Hepatic steatosis and metabolic risk factors among patients with chronic hepatitis B: The multicentre, prospective CAP‐Asia study

Author:

Leow Yong‐Wen1,Chan Wah‐Kheong1,Goh George Boon‐Bee2,Wong Vincent Wai‐Sun3,Fan Jian Gao4,Kim Young Seok5,Kim Seung Up6ORCID,Nakajima Atsushi7,Seto Wai‐Kay8ORCID,Lee I‐Cheng910,Huang Yi‐Hsiang91011ORCID,Kim Yoon Jun12ORCID,Young Jang Jae13,Chow Wan Cheng2

Affiliation:

1. Gastroenterology and Hepatology Unit, Department of Medicine, Faculty of Medicine University of Malaya Kuala Lumpur Malaysia

2. Department of Gastroenterology and Hepatology Singapore General Hospital Singapore Singapore

3. Department of Medicine and Therapeutics, Faculty of Medicine The Chinese University of Hong Kong Hong Kong Hong Kong

4. Department of Gastroenterology and Hepatology Shanghai Jiaotong University School of Medicine Xinhua Hospital Shanghai China

5. Division of Gastroenterology and Hepatology, Department of Internal Medicine SoonChunHyang University, Bucheon Hospital Bucheon‐si Korea

6. Division of Gastroenterology, Department of Internal Medicine Severance Hospital Seoul Korea

7. Department of Gastroenterology and Hepatology Yokohama City University Graduate School of Medicine Yokohama Japan

8. Department of Medicine School of Clinical Medicine, The University of Hong Kong Hong Kong Hong Kong

9. Division of Gastroenterology and Hepatology, Department of Medicine Taipei Veterans General Hospital Taipei Taiwan

10. School of Medicine, National Yang Ming Chiao Tung University Taipei Taiwan

11. Institute of Clinical Medicine, National Yang Ming Chiao Tung University Taipei Taiwan

12. Department of Internal Medicine Liver Research Institute, Seoul National University College of Medicine Seoul Korea

13. Soon Chun Hyang University Seoul Hospital Seoul Korea

Abstract

AbstractWe aimed to compare the severity of liver disease, metabolic profile and cardiovascular disease (CVD) risk of chronic hepatitis B (CHB) patients with and without hepatic steatosis and patients with non‐alcoholic fatty liver disease (NAFLD). Patients with NAFLD and CHB were prospectively enrolled from 10 Asian centres. Fibroscan was performed for all patients and hepatic steatosis was defined based on controlled attenuation parameter >248 dB/m. CVD risk was assessed using the Framingham risk score. The data for 1080 patients were analysed (67% NAFLD, 33% CHB). A high proportion (59%) of CHB patients had hepatic steatosis. There was a significant stepwise increase in alanine aminotransferase, aspartate aminotransferase, gamma‐glutamyl transpeptidase, controlled attenuation parameter and liver stiffness measurement, from CHB patients without hepatic steatosis to CHB patients with hepatic steatosis to NAFLD patients (p < 0.001 for all comparisons). There was a significant stepwise increase in the proportion of patients with metabolic syndrome and in CVD risk, with very high or extreme CVD risk seen in 20%, 48% and 61%, across the groups (p < 0.001 between CHB patients with and without hepatic steatosis and p < 0.05 between CHB patients with hepatic steatosis and NAFLD patients). In conclusion, there was a high proportion of CHB patients with hepatic steatosis, which should be diagnosed, as they may have more severe liver disease, so that this and their metabolic risk factors can be assessed and managed accordingly for a better long‐term outcome

Funder

Gilead Sciences

Publisher

Wiley

Subject

Virology,Infectious Diseases,Hepatology

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