Metabolic impact of pheochromocytoma/paraganglioma: targeted metabolomics in patients before and after tumor removal

Author:

Erlic Zoran1,Kurlbaum Max23,Deutschbein Timo3,Nölting Svenja4,Prejbisz Aleksander5,Timmers Henri6,Richter Susan7,Prehn Cornelia8,Weismann Dirk3,Adamski Jerzy891011,Januszewicz Andrzej5,Reincke Martin4,Fassnacht Martin2312,Robledo Mercedes13,Eisenhofer Graeme7,Beuschlein Felix14,Kroiss Matthias2312

Affiliation:

1. 1Klinik für Endokrinologie, Diabetologie und Klinische Ernährung, Universitätsspital Zürich, Zürich, Switzerland

2. 2Core Unit Clinical Mass Spectrometry, University Hospital Würzburg, Würzburg, Germany

3. 3Division of Endocrinology and Diabetology, Department of Internal Medicine I, Universitätsklinikum Würzburg, Würzburg, Germany

4. 4Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, München, Germany

5. 5Department of Hypertension, Institute of Cardiology, Warsaw, Poland

6. 6Department of Internal Medicine, Radboud University Medical Centre, Nijmegen, The Netherlands

7. 7Institut für Klinische Chemie und Labormedizin, Universitätsklinikum Carl Gustav Carus, Dresden, Germany

8. 8Helmholtz Zentrum München, Research Unit Molecular Endocrinology and Metabolism, Neuherberg, Germany

9. 9German Center for Diabetes Research (DZD), München-Neuherberg, Germany

10. 10Chair for Experimental Genetics, Technical University of Munich, Freising-Weihenstephan, Germany

11. 13Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore

12. 11Comprehensive Cancer Center Mainfranken, Universität Würzburg, Würzburg, Germany

13. 12Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO) and ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Madrid, Spain

Abstract

Objective Excess catecholamine release by pheochromocytomas and paragangliomas (PPGL) leads to characteristic clinical features and increased morbidity and mortality. The influence of PPGLs on metabolism is ill described but may impact diagnosis and management. The objective of this study was to systematically and quantitatively study PPGL-induced metabolic changes at a systems level. Design Targeted metabolomics by liquid chromatography-tandem mass spectrometry of plasma specimens in a clinically well-characterized prospective cohort study. Methods Analyses of metabolic profiles of plasma specimens from 56 prospectively enrolled and clinically well-characterized patients (23 males, 33 females) with catecholamine-producing PPGL before and after surgery, as well as measurement of 24-h urinary catecholamine using LC-MS/MS. Results From 127 analyzed metabolites, 15 were identified with significant changes before and after surgery: five amino acids/biogenic amines (creatinine, histidine, ornithine, sarcosine, tyrosine) and one glycerophospholipid (PCaeC34:2) with increased concentrations and six glycerophospholipids (PCaaC38:1, PCaaC42:0, PCaeC40:2, PCaeC42:5, PCaeC44:5, PCaeC44:6), two sphingomyelins (SMC24:1, SMC26:1) and hexose with decreased levels after surgery. Patients with a noradrenergic tumor phenotype had more pronounced alterations compared to those with an adrenergic tumor phenotype. Weak, but significant correlations for 8 of these 15 metabolites with total urine catecholamine levels were identified. Conclusions This first large prospective metabolomics analysis of PPGL patients demonstrates broad metabolic consequences of catecholamine excess. Robust impact on lipid and amino acid metabolism may contribute to increased morbidity of PPGL patients.

Publisher

Bioscientifica

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

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