Corticosterone is a glucocorticoid steroid hormone synthesized from cholesterol in the adrenal cortex. It serves primarily as a precursor to aldosterone, a key regulator of blood pressure, and exhibits weak mineralocorticoid activity.
Although corticosterone's glucocorticoid effects are much weaker than cortisol's, it still plays a role in anti-inflammatory actions, glucose metabolism, and HPA axis regulation.
In humans, corticosterone is also an important marker for diagnosing conditions such as 11-beta hydroxylase deficiency and glucocorticoid-responsive hyperaldosteronism.
Accurate measurement of corticosterone is crucial for assessing adrenal function and stress responses.
Common methods include blood, urine, and saliva testing, each with its own benefits and drawbacks. Blood tests provide a snapshot of total corticosterone levels, while urine tests offer a 24-hour integrated measure. Saliva tests are non-invasive and reflect bioavailable hormone levels.
Understanding corticosterone levels, alongside related biomarkers like ACTH, aldosterone, and cortisol, helps in diagnosing and managing adrenal disorders effectively.
Corticosterone plays a pivotal role in the endocrine system, influencing various physiological processes.
Corticosterone is a glucocorticoid steroid hormone that is synthesized from cholesterol in the zona fasciculata of the adrenal cortex.
Corticosterone is produced via steroidogenesis. Steroidogenesis is the biosynthetic process through which cholesterol is converted into steroid hormones.
The process begins with cholesterol's conversion to pregnenolone, catalyzed by the enzyme cytochrome P450scc (CYP11A1) within the mitochondria. Pregnenolone is further processed by oxidative enzymes in both the mitochondria and endoplasmic reticulum to produce various steroids.
For corticosterone specifically, pregnenolone is converted to progesterone, which is then hydroxylated by 21-hydroxylase to form 11-deoxycorticosterone. 11-Deoxycorticosterone is further processed by 11-beta hydroxylase to produce corticosterone.
Corticosterone is primarily recognized as a precursor for aldosterone, an important mineralocorticoid that regulates blood pressure. [13.] Corticosterone is converted to aldosterone by the enzyme 11-beta hydroxylase 2, a subtype of 11-beta hydroxylase. [4.]
As a direct precursor to aldosterone, corticosterone does have some weak mineralocorticoid activity, although much less than that of aldosterone. [11.]
In addition to its important role as a precursor for aldosterone, corticosterone has its own biological activity as a glucocorticoid, although it is much weaker than that of cortisol. This is in contrast to steroidogenesis in rats: in rats, corticosterone is a main glucocorticoid so it exerts cortisol-like effects on their physiology.
Corticosterone exerts anti-inflammatory actions similar to those of cortisol, although much more weakly. [20.]
Similarly, it may have the same effects on glucose metabolism, protein catabolism, HPA axis regulation and immunosuppression as cortisol, although its effects are much weaker than those of cortisol in humans. [6., 9.]
Corticosterone can also have mineralocorticoid and glucocorticoid effects on the brain, at much lower levels than aldosterone and cortisol. [5.]
In humans, corticosterone is primarily considered a precursor to aldosterone as well as a marker of 11-beta hydroxylase deficiency. [2.]
Accurate measurement of corticosterone levels is essential for diagnosing and managing conditions related to adrenal function and stress responses.
Corticosterone levels can be measured in blood, saliva, and urine, with blood being the most common medium.
Blood testing for corticosterone involves drawing a blood sample from a vein, usually in the arm. This method measures the total corticosterone concentration in the bloodstream, providing a snapshot of cortisol levels at the time of the test.
Benefits:
Drawbacks:
Urine testing for corticosterone involves collecting a urine sample over a specified period, usually 24 hours, to measure the total corticosterone excretion. This method provides an integrated measure of corticosterone production over time and is less invasive than blood testing.
Urine testing can also show cortisol, cortisone, and metabolized cortisol levels.
Benefits:
Drawbacks:
Saliva testing for corticosterone involves collecting saliva samples at specific times throughout the day.
Benefits:
Drawbacks:
Optimal levels will vary depending on the laboratory and sample type used. It is essential to contact the laboratory company used to determine their recommended reference ranges.
As an example, one company reports a reference range in urine testing of: 10-47 ng/mg creatinine/day [16.]
Another company reports a reference range in salivary testing of: 11-66 pg/mL [17.]
Generally, optimal levels are well within the reference range, because higher or lower levels of corticosterone may affect blood pressure due to aldosterone production.
Commonly, corticosterone testing is used to confirm rare aldosterone deficiency due to 18-hydroxylase deficiency, which shows elevated corticosterone levels. [15.]
Corticosterone levels are also typically elevated in cases of suspected or confirmed 11β-hydroxylase (CYP11B1) deficiency, as well as in glucocorticoid-responsive hyperaldosteronism, while they may be normal or only mildly elevated in aldosterone synthase (CYP11B2) deficiency. In these settings, prompt assessment by an endocrinologist is recommended.
Functionally, elevated corticosterone levels can also be seen in chronic stress. [12.] In this setting, they are associated with metabolic disturbances like insulin resistance, visceral adiposity, and impaired glucose tolerance that also are commonly seen in chronic stress.
Because of its action as a mineralocorticoid, it may also contribute to cardiovascular complications such as hypertension and atherosclerosis.
Decreased corticosterone levels should prompt further assessment by an endocrinologist, especially if other adrenal hormone levels are out of range, and/or if symptoms of hypoaldosteronism are present.
