An Aging Population of Chronic Hepatitis B With Increasing Comorbidities: A Territory‐Wide Study From 2000 to 2017

Patients with chronic hepatitis B (CHB) are aging because of improved survival under better health care. This has an important implication on the choice of antiviral treatment (AVT), given that long‐term safety would be a concern in the presence of multiple comorbidities. We aimed to determine the prevalence of key comorbidities and concomitant medications in a territory‐wide CHB cohort in Hong Kong in 2000‐2017. CHB patients who have been under the care at primary, secondary, and tertiary medical centers in the public sector were identified through the Clinical Data Analysis and Reporting System of the Hospital Authority, Hong Kong. The demographics and prevalence of key comorbidities, including diabetes mellitus, hypertension, chronic kidney disease, osteopenia/osteoporosis based on diagnosis codes, relevant medications, and/or laboratory parameters, were determined according to CHB patients’ first appearance in four time periods: 2000‐2004, 2005‐2009, 2010‐2013, and 2014‐2017. In the final analysis, 135,395 CHB patients were included; the mean age increased with time: 41 ± 15 years in 2000‐2004; 46 ± 17 years in 2005‐2009; 51 ± 16 years in 2010‐2013; and 55 ± 15 years in 2014‐2017. There was a trend of increasing prevalence of several common comorbidities over the four periods: hypertension 25.5%, 23.8%, 27.2%, and 28.6%; diabetes mellitus 10.6%, 12.5%, 16.1%, and 20.1%; cardiovascular disease 12.5%, 16.9%, 20.9%, and 22.2%; and malignancy 7.0%, 13.2%, 17.3%, and 23.6%, respectively (all P < 0.001). Conclusion: CHB patients are getting older with increasing prevalence of common comorbidities. These comorbidities should be taken into account when choosing AVT.

[1]  Wang Xiaoxiao,et al.  Durability of hepatitis B surface antigen seroclearance and subsequent risk for hepatocellular carcinoma: A meta‐analysis , 2021, Journal of viral hepatitis.

[2]  M. Yuen,et al.  A Territorywide Prevalence Study on Blood-Borne and Enteric Viral Hepatitis in Hong Kong. , 2019, The Journal of infectious diseases.

[3]  G. Wong,et al.  Unmet need in chronic hepatitis B management , 2019, Clinical and molecular hepatology.

[4]  G. Dusheiko,et al.  Advancing Age and Comorbidity in a US Insured Population‐Based Cohort of Patients With Chronic Hepatitis B , 2019, Hepatology.

[5]  2. Classification and Diagnosis of Diabetes: Standards of Medical Care in Diabetes—2019 , 2018, Diabetes Care.

[6]  V. Wong,et al.  Normal on-treatment ALT during antiviral treatment is associated with a lower risk of hepatic events in patients with chronic hepatitis B. , 2018, Journal of hepatology.

[7]  V. Wong,et al.  Chronic kidney disease progression in patients with chronic hepatitis B on tenofovir, entecavir, or no treatment , 2018, Alimentary pharmacology & therapeutics.

[8]  M. Buti,et al.  No Resistance to Tenofovir Alafenamide Detected through 96 Weeks of Treatment in Patients with Chronic Hepatitis B Infection , 2018, Antimicrobial Agents and Chemotherapy.

[9]  S. Alavian,et al.  Global prevalence, treatment, and prevention of hepatitis B virus infection in 2016: a modelling study. , 2018, The lancet. Gastroenterology & hepatology.

[10]  B. McMahon,et al.  Update on prevention, diagnosis, and treatment of chronic hepatitis B: AASLD 2018 hepatitis B guidance , 2018, Hepatology.

[11]  M. Buti,et al.  96 weeks treatment of tenofovir alafenamide vs. tenofovir disoproxil fumarate for hepatitis B virus infection. , 2018, Journal of hepatology.

[12]  M. Yuen,et al.  Review article: long‐term safety of oral anti‐viral treatment for chronic hepatitis B , 2018, Alimentary pharmacology & therapeutics.

[13]  V. Wong,et al.  Impact of age and gender on risk of hepatocellular carcinoma after hepatitis B surface antigen seroclearance. , 2017, Journal of hepatology.

[14]  G. Wong,et al.  Statins reduce the risk of liver decompensation and death in chronic viral hepatitis: a propensity score weighted landmark analysis , 2017, Alimentary pharmacology & therapeutics.

