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慢性乙型肝炎合并脂肪性肝病患者的全因死亡率和特定病因死亡率。

All-cause and cause-specific mortality in patients with chronic hepatitis B and concurrent steatotic liver disease.

作者信息

Huang Shang-Chin, Su Tung-Hung, Tseng Tai-Chung, Hsu Shih-Jer, Hong Chun-Ming, Lan Ting-Yuan, Liu Chen-Hua, Yang Hung-Chih, Liu Chun-Jen, Kao Jia-Horng

机构信息

Department of Internal Medicine, National Taiwan University Hospital Bei-Hu Branch, Taipei, Taiwan; Division of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan; Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan; Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine, Taipei, Taiwan.

Division of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan; Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan.

出版信息

J Hepatol. 2024 Dec 14. doi: 10.1016/j.jhep.2024.12.009.

Abstract

BACKGROUND & AIMS: Steatotic liver disease (SLD) is prevalent among patients with chronic hepatitis B (CHB). However, the effects of metabolic dysfunction-associated SLD (MASLD) on the long-term survival of such patients remain unknown. Accordingly, this study investigated the mortality risks in patients with CHB and concurrent SLD.

METHODS

Consecutive patients with CHB and concurrent SLD were retrospectively recruited at National Taiwan University Hospital. MASLD was defined by the presence of cardiometabolic risk factors. The cumulative incidences of all-cause and cause-specific mortality were compared.

RESULTS

A total of 8,718 patients with CHB and concurrent SLD were included from 2006 to 2021. At baseline, the MASLD group (n = 6,562) was older and had a lower proportion of HBeAg positivity and lower HBV DNA levels compared with the non-MASLD group (n = 2,156). After a median follow-up period of 9.1 years, the MASLD group exhibited a higher risk of all-cause mortality compared with the non-MASLD group (adjusted hazard ratio 1.79, 95% CI 1.24-2.58, p = 0.002). Furthermore, cumulative cardiometabolic risk factors dose-dependently elevated the risks of all-cause, liver-related, and cardiovascular mortality (all p <0.05). During the follow-up period, new-onset diabetes mellitus, hypertension, and significant weight gain further increased the risks of all-cause and liver-related mortality (all p <0.05). However, patients with SLD had a lower mortality risk than those without SLD after propensity score matching (hazard ratio 0.62, 95% CI 0.53-0.74, p <0.001).

CONCLUSIONS

Among patients with CHB and SLD, metabolic burden dose-dependently increases all-cause, liver-related, and cardiovascular mortality risks. Patients with SLD have a lower mortality risk than those without SLD. Identifying these metabolic dysfunctions is crucial for stratifying the level of risk in daily care.

IMPACT AND IMPLICATIONS

Concurrent steatotic liver disease (SLD) is prevalent among patients with chronic hepatitis B (CHB); however, the effects of the associated cardiometabolic risk factors on all-cause and cause-specific mortality remain unknown. This study demonstrated that cumulative metabolic burden dose-dependently increased the risks of all-cause, liver-related, and cardiovascular mortality in patients with CHB and SLD. Moreover, new-onset diabetes mellitus, hypertension, and weight gain during the follow-up period further exacerbated these risks. However, patients with SLD had a lower risk of mortality than those without SLD. Thus, routine screening and monitoring of metabolic dysfunctions constitute a key element of daily care for patients with CHB.

摘要

背景与目的

脂肪性肝病(SLD)在慢性乙型肝炎(CHB)患者中很常见。然而,代谢功能障碍相关的SLD(MASLD)对此类患者长期生存的影响尚不清楚。因此,本研究调查了CHB合并SLD患者的死亡风险。

方法

在台湾大学医院回顾性招募连续的CHB合并SLD患者。MASLD由存在心脏代谢危险因素定义。比较全因死亡率和特定病因死亡率的累积发生率。

结果

2006年至2021年共纳入8718例CHB合并SLD患者。基线时,与非MASLD组(n = 2156)相比,MASLD组(n = 6562)年龄更大,HBeAg阳性比例更低,HBV DNA水平更低。中位随访9.1年后,MASLD组与非MASLD组相比全因死亡风险更高(调整后风险比1.79,95%CI 1.24 - 2.58,p = 0.002)。此外,累积的心脏代谢危险因素剂量依赖性地增加全因、肝脏相关和心血管死亡风险(所有p < 0.05)。随访期间,新发糖尿病、高血压和显著体重增加进一步增加全因和肝脏相关死亡风险(所有p < 0.05)。然而,倾向评分匹配后,SLD患者的死亡风险低于无SLD患者(风险比0.62,95%CI 0.53 - 0.74,p < 0.001)。

结论

在CHB合并SLD患者中,代谢负担剂量依赖性地增加全因、肝脏相关和心血管死亡风险。SLD患者的死亡风险低于无SLD患者。识别这些代谢功能障碍对于在日常护理中分层风险水平至关重要。

影响与意义

合并脂肪性肝病(SLD)在慢性乙型肝炎(CHB)患者中很常见;然而,相关心脏代谢危险因素对全因和特定病因死亡率的影响尚不清楚。本研究表明,累积代谢负担剂量依赖性地增加CHB合并SLD患者的全因、肝脏相关和心血管死亡风险。此外,随访期间新发糖尿病、高血压和体重增加进一步加剧了这些风险。然而,SLD患者的死亡风险低于无SLD患者。因此,对代谢功能障碍进行常规筛查和监测是CHB患者日常护理的关键要素。

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