Literature DB >> 21147885

Age at diagnosis of pheochromocytoma differs according to catecholamine phenotype and tumor location.

Graeme Eisenhofer1, Henri J Timmers, Jacques W M Lenders, Stefan R Bornstein, Oliver Tiebel, Massimo Mannelli, Kathryn S King, Cathy D Vocke, W Marston Linehan, Gennady Bratslavsky, Karel Pacak.   

Abstract

CONTEXT: Pheochromocytomas and paragangliomas (PPGLs) are diagnosed earlier in patients with hereditary than sporadic disease. Whether other factors influence age at diagnosis is unclear.
OBJECTIVE: We examined ages at which PPGLs were diagnosed according to different catecholamine phenotypes and locations of tumors. DESIGN &
SETTING: Retrospective multicenter study. PATIENTS: Patients with PPGLs included 172 with and 183 without identified germline mutations or hereditary syndromes. BIOCHEMICAL MEASUREMENTS: Differences in plasma concentrations of metanephrine, a metabolite of epinephrine, were used to distinguish epinephrine-producing tumors from those lacking epinephrine production.
RESULTS: Patients with epinephrine-producing tumors were diagnosed 11 yr later (P < 0.001) than those with tumors lacking appreciable epinephrine production. Among patients without evidence of a hereditary condition, those with and without epinephrine-producing tumors had respective mean ± se ages of 50 ± 2 and 42 ± 2 yr (P < 0.001) at diagnosis. Patients with multiple endocrine neoplasia type 2 and neurofibromatosis type 1, all with epinephrine-producing tumors, were similarly diagnosed with disease at a later age than patients with tumors that lacked appreciable epinephrine production secondary to mutations of von Hippel-Lindau and succinate dehydrogenase genes (40 ± 2 vs. 31 ± 1 yr, P < 0.001). Among the latter patients, those with multifocal tumors were diagnosed earlier than those with solitary tumors (19 ± 3 vs. 34 ± 2 yr, P < 0.001).
CONCLUSIONS: The variations in ages at diagnosis associated with different tumor catecholamine phenotypes and locations suggest origins of PPGLs from different chromaffin progenitor cells with variable susceptibility to disease causing mutations. Different optimal age cut-offs for mutation testing are indicated for patients with and without epinephrine-producing tumors (44-49 vs. 30-35 yr, respectively).

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Year:  2010        PMID: 21147885      PMCID: PMC3048320          DOI: 10.1210/jc.2010-1588

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  28 in total

1.  Genetics of pheochromocytoma and paraganglioma in Spanish patients.

Authors:  Alberto Cascón; Guillermo Pita; Nelly Burnichon; Iñigo Landa; Elena López-Jiménez; Cristina Montero-Conde; Susanna Leskelä; Luis Javier Leandro-García; Rocío Letón; Cristina Rodríguez-Antona; José Angel Díaz; Emilio López-Vidriero; Anna González-Neira; Ana Velasco; Xavier Matias-Guiu; Anne-Paule Gimenez-Roqueplo; Mercedes Robledo
Journal:  J Clin Endocrinol Metab       Date:  2009-03-03       Impact factor: 5.958

Review 2.  Review: the role of neural crest cells in the endocrine system.

Authors:  Meghan Sara Adams; Marianne Bronner-Fraser
Journal:  Endocr Pathol       Date:  2009       Impact factor: 3.943

3.  Expression of HIF-1alpha, HIF-2alpha (EPAS1), and their target genes in paraganglioma and pheochromocytoma with VHL and SDH mutations.

