Evidence map›Paper›PMID 41934517›Full record

ArticlePituitary2026

Adverse hepato-biliary-pancreatic events in acromegaly patients treated with first generation somatostatin receptor ligands.

Francesco Ferraù, Elena Sofia Blanca, Marta Ragonese, Angela Alibrandi, Marianna Martino, Giorgio Arnaldi, Luigi Simone Aversa, Daniela Cuboni, Silvia Grottoli, Francesco Giorgino and 9 more

Abstract readMulticenter Study
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In one paragraph

Article in Pituitary, 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

19 authors.

Francesco Ferraù *Endocrinology Unit, University Hospital "G. Martino", Messina, Italy. fferrau@unime.it.
Elena Sofia Blanca *Endocrinology Unit, University Hospital "G. Martino", Messina, Italy.
Marta RagoneseEndocrinology Unit, University Hospital "G. Martino", Messina, Italy.
Angela AlibrandiDepartment of Economics, Unit of Statistical and Mathematical Sciences, University of Messina, Messina, Italy.
Marianna MartinoDivision of Endocrinology, Marche University Hospital, Ancona, Italy.
Giorgio ArnaldiEndocrine, Metabolic and Nutritional Diseases, Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties (PROMISE), University Hospital Policlinico P. Giaccone, Palermo, Italy.
Luigi Simone AversaEndocrinology, Diabetes and Metabolism, Department of Medical Sciences, University of Turin, Turin, Italy.
Daniela CuboniEndocrinology, Diabetes and Metabolism, Department of Medical Sciences, University of Turin, Turin, Italy.
Silvia GrottoliEndocrinology, Diabetes and Metabolism, Department of Medical Sciences, University of Turin, Turin, Italy.
Francesco GiorginoDepartment of Precision and Regenerative Medicine and Ionian Area, Section of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, University of Bari Aldo Moro, Bari, Italy.
Anna LeonardiniDepartment of Precision and Regenerative Medicine and Ionian Area, Section of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, University of Bari Aldo Moro, Bari, Italy.
Ylenia AlessiEndocrinology Unit, University Hospital "G. Martino", Messina, Italy.
Carla Paola CostaEndocrinology Unit, University Hospital "G. Martino", Messina, Italy.
Giordana SiracusanoEndocrinology Unit, University Hospital "G. Martino", Messina, Italy.
Giovanni SquadritoUnit of Internal Medicine, Department of Clinical and Experimental Medicine, University Hospital G. Martino, University of Messina, Messina, Italy.
Giulia CarosiEndocrinology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Alessandra MangoneEndocrinology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Giovanna MantovaniEndocrinology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Salvatore CannavòEndocrinology Unit, University Hospital "G. Martino", Messina, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

First-generation somatostatin receptor ligands (SRLs) are first-line medical therapy for acromegaly. During long-term treatment, hepato-biliary-pancreatic adverse events can occur. This study aimed to evaluate the prevalence and predictors of hepato-biliary-pancreatic adverse events during SRL-treatment.In this multicenter study, data of 371 acromegaly patients (223 females) were retrospectively collected at the start of SRL therapy (T0), and at the last follow-up visit (120 ± 97.31 months). The occurrence of hepato-biliary-pancreatic adverse events and their relationship with features at T0 were investigated.Sixty-one patients (16.4%) underwent cholecystectomy (CH-Tx), cholecystitis (CH) occurred in 3.8%, severe or mild hyperlipasemia/hyperamylasemia in 2.2% and in 5.1%, severe or mild hypertransaminasemia in 1.1% and in 6.4%,respectively. No significant differences emerged after patient stratification by gender or age (≤/>50yrs). BMI, GH and IGF1 values were not associated with a higher risk of biliary complications. Patients undergoing CH-Tx or CH had a higher prevalence of cholelithiasis at T0 (p = 0.002 and p = 0.005). Cholelithiasis (p = 0.040) and biliary sludge (p = 0.014) at T0 were independent predictors of cholecystectomy. Cholelithiasis also strongly predicted cholecystitis in both univariable (p = 0.012) and multivariable (p = 0.025) analyses. Ursodeoxycholic acid (UDCA) treatment was associated with cholecystitis (p = 0.007) and mild-hypertransaminasemia (p = 0.035). When considering overall hepato-biliary-pancreatic adverse events, cholelithiasis, biliary sludge and age at T0 were significant predictors in both univariate (p = 0.006,p = 0.010,p = 0.013) and multivariable analysis (p = 0.029,p = 0.028,p = 0.044).Hepato-biliary-pancreatic adverse events are not infrequent during long-term SRLs therapy and are influenced overall by older age, cholelithiasis and biliary sludge.

Indexed as

AcromegalyReceptors, SomatostatinAdultAgedCabergolineCholecystectomyCholecystitisCholelithiasisFemaleHumansLigandsMaleMiddle AgedOctreotidePeptides, CyclicRetrospective StudiesCabergolineLigandsOctreotidepasireotidePeptides, CyclicReceptors, SomatostatinSomatostatinAcromegalyCholelithiasisHepato-biliary-pancreatic adverse eventsSomatostatin analogues

Identifiers

PMID41934517

What Socratic 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 Socratic graph.