Evidence mapPaperPMID 39745823Full record

ArticleThe Journal of clinical endocrinology and metabolism2025

Long-Term Persistence of Glycemic Dysregulation in Patients With a History of Pheochromocytoma/Paraganglioma.

Alessa Fischer, Hanna Remde, Christina Pamporaki, Ulrich Dischinger, Nicole Bechmann, Mercedes Robledo, Katharina Wang, Diana Vetter, José Oberholzer, Grégoire B Morand and 12 more

Abstract readMulticenter Study
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 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. 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

22 authors.

Alessa FischerDepartment of Endocrinology, Diabetology and Clinical Nutrition, University Hospital Zurich (USZ), University of Zurich (UZH), Zurich 8091, Switzerland.ORCID 0000-0003-4555-8334
Hanna RemdeDepartment of Internal Medicine I, Division of Endocrinology and Diabetes, University Hospital, University of Würzburg, Würzburg 97080, Germany.ORCID 0000-0002-3499-5910
Christina PamporakiDepartment of Internal Medicine III, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden 01307, Germany.ORCID 0000-0003-0772-1604
Ulrich DischingerDepartment of Internal Medicine I, Division of Endocrinology and Diabetes, University Hospital, University of Würzburg, Würzburg 97080, Germany.
Nicole BechmannInstitute of Clinical Chemistry and Laboratory Medicine, University Hospital Carl Gustav Carus, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden 01307, Germany.ORCID 0000-0002-6932-333X
Mercedes RobledoHereditary Endocrine Cancer Group, Spanish National Cancer Research Center (CNIO), Madrid 28029, Spain.ORCID 0000-0001-6256-5902
Katharina WangDepartment of Medicine IV, University Hospital, Ludwig-Maximilians-University Munich, Munich 80336, Germany.ORCID 0000-0002-7795-1395
Diana VetterDepartment of Visceral and Transplantation Surgery, University Hospital, Zurich 8091, Switzerland.
José OberholzerDepartment of Visceral and Transplantation Surgery, University Hospital, Zurich 8091, Switzerland.
Grégoire B MorandDepartment of Otorhinolaryngology, University Hospital, Zurich 8091, Switzerland.ORCID 0000-0002-6150-6772
Simon Andreas MuellerDepartment of Otorhinolaryngology, University Hospital, Zurich 8091, Switzerland.
Alexander HuberDepartment of Otorhinolaryngology, University Hospital, Zurich 8091, Switzerland.
Ralph FritschDepartment of Medical Oncology and Hematology, University Hospital, Zurich 8091, Switzerland.ORCID 0000-0001-9639-3213
Sven GruberDepartment of Endocrinology, Diabetology and Clinical Nutrition, University Hospital Zurich (USZ), University of Zurich (UZH), Zurich 8091, Switzerland.
Constanze HantelDepartment of Endocrinology, Diabetology and Clinical Nutrition, University Hospital Zurich (USZ), University of Zurich (UZH), Zurich 8091, Switzerland.ORCID 0009-0000-8906-2563
Kathrin ZitzmannDepartment of Medicine IV, University Hospital, Ludwig-Maximilians-University Munich, Munich 80336, Germany.ORCID 0009-0001-2341-3161
Martin ReinckeDepartment of Medicine IV, University Hospital, Ludwig-Maximilians-University Munich, Munich 80336, Germany.ORCID 0000-0002-9817-9875
Christoph J AuernhammerDepartment of Medicine IV, University Hospital, Ludwig-Maximilians-University Munich, Munich 80336, Germany.ORCID 0000-0001-8087-3722
Karel PacakAKESO, Prague 5, Czech Republic.ORCID 0000-0002-3541-3767
Ashley B GrossmanGreen Templeton College, University of Oxford, Oxford OX2 6HG, UK.ORCID 0000-0003-1176-6186
Felix BeuschleinDepartment of Endocrinology, Diabetology and Clinical Nutrition, University Hospital Zurich (USZ), University of Zurich (UZH), Zurich 8091, Switzerland.ORCID 0000-0001-7826-3984
Svenja NöltingDepartment of Endocrinology, Diabetology and Clinical Nutrition, University Hospital Zurich (USZ), University of Zurich (UZH), Zurich 8091, Switzerland.ORCID 0000-0002-7064-590X

Funding

CRC/Transregio 205/2CRC/Transregio 314061271CRC/Transregio TRR 205CRC/Transregio "Young Talents in Clinical Research"German Research FoundationG. & J. Bangerter-Rhyner Foundation
6 · The paper itself

Abstract

contextPheochromocytomas and paragangliomas (PPGLs) are rare endocrine tumors that frequently produce catecholamines. Catecholamine-induced cardiometabolic complications substantially contribute to increased morbidity and mortality in PPGL patients prior to surgical resection.

objectiveTo determine whether markers of elevated cardiometabolic risk persist in patients following PPGL resection.

methodsIn this retrospective analysis of a multicenter cohort of patients with PPGLs participating in the prospective ProsPheo study and the ENS@T registry, cardiometabolic risk factors, including glycemic status, dyslipidemia, and body mass index (BMI), were assessed in patients with PPGL at diagnosis and during follow-up. Patients with a history of resected PPGL were compared to a control group with nonfunctioning adrenal adenomas from the ENS@T registry.

resultsPatients with a present PPGL or a history of PPGL (n = 188), a metastatic PPGL (n = 27), or a known susceptibility gene pathogenic variant (PV) for the development of PPGL without a history of PPGL (n = 44) were included. We compared the asymptomatic PV carriers to patients with a history of PPGL: those with a history of PPGL showed a significantly higher prevalence of hyperglycemic disorders (P = .013) compared with asymptomatic PV carriers. In patients with a history of PPGL and at least 12 months of follow-up post surgery (n = 113), the prevalence of hyperglycemic disorders (P < .001), as well as the mean HbA1c (5.63%, SD 0.43%), were significantly higher, compared to a control group with nonfunctioning adrenal adenomas (n = 76) of similar age and BMI (HbA1c 5.45%, SD 0.40%; P = .004).

conclusionGlycemic disturbances persist long-term after the resection of PPGL.

Indexed as

Adrenal Gland NeoplasmsParagangliomaPheochromocytomaAdultAgedBlood GlucoseCardiometabolic Risk FactorsFemaleFollow-Up StudiesHumansMaleMiddle AgedProspective StudiesRetrospective StudiesBlood Glucosecardiometabolic riskdiabetesglucose intoleranceHbA1cparagangliomapheochromocytoma

Identifiers

PMID39745823
PMCPMC12342352

What Socratic holds

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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.