Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line<i>AIP</i>Mutations and Pituitary Adenomas: An International Collaborative Study

Adrian Daly(University of Liège), María A. Tichomirowa(University of Liège), Patrick Pétrossians(University of Liège), Elina Heliövaara(University of Helsinki), Marie‐Lise Jaffrain‐Rea(University of L'Aquila), Anne Barlier(Centre National de la Recherche Scientifique), Luciana Ansaneli Naves(Universidade de Brasília), Tapani Ebeling(Oulu University Hospital), Auli Karhu(University of Helsinki), Antti Raappana(Oulu University Hospital), Laure Cazabat(Inserm), Ernesto De Menis, Carmen Fajardo Montañana(Hospital de La Ribera), Gérald Raverot(Hôpital Lyon Sud), Robert J. Weil(Cleveland Clinic), Timo Sane(Helsinki University Hospital), Dominique Maiter(UCLouvain), Sebastian Neggers(Erasmus University Rotterdam), Maria Yaneva(Medical University of Sofia), Antoine Tabarin(Centre Hospitalier Universitaire de Bordeaux), Elisa Verrua(Ospedale Maggiore), Eija Eloranta(Oulu University Hospital), Arnaud Murat(Centre Hospitalier Universitaire de Nantes), Outi Vierimaa(Oulu University Hospital), Pasi Salmela(Oulu University Hospital), Philippe Émy(Centre hospitalier universitaire d'Orléans), Rodrigo A. Toledo(Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo), Maria Sabaté(Austral University), Chiara Villa(Inserm), Marc Popelier, Roberto Salvatori(Johns Hopkins University), Juliet Jennings(Royal Children's Hospital), A Ferrández Longás(Hospital Universitario Miguel Servet), José Ignacio Labarta Aizpún(Hospital Universitario Miguel Servet), Marianthi Georgitsi(Universidad de Buenos Aires), Ralf Paschke(Leipzig University), Cristina L. Ronchi(Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda), Matti Välimäki(Helsinki University Hospital), Carola Saloranta(Helsinki University Hospital), Wouter W. de Herder(Erasmus University Rotterdam), Renato Cozzi(Ospedale Maggiore), Mirtha Guitelman(University of Helsinki), Flavia Magri(University of Pavia), Maria Stefania Lagonigro(University of Pavia), Georges Halaby(Hôtel-Dieu de France), Vinciane Corman(Centre hospitalier régional de la Citadelle), Marie-Thérèse Hagelstein(University of Liège), Jean-François Vanbellinghen(University of Liège), Gustavo Barcelos Barra(Sabin Medicina Diagnostica (Brazil)), Anne‐Paule Gimenez‐Roqueplo(Délégation Paris 5), Fergus Cameron(Royal Children's Hospital), Françoise Borson‐Chazot(Hôpital Lyon Sud), I. M. Holdaway(Greenlane Clinical Centre), S. P. A. Toledo(Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo), Günter K. Stalla(Max Planck Institute of Psychiatry), Anna Spada(Ospedale Maggiore), Sabina Zacharieva(Medical University of Sofia), Jérôme Bertherat(Inserm), Thierry Brue(Hôpital de la Timone), Vincent Bours(University of Liège), Philippe Chanson(Université Paris-Sud), Lauri A. Aaltonen(University of Helsinki), Albert Beckers(University of Liège)
The Journal of Clinical Endocrinology & Metabolism
August 5, 2010
Cited by 369Open Access
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Abstract

CONTEXT: AIP mutations (AIPmut) give rise to a pituitary adenoma predisposition that occurs in familial isolated pituitary adenomas and less often in sporadic cases. The clinical and therapeutic features of AIPmut-associated pituitary adenomas have not been studied comprehensively. OBJECTIVE: The objective of the study was to assess clinical/therapeutic characteristics of AIPmut pituitary adenomas. DESIGN: This study was an international, multicenter, retrospective case collection/database analysis. SETTING: The study was conducted at 36 tertiary referral endocrine and clinical genetics departments. PATIENTS: Patients included 96 patients with germline AIPmut and pituitary adenomas and 232 matched AIPmut-negative acromegaly controls. RESULTS: The AIPmut population was predominantly young and male (63.5%); first symptoms occurred as children/adolescents in 50%. At diagnosis, most tumors were macroadenomas (93.3%); extension and invasion was common. Somatotropinomas comprised 78.1% of the cohort; there were also prolactinomas (n = 13), nonsecreting adenomas (n = 7), and a TSH-secreting adenoma. AIPmut somatotropinomas were larger (P = 0.00026), with higher GH levels (P = 0.00068), more frequent extension (P = 0.018) and prolactin cosecretion (P = 0.00023), and occurred 2 decades before controls (P < 0.000001). Gigantism was more common in the AIPmut group (P < 0.000001). AIPmut somatotropinoma patients underwent more surgical interventions (P = 0.00069) and had lower decreases in GH (P = 0.00037) and IGF-I (P = 0.028) and less tumor shrinkage with somatostatin analogs (P < 0.00001) vs. controls. AIPmut prolactinomas occurred generally in young males and frequently required surgery or radiotherapy. CONCLUSIONS: AIPmut pituitary adenomas have clinical features that may negatively impact treatment efficacy. Predisposition for aggressive disease in young patients, often in a familial setting, suggests that earlier diagnosis of AIPmut pituitary adenomas may have clinical utility.


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