Evidence map›Paper›PMID 39738706›Full record

ReviewPituitary2024

Treatment of acromegaly-induced diabetes: an updated proposal.

Betina Biagetti, Marta Araujo-Castro, Mónica Marazuela, Manel Puig-Domingo

Abstract readReview
PubMed Publisher
In one paragraph

Review in Pituitary, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Approach to the patient: precision medicine-guided evaluation and treatment of acromegaly.The Journal of clinical endocrinology and metabolism · 2026
    Review
  2. Review
  3. Article
  4. Review
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

4 authors.

Betina BiagettiEndocrinology & Nutrition Department, Hospital Universitario Vall de Hebrón. CIBERER U747 (ISCIII), ENDO-ERN, Barcelona, Spain. betinaloys.biagetti@vallhebron.cat.ORCID http://orcid.org/0000-0002-8837-4343
Marta Araujo-CastroDepartment of Endocrinology and Nutrition, Hospital Universitario Ramón y Cajal, Madrid, Spain.ORCID http://orcid.org/0000-0002-0519-0072
Mónica MarazuelaEndocrinology & Nutrition Department, Hospital Universitario La Princesa Madrid, Madrid, Spain.ORCID http://orcid.org/0000-0003-1158-9618
Manel Puig-DomingoEndocrinology & Nutrition Department, Hospital Universitario Germans Trias i Pujol. CIBERER U747 (ISCIII), Universitat Autònoma de Barcelona, Badalona, Spain. mpuigd@igtp.cat.ORCID http://orcid.org/0000-0002-6744-7195

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acromegaly-induced diabetes presents unique features due to the direct effects of excess growth hormone (GH) and insulin-like growth factor 1 (IGF-) on glucose metabolism, especially insulin resistance in association to low body fat content and water retention. Increased cardiovascular risk is much higher when acromegaly is complicated with diabetes, thus requiring a holistic management that addresses also these specific characteristics which differ from those of classical type 2 diabetes.The optimal management of diabetes in acromegaly requires not only an effective control of carbohydrate disturbances per se, but also the concurrent control of GH hypersecretion as it will directly impact on glucose control. If surgical treatment is not effective to normalize GH and IGF-1 levels, pharmacologic therapy for acromegaly must consider the metabolic effects that the different drugs may induce, as some of them may worsen carbohydrate metabolism. When treating acromegaly-induced diabetes, a comprehensive approach is essential, incorporating medications that may also protect against acromegaly associated comorbidities. Metformin remains the first-line therapy due to its ability to reduce hepatic glucose production enhance insulin sensitivity and its cost effectiveness. The newer drug classes, such as glucagon-like peptide-1 receptor agonists and sodium-glucose cotransporter-2 inhibitors, offer benefits similar to those seen in type 2 diabetes, but the unique metabolic profile of acromegaly-including an enhanced ketogenic state and the effects of incretins on GH secretion-have to be considered as it may influence outcomes. Understanding the distinct pathophysiology of acromegaly-induced diabetes and the benefits of these newer drug classes for the patient with acromegaly is crucial for optimizing treatment outcomes and improving the quality of life.

Indexed as

AcromegalyDiabetes Mellitus, Type 2Diabetes MellitusHuman Growth HormoneHumansHypoglycemic AgentsInsulin-Like Growth Factor IMetforminHuman Growth HormoneHypoglycemic AgentsInsulin-Like Growth Factor IMetforminAcromegalyDiabetesGLP-1GuidelineHyperglycemiaSGLT2i

Identifiers

What OpenQuestion holds

Texttitle and abstract
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.