Evidence map›Paper›PMID 42611413›Full record

Observational studyPituitary2026

Cardiometabolic effects of sequential prolactin states in dopamine agonist-treated prolactinoma patients: a retrospective longitudinal study.

Pedro Iglesias, María Dolores Moure Rodríguez, Fernando Guerrero-Pérez, Andreu Simó-Servat, Laura González Fernández, Eva Fernández-Rodríguez, Patricia Pérez Castro, Rocío Villar-Taibo, Betina Biagetti, Aida Orois and 16 more

Abstract readMulticenter StudyObservational Study
PubMed Publisher
In one paragraph

Observational study 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.

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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

26 authors.

Pedro IglesiasEndocrinology & Nutrition Department, Hospital Universitario Puerta de Hierro Majadahonda, C. Joaquín Rodrigo 1, 28222 Majadahonda, Madrid, Spain. piglo65@gmail.com.
María Dolores Moure RodríguezEndocrinology & Nutrition Department, Instituto Investigación Sanitaria Biobizkaia (IIS Biobizkaia), Hospital Universitario Cruces, Universidad del País Vasco UPV/EHU, Bilbao, Spain.
Fernando Guerrero-PérezEndocrinology & Nutrition Department, Hospital Universitari de Bellvitge, L'Hospitalet de Llobregat, Barcelona, Spain.
Andreu Simó-ServatEndocrinology & Nutrition Department, Hospital Universitari MutuaTerrassa and Terrassa Health Consortium, Terrassa, Spain.
Laura González FernándezEndocrinology & Nutrition Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Eva Fernández-RodríguezEndocrinology & Nutrition Department, Complexo Hospitalario Universitario de Ourense, Ourense, Spain.
Patricia Pérez CastroEndocrinology & Nutrition Department, Complejo Hospitalario Universitario de Vigo, Vigo, Spain.
Rocío Villar-TaiboEndocrinology & Nutrition Department, Hospital Universitario de Santiago, Santiago de Compostela, Spain.
Betina BiagettiEndocrinology & Nutrition Department, Hospital Universitario Vall de Hebrón, CIBERER U747 (ISCIII), ENDO-ERN, Universitat Autónoma de Barcelona, Barcelona, Spain.
Aida OroisEndocrinology & Nutrition Department, Hospital Clínic de Barcelona, Barcelona, Spain.
Sara DonatoEndocrinology & Nutrition Department, Hospital Universitario Ramón y Cajal, Madrid, Spain.
Victoria Alcázar LázaroEndocrinology & Nutrition Department, Hospital Universitario Severo Ochoa, Madrid, Spain.
Noel Roig-MarínEndocrinology & Nutrition Department, Complejo Hospitalario Universitario de Albacete, Albacete, Spain.
Guillermo SerraEndocrinology & Nutrition Department, Hospital Universitario Son Espases, Palma de Mallorca, Spain.
Soralla CivantosEndocrinology & Nutrition Department, Hospital Universitario de Fuenlabrada, Madrid, Spain.
Gonzalo RiveroEndocrinology & Nutrition Department, Hospital Universitario Puerta de Hierro Majadahonda, C. Joaquín Rodrigo 1, 28222 Majadahonda, Madrid, Spain.
Carmen María Fernandez de AraozEndocrinology & Nutrition Department, Hospital Universitario de Getafe, Madrid, Spain.
Isabel Pavón de PazEndocrinology & Nutrition Department, Hospital Universitario de Getafe, Madrid, Spain.
Elena Outeiriño-BlancoEndocrinology & Nutrition Department, Hospital Universitario A Coruña, University of A Coruña, A Coruña, Spain.
Fernando CordidoEndocrinology & Nutrition Department, Hospital Universitario A Coruña, University of A Coruña, A Coruña, Spain.
Rogelio García CentenoEndocrinology & Nutrition Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Marta Araujo-CastroEndocrinology & Nutrition Department, Hospital Universitario Ramón y Cajal, Madrid, Spain.
Cristina LamasEndocrinology & Nutrition Department, Complejo Hospitalario Universitario de Albacete, Albacete, Spain.
Miguel PajaEndocrinology & Nutrition, Biobizkaia Health Research Institute; Osakidetza, Basurto University Hospital; EHU, Basque Country University, Bilbao, Bizkaia, Spain.
Felicia Alexandra HanzuEndocrinology & Nutrition Department, Hospital Clinic. University of Barcelona. IDIPAS, Barcelona, Spain.
Juan J DíezEndocrinology & Nutrition Department, Hospital Universitario Puerta de Hierro Majadahonda, C. Joaquín Rodrigo 1, 28222 Majadahonda, Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeHyperprolactinemia has been associated with adverse cardiometabolic alterations, whereas the metabolic consequences of treatment-induced hypoprolactinemia remain uncertain. We aimed to evaluate longitudinal cardiometabolic changes across sequential prolactin states in dopamine agonist-treated prolactinoma patients.

methodsWe conducted a retrospective multicentre longitudinal cohort study including 47 prolactinoma patients from 19 tertiary hospitals in Spain. All patients sequentially transitioned from hyperprolactinemia (HyperPRL) to normoprolactinemia (NormoPRL) and subsequently to hypoprolactinemia (HypoPRL) during cabergoline therapy. Longitudinal changes in anthropometric, hemodynamic, and metabolic parameters were assessed using repeated-measures analyses and generalized estimating equation (GEE) models. Correlation and multivariable regression analyses were performed to evaluate associations between prolactin reduction and metabolic changes.

resultsTransition from HyperPRL to NormoPRL was associated with significant reductions in body weight (80.4 ± 23.6 vs. 78.7 ± 22.8 kg; p = 0.009), body mass index (29.3 ± 7.4 vs. 28.4 ± 7.3 kg/m²; p = 0.034), and total cholesterol (194.3 ± 36.5 vs. 178.7 ± 34.8 mg/dL; p = 0.006). Triglyceride concentrations showed a trend toward reduction across prolactin states, with a significant decrease observed between HyperPRL and NormoPRL. No additional cardiometabolic improvements were detected after transition from NormoPRL to HypoPRL. GEE analyses confirmed significant longitudinal reductions in body weight and total cholesterol after adjustment for age, sex, and initial cabergoline dose, and results remained unchanged in sensitivity analyses additionally accounting for treatment duration. Although percentage prolactin reduction showed a weak inverse association with body weight change in exploratory analyses, no independent associations were identified after multivariable adjustment.

conclusionsNormalization of prolactin concentrations was associated with significant improvements in body weight, BMI, and total cholesterol concentrations. In contrast, no significant cardiometabolic improvements were detected following the subsequent development of treatment-induced hypoprolactinemia. Furthermore, the magnitude of prolactin reduction was not independently associated with changes in anthropometric or metabolic parameters after multivariable adjustment. These findings suggest that the main cardiometabolic changes occur during the transition from hyperprolactinemia to normoprolactinemia. However, the specific cardiometabolic effects of treatment-induced hypoprolactinemia require confirmation in larger prospective studies.

Indexed as

Dopamine AgonistsHyperprolactinemiaPituitary NeoplasmsProlactinProlactinomaAdultCabergolineErgolinesFemaleHumansLongitudinal StudiesMaleMiddle AgedRetrospective StudiesCabergolineDopamine AgonistsErgolinesProlactinCardiometabolic riskDopamine agonistsHyperprolactinemiaHypoprolactinemiaProlactin homeostasisProlactinoma

Identifiers

PMID42611413

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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.