ReviewWorld journal of hepatology2025
Gray zone and the need for expansion in chronic hepatitis B: From theory to clinical practice.
Review in World journal of hepatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Heterogeneity Analysis of HBeAg-Positive Chronic Hepatitis B Patients with Ultra-High Viral Load (HBV DNA ≥ 7.0 logJournal of clinical medicine · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Chronic hepatitis B (CHB) remains a significant global health challenge. The natural course of CHB is traditionally divided into four phases: (1) Immune tolerance; (2) Immune activation; (3) Immune control; and (4) Immune escape. However, approximately 20%-30% of patients referred to as the "gray zone" (GZ) do not fit neatly into these categories. These patients often exhibit elevated hepatitis B virus DNA levels alongside normal or mildly elevated alanine aminotransferase levels, placing them at significant risk for liver fibrosis, cirrhosis, and hepatocellular carcinoma. However, current clinical guidelines generally do not recommend antiviral therapy for GZ patients, increasing their vulnerability to adverse outcomes. This mini-review explores the challenges and gaps in CHB management, focusing on GZ patients. It also highlights recent advancements in therapeutic strategies and updates in clinical guidelines, emphasizing the need for a more inclusive, risk-adapted approach to treatment. By leveraging novel biomarkers, noninvasive fibrosis assessment tools, and artificial intelligence-driven predictive models, this article advocates for early intervention to mitigate disease progression and improve clinical outcomes in this overlooked population.
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Registered trials
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.