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Clinical Factors Predicting Multiple Endocrine Neoplasia Type 1 and Type 4 in Patients with Neuroendocrine Tumors

The aim of this study is to evaluate the predictive role of specific clinical factors for the diagnosis of Multiple Endocrine Neoplasia type-1 (MEN1) and type-4 (MEN4) in patients with an initial diagnosis of gastrointestinal, bronchial, or thymic neuroendocrine tumor (NET). Methods: Patients referr...

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Autores principales: Faggiano, Antongiulio, Fazzalari, Beatrice, Mikovic, Nevena, Russo, Flaminia, Zamponi, Virginia, Mazzilli, Rossella, Guarnieri, Vito, Piane, Maria, Visco, Vincenzo, Petrucci, Simona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531237/
https://www.ncbi.nlm.nih.gov/pubmed/37761922
http://dx.doi.org/10.3390/genes14091782
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author Faggiano, Antongiulio
Fazzalari, Beatrice
Mikovic, Nevena
Russo, Flaminia
Zamponi, Virginia
Mazzilli, Rossella
Guarnieri, Vito
Piane, Maria
Visco, Vincenzo
Petrucci, Simona
author_facet Faggiano, Antongiulio
Fazzalari, Beatrice
Mikovic, Nevena
Russo, Flaminia
Zamponi, Virginia
Mazzilli, Rossella
Guarnieri, Vito
Piane, Maria
Visco, Vincenzo
Petrucci, Simona
author_sort Faggiano, Antongiulio
collection PubMed
description The aim of this study is to evaluate the predictive role of specific clinical factors for the diagnosis of Multiple Endocrine Neoplasia type-1 (MEN1) and type-4 (MEN4) in patients with an initial diagnosis of gastrointestinal, bronchial, or thymic neuroendocrine tumor (NET). Methods: Patients referred to the NET Unit between June 2021 and December 2022 with a diagnosis of NET and at least one clinical criterion of suspicion for MEN1 and MEN4 underwent molecular analysis of the MEN1 and CDKN1B genes. Phenotypic criteria were: (1) age ≤ 40 years; (2) NET multifocality; (3) MEN1/4-associated manifestations other than NETs; and (4) endocrine syndrome related to NETs or pituitary/adrenal tumors. Results: A total of 22 patients were studied. In 18 patients (81.8%), the first-level genetic test was negative (Group A), while four patients (25%) were positive for MEN1 (Group B). No patient was positive for MEN4. In Group A, 10 cases had only one clinical criterion, and three patients met three criteria. In Group B, three patients had three criteria, and one met all criteria. Conclusion: These preliminary data show that a diagnosis of NET in patients with a negative family history is suggestive of MEN1 in the presence of ≥three positive phenotypic criteria, including early age, multifocality, multiple MEN-associated manifestations, and endocrine syndromes. This indication may allow optimization of the diagnosis of MEN in patients with NET.
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spelling pubmed-105312372023-09-28 Clinical Factors Predicting Multiple Endocrine Neoplasia Type 1 and Type 4 in Patients with Neuroendocrine Tumors Faggiano, Antongiulio Fazzalari, Beatrice Mikovic, Nevena Russo, Flaminia Zamponi, Virginia Mazzilli, Rossella Guarnieri, Vito Piane, Maria Visco, Vincenzo Petrucci, Simona Genes (Basel) Article The aim of this study is to evaluate the predictive role of specific clinical factors for the diagnosis of Multiple Endocrine Neoplasia type-1 (MEN1) and type-4 (MEN4) in patients with an initial diagnosis of gastrointestinal, bronchial, or thymic neuroendocrine tumor (NET). Methods: Patients referred to the NET Unit between June 2021 and December 2022 with a diagnosis of NET and at least one clinical criterion of suspicion for MEN1 and MEN4 underwent molecular analysis of the MEN1 and CDKN1B genes. Phenotypic criteria were: (1) age ≤ 40 years; (2) NET multifocality; (3) MEN1/4-associated manifestations other than NETs; and (4) endocrine syndrome related to NETs or pituitary/adrenal tumors. Results: A total of 22 patients were studied. In 18 patients (81.8%), the first-level genetic test was negative (Group A), while four patients (25%) were positive for MEN1 (Group B). No patient was positive for MEN4. In Group A, 10 cases had only one clinical criterion, and three patients met three criteria. In Group B, three patients had three criteria, and one met all criteria. Conclusion: These preliminary data show that a diagnosis of NET in patients with a negative family history is suggestive of MEN1 in the presence of ≥three positive phenotypic criteria, including early age, multifocality, multiple MEN-associated manifestations, and endocrine syndromes. This indication may allow optimization of the diagnosis of MEN in patients with NET. MDPI 2023-09-10 /pmc/articles/PMC10531237/ /pubmed/37761922 http://dx.doi.org/10.3390/genes14091782 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Faggiano, Antongiulio
Fazzalari, Beatrice
Mikovic, Nevena
Russo, Flaminia
Zamponi, Virginia
Mazzilli, Rossella
Guarnieri, Vito
Piane, Maria
Visco, Vincenzo
Petrucci, Simona
Clinical Factors Predicting Multiple Endocrine Neoplasia Type 1 and Type 4 in Patients with Neuroendocrine Tumors
title Clinical Factors Predicting Multiple Endocrine Neoplasia Type 1 and Type 4 in Patients with Neuroendocrine Tumors
title_full Clinical Factors Predicting Multiple Endocrine Neoplasia Type 1 and Type 4 in Patients with Neuroendocrine Tumors
title_fullStr Clinical Factors Predicting Multiple Endocrine Neoplasia Type 1 and Type 4 in Patients with Neuroendocrine Tumors
title_full_unstemmed Clinical Factors Predicting Multiple Endocrine Neoplasia Type 1 and Type 4 in Patients with Neuroendocrine Tumors
title_short Clinical Factors Predicting Multiple Endocrine Neoplasia Type 1 and Type 4 in Patients with Neuroendocrine Tumors
title_sort clinical factors predicting multiple endocrine neoplasia type 1 and type 4 in patients with neuroendocrine tumors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531237/
https://www.ncbi.nlm.nih.gov/pubmed/37761922
http://dx.doi.org/10.3390/genes14091782
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