[15]  Thomas Berg,et al.  EASL 2017 Clinical Practice Guidelines on the management of hepatitis B virus infection. , 2017, Journal of hepatology.

[16]  John F. Flaherty,et al.  Tenofovir alafenamide versus tenofovir disoproxil fumarate for the treatment of patients with HBeAg-negative chronic hepatitis B virus infection: a randomised, double-blind, phase 3, non-inferiority trial. , 2016, The lancet. Gastroenterology & hepatology.

[17]  V. Wong,et al.  Metabolic syndrome increases cardiovascular events but not hepatic events and death in patients with chronic hepatitis B , 2016, Hepatology.

[18]  M. Kumar,et al.  Asian-Pacific clinical practice guidelines on the management of hepatitis B: a 2015 update , 2015, Hepatology International.

[19]  V. Wong,et al.  Long‐term safety of oral nucleos(t)ide analogs for patients with chronic hepatitis B: A cohort study of 53,500 subjects , 2015, Hepatology.

[20]  V. Wong,et al.  Adverse effects of vitamin D deficiency on outcomes of patients with chronic hepatitis B. , 2015, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

[21]  G. Wong,et al.  Current developments in nucleoside/nucleotide analogues for hepatitis B , 2014, Expert review of gastroenterology & hepatology.

[22]  B. C. Kwan,et al.  Metabolic syndrome in peritoneal dialysis patients: choice of diagnostic criteria and prognostic implications. , 2014, Clinical journal of the American Society of Nephrology : CJASN.

[23]  A. Chan,et al.  Coincidental metabolic syndrome increases the risk of liver fibrosis progression in patients with chronic hepatitis B – a prospective cohort study with paired transient elastography examinations , 2014, Alimentary pharmacology & therapeutics.

[24]  V. Wong,et al.  Entecavir treatment reduces hepatic events and deaths in chronic hepatitis B patients With liver cirrhosis , 2013, Hepatology.

[25]  V. Wong,et al.  Accuracy of risk scores for patients with chronic hepatitis B receiving entecavir treatment. , 2013, Gastroenterology.

[26]  John F. Flaherty,et al.  Regression of cirrhosis during treatment with tenofovir disoproxil fumarate for chronic hepatitis B: a 5-year open-label follow-up study , 2013, The Lancet.

[27]  V. Wong,et al.  Hepatitis B virus infection and fatty liver in the general population. , 2012, Journal of hepatology.

[28]  Vincent Wai-Sun Wong,et al.  Prevalence of non-alcoholic fatty liver disease and advanced fibrosis in Hong Kong Chinese: a population study using proton-magnetic resonance spectroscopy and transient elastography , 2011, Gut.

[29]  G. Wong,et al.  Development of a non‐invasive algorithm with transient elastography (Fibroscan) and serum test formula for advanced liver fibrosis in chronic hepatitis B , 2010, Alimentary pharmacology & therapeutics.

[30]  V. Wong,et al.  Metabolic syndrome increases the risk of liver cirrhosis in chronic hepatitis B , 2008, Gut.

[31]  H. Chan,et al.  Genotype C hepatitis B virus infection is associated with an increased risk of hepatocellular carcinoma , 2004, Gut.

[32]  Robert Gray,et al.  A Proportional Hazards Model for the Subdistribution of a Competing Risk , 1999 .

[33]  F. Lai,et al.  Membranous nephropathy related to hepatitis B virus in adults. , 1991, The New England journal of medicine.

[34]  M. Buti,et al.  Improved bone and renal safety of switching from tenofovir disoproxil fumarate to tenofovir alafenamide: preliminary results from 2 phase 3 studies in HBeAg-positive and HBeAg-negative patients with chronic hepatitis B , 2017 .

[35]  V. Wong,et al.  Durability of hepatitis B surface antigen seroclearance in untreated and nucleos(t)ide analogue-treated patients. , 2017, Journal of hepatology.

[36]  John F. Flaherty,et al.  Tenofovir alafenamide versus tenofovir disoproxil fumarate for the treatment of HBeAg-positive chronic hepatitis B virus infection: a randomised, double-blind, phase 3, non-inferiority trial. , 2016, The lancet. Gastroenterology & hepatology.