Evidence map›Paper›PMID 40726561›Full record

ArticleGE Portuguese journal of gastroenterology2025

Disorder of Glucose Metabolism and Therapy: Implications on the Natural History of Advanced Chronic Liver Disease.

Sofia Garcês Soares, Tereza Frazão, Célia Tuna, Margarida Montes, Ana Rocha, Lígia Rodrigues Santos, Paulo Carrola, Sónia Carvalho, Inês Pinho, Luís Nogueira and 2 more

Abstract read
In one paragraph

Article in GE Portuguese journal of gastroenterology, 2025. 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. Hepatogenous Diabetes - Let us Shun the Neglect!Indian journal of endocrinology and metabolism
    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

12 authors.

Sofia Garcês SoaresInternal Medicine Department, Unidade Local de Saúde Tâmega e Sousa, Penafiel, Portugal.
Tereza FrazãoInternal Medicine Department, Unidade Local de Saúde Alto Ave, Guimarães, Portugal.
Célia TunaInternal Medicine Department, Unidade Local de Saúde Cova da Beira, Covilhã, Portugal.
Margarida MontesInternal Medicine Department, Unidade Local de Saúde Trás-os Montes e Alto Douro, Vila Real, Portugal.
Ana RochaInternal Medicine Department, Unidade Local de Saúde Tâmega e Sousa, Penafiel, Portugal.
Lígia Rodrigues SantosInternal Medicine Department, Unidade Local de Saúde Gaia e Espinho, Vila Nova de Gaia, Portugal.
Paulo CarrolaLiver Unit, Internal Medicine Department, Unidade Local de Saúde Trás-os-Montes e Alto Douro, Vila Real, Portugal.
Sónia CarvalhoLiver Unit, Internal Medicine Department, Unidade Local de Saúde Trás-os-Montes e Alto Douro, Vila Real, Portugal.
Inês PinhoLiver Unit, Internal Medicine Department, Unidade Local de Saúde Trás-os-Montes e Alto Douro, Vila Real, Portugal.
Luís NogueiraInternal Medicine Department, Unidade Local de Saúde Tâmega e Sousa, Penafiel, Portugal.
Manuel Marques-CruzDepartment of Community Medicine, Information and Health Decision Sciences (MEDCIDS), Faculty of Medicine, University of Porto, Porto, Portugal.
José PresaLiver Unit, Internal Medicine Department, Unidade Local de Saúde Trás-os-Montes e Alto Douro, Vila Real, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Hepatogenous diabetes (HD) is a disorder of glucose metabolism (DGM) that develops as a complication of advanced chronic liver disease (ACLD) with an estimated prevalence of 20-70%. It appears to be associated with a larger number of decompensations, but its impact on the natural history of the disease is unclear. The treatment of DGM is hampered by the fact that some therapeutic agents are associated with a risk of complications in ACLD. The aim of this work was to study DGM in a population of patients with ACLD: prevalence, liver disease decompensation episodes, mortality analysis and study of the impact of antidiabetic therapies in patients with ACLD who developed DGM. Materials and Methods: A cohort of consecutive patients with ACLD without previous DGM, who attended a Hepatology clinic in the period of January to June 2015 was selected. Follow-up was carried out for 5 years. Data on age, gender, date of diagnosis and etiology of ACLD, Child-Pugh and MELD-Na classifications at enrollment, development of DGM, and antidiabetic therapy were collected. Logistic regression models for hospitalizations due to decompensated ACLD, ascites, hepatic encephalopathy (HE), upper gastrointestinal bleeding (UGB), hepatocellular carcinoma (HCC), portal vein thrombosis (PVT), infectious complications, acute-on-chronic liver failure (ACLF), and death were built. A survival analysis for patients with and without DGM was also performed. Treatment effectiveness for patients with DGM was assessed. Results: Initially, 221 patients were included, 154 (69.7%) of whom developed DGM after the diagnosis of ACLD. DGM patients presented a significantly higher number of hospitalizations. Odds ratio (OR) for death was not significantly related with DGM. At 5 years of follow-up, 68.9% of patients with DGM were alive, against 81.8% without DGM ( Conclusion: DGM occurs with high prevalence in patients with ACLD and it seems to be related to more hospitalizations, which highlights the importance of its early identification and appropriate therapeutic approach. In the absence of contraindications, biguanides should be considered for treatment of patients with ACLD and DGM as they appear to be associated with a tendency to better outcomes and may present some advantage in terms of survival.

Indexed as

BiguanidesChronic liver diseaseGlucose intoleranceHepatogenous diabetes

Identifiers

PMID40726561
PMCPMC12296221

What Socratic holds

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Registered trials

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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 Socratic graph.