Evidence map›Paper›PMID 42010908›Full record

ArticleAlimentary pharmacology & therapeutics2026

Baseline HDV-RNA Levels Could Stratify Clinical Risk Before, But Not After, Cirrhosis in Chronic Hepatitis D: A Multicentre European Study.

Adriana Palom, Elisabetta Degasperi, Barbara Coco, Alessandro Loglio, Alessia Ciancio, Grazia Anna Niro, Mar Riveiro-Barciela, Angela Carvalho-Gomes, Javier García-Samaniego, Sabela Lens and 8 more

Abstract readMulticenter Study
In one paragraph

Article in Alimentary pharmacology & therapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Adriana PalomLiver Unit, Hospital Univesitari Vall d'Hebron, Barcelona, Spain.
Elisabetta DegasperiDivision of Gastroenterology and Hepatology, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.ORCID https://orcid.org/0000-0002-9899-4669
Barbara CocoHepatology Unit, University Hospital, Pisa, Italy.
Alessandro LoglioGastroenterology Hepatology and Transplantation Unit, ASST Papa Giovanni XXIII, Bergamo, Italy.ORCID https://orcid.org/0000-0001-8022-8803
Alessia CiancioCitta della Salute e della Scienza di Torino (City of Health and Science of Turin), School of Medicine, Department of Medical Sciences, University of Turin Department of Medical Sciences, University of Turin, Turin, Italy.
Grazia Anna NiroDivision of Gastroenterology and Endoscopy, Fondazione Casa Sollievo della Sofferenza, IRCCS, San Giovanni Rotondo, Italy.
Mar Riveiro-BarcielaLiver Unit, Hospital Univesitari Vall d'Hebron, Barcelona, Spain.
Angela Carvalho-GomesCIBERehd, Madrid, Spain.ORCID https://orcid.org/0000-0001-5424-3479
Javier García-SamaniegoLiver Unit, Hospital Universitario La Paz, IdiPAZ, Universidad Autónoma de Madrid, Madrid, Spain.
Sabela LensCIBERehd, Madrid, Spain.
Ariadna Rando-SeguraCIBERehd, Madrid, Spain.
Dana SambarinoDivision of Gastroenterology and Hepatology, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Rosa CotugnoDivision of Gastroenterology and Endoscopy, Fondazione Casa Sollievo della Sofferenza, IRCCS, San Giovanni Rotondo, Italy.
Loretta A KondiliNational Center for Global Health, Istituto Superiore di Sanità (Italian Institute of Health), Italy.ORCID https://orcid.org/0000-0003-2656-224X
Maurizia BrunettoHepatology Unit, University Hospital, Pisa, Italy.
Mauro ViganòGastroenterology Hepatology and Transplantation Unit, ASST Papa Giovanni XXIII, Bergamo, Italy.ORCID https://orcid.org/0000-0003-0769-1767
Pietro LamperticoDivision of Gastroenterology and Hepatology, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.ORCID https://orcid.org/0000-0002-1026-7476
Maria ButiLiver Unit, Hospital Univesitari Vall d'Hebron, Barcelona, Spain.

Funding

Instituto de Salud Carlos III PI20/01692Instituto de Salud Carlos III PI23/01065
6 · The paper itself

Abstract

BACKGROUND AND

aimsChronic hepatitis D (CHD) is associated with rapid progression to liver cirrhosis. However, the prognostic relevance of quantitative serum HDV-RNA remains incompletely defined. We aimed to evaluate whether baseline HDV-RNA levels are associated with the risk of liver-related events in untreated patients with CHD and to validate these findings in two independent European cohorts.

methodsWe conducted a multicentre retrospective-prospective cohort study including 260 untreated adults with CHD and detectable HDV-RNA. Patients were derived from a Spanish derivation cohort (n = 98) and two Italian validation cohorts (n = 100 and n = 62). Baseline serum qHDV-RNA was categorized in 1-log increments starting from 6 IU/mL.

resultsDuring a median follow-up of 4.1 years, 74 patients (28%) experienced at least one liver-related event, with a significantly higher incidence in patients with cirrhosis than in those without cirrhosis (p < 0.001). Among noncirrhotic patients, increasing baseline HDV-RNA levels were consistently associated with a higher proportion of liver-related events across derivation and validation cohorts, whereas no events occurred at the lowest HDV-RNA category. In contrast, among patients with established cirrhosis, baseline HDV-RNA levels were not associated with the occurrence of liver-related events, and cumulative incidence was comparable across viral load categories.

conclusionsBaseline quantitative HDV-RNA allows early risk stratification in untreated patients with chronic hepatitis D before the development of liver cirrhosis. Once cirrhosis is established, clinical outcomes are largely independent of viral replication, emphasising the need to prioritise timely antiviral intervention and close surveillance at earlier disease stages.

Indexed as

Hepatitis D, ChronicHepatitis Delta VirusLiver CirrhosisRNA, ViralAdultAgedDisease ProgressionFemaleHumansItalyMaleMiddle AgedPrognosisProspective StudiesRetrospective StudiesRisk FactorsRNA, Viralchronic hepatitis Dcohort validationliver‐related outcomesquantitative HDV‐RNA

Identifiers

PMID42010908
PMCPMC13356362

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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.