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Addison’s Disease: Diagnosis and Management Strategies
We aim to overview Addison’s disease (AD) with regard to current diagnosis and management. This is a narrative review of full-length articles published in English between January 2022 and December 2022 (including online ahead of print versions) in PubMed-indexed journals. We included original studie...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10243343/ https://www.ncbi.nlm.nih.gov/pubmed/37287503 http://dx.doi.org/10.2147/IJGM.S390793 |
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author | Carsote, Mara Nistor, Claudiu |
author_facet | Carsote, Mara Nistor, Claudiu |
author_sort | Carsote, Mara |
collection | PubMed |
description | We aim to overview Addison’s disease (AD) with regard to current diagnosis and management. This is a narrative review of full-length articles published in English between January 2022 and December 2022 (including online ahead of print versions) in PubMed-indexed journals. We included original studies in living humans regardless of the level of statistical significance starting from the key search terms “Addison’s disease” or “primary adrenal insufficiency” in title or abstract. We excluded articles with secondary adrenal insufficiency. Briefly, 199 and 355 papers, respectively were identified; we manually checked each of them, excluded the duplicates, and then selected 129 based on their clinical relevance in order to address our 1-year analysis. We organized the data in different subsections covering all published aspects on the subject of AD. To our knowledge, this is the largest AD retrospective from 2022 on published data. A massive role of genetic diagnosis especially in pediatric cases is highlighted; the importance of both pediatric and adult awareness remains since unusual presentations continue to be described. COVID-19 infection is a strong player amid this third year of pandemic although we still not do have large cohorts in this particular matter as seen, for instance, in thyroid anomalies. In our opinion, the most important topic for research is immune checkpoint inhibitors, which cause a large panel of endocrine side effects, AD being one of them. |
format | Online Article Text |
id | pubmed-10243343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-102433432023-06-07 Addison’s Disease: Diagnosis and Management Strategies Carsote, Mara Nistor, Claudiu Int J Gen Med Review We aim to overview Addison’s disease (AD) with regard to current diagnosis and management. This is a narrative review of full-length articles published in English between January 2022 and December 2022 (including online ahead of print versions) in PubMed-indexed journals. We included original studies in living humans regardless of the level of statistical significance starting from the key search terms “Addison’s disease” or “primary adrenal insufficiency” in title or abstract. We excluded articles with secondary adrenal insufficiency. Briefly, 199 and 355 papers, respectively were identified; we manually checked each of them, excluded the duplicates, and then selected 129 based on their clinical relevance in order to address our 1-year analysis. We organized the data in different subsections covering all published aspects on the subject of AD. To our knowledge, this is the largest AD retrospective from 2022 on published data. A massive role of genetic diagnosis especially in pediatric cases is highlighted; the importance of both pediatric and adult awareness remains since unusual presentations continue to be described. COVID-19 infection is a strong player amid this third year of pandemic although we still not do have large cohorts in this particular matter as seen, for instance, in thyroid anomalies. In our opinion, the most important topic for research is immune checkpoint inhibitors, which cause a large panel of endocrine side effects, AD being one of them. Dove 2023-06-02 /pmc/articles/PMC10243343/ /pubmed/37287503 http://dx.doi.org/10.2147/IJGM.S390793 Text en © 2023 Carsote and Nistor. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Review Carsote, Mara Nistor, Claudiu Addison’s Disease: Diagnosis and Management Strategies |
title | Addison’s Disease: Diagnosis and Management Strategies |
title_full | Addison’s Disease: Diagnosis and Management Strategies |
title_fullStr | Addison’s Disease: Diagnosis and Management Strategies |
title_full_unstemmed | Addison’s Disease: Diagnosis and Management Strategies |
title_short | Addison’s Disease: Diagnosis and Management Strategies |
title_sort | addison’s disease: diagnosis and management strategies |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10243343/ https://www.ncbi.nlm.nih.gov/pubmed/37287503 http://dx.doi.org/10.2147/IJGM.S390793 |
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