Evidence map›Paper›PMID 39557789›Full record

ArticleDigestive diseases and sciences2025

Predicting Immune Flares in Untreated Chronic Hepatitis B Patients Using Novel Risk Factors and the FLARE-B Score.

Danny Con, Daniel Clayton-Chubb, Steven Tu, John S Lubel, Amanda Nicoll, Stephen Bloom, Rohit Sawhney

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Article in Digestive diseases and sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Danny ConDepartment of Gastroenterology, Eastern Health, Box Hill Hospital, 8 Arnold Street, Box Hill, Melbourne, Victoria, 3128, Australia. dannycon302@gmail.com.
Daniel Clayton-ChubbDepartment of Gastroenterology, Alfred Health, Melbourne, Victoria, Australia.
Steven TuDepartment of Gastroenterology, Eastern Health, Box Hill Hospital, 8 Arnold Street, Box Hill, Melbourne, Victoria, 3128, Australia.
John S LubelDepartment of Gastroenterology, Alfred Health, Melbourne, Victoria, Australia.
Amanda NicollDepartment of Gastroenterology, Eastern Health, Box Hill Hospital, 8 Arnold Street, Box Hill, Melbourne, Victoria, 3128, Australia.
Stephen BloomDepartment of Gastroenterology, Eastern Health, Box Hill Hospital, 8 Arnold Street, Box Hill, Melbourne, Victoria, 3128, Australia.
Rohit SawhneyDepartment of Gastroenterology, Eastern Health, Box Hill Hospital, 8 Arnold Street, Box Hill, Melbourne, Victoria, 3128, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsRisk factors of chronic hepatitis B (CHB) immune flares are poorly understood. The primary aim of this study was to discover predictors of the CHB flare in non-cirrhotic, untreated CHB patients and develop a simple risk-stratifying score to predict the CHB flare. The secondary aim was to compare different machine learning methods for prediction.

methodsA retrospective cohort of untreated, non-cirrhotic CHB patients with normal baseline ALT was followed up over time until an immune flare as defined by ALT twice the upper limit of normal. Statistical learning and machine learning algorithms were used to develop predictive models using baseline variables. Bootstrap validation was used to internally validate the models.

resultsOf 405 patients (median age 44y; 41% male, 10% HBeAg positive), 67 (17%) experienced an immune flare by 5 years (annual incidence 4.0%). Predictors of flare included raised serum globulin, younger age, HBeAg positive status, higher viral load and raised liver stiffness. A simple predictive model "FLARE-B" had optimism-adjusted 1, 3 and 5-year AUCs of 0.813, 0.728 and 0.702, respectively. The random survival forest algorithm had the highest optimism-adjusted AUCs of 0.861, 0.766 and 0.725, respectively.

conclusionsNew, novel predictors of the CHB flare include a raised serum globulin and possibly raised liver stiffness and the absence of liver steatosis. FLARE-B can be used to risk-stratify individuals and potentially guide personalized management strategies such as monitoring schedules and proactive antiviral treatment in high-risk patients.

Indexed as

Hepatitis B, ChronicAdultAlanine TransaminaseFemaleHepatitis B e AntigensHumansMachine LearningMaleMiddle AgedPredictive Value of TestsRetrospective StudiesRisk AssessmentRisk FactorsSymptom Flare UpViral LoadAlanine TransaminaseHepatitis B e AntigensAlanine aminotransferaseHBVHepatitis B virus

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.