Authors:  Patrick J Pollard; Mona El-Bahrawy; Richard Poulsom; George Elia; Pip Killick; Gavin Kelly; Toby Hunt; Rosemary Jeffery; Pooja Seedhar; Julian Barwell; Farida Latif; Michael J Gleeson; Shirley V Hodgson; Gordon W Stamp; Ian P M Tomlinson; Eamonn R Maher
Journal:  J Clin Endocrinol Metab       Date:  2006-09-05       Impact factor: 5.958

4.  Genetic testing in pheochromocytoma: increasing importance for clinical decision making.

Authors:  Stefan R Bornstein; Anne-Paule Gimenez-Roqueplo
Journal:  Ann N Y Acad Sci       Date:  2006-08       Impact factor: 5.691

5.  Germline mutations in TMEM127 confer susceptibility to pheochromocytoma.

Authors:  Yuejuan Qin; Li Yao; Elizabeth E King; Kalyan Buddavarapu; Romina E Lenci; E Sandra Chocron; James D Lechleiter; Meghan Sass; Neil Aronin; Francesca Schiavi; Francesca Boaretto; Giuseppe Opocher; Rodrigo A Toledo; Sergio P A Toledo; Charles Stiles; Ricardo C T Aguiar; Patricia L M Dahia
Journal:  Nat Genet       Date:  2010-02-14       Impact factor: 38.330

6.  The kinesin KIF1Bbeta acts downstream from EglN3 to induce apoptosis and is a potential 1p36 tumor suppressor.

Authors:  Susanne Schlisio; Rajappa S Kenchappa; Liesbeth C W Vredeveld; Rani E George; Rodney Stewart; Heidi Greulich; Kristina Shahriari; Nguyen V Nguyen; Pascal Pigny; Patricia L Dahia; Scott L Pomeroy; John M Maris; A Thomas Look; Matthew Meyerson; Daniel S Peeper; Bruce D Carter; William G Kaelin
Journal:  Genes Dev       Date:  2008-03-11       Impact factor: 11.361

7.  Clinically guided genetic screening in a large cohort of italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas.

Authors:  Massimo Mannelli; Maurizio Castellano; Francesca Schiavi; Sebastiano Filetti; Mara Giacchè; Luigi Mori; Viviana Pignataro; Gianpaolo Bernini; Valentino Giachè; Alessandra Bacca; Bernadette Biondi; Giovanni Corona; Giuseppe Di Trapani; Erika Grossrubatscher; Giuseppe Reimondo; Giorgio Arnaldi; Gilberta Giacchetti; Franco Veglio; Paola Loli; Annamaria Colao; Maria Rosaria Ambrosio; Massimo Terzolo; Claudio Letizia; Tonino Ercolino; Giuseppe Opocher
Journal:  J Clin Endocrinol Metab       Date:  2009-02-17       Impact factor: 5.958

8.  Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients.

Authors:  Zoran Erlic; Lisa Rybicki; Mariola Peczkowska; Henriette Golcher; Peter H Kann; Michael Brauckhoff; Karsten Müssig; Michaela Muresan; Andreas Schäffler; Nicole Reisch; Matthias Schott; Martin Fassnacht; Giuseppe Opocher; Silke Klose; Christian Fottner; Flavio Forrer; Ursula Plöckinger; Stephan Petersenn; Dimitry Zabolotny; Oleg Kollukch; Svetlana Yaremchuk; Andrzej Januszewicz; Martin K Walz; Charis Eng; Hartmut P H Neumann
Journal:  Clin Cancer Res       Date:  2009-10-13       Impact factor: 12.531

9.  Conditional inactivation of glucocorticoid receptor gene in dopamine-beta-hydroxylase cells impairs chromaffin cell survival.

Authors:  Rosanna Parlato; Christiane Otto; Jan Tuckermann; Stefanie Stotz; Sylvia Kaden; Hermann-Josef Gröne; Klaus Unsicker; Günther Schütz
Journal:  Endocrinology       Date:  2008-11-26       Impact factor: 4.736

10.  Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD.

