ID | 109656 |
タイトル別表記 | Landscape of FIPA : AIP and Prospective Diagnosis
|
著者 |
Hernández-Ramírez, Laura C.
Queen Mary University of London
Gabrovska, Plamena
Queen Mary University of London
Dénes, Judit
Queen Mary University of London
Stals, Karen
Royal Devon and Exeter National Health Service Foundation Trust
Trivellin, Giampaolo
Queen Mary University of London|National Institutes of Health
Tilley, Daniel
Queen Mary University of London
Ferraù, Francesco
Queen Mary University of London
Evanson, Jane
Queen Mary University of London
Ellard, Sian
Royal Devon and Exeter National Health Service Foundation Trust
Grossman, Ashley B.
Churchill Hospital
Roncaroli, Federico
Imperial College
Gadelha, Mônica R.
Federal University of Rio de Janeiro
Korbonits, Márta
Queen Mary University of London
|
資料タイプ |
学術雑誌論文
|
抄録 | Context: Familial isolated pituitary adenoma (FIPA) due to aryl hydrocarbon receptor interacting protein (AIP) gene mutations is an autosomal dominant disease with incomplete penetrance. Clinical screening of apparently unaffected AIP mutation (AIPmut) carriers could identify previously unrecognized disease.
Objective: To determine the AIP mutational status of FIPA and young pituitary adenoma patients, analyzing their clinical characteristics, and to perform clinical screening of apparently unaffected AIPmut carrier family members. Design: This was an observational, longitudinal study conducted over 7 years. Setting: International collaborative study conducted at referral centers for pituitary diseases. Participants: FIPA families (n = 216) and sporadic young-onset (≤30 y) pituitary adenoma patients (n = 404) participated in the study. Interventions: We performed genetic screening of patients for AIPmuts, clinical assessment of their family members, and genetic screening for somatic GNAS1 mutations and the germline FGFR4 p.G388R variant. Main Outcome Measure(s): We assessed clinical disease in mutation carriers, comparison of characteristics of AIPmut positive and negative patients, results of GNAS1, and FGFR4 analysis. Results: Thirty-seven FIPA families and 34 sporadic patients had AIPmuts. Patients with truncating AIPmuts had a younger age at disease onset and diagnosis, compared with patients with nontruncating AIPmuts. Somatic GNAS1 mutations were absent in tumors from AIPmut-positive patients, and the studied FGFR4 variant did not modify the disease behavior or penetrance in AIPmut-positive individuals.Atotal of 164 AIPmut-positive unaffected family members were identified; pituitary disease was detected in 18 of those who underwent clinical screening. Conclusions: A quarter of the AIPmut carriers screened were diagnosed with pituitary disease, justifying this screening and suggesting a variable clinical course for AIPmut-positive pituitary adenomas. |
掲載誌名 |
The Journal of Clinical Endocrinology & Metabolism
|
ISSN | 0021972X
19457197
|
cat書誌ID | AA00695484
AA1203774X
|
出版者 | The Endocrine Society|Oxford University Press
|
巻 | 100
|
号 | 9
|
開始ページ | E1242
|
終了ページ | E1254
|
発行日 | 2015-07-17
|
備考 | Collaborators : Members of the FIPA consortium are listed at http://www.fipapatients.org/fipaconsortium/.
|
権利情報 | Copyright © 2015 by the Endocrine Society
This article has been published under the terms of the Creative Commons Attribution License (CC-BY; https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Copyright for this article is retained by the author(s). |
EDB ID | |
出版社版DOI | |
出版社版URL | |
フルテキストファイル | |
言語 |
eng
|
著者版フラグ |
出版社版
|
部局 |
歯学系
|