Literature DB >> 28132167

Multiple endocrine neoplasia syndrome type 1: institution, management, and data analysis of a nationwide multicenter patient database.

Francesca Giusti1, Luisella Cianferotti1, Francesca Boaretto2, Filomena Cetani3, Federica Cioppi1, Annamaria Colao4, Maria Vittoria Davì5, Antongiulio Faggiano6, Giuseppe Fanciulli7, Piero Ferolla8, Diego Ferone9, Caterina Fossi1, Francesco Giudici1, Giorgio Gronchi1, Paola Loli10, Franco Mantero11, Claudio Marcocci3, Francesca Marini1, Laura Masi1, Giuseppe Opocher2, Paolo Beck-Peccoz12, Luca Persani13,14, Alfredo Scillitani15, Giovanna Sciortino13,14, Anna Spada16, Paola Tomassetti17, Francesco Tonelli1, Maria Luisa Brandi18.   

Abstract

OBJECTIVE: The aim of this study was to integrate European epidemiological data on patients with multiple endocrine neoplasia type 1 by creating an Italian registry of this syndrome, including clinical and genetic characteristics and therapeutic management.
METHODS: Clinical, familial and genetic data of patients with multiple endocrine neoplasia type 1, diagnosed, treated, and followed-up for a mean time of 11.3 years, in 14 Italian referral endocrinological centers, were collected, over a 3-year course (2011-2013), to build a national electronic database.
RESULTS: The Italian multiple endocrine neoplasia type 1 database includes 475 patients (271 women and 204 men), of whom 383 patients (80.6%) were classified as familial cases (from 136 different pedigrees), and 92 (19.4%) patients were sporadic cases. A MEN1 mutation was identified in 92.6% of familial cases and in 48.9% of sporadic cases. Four hundred thirty-six patients were symptomatic, presenting primary hyperparathyroidism, gastroenteropancreatic neuroendocrine tumors and pituitary tumors in 93, 53, and 41% of cases, respectively. Thirty-nine subjects, belonging to affected pedigrees positive for a MEN1 mutation, were asymptomatic at clinical and biochemical screening. Age at diagnosis of multiple endocrine neoplasia type 1 probands was similar for both familial and simplex cases (mean age 47.2 ± 15.3 years). In familial cases, diagnosis of multiple endocrine neoplasia type 1 in relatives of affected probands was made more than 10 years in advance (mean age at diagnosis 36.5 ± 17.6 years).
CONCLUSIONS: The analysis of Italian registry of multiple endocrine neoplasia type 1 patients revealed that clinical features of Italian multiple endocrine neoplasia type 1 patients are similar to those of other western countries, and confirmed that the genetic test allowed multiple endocrine neoplasia type 1 diagnosis 10 years earlier than biochemical or clinical diagnosis.

Entities:  

Keywords:  Gastroenteropancreatic tumors; Italian registry; MEN1; MEN1 genetic test; Pituitary adenomas; Primary hyperparathyroidism

Mesh:

Substances:

Year:  2017        PMID: 28132167     DOI: 10.1007/s12020-017-1234-4

Source DB:  PubMed          Journal:  Endocrine        ISSN: 1355-008X            Impact factor:   3.633


  28 in total

1.  Surgery increases survival in patients with gastrinoma.

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Journal:  Ann Surg       Date:  2006-09       Impact factor: 12.969

2.  Unraveling the intrafamilial correlations and heritability of tumor types in MEN1: a Groupe d'étude des Tumeurs Endocrines study.

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Journal:  Eur J Endocrinol       Date:  2015-09-21       Impact factor: 6.664

Review 3.  Guidelines for diagnosis and therapy of MEN type 1 and type 2.

