Glucocorticoid deficiency is a condition where the body doesn't produce enough glucocorticoid hormones.
Signs and symptoms
editSymptoms of glucocorticoid deficiency (having not enough hormones that are classified as glucocorticoids, and mostly consisting of cortisol) vary depending on the underlying cause and severity—common signs and symptoms may include fatigue, weakness, weight loss, decreased appetite, low blood pressure, salt cravings, dizziness upon standing (orthostatic hypotension), muscle aches and pains, joint pain or stiffness, nausea or vomiting. In severe cases, individuals may experience abdominal pain, confusion or delirium.[1][2]
Complications
editIf left untreated or inadequately treated, glucocorticoid deficiency can lead to severe complications such as adrenal crisis (a life-threatening condition characterized by extreme fatigue, dehydration, and electrolyte imbalances), low blood sugar (hypoglycemia), and recurrent infections due to impaired immune function.[2][1]
Causes
editGlucocorticoid deficiency can be caused by inherited genetic disorders that affect the production of cortisol in the adrenal glands, such as familial glucocorticoid deficiency (FGD).[3] FGD is a group of monogenic recessive disorders caused by disease-causing variants in genes involved in cortisol biosynthesis.[4] FGD is categorized into type 1, also called Glucocorticoid deficiency 1, where genes associated with ACTH have disease-causing variants, type 2, where ACTH receptors are normal,[5] and there are other types: 3, 4 and 5, associated with various causes. Glucocorticoid deficiency can also be acquired after birth due to damage or dysfunction of the hypothalamus-pituitary-adrenal axis (HPA axis), which regulates cortisol production.[4] Common causes of acquired glucocorticoid deficiency include autoimmune conditions affecting the HPA axis (such as autoimmune adrenalitis) and infections, such as tuberculosis, that affect the adrenal glands directly.[2]
Risk factors
editRisk factors for developing glucocorticoid deficiency include having a family history of inherited genetic disorders affecting cortisol biosynthesis by the body; having autoimmune conditions such as Addison's disease; having infections that specifically target the adrenal glands; undergoing surgery involving removal of the pituitary gland or parts of it.[1]
Triggers
editGlucocorticoid deficiency can be triggered by stressors such as illness/infection/surgery/trauma, which increase demand for cortisol production from the adrenals.[4][6] In individuals with already compromised HPA axis function or inadequate cortisol reserve, this increased demand for glucocorticoid hormones cannot be met, leading to acute exacerbation of glucocorticoid insufficiency/adrenal crisis.[4]
Diagnosis
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Prevention
editThere are no specific measures known for preventing primary forms of glucocorticoid deficiency unless there is an identified genetic mutation causing it. For secondary forms, prevention includes prompt treatment, i.e., addressing underlying causes such as infection and autoimmune diseases.[1][4]
Treatment
editThe treatment of glucocorticoid deficiency involves replacing the deficient cortisol through exogenous glucocorticoid therapy. This typically includes oral administration of synthetic glucocorticoids such as hydrocortisone or prednisone, which aim to mimic the normal physiological secretion of cortisol. The dosage and timing of medication may vary depending on individual needs and circumstances.[1][7][4]
Prognosis
editWith appropriate treatment, most individuals with glucocorticoid deficiency can lead normal lives and have a good prognosis.[4] However, it is important to closely monitor hormone levels and adjust medication accordingly to prevent complications such as adrenal crisis or over-replacement side effects.[1]
Epidemiology
editThe exact incidence and prevalence of glucocorticoid deficiency are not well established due to its heterogeneity in causes and clinical presentation.[4] Familial Glucocorticoid Deficiency is considered rare but more common than previously thought due to underdiagnosis and lack of awareness about the condition.[1][3]
References
edit- ^ a b c d e f g Garrahy A, Thompson CJ (2019). "Hyponatremia and Glucocorticoid Deficiency". Front Horm Res. Frontiers of Hormone Research. 52: 80–92. doi:10.1159/000493239. ISBN 978-3-318-06382-0. PMID 32097946. S2CID 81490257.
- ^ a b c Timmermans S, Souffriau J, Libert C (2019). "A General Introduction to Glucocorticoid Biology". Front Immunol. 10: 1545. doi:10.3389/fimmu.2019.01545. PMC 6621919. PMID 31333672.
- ^ a b Maharaj AV (2023). "Familial Glucocorticoid Deficiency: the changing landscape of an eponymous syndrome". Front Endocrinol (Lausanne). 14: 1268345. doi:10.3389/fendo.2023.1268345. PMC 10771341. PMID 38189052.
- ^ a b c d e f g h Dineen R, Martin-Grace J, Thompson CJ, Sherlock M (June 2020). "The management of glucocorticoid deficiency: Current and future perspectives". Clin Chim Acta. 505: 148–159. doi:10.1016/j.cca.2020.03.006. PMID 32145273. S2CID 212629520.
- ^ Gupta RK, Khera S, Kanitkar M (January 2011). "Familial Glucocorticoid Deficiency". Med J Armed Forces India. 67 (1): 69–71. doi:10.1016/S0377-1237(11)80021-3. PMC 4920607. PMID 27365766.
- ^ Feingold KR, et al. (October 19, 2018). Glucocorticoid Therapy and Adrenal Suppression. PMID 25905379.
- ^ Maharaj A, Maudhoo A, Chan LF, Novoselova T, Prasad R, Metherell LA, Guasti L (May 2019). "Isolated glucocorticoid deficiency: Genetic causes and animal models". J Steroid Biochem Mol Biol. 189: 73–80. doi:10.1016/j.jsbmb.2019.02.012. PMID 30817990. S2CID 72333617. Archived from the original on 2024-03-04. Retrieved 2024-03-04.
Further reading
edit- Metwalley KA, Farghaly HS (2012). "Familial glucocorticoid deficiency presenting with generalized hyperpigmentation in an Egyptian child: a case report". Journal of Medical Case Reports. 6 (1): 110. doi:10.1186/1752-1947-6-110. ISSN 1752-1947. PMC 3369203. PMID 22507176.
- Meimaridou E, Hughes CR, Kowalczyk J, Guasti L, Chapple JP, King PJ, Chan LF, Clark AJ, Metherell LA (2013). "Familial glucocorticoid deficiency: New genes and mechanisms". Molecular and Cellular Endocrinology. 371 (1–2). Elsevier BV: 195–200. doi:10.1016/j.mce.2012.12.010. ISSN 0303-7207. PMID 23279877.