Evidence map›Paper›PMID 42588698›Full record

ArticleCancers2026

Interpreting Circulating Bile Acid Profiles in Pancreatic Cancer: The Role of Cholestasis and Its Management.

Elisa Danese, Alessandro Esposito, Matteo De Pastena, Fabio Del Ben, Gabriella Lionetto, Alessia Scirpoli, Mariateresa Rizza, Roberto Salvia, Giuseppe Lippi

Abstract read
In one paragraph

Article in Cancers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Elisa DaneseSection of Clinical Biochemistry, Department of Engineering for Innovation Medicine, University of Verona, 37129 Verona, Italy.ORCID 0000-0002-2454-0410
Alessandro EspositoDepartment of General and Pancreatic Surgery, Pancreas Institute, University of Verona Hospital Trust, 37129 Verona, Italy.ORCID 0000-0003-0079-2311
Matteo De PastenaDepartment of General and Pancreatic Surgery, Pancreas Institute, University of Verona Hospital Trust, 37129 Verona, Italy.ORCID 0000-0001-5244-4357
Fabio Del BenImmunopathology and Cancer Biomarkers Unit, Department of Cancer Research and Advanced Diagnostics, CRO Aviano National Cancer Institute IRCCS, 33081 Aviano, Italy.ORCID 0000-0002-1880-0669
Gabriella LionettoDepartment of General and Pancreatic Surgery, Pancreas Institute, University of Verona Hospital Trust, 37129 Verona, Italy.ORCID 0000-0003-4635-3680
Alessia ScirpoliDepartment of General and Pancreatic Surgery, Pancreas Institute, University of Verona Hospital Trust, 37129 Verona, Italy.ORCID 0009-0004-5732-7327
Mariateresa RizzaSection of Clinical Biochemistry, Department of Engineering for Innovation Medicine, University of Verona, 37129 Verona, Italy.
Roberto SalviaDepartment of General and Pancreatic Surgery, Pancreas Institute, University of Verona Hospital Trust, 37129 Verona, Italy.ORCID 0000-0002-3514-8473
Giuseppe LippiSection of Clinical Biochemistry, Department of Engineering for Innovation Medicine, University of Verona, 37129 Verona, Italy.ORCID 0000-0001-9523-9054

Funding

Italian Ministry of Health through Fondazione Italiana Malattie Pancreas FIMP_CUP E37G25000440001
6 · The paper itself

Abstract

backgroundCirculating bile acid (BA) profiles are increasingly explored in pancreatic cancer, although their interpretation is often complicated by biliary obstruction and its clinical management. In this study, we characterized plasma BA profiles in pancreatic ductal adenocarcinoma (PDAC) and assessed the relative contributions of tumor localization, histological subtype, cholestasis, and cholestasis-related interventions.

methodsPlasma BAs were quantified by LC-MS/MS in patients with PDAC of the pancreatic head (hPDAC,

resultsUDCA therapy was associated with markedly increased circulating UDCA, higher total BA concentrations, and enrichment of secondary BA species. Direct bilirubin explained more variability in BA composition than binary jaundice classification and showed a non-linear association with BA remodeling, with a distinct metabolic profile emerging only at high bilirubin levels. Longitudinally, BA profiles changed substantially over time in hPDAC, largely in parallel with bilirubin, whereas they remained comparatively stable in tPDAC. After adjustment for bilirubin, tumor-related differences were modest and context-dependent.

conclusionsOverall, circulating BA profiles in pancreatic cancer appear to be driven predominantly by cholestasis and its management rather than by tumor-related features alone.

Indexed as

bile acidbilirubincholestasispancreatic ductal adenocarcinomaUDCA

Identifiers

PMID42588698
PMCPMC13463877

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.