Authors:  M L Brandi; R F Gagel; A Angeli; J P Bilezikian; P Beck-Peccoz; C Bordi; B Conte-Devolx; A Falchetti; R G Gheri; A Libroia; C J Lips; G Lombardi; M Mannelli; F Pacini; B A Ponder; F Raue; B Skogseid; G Tamburrano; R V Thakker; N W Thompson; P Tomassetti; F Tonelli; S A Wells; S J Marx
Journal:  J Clin Endocrinol Metab       Date:  2001-12       Impact factor: 5.958

4.  Long-Term Natural Course of Pituitary Tumors in Patients With MEN1: Results From the DutchMEN1 Study Group (DMSG).

Authors:  Joanne M de Laat; Olaf M Dekkers; Carolina R C Pieterman; Wouter P Kluijfhout; Ad R Hermus; Alberto M Pereira; Anouk N van der Horst-Schrivers; Madeleine L Drent; Peter H Bisschop; Bas Havekes; Wouter W de Herder; Gerlof D Valk
Journal:  J Clin Endocrinol Metab       Date:  2015-06-30       Impact factor: 5.958

5.  Adrenal involvement in MEN1. Analysis of 715 cases from the Groupe d'etude des Tumeurs Endocrines database.

Authors:  B Gatta-Cherifi; O Chabre; A Murat; P Niccoli; C Cardot-Bauters; V Rohmer; J Young; B Delemer; H Du Boullay; M F Verger; J M Kuhn; J L Sadoul; Ph Ruszniewski; A Beckers; M Monsaingeon; E Baudin; P Goudet; A Tabarin
Journal:  Eur J Endocrinol       Date:  2011-11-14       Impact factor: 6.664

6.  Genotype-phenotype analysis in multiple endocrine neoplasia type 1.

Authors:  Maria A Kouvaraki; Jeffrey E Lee; Suzanne E Shapiro; Robert F Gagel; Steven I Sherman; Rena V Sellin; Gilbert J Cote; Douglas B Evans
Journal:  Arch Surg       Date:  2002-06

7.  Clinical genetic testing and early surgical intervention in patients with multiple endocrine neoplasia type 1 (MEN 1).

Authors:  Terry C Lairmore; Linda D Piersall; Mary K DeBenedetti; William G Dilley; Matthew G Mutch; Alison J Whelan; Barbara Zehnbauer
Journal:  Ann Surg       Date:  2004-05       Impact factor: 12.969

8.  Screening of patients with multiple endocrine neoplasia type 1 (MEN-1): a critical analysis of its value.

Authors:  Jens Waldmann; Volker Fendrich; Nils Habbe; Detlef K Bartsch; Emily P Slater; Peter H Kann; Matthias Rothmund; Peter Langer
Journal:  World J Surg       Date:  2009-06       Impact factor: 3.352

9.  Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d'etude des Tumeurs Endocrines (GTE) cohort study.

Authors:  Julien Thevenon; Abderrahmane Bourredjem; Laurence Faivre; Catherine Cardot-Bauters; Alain Calender; Arnaud Murat; Sophie Giraud; Patricia Niccoli; Marie-Françoise Odou; Françoise Borson-Chazot; Anne Barlier; Catherine Lombard-Bohas; Eric Clauser; Antoine Tabarin; Béatrice Parfait; Olivier Chabre; Emilie Castermans; Albert Beckers; Philippe Ruszniewski; Morgane Le Bras; Brigitte Delemer; Philippe Bouchard; Isabelle Guilhem; Vincent Rohmer; Bernard Goichot; Philippe Caron; Eric Baudin; Philippe Chanson; Lionel Groussin; Hélène Du Boullay; Georges Weryha; Pierre Lecomte; Alfred Penfornis; Hélène Bihan; Françoise Archambeaud; Véronique Kerlan; Françoise Duron; Jean-Marc Kuhn; Bruno Vergès; Michel Rodier; Michel Renard; Jean-Louis Sadoul; Christine Binquet; Pierre Goudet
Journal:  Hum Mol Genet       Date:  2013-01-31       Impact factor: 6.150

Review 10.  Variable clinical expression in patients with a germline MEN1 disease gene mutation: clues to a genotype-phenotype correlation.

