Recompensation in Patients With Alcohol-Related Liver Disease—A Multicenter Study

IF 3.3
Gastro hep advances Pub Date : 2026-01-01 Epub Date: 2026-02-06 DOI:10.1016/j.gastha.2026.100897
Anand V. Kulkarni , Madhumita Premkumar , Karan Kumar , Akash Roy , Suprabhat Giri , Ashirvad Pasumarthy , Mithun Sharma , Shantan Venishetty , Sowmya Iyengar , Manasa Alla , Rakesh Kalapala , Padaki Nagaraj Rao , Duvvur Nageshwar Reddy , Ashwani K. Singal , K. Rajender Reddy
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Abstract

Background and Aims

Removal of etiology of cirrhosis may lead to recompensation in decompensated cirrhosis. Few studies have reported on rates of recompensation, as per Baveno VII criteria, in viral etiology-related decompensated cirrhosis. Our aim was to assess the rate and predictors of recompensation in the spectrum of alcohol-related liver disease (ALD).

Methods

Retrospective multicenter cohort study across 5 Indian centers included patients with a spectrum of ALD from January 2018 to November 2024. Clinical and biochemical data were collected and patients followed, and end points of recompensation, mortality, and transplant-free survival were evaluated.

Results

Among 344 patients (age: 41.2 ± 8.4 years; Model for End-Stage Liver Disease: 23.9 ± 6.2; men: 98.3%), 242 had decompensated cirrhosis with alcohol-associated hepatitis (DC + AAH), and 102 had decompensated cirrhosis without alcohol-associated hepatitis (DC-AAH). Twenty percent (69/344) achieved recompensation as per Baveno VII criteria over 21 (range, 12–67) months. The recompensation rate was higher among those with DC-AAH (30.4%; 31/102) compared to DC + AAH (15.7%; 38/242; P = .002). Transplant-free survival was higher among those who recompensated (DC + AAH: 92.1% vs 77.9%; DC-AAH: 93.5% vs 76.1%). On competing risk regression analysis, duration of abstinence (subdistribution hazard ratio, 1.03 [95% confidence interval, 1.01–1.05]; P = .04) and Child score (subdistribution hazard ratio 0.83 [95% confidence interval, 0.71–0.98]; P = .03) predicted recompensation. Model for End-Stage Liver Disease (hazard ratio, 1.09 [1.09–1.16]; P = .001) and recompensation (hazard ratio, 0.14 [0.04–0.49]; P = .002) predicted mortality.

Conclusion

Twenty percent of patients in the spectrum of ALD demonstrated recompensation, which was associated with improved survival.

Abstract Image

酒精相关性肝病患者的再代偿——一项多中心研究
背景与目的消除肝硬化的病因可能导致失代偿肝硬化的再代偿。根据Baveno VII标准,很少有研究报道与病毒病因相关的失代偿性肝硬化的再代偿率。我们的目的是评估酒精相关性肝病(ALD)谱系中再代偿的比率和预测因素。方法回顾性多中心队列研究纳入了2018年1月至2024年11月印度5个中心的ALD患者。收集临床和生化数据,随访患者,评估再补偿、死亡率和无移植生存的终点。结果344例患者(年龄:41.2±8.4岁;终末期肝病模型:23.9±6.2;男性:98.3%)中,242例失代偿性肝硬化伴酒精相关性肝炎(DC + AAH), 102例失代偿性肝硬化伴酒精相关性肝炎(DC-AAH)。20%(69/344)的患者在21个月(范围12-67个月)的时间内按照《巴韦诺VII》标准获得了补偿。DC-AAH患者的再代偿率(30.4%,31/102)高于DC + AAH患者(15.7%,38/242,P = 0.002)。无移植生存率在获得补偿的患者中更高(DC + AAH: 92.1% vs 77.9%; DC-AAH: 93.5% vs 76.1%)。在竞争风险回归分析中,戒断时间(亚分布风险比1.03[95%置信区间,1.01-1.05];P = 0.04)和儿童评分(亚分布风险比0.83[95%置信区间,0.71-0.98];P = 0.03)预测再补偿。终末期肝病模型(风险比1.09 [1.09 - 1.16];P = .001)和再补偿模型(风险比0.14 [0.04-0.49];P = .002)预测死亡率。结论20%的ALD患者表现出再代偿,这与生存率的提高有关。
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来源期刊
Gastro hep advances
Gastro hep advances Gastroenterology
CiteScore
0.80
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审稿时长
64 days
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