU - Liu, Lucie
AU - Kaznowski, Diana
AU - Chen, Jiayun
AU - Huang, Fengfei
AU - Vladutu, Doinita
AU - Cerocchi, Orlando
AU - Rowan, Debra
AU - Bass, Sheila
AU - Lilly, Barbara
AU - French, Samuel
AU - Peacock, Velma
AU - Peters, Marion
AU - Shobe, Ashley
AU - Davis, Rayshawnda
AU - Lee, William M.
AU - Murakami, Carol S.
N1 - Funding Information:
The Hepatitis B Research Network (HBRN) was funded by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) in 2008 to investigate clinical, virological, and immunological characteristics of patients with HBV infection in the United States and Canada. The HBRN cohort study enrolled persons with chronic HBV infection who were not receiving AVT and followed them prospectively per standard of care, which included initiating AVT during follow‐up if necessary. We analyzed data from the HBRN Adult Cohort Study to determine the incidence and factors associated with clinical outcomes in this large and diverse population of persons with chronic HBV infection.
Publisher Copyright:
© 2020 by the American Association for the Study of Liver Diseases.
PY - 2020
Y1 - 2020
N2 - Background and Aims: Outcomes of persons with chronic hepatitis B virus (HBV) infection in the era of antiviral therapy (AVT) are not well characterized. We determined the incidence and factors associated with clinical outcomes in a multiethnic, North American cohort of adults with chronic HBV infection, who were not on AVT at enrollment. Approach and Results: Adults with chronic HBV infection, not receiving AVT, and without a history of decompensation, HCC, or liver transplantation (LT), were prospectively followed. Participants with known human immunodeficiency virus (HIV), hepatitis C virus, or hepatitis D virus (HDV) coinfection were excluded. During follow-up, treatment could be initiated per standard of care. Clinical outcomes included: incident cirrhosis, decompensation, HCC, OLT, and HBV-related death. Among 1,418 participants analyzed, 51.5% were women, median age was 41.1 years, 75% were Asian, 10% White, 13% Black, 24% HBeAg(+), and 1.5% cirrhosis at baseline. During the study, 274 started treatment, 83 had an alanine aminotransferase flare, 118 of 330 initially HBeAg(+) became HBeAg(−), and 90 of 1,329 became HBsAg(−). After 6,641 person-years follow-up, 8 participants (4 of 21 with baseline cirrhosis) had 12 clinical outcomes (2 decompensation, 5 HCC, 2 OLT, and 3 HBV-related deaths) and 19 of 1,397 had incident cirrhosis. Twenty-one of 26 participants had first outcome before treatment, none had become HBsAg(−), whereas 5/9 HBeAg(+) had become HBeAg(−) at time of first outcome. Cumulative percentage of clinical outcomes was 16% at year 4 in participants with baseline cirrhosis and 2% (including incident cirrhosis) at year 7 in those without. Conclusions: Incidence of adverse outcomes was low in this closely monitored, large cohort of North American adults with predominantly inactive, chronic HBV without cirrhosis. Our data highlight the benefits of HBsAg loss and the importance of early diagnosis and treatment to prevent cirrhosis and other complications of chronic HBV infection.
AB - Background and Aims: Outcomes of persons with chronic hepatitis B virus (HBV) infection in the era of antiviral therapy (AVT) are not well characterized. We determined the incidence and factors associated with clinical outcomes in a multiethnic, North American cohort of adults with chronic HBV infection, who were not on AVT at enrollment. Approach and Results: Adults with chronic HBV infection, not receiving AVT, and without a history of decompensation, HCC, or liver transplantation (LT), were prospectively followed. Participants with known human immunodeficiency virus (HIV), hepatitis C virus, or hepatitis D virus (HDV) coinfection were excluded. During follow-up, treatment could be initiated per standard of care. Clinical outcomes included: incident cirrhosis, decompensation, HCC, OLT, and HBV-related death. Among 1,418 participants analyzed, 51.5% were women, median age was 41.1 years, 75% were Asian, 10% White, 13% Black, 24% HBeAg(+), and 1.5% cirrhosis at baseline. During the study, 274 started treatment, 83 had an alanine aminotransferase flare, 118 of 330 initially HBeAg(+) became HBeAg(−), and 90 of 1,329 became HBsAg(−). After 6,641 person-years follow-up, 8 participants (4 of 21 with baseline cirrhosis) had 12 clinical outcomes (2 decompensation, 5 HCC, 2 OLT, and 3 HBV-related deaths) and 19 of 1,397 had incident cirrhosis. Twenty-one of 26 participants had first outcome before treatment, none had become HBsAg(−), whereas 5/9 HBeAg(+) had become HBeAg(−) at time of first outcome. Cumulative percentage of clinical outcomes was 16% at year 4 in participants with baseline cirrhosis and 2% (including incident cirrhosis) at year 7 in those without. Conclusions: Incidence of adverse outcomes was low in this closely monitored, large cohort of North American adults with predominantly inactive, chronic HBV without cirrhosis. Our data highlight the benefits of HBsAg loss and the importance of early diagnosis and treatment to prevent cirrhosis and other complications of chronic HBV infection.
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U2 - 10.1002/hep.31554
DO - 10.1002/hep.31554
M3 - Article
C2 - 32936969
AN - SCOPUS:85108741971
JO - Hepatology
JF - Hepatology
SN - 0270-9139
ER -