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Adrenal gland
A Contemporary Approach to the Diagnosis and Management of Adrenal Insufficiency
Suranut Charoensri, Richard J. Auchus
Endocrinol Metab. 2024;39(1):73-82.   Published online January 22, 2024
DOI: https://doi.org/10.3803/EnM.2024.1894
  • 48,230 View
  • 2,270 Download
  • 11 Web of Science
  • 16 Crossref
AbstractAbstract PDFPubReader   ePub   
Adrenal insufficiency (AI) can be classified into three distinct categories based on its underlying causes: primary adrenal disorders, secondary deficiencies in adrenocorticotropin, or hypothalamic suppression from external factors, most commonly glucocorticoid medications used for anti-inflammatory therapy. The hallmark clinical features of AI include fatigue, appetite loss, unintentional weight loss, low blood pressure, and hyponatremia. Individuals with primary AI additionally manifest skin hyperpigmentation, hyperkalemia, and salt craving. The diagnosis of AI is frequently delayed due to the non-specific symptoms and signs early in the disease course, which poses a significant challenge to its early detection prior to an adrenal crisis. Despite the widespread availability of lifesaving glucocorticoid medications for decades, notable challenges persist, particularly in the domains of timely diagnosis while simultaneously avoiding misdiagnosis, patient education for averting adrenal crises, and the determination of optimal replacement therapies. This article reviews recent advancements in the contemporary diagnostic strategy and approaches to optimal treatment for AI.

Citations

Citations to this article as recorded by  
  • Determining the comparative pharmacodynamic equivalence of a non-invasive diagnostic test for patients with adrenal insufficiency using a randomised 2-way crossover trial: the STARLIT-3 study protocol
    Kathryn Date, Kathleen Baster, Sharon Caunt, Judith Cohen, Miguel Debono, Jane Fearnside, Trevor N Johnson, Peter Laud, Richard J Ross, Rosie Taylor, Charlotte Jane Elder
    BMJ Open.2026; 16(2): e112708.     CrossRef
  • Post-ACTH peak cortisol response is associated with genotype in children with nonclassic congenital adrenal hyperplasia
    Allie N. Dayno, Marissa J. Kilberg, Erin Gonter, Robert Gallop, Jacob Squicciarini, Carolina Montano, Maria G. Vogiatzi
    Frontiers in Endocrinology.2026;[Epub]     CrossRef
  • Metabolic Effects of Modified‐Release Hydrocortisone Versus Short Acting Conventional Oral Glucocorticoids in Adrenal Insufficiency: A Systematic Review and Meta‐Analysis
    Mohammad Ehab Abdelsattar, Mai Abdallah, Ola Khaled, Heba Aboeldahab, Nour Mohyeldin Ahmed, Yusuf Abdeen, Nada Altayeb, Yousef Mousa, Ahmed Gaballa Ali, Mohammed Tarek Hasan
    Clinical Endocrinology.2026;[Epub]     CrossRef
  • Adrenal insufficiency in severely wounded men with combat gunshot injury
    N.Yu. Seliukova, K.V. Misiura, E.M. Khoroshun, V.V. Makarov, V.V. Nehoduiko, O.I. Zalyubovska, E. Szucsik
    INTERNATIONAL JOURNAL OF ENDOCRINOLOGY (Ukraine).2025; 20(8): 573.     CrossRef
  • A deep learning algorithm for automated adrenal gland segmentation on non-contrast CT images
    Fanxing Meng, Tuo Zhang, Yukun Pan, Xiaojing Kan, Yuwei Xia, Mengyuan Xu, Jin Cai, Fangbin Liu, Yinghui Ge
    BMC Medical Imaging.2025;[Epub]     CrossRef
  • Metabolic and endocrine dysfunctions in traumatic brain injury: Implications for cognitive recovery and therapeutic strategies
    Jigar Manilal Haria, Naveen Kumar Singh, Jayballabh Kumar, Sanjeev Kumar Jain, DattaSai Pamidimarri
    Behavioural Brain Research.2025; 493: 115697.     CrossRef
  • Recurrent Hyponatremia Mimicking Syndrome of Inappropriate Antidiuretic Hormone Secretion: A Case of Partial Empty Sella Syndrome With Isolated Adrenocorticotropic Hormone Deficiency
    Revathi Rajendran, Amirthalingeswaran Govindan
    Cureus.2025;[Epub]     CrossRef
  • Management of Primary Adrenal Insufficiency and Overt Hypothyroidism in an HIV‐Positive Patient in a Resource‐Limited Setting: A Case Report
    Majani Edward, Witness John, Dominick M. Raphael
    Clinical Case Reports.2025;[Epub]     CrossRef
  • A practical approach to diagnosis and treatment in children with primary adrenal insufficiency
    Donatella Capalbo, Sara Illiano, Sara Vasaturo, Paola Lorello, Francesca Romana Rotondo, Raffaella Di Mase, Carla Bizzarri, Mariacarolina Salerno
    European Journal of Endocrinology.2025; 193(5): R45.     CrossRef
  • The Effect of Whitening Creams Usage on the Adrenal Gland 
    Fadheelah Salman Azeez, Noor Faisal Noaman, Ahmed Neema AL-Mussawy
    F1000Research.2025; 14: 1434.     CrossRef
  • Unintentional discontinuation of topical corticosteroids after emergency hospitalization can exacerbate adrenal insufficiency
    Hiroya Kitsunai, Yumika Watanabe, Eisuke Nishikawa, Fumika Maruyama, Hiroshi Nomoto
    Endocrine Journal.2025; 72(12): 1377.     CrossRef
  • Diagnostic pharmacology: Drugs that uncover diseases
    K. Saranraj, Gollapudi Poojitha Siri Chandana
    National Journal of Pharmacology and Therapeutics.2025; 3(3): 197.     CrossRef
  • Post-Traumatic Hypopituitarism
    Nissa Blocher
    Current Physical Medicine and Rehabilitation Reports.2024; 12(4): 405.     CrossRef
  • Severe Fatigue in Uncontrolled Asthma: Contributing Factors and Impact of Rehabilitation
    Karin B. Fieten, Lianne ten Have, Linde N. Nijhof, Lucia Rijssenbeek-Nouwens, Anneke ten Brinke
    The Journal of Allergy and Clinical Immunology: In Practice.2024; 12(12): 3292.     CrossRef
  • Adrenal Insufficiency in Patients with Beta Thalassemia: A Meta-Analysis
    Christos Savvidis, Dimitra Ragia, Sophia Delicou, Aikaterini Xydaki, Manfredi Rizzo, Ioannis Ilias
    Medicina.2024; 60(10): 1571.     CrossRef
  • 長期間の呼吸管理および遷延する低血圧から診断に至ったACTH単独欠損症の1例(A case of isolated ACTH deficiency diagnosed after long–term respiratory management and persistent hypotension)
    古谷 慎太郎, 神山 治郎, 多喜 亘, 山本 大輔, 五木田 昌士, 田口 茂正, 清田 和也
    Nihon Kyukyu Igakukai Zasshi: Journal of Japanese Association for Acute Medicine.2024; 35(12): 965.     CrossRef
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Adrenal gland
Molecular Mechanisms of Primary Aldosteronism
Sergei G. Tevosian, Shawna C. Fox, Hans K. Ghayee
Endocrinol Metab. 2019;34(4):355-366.   Published online December 23, 2019
DOI: https://doi.org/10.3803/EnM.2019.34.4.355
  • 14,392 View
  • 175 Download
  • 7 Web of Science
  • 7 Crossref
AbstractAbstract PDFPubReader   ePub   

