Evidence map›Paper›PMID 40960781›Full record

ArticleEinstein (Sao Paulo, Brazil)2025

A new and useful tool for differentiating prolactinomas from non-functioning pituitary adenomas: a pilot study of the cabergoline disconnection test.

Stefano Alvarenga Galliano, Matheo Augusto Morandi Stumpf, Nara L Queiroz, Eduardo Henrique Rodrigues Ferreira, Flora Ladeira Craveiro, Christiane Gruetzmacher, Gilberto Ochman da Silva, Valter Angelo Sperling Cescato, Eduardo Arnaldo Silva Vellutini, Malebranche Berardo Carneiro Cunha-Neto and 2 more

Abstract read
In one paragraph

Article in Einstein (Sao Paulo, Brazil), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Stefano Alvarenga GallianoEndocrinology and Metabolism Discipline, Neuroendocrinology Unit, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0003-0265-6604
Matheo Augusto Morandi StumpfEndocrinology and Metabolism Discipline, Neuroendocrinology Unit, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-6465-0972
Nara L QueirozEndocrinology and Metabolism Discipline, Neuroendocrinology Unit, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.ORCID http://orcid.org/0009-0009-1597-6616
Eduardo Henrique Rodrigues FerreiraEndocrinology and Metabolism Discipline, Neuroendocrinology Unit, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.
Flora Ladeira CraveiroEndocrinology and Metabolism Discipline, Neuroendocrinology Unit, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0003-1085-5689
Christiane GruetzmacherEndocrinology and Metabolism Discipline, Neuroendocrinology Unit, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.ORCID http://orcid.org/0009-0008-0775-2711
Gilberto Ochman da SilvaNeuroendocrinology Group, Neurosurgery Division, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.ORCID http://orcid.org/0009-0007-2819-8281
Valter Angelo Sperling CescatoNeuroendocrinology Group, Neurosurgery Division, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.ORCID http://orcid.org/0009-0002-8005-5476
Eduardo Arnaldo Silva VellutiniNeuroendocrinology Group, Neurosurgery Division, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0003-1323-6488
Malebranche Berardo Carneiro Cunha-NetoEndocrinology and Metabolism Discipline, Neuroendocrinology Unit, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.ORCID http://orcid.org/0009-0007-8263-374X
Rafael Loch BatistaEndocrinology and Metabolism Discipline, Neuroendocrinology Unit, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-5461-0301
Andrea GlezerEndocrinology and Metabolism Discipline, Neuroendocrinology Unit, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-8201-6756

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveClinical, imaging, and laboratory differentiation between non-functioning pituitary adenomas (NFPAs) and prolactinomas can be challenging in clinical practice because of their similar presentation and eventual overlap in prolactin levels. The degree of prolactin suppression after a single low-dose cabergoline administration may be useful as a test to discriminate between these two clinical conditions and to determine the choice of therapy (dopamine agonist versus neurosurgery).

methodsThis retrospective cohort study included 19 patients with macroadenomas (11 NFPAs and 8 prolactinomas) whose prolactin levels were evaluated at baseline and 48 h after receiving a single dose of 0.25mg cabergoline. A receiver operating characteristic curve was generated for sensitivity and specificity analyses.

resultsThe baseline median prolactin level was 58ng/mL (range, 32.5-151.2ng/mL) in the NFPA Group, which was significantly lower than that observed in the Prolactinoma Group (733.7 [range, 180-6941ng/mL]) (p<0.001). After the cabergoline disconnection test, the NFPA Group exhibited a lower absolute prolactin level (p<0.001) and a higher percentage of prolactin reduction (p=0.004). The post-test prolactin level ≥26.3ng/mL had 100% sensitivity and specificity in identifying prolactinomas. When using the percentage of reduction, post-test prolactin reduction ≥85.6% had 54.5% sensitivity and 100% specificity to differentiate NFPAs from prolactinomas.

conclusionA single low-dose oral cabergoline is a fast and inexpensive test for use in daily clinical practice to discriminate between hyperprolactinemia due to NFPAs and prolactinomas, with high sensitivity and specificity.

Indexed as

AdenomaDopamine AgonistsErgolinesPituitary NeoplasmsProlactinProlactinomaAdultAgedCabergolineDiagnosis, DifferentialFemaleHumansMaleMiddle AgedPilot ProjectsRetrospective StudiesCabergolineDopamine AgonistsErgolinesProlactin

Identifiers

PMID40960781
PMCPMC12539812

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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 OpenQuestion graph.