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      False-positive results for pheochromocytoma associated with norepinephrine reuptake blockade

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          Abstract

          Measurements of plasma metanephrines and methoxytyramine provide a sensitive test for diagnosis of pheochromocytoma/paraganglioma. False-positive results remain a problem, particularly in patients taking norepinephrine reuptake-blocking drugs. Therefore, in this retrospective observational study, we measured plasma metanephrines and methoxytyramine in 61 patients taking norepinephrine reuptake blockers (tricyclic antidepressants or serotonin–norepinephrine reuptake inhibitors) and 17 others taking selective serotonin reuptake inhibitors, all without pheochromocytoma/paraganglioma. We highlight a singular case with strongly elevated plasma normetanephrine and methoxytyramine concentrations associated with norepinephrine reuptake blockade. Data were compared to results from 252 and 1804 respective patients with and without tumors. Plasma normetanephrine was 40% higher ( P < 0.0001) in patients on norepinephrine reuptake blockers and methoxytyramine was 127% higher ( P = 0.0062) in patients taking tricyclic antidepressants compared to patients not taking uptake blockers and without tumors. The corresponding false-positive rates rose ( P < 0.0001) from 4.8% to 23.0% for normetanephrine and from 0.9% to 28.6% for methoxytyramine. Selective serotonin reuptake inhibitors did not increase plasma concentrations of metabolites. In the highlighted case, plasma normetanephrine and methoxytyramine were elevated more than six times above upper reference limits. A pheochromocytoma/paraganglioma, however, was excluded by functional imaging. All biochemical test results normalized after discontinuation of norepinephrine reuptake blockers. These findings clarify that norepinephrine reuptake blockers usually result in mild elevations of normetanephrine and methoxytyramine that, nevertheless, significantly increase the number of false-positive results. There can, however, be exceptions where increases in normetanephrine and methoxytyramine reach pathological levels. Such exceptions may reflect failure of centrally mediated sympathoinhibition that normally occurs with the norepinephrine reuptake blockade.

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          Most cited references34

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          CARE 2013 Explanations and Elaborations: Reporting Guidelines for Case Reports.

          Well-written and transparent case reports (1) reveal early signals of potential benefits, harms, and information on the use of resources; (2) provide information for clinical research and clinical practice guidelines (CPGs), and (3) inform medical education. High-quality case reports are more likely when authors follow reporting guidelines. During 2011-2012 a group of clinicians, researchers, and journal editors developed recommendations for the accurate reporting of information in case reports that resulted in the CARE (CAse REport) Statement and Checklist. They were presented at the 2013 International Congress on Peer Review and Biomedical Publication, have been endorsed by multiple medical journals, and translated into nine languages. This explanation and elaboration document has the objective to increase the use and dissemination of the CARE Checklist in writing and publishing case reports. Each item from the CARE Checklist is explained and accompanied by published examples. The explanations and examples in this document are designed to support the writing of high-quality case reports by authors and their critical appraisal by editors, peer reviewers, and readers. This article and the 2013 CARE Statement and Checklist, available from the CARE website [www.care-statement.org] and the EQUATOR Network, [www.equator-network.org] are resources for improving the completeness and transparency of case reports.
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            Pharmacological profile of antidepressants and related compounds at human monoamine transporters.

            Using radioligand binding assays, we determined the equilibrium dissociation constants (KD's) for 37 antidepressants, three of their metabolites (desmethylcitalopram, desmethylsertraline, and norfluoxetine), some mood stabilizers, and assorted other compounds (some antiepileptics, Ca2+ channel antagonists, benzodiazepines, psychostimulants, antihistamines, and monoamines) for the human serotonin, norepinephrine, and dopamine transporters. Among the compounds that we tested, mazindol was the most potent at the human norepinephrine and dopamine transporters with KD's of 0.45 +/- 0.03 nM and 8.1 +/- 0.4 nM, respectively. Sertraline (KD = 25 +/- 2 nM) and nomifensine (56 +/- 3 nM) were the two most potent antidepressants at the human dopamine transporter. We showed significant correlations for antidepressant affinities at binding to serotonin (R = 0.93), norepinephrine (R = 0.97), and dopamine (R = 0.87) transporters in comparison to their respective values for inhibiting uptake of monoamines into rat brain synaptosomes. These data are useful in predicting some possible adverse effects and drug-drug interactions of antidepressants and related compounds.
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              Biochemical diagnosis of pheochromocytoma: how to distinguish true- from false-positive test results.