Primary aldosteronism (PA) results from excess production of mineralocorticoid hormone aldosterone by the adrenal cortex. It is normally caused either by unilateral aldosterone-producing adenoma (APA) or by bilateral aldosterone excess as a result of bilateral adrenal hyperplasia. PA is the most common cause of secondary hypertension and associated morbidity and mortality. While most cases of PA are sporadic, an important insight into this debilitating disease has been derived through investigating the familial forms of the disease that affect only a minor fraction of PA patients. The advent of gene expression profiling has shed light on the genes and intracellular signaling pathways that may play a role in the pathogenesis of these tumors. The genetic basis for several forms of familial PA has been uncovered in recent years although the list is likely to expand. Recently, the work from several laboratories provided evidence for the involvement of mammalian target of rapamycin pathway and inflammatory cytokines in APAs; however, their mechanism of action in tumor development and pathophysiology remains to be understood.

Citations

Citations to this article as recorded by  
  • Mineralocorticoid Receptor and Aldosterone: Interaction Between NR3C2 Genetic Variants, Sex, and Age in a Mixed Cohort
    Mahyar Heydarpour, Wasita W Parksook, Luminita H Pojoga, Gordon H Williams, Jonathan S Williams
    The Journal of Clinical Endocrinology & Metabolism.2024; 110(1): e140.     CrossRef
  • Subunit-Specific Developmental Roles of PI3K in SF1-Expressing Cells
    My Khanh Q. Huynh, Sang Hee Lyoo, Dong Joo Yang, Yun-Hee Choi, Ki Woo Kim
    Endocrinology and Metabolism.2024; 39(5): 793.     CrossRef
  • Proteomic analysis of urinary extracellular vesicles highlights specific signatures for patients with primary aldosteronism
    Lorenzo Bertolone, Annalisa Castagna, Marcello Manfredi, Domenica De Santis, Francesca Ambrosani, Elisa Antinori, Paolo Mulatero, Elisa Danese, Emilio Marengo, Elettra Barberis, Mariangela Veneri, Nicola Martinelli, Simonetta Friso, Francesca Pizzolo, Oli
    Frontiers in Endocrinology.2023;[Epub]     CrossRef
  • Focus on adrenal and related causes of hypertension in childhood and adolescence: Rare or rarely recognized?
    Flávia A. Costa-Barbosa, Rafael B. Giorgi, Claudio E. Kater
    Archives of Endocrinology and Metabolism.2022;[Epub]     CrossRef
  • Diseases caused by mutations in the Na+/K+ pump α1 gene ATP1A1
    Elisa D. Biondo, Kerri Spontarelli, Giovanna Ababioh, Lois Méndez, Pablo Artigas
    American Journal of Physiology-Cell Physiology.2021; 321(2): C394.     CrossRef
  • Aldosterone Inhibits In Vitro Myogenesis by Increasing Intracellular Oxidative Stress via Mineralocorticoid Receptor
    Jin Young Lee, Da Ae Kim, Eunah Choi, Yun Sun Lee, So Jeong Park, Beom-Jun Kim
    Endocrinology and Metabolism.2021; 36(4): 865.     CrossRef
  • Progress on Genetic Basis of Primary Aldosteronism
    Izabela Karwacka, Łukasz Obołończyk, Sonia Kaniuka-Jakubowska, Michał Bohdan, Krzysztof Sworczak
    Biomedicines.2021; 9(11): 1708.     CrossRef
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