Prevalence and risk factors of significant fibrosis in chronic hepatitis B patients with concurrent metabolic dysfunction-associated steatotic liver disease

被引:6
作者
Hong, Shan [1 ]
Hao, Yiwei [2 ]
Sun, Lei [3 ]
Li, Ping [1 ]
Yang, Junru [1 ]
Zhang, Fuyang [1 ]
He, Lingling [1 ]
Zhang, Jing [4 ]
Wei, Hongshan [1 ]
机构
[1] Capital Med Univ, Beijing Ditan Hosp, Dept Gastroenterol, Beijing 100015, Peoples R China
[2] Capital Med Univ, Beijing Ditan Hosp, Dept Med Records & Stat, Beijing 100015, Peoples R China
[3] Capital Med Univ, Beijing Ditan Hosp, Dept Pathol, Beijing 100015, Peoples R China
[4] Capital Med Univ, Beijing YouAn Hosp, Dept Hepatol, Beijing 100069, Peoples R China
基金
中国国家自然科学基金;
关键词
Non-alcoholic fatty liver disease; Metabolic diseases; Liver biopsy; Hepatic steatosis; Hepatitis B; HEPATOCELLULAR-CARCINOMA; STEATOHEPATITIS; SEROCLEARANCE; EPIDEMIOLOGY; GUIDELINES; INDEX; MEN;
D O I
10.1016/j.aohep.2024.101589
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Introduction and objectives: Significant fibrosis is an indicator of clinical intervention for both chronic hepatitis B (CHB) and metabolic dysfunction-associated steatotic liver disease (MASLD). There remains a paucity of data regarding the clinical impact of biopsy-defined MASLD on significant fibrosis in CHB patients. The current study aims to elucidate whether patients with concomitant MASLD are at higher risk of significant fibrosis in patients with CHB. Patients and methods: This retrospective research of two tertiary hospitals comprised 1818 patients between 2009 and 2021 with CHB and hepatic steatosis who had not received antiviral therapy. Pathologic findings by liver biopsy were contrasted between CHB group (n = 844) and CHB + MASLD (n = 974) group. METAVIR values of F >= 2 were used to categorize significant fibrosis. Results: Patients with CHB + MASLD had more significant fibrosis (35.5 % vs. 23.5 %, p < 0.001) than CHB group. The presence of MASLD [adjusted odds ratio (aOR) 2.055, 95 % confidence interval (CI) 1.635-2.584; p < 0.001] was strongly associated with significant fibrosis in all CHB patients. There was a trend for patients with more cardiometabolic risk factors (CMRFs) to have a higher prevalence of significant fibrosis: (25.7 % in CMRF1 subgroup v.s. 34.9 % in CMRF2 subgroup v.s. 53.7 % in CMRF >= 3 subgroup, p < 0.001). Patients with CMRF >= 3 had a three-fold higher significant fibrosis than those with just one CMRF. Conclusions: MASLD was associated with higher fibrosis stage in patients with CHB. Early detection and intervention are crucial to patients with three or more cardiometabolic risk factors. (c) 2024 Fundaci & oacute;n Cl & iacute;nica M & eacute;dica Sur, A.C. Published by Elsevier Espa & ntilde;a, S.L.U. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
引用
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页数:8
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