              Measurements of plasma normetanephrine and metanephrine provide a highly sensitive test for diagnosis of pheochromocytoma, but false-positive results remain a problem. We therefore assessed medication-associated false-positive results and use of supplementary tests, including plasma normetanephrine responses to clonidine, to distinguish true- from false-positive results. The study included 208 patients with pheochromocytoma and 648 patients in whom pheochromocytoma was excluded. Clonidine-suppression tests were carried out in 48 patients with and 49 patients without the tumor. Tricyclic antidepressants and phenoxybenzamine accounted for 41% of false-positive elevations of plasma normetanephrine and 44-45% those of plasma and urinary norepinephrine. High plasma normetanephrine to norepinephrine or metanephrine to epinephrine ratios were strongly predictive of pheochromocytoma. Lack of decrease and elevated plasma levels of norepinephrine or normetanephrine after clonidine also confirmed pheochromocytoma with high specificity. However, 16 of 48 patients with pheochromocytoma had normal levels or decreases of norepinephrine after clonidine. In contrast, plasma normetanephrine remained elevated in all but 2 patients, indicating more reliable diagnosis using normetanephrine than norepinephrine responses to clonidine. Thus, in patients with suspected pheochromocytoma and positive biochemical results, false-positive elevations due to medications should first be eliminated. Patterns of biochemical test results and responses of plasma normetanephrine to clonidine can then help distinguish true- from false-positive results.

                Author and article information

                Journal
                Endocr Relat Cancer
                Endocr Relat Cancer
                ERC
                Endocrine-Related Cancer
                Bioscientifica Ltd (Bristol )
                1351-0088
                1479-6821
                01 December 2023
                13 November 2023
                01 January 2024
                : 31
                : 1
                : e230063
                Affiliations
                [1 ]Division of Endocrinology and Diabetes , Department of Internal Medicine, University of Leipzig, Leipzig, Germany
                [2 ]TU Dresden , Medical Clinic III, University Hospital Carl Gustav Carus, Dresden, Germany
                [3 ]TU Dresden , Institute of Clinical Chemistry and Laboratory Medicine, Dresden, Germany
                [4 ]Center of Surgery , Division of Endocrine Surgery, Department for Visceral, Transplant, Thoracic, and Vascular Surgery, University of Leipzig, Leipzig, Germany
                [5 ]Department of Nuclear Medicine , University of Leipzig, Leipzig, Germany
                [6 ]Center of Surgery , Department for Visceral, Transplant, Thoracic, and Vascular Surgery, University of Leipzig, Leipzig, Germany
                [7 ]Center of Surgery , Department for Vascular Surgery, Diakonissen Hospital of Leipzig, Leipzig, Germany
                [8 ]Institute of Clinical Chemistry and Laboratory Medicine , University of Leipzig, Leipzig, Germany
                Author notes
                Correspondence should be addressed to R Schürfeld: robin.schuerfeld@ 123456medizin.uni-leipzig.de

                *(R Schürfeld and C Pamporaki contributed equally to this work)

                †(A Tönjes and G Eisenhofer contributed equally to this work as senior authors)

                This paper is part of a themed collection on Advances and Future Directions in Pheochromocytoma and Paraganglioma. The collection editors for this collection are Karel Pacak (NICHHD, USA) and Roderick Clifton-Bligh (University of Sydney, Australia).

                Author information
                http://orcid.org/0000-0002-7488-916X
                http://orcid.org/0000-0002-8601-9903
                Article
                ERC-23-0063
                10.1530/ERC-23-0063
                10762534
                37955319
                0e15a383-ff88-40e8-b082-3b0237148e33
                © the author(s)

                This work is licensed under a Creative Commons Attribution 4.0 International License.

                History
                : 10 March 2023
                : 13 November 2023
                Funding
                Funded by: Deutsche Forschungsgemeinschaft, doi http://dx.doi.org/10.13039/501100001659;
                Funded by: Deutsche Forschungsgemeinschaft, doi http://dx.doi.org/10.13039/501100001659;
                Funded by: Deutsche Forschungsgemeinschaft, doi http://dx.doi.org/10.13039/501100001659;
                Categories
                Thematic Research

                Oncology & Radiotherapy
                pheochromocytoma,false-positive,doxepin,duloxetine,metanephrines,normetanephrine,tricyclic antidepressant,serotonin–norepinephrine reuptake inhibitor,metanephrine,methoxytyramine,clonidine

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