To gain a comprehensive understanding of adrenal function and stress responses, it is often necessary to measure other related biomarkers alongside corticosterone.
Click here to compare testing options and order testing for corticosterone levels.
[1.] Chakraborty, S., Pramanik, J. & Mahata, B. Revisiting steroidogenesis and its role in immune regulation with the advanced tools and technologies. Genes Immun 22, 125–140 (2021). https://doi.org/10.1038/s41435-021-00139-3
[2.] CORTC - Overview: Corticosterone, Serum. @mayocliniclabs. Published 2017. Accessed May 22, 2024. https://www.mayocliniclabs.com/test-catalog/overview/88221
[3.] Corticosterone | hormone | Britannica. www.britannica.com. Accessed May 22, 2024. https://www.britannica.com/science/corticosterone
[4.] Itcho K, Oki K, Ohno H, Yoneda M. Update on Genetics of Primary Aldosteronism. Biomedicines. 2021;9(4):409. doi:https://doi.org/10.3390/biomedicines9040409
[5.] Jimeno B, Hau M, Verhulst S. Corticosterone levels reflect variation in metabolic rate, independent of 'stress'. Sci Rep. 2018 Aug 29;8(1):13020. doi: 10.1038/s41598-018-31258-z. PMID: 30158537; PMCID: PMC6115469.
[6.] Joëls M, Karst H, Sarabdjitsingh RA. The stressed brain of humans and rodents. Acta Physiol (Oxf). 2018 Jun;223(2):e13066. doi: 10.1111/apha.13066. Epub 2018 Apr 16. PMID: 29575542; PMCID: PMC5969253.
[7.] Kinlein SA, Phillips DJ, Keller CR, Karatsoreos IN. Role of corticosterone in altered neurobehavioral responses to acute stress in a model of compromised hypothalamic-pituitary-adrenal axis function. Psychoneuroendocrinology. 2019 Apr;102:248-255. doi: 10.1016/j.psyneuen.2018.12.010. Epub 2018 Dec 11. PMID: 30594817; PMCID: PMC7649055.
[8.] Matallana-Rhoades AM, Corredor-Castro JD, Bonilla-Escobar FJ, Mecias-Cruz BV, Mejia de Beldjena L. Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: description of a new mutation, R384X. Colomb Med (Cali). 2016 Sep 30;47(3):172-175. PMID: 27821898; PMCID: PMC5091277.
[9.] McKay LI, Cidlowski JA. Physiologic and Pharmacologic Effects of Corticosteroids. In: Kufe DW, Pollock RE, Weichselbaum RR, et al., editors. Holland-Frei Cancer Medicine. 6th edition. Hamilton (ON): BC Decker; 2003. Available from: https://www.ncbi.nlm.nih.gov/books/NBK13780/
[10.] Momodu II, Lee B, Singh G. Congenital Adrenal Hyperplasia. [Updated 2023 Jul 17]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK448098/
[11.] Morris DJ, Souness GW, Brem AS, Oblin ME. Interactions of mineralocorticoids and glucocorticoids in epithelial target tissues. Kidney International. 2000;57(4):1370-1373. doi:https://doi.org/10.1046/j.1523-1755.2000.00977.x
[12.] M.S. Oitzl. Avoidance. Elsevier eBooks. Published online January 1, 2007:297-301. doi:https://doi.org/10.1016/b978-012373947-6.00050-7
[13.] Payne AH, Hales DB. Overview of steroidogenic enzymes in the pathway from cholesterol to active steroid hormones. Endocrine reviews. 2004;25(6):947-970. doi:https://doi.org/10.1210/er.2003-0030
[14.] Peter M. Congenital adrenal hyperplasia: 11beta-hydroxylase deficiency. Semin Reprod Med. 2002 Aug;20(3):249-54. doi: 10.1055/s-2002-35389. PMID: 12428205.
[15.] Quest Diagnostics: Test Directory. testdirectory.questdiagnostics.com. Accessed May 22, 2024. https://testdirectory.questdiagnostics.com/test/test-detail/6547/corticosterone?cc=MASTER
[16.] Rupa Health. Adrenal Corticoids Profile Sample Report.pdf. Google Docs. https://drive.google.com/file/d/1DA16VPe0rRVDXhXe-F2_g-_JadGyhw5-/view
[17.] Rupa Health. LCMS Saliva Profile Sample Report.pdf. Google Docs. https://drive.google.com/file/d/1I7j4bnY7oT1IrThBO0QyTbnhzhTs6Pzr/view
[18.] Turcu AF, Wannachalee T, Tsodikov A, Nanba AT, Ren J, Shields JJ, O'Day PJ, Giacherio D, Rainey WE, Auchus RJ. Comprehensive Analysis of Steroid Biomarkers for Guiding Primary Aldosteronism Subtyping. Hypertension. 2020 Jan;75(1):183-192. doi: 10.1161/HYPERTENSIONAHA.119.13866. Epub 2019 Dec 2. PMID: 31786984; PMCID: PMC7034384.
[19.] Xing Y, Edwards MA, Ahlem C, et al. The effects of ACTH on steroid metabolomic profiles in human adrenal cells. The Journal of Endocrinology. 2011;209(3):327-335. doi:https://doi.org/10.1530/JOE-10-0493
[20.] Yoshinao Katsu, Baker ME. Corticosterone. Elsevier eBooks. Published online January 1, 2021:935-937. doi:https://doi.org/10.1016/b978-0-12-820649-2.00258-8