Evidence map›Paper›PMID 39969799›Full record

ArticleLiver international : official journal of the International Association for the Study of the Liver2025

Insights Into Hepatic Sarcoidosis: Analysis of Histological Patterns, Hepatic Complications and Therapeutic Approaches.

Ludwig J Horst, Katharina Zimmermann, Johanna Lutz, Sören Weidemann, Stefan Lüth, Ansgar W Lohse, Julian Schulze Zur Wiesch, Christoph Schramm, Malte H Wehmeyer, Martina Müller and 1 more

Abstract readMulticenter Study
In one paragraph

Article in Liver international : official journal of the International Association for the Study of the Liver, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Cirrhosis Risk in Sarcoidosis Without Documented Hepatic Involvement-A Large Nationwide Population-Based Cohort Study.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Article
  3. Article
  4. Article
  5. 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

11 authors.

Ludwig J HorstI. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-0344-6337
Katharina ZimmermannDepartment of Internal Medicine I, University Hospital Regensburg, Regensburg, Germany.
Johanna LutzI. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Sören WeidemannInstitute for Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Stefan LüthDepartment of Gastroenterology, Hepatology and Diabetology, Center of Internal Medicine II, University Hospital Brandenburg an der Havel, Brandenburg an der Havel, Germany.
Ansgar W LohseI. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Julian Schulze Zur WieschI. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Christoph SchrammI. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Malte H WehmeyerI. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-3606-3818
Martina MüllerDepartment of Internal Medicine I, University Hospital Regensburg, Regensburg, Germany.
Marcial SebodeI. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-5163-6979

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsSarcoidosis is a granulomatous multi-systemic disorder of uncertain aetiology frequently involving the liver. This study aimed to delineate the histological characteristics, treatment effectiveness and factors predictive of liver-related complications in individuals with hepatic sarcoidosis.

methodsThis retrospective cohort study included patients diagnosed with hepatic sarcoidosis by liver biopsy, which was conducted at two tertiary care centres from January 2009 to December 2023. We analysed demographic, clinical and laboratory parameters, treatment response and outcome.

resultsWe enrolled 70 hepatic sarcoidosis patients with a median follow-up of 45 months (IQR 11-97 months), including 37 males with a median age of 48 years (IQR 37-59 years). Elevated GGT (94%) and ALP (81%) were the most common liver-specific biochemical alterations observed. Using mini-laparoscopy for liver biopsy made it possible to macroscopically identify granulomatous disease in 71% of patients. While at baseline, 16% of the cohort showed evidence of potential portal hypertension, at the last follow-up, 23% of patients developed complications related to portal hypertension. In addition to granulomatous changes, bile duct irregularities were found in 57% of liver biopsies, indicating cholangiopathy being part of the hepatic manifestation of sarcoidosis. Treatment with Ursodeoxycholic acid and prednisolone resulted in a significantly more pronounced decrease in ALT and ALP compared to untreated patients.

conclusionsPatients with hepatic sarcoidosis require careful assessment of disease manifestation with a particular focus on portal hypertension. Treatment with UDCA and prednisolone leads to a reduction of biochemical parameters in a significant proportion of these patients.

Indexed as

LiverLiver DiseasesSarcoidosisAdultAlkaline PhosphataseBiopsyFemaleHumansHypertension, PortalMaleMiddle AgedRetrospective StudiesTreatment OutcomeUrsodeoxycholic AcidAlkaline PhosphataseUrsodeoxycholic Acidcirrhosiselevated liver enzymesgranulomatous liver diseasemini‐laparoscopyportal hypertension

Identifiers

PMID39969799
PMCPMC11837985

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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.