Authors:  Cornelis J Lips; Koen M Dreijerink; Jo W Höppener
Journal:  Clinics (Sao Paulo)       Date:  2012       Impact factor: 2.365

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  29 in total

1.  The need for national registries for rare endocrine tumor syndromes.

Authors:  Rachel S van Leeuwaarde; Wouter W de Herder; Gerlof D Valk
Journal:  Endocrine       Date:  2017-04-17       Impact factor: 3.633

2.  Children with MEN1 gene mutations may present first (and at a young age) with Cushing disease.

Authors:  Angeliki Makri; Maria Belen Bonella; Margaret F Keil; Laura Hernandez-Ramirez; Gabriella Paluch; Amit Tirosh; Carolina Saldarriaga; Prashant Chittiboina; Stephen J Marx; Constantine A Stratakis; Maya Lodish
Journal:  Clin Endocrinol (Oxf)       Date:  2018-07-20       Impact factor: 3.478

Review 3.  Clinical aspects of multiple endocrine neoplasia type 1.

Authors:  Abdallah Al-Salameh; Guillaume Cadiot; Alain Calender; Pierre Goudet; Philippe Chanson
Journal:  Nat Rev Endocrinol       Date:  2021-02-09       Impact factor: 43.330

4.  Multiple endocrine neoplasia type 1: analysis of germline MEN1 mutations in the Italian multicenter MEN1 patient database.

Authors:  Francesca Marini; Francesca Giusti; Caterina Fossi; Federica Cioppi; Luisella Cianferotti; Laura Masi; Francesca Boaretto; Stefania Zovato; Filomena Cetani; Annamaria Colao; Maria Vittoria Davì; Antongiulio Faggiano; Giuseppe Fanciulli; Piero Ferolla; Diego Ferone; Paola Loli; Franco Mantero; Claudio Marcocci; Giuseppe Opocher; Paolo Beck-Peccoz; Luca Persani; Alfredo Scillitani; Fabiana Guizzardi; Anna Spada; Paola Tomassetti; Francesco Tonelli; Maria Luisa Brandi
Journal:  Endocrine       Date:  2018-03-01       Impact factor: 3.633

Review 5.  Cushing's disease in children: unique features and update on genetics.

Authors:  Constantine A Stratakis
Journal:  Pituitary       Date:  2022-06-24       Impact factor: 3.599

Review 6.  Neuroendocrine neoplasms in the context of inherited tumor syndromes: a reappraisal focused on targeted therapies.

Authors:  R M Ruggeri; E Benevento; F De Cicco; B Fazzalari; E Guadagno; I Hasballa; M G Tarsitano; A M Isidori; A Colao; A Faggiano
Journal:  J Endocrinol Invest       Date:  2022-08-30       Impact factor: 5.467

Review 7.  The future: genetics advances in MEN1 therapeutic approaches and management strategies.

Authors:  Sunita K Agarwal
Journal:  Endocr Relat Cancer       Date:  2017-10       Impact factor: 5.678

8.  A large Turkish pedigree with multiple endocrine neoplasia type 1 syndrome carrying a rare mutation: c.1680_1683 del TGAG.

Authors:  Coşkun Özer Demirtaş; Pınar Ata; Ali Çetin; Ayberk Türkyılmaz; Deniz Guney Duman
Journal:  Turk J Gastroenterol       Date:  2020-07       Impact factor: 1.852

Review 9.  Multiple Endocrine Neoplasia Type 1: Latest Insights.

Authors:  Maria Luisa Brandi; Sunita K Agarwal; Nancy D Perrier; Kate E Lines; Gerlof D Valk; Rajesh V Thakker
Journal:  Endocr Rev       Date:  2021-03-15       Impact factor: 19.871

10.  A Direct Comparison of Patients With Hereditary and Sporadic Pancreatic Neuroendocrine Tumors: Evaluation of Clinical Course, Prognostic Factors and Genotype-Phenotype Correlations.

Authors:  Przemysław Soczomski; Beata Jurecka-Lubieniecka; Aleksandra Krzywon; Alexander Jorge Cortez; Stanisław Zgliczynski; Natalia Rogozik; Małgorzata Oczko-Wojciechowska; Agnieszka Pawlaczek; Tomasz Bednarczuk; Barbara Jarzab
Journal:  Front Endocrinol (Lausanne)       Date:  2021-05-28       Impact factor: 5.555

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