Authors:  Christopher J Ricketts; Julia R Forman; Eleanor Rattenberry; Nicola Bradshaw; Fiona Lalloo; Louise Izatt; Trevor R Cole; Ruth Armstrong; V K Ajith Kumar; Patrick J Morrison; A Brew Atkinson; Fiona Douglas; Steve G Ball; Jackie Cook; Umasuthan Srirangalingam; Pip Killick; Gail Kirby; Simon Aylwin; Emma R Woodward; D Gareth R Evans; Shirley V Hodgson; Vicky Murday; Shern L Chew; John M Connell; Tom L Blundell; Fiona Macdonald; Eamonn R Maher
Journal:  Hum Mutat       Date:  2010-01       Impact factor: 4.878

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  27 in total

1.  Von Hippel-Lindau disease type 2 in a Chinese family with a VHL p.W88X truncation.

Authors:  Min Zhang; Jie Wang; Jingjing Jiang; Xiaohui Zhan; Yan Ling; Zhiqiang Lu; Jianming Guo; Xin Gao
Journal:  Endocrine       Date:  2014-07-29       Impact factor: 3.633

2.  Genetic screening for von Hippel-Lindau gene mutations in non-syndromic pheochromocytoma: low prevalence and false-positives or misdiagnosis indicate a need for caution.

Authors:  G Eisenhofer; C D Vocke; A Elkahloun; T-T Huynh; T Prodanov; J W M Lenders; H J Timmers; J N Benhammou; W M Linehan; K Pacak
Journal:  Horm Metab Res       Date:  2012-03-21       Impact factor: 2.936

Review 3.  Pheochromocytomas and paragangliomas: assessment of malignant potential.

Authors:  Tim I M Korevaar; Ashley B Grossman
Journal:  Endocrine       Date:  2011-10-25       Impact factor: 3.633

Review 4.  Role of hypoxia and HIF2α in development of the sympathoadrenal cell lineage and chromaffin cell tumors with distinct catecholamine phenotypic features.

Authors:  Susan Richter; Nan Qin; Karel Pacak; Graeme Eisenhofer
Journal:  Adv Pharmacol       Date:  2013

Review 5.  Management of medullary thyroid carcinoma and MEN2 syndromes in childhood.

Authors:  Steven G Waguespack; Thereasa A Rich; Nancy D Perrier; Camilo Jimenez; Gilbert J Cote
Journal:  Nat Rev Endocrinol       Date:  2011-08-23       Impact factor: 43.330

Review 6.  Diagnostic tests and biomarkers for pheochromocytoma and extra-adrenal paraganglioma: from routine laboratory methods to disease stratification.

Authors:  Graeme Eisenhofer; Arthur S Tischler; Ronald R de Krijger
Journal:  Endocr Pathol       Date:  2012-03       Impact factor: 3.943

Review 7.  What Have We Learned from Molecular Biology of Paragangliomas and Pheochromocytomas?

Authors:  Thomas G Papathomas; Diederik P D Suurd; Alfred K Lam; Ronald R de Krijger; Karel Pacak; Arthur S Tischler; Menno R Vriens
Journal:  Endocr Pathol       Date:  2021-01-12       Impact factor: 3.943

8.  Pheochromocytoma - update on disease management.

Authors:  Roland Därr; Jacques W M Lenders; Lorenz C Hofbauer; Bernd Naumann; Stefan R Bornstein; Graeme Eisenhofer
Journal:  Ther Adv Endocrinol Metab       Date:  2012-02       Impact factor: 3.565

Review 9.  PRECISION MEDICINE: AN UPDATE ON GENOTYPE/BIOCHEMICAL PHENOTYPE RELATIONSHIPS IN PHEOCHROMOCYTOMA/PARAGANGLIOMA PATIENTS.

Authors:  Garima Gupta; Karel Pacak
Journal:  Endocr Pract       Date:  2017-03-23       Impact factor: 3.443

10.  Genitourinary paraganglioma: Demographic, pathologic, and clinical characteristics in the surveillance, epidemiology, and end results database (2000-2012).

Authors:  Stephanie Purnell; Abhinav Sidana; Mahir Maruf; Campbell Grant; Piyush K Agarwal
Journal:  Urol Oncol       Date:  2017-03-18       Impact factor: 3.498

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