Management of patients with glucocorticoid deficiency (original) (raw)
- Viewpoint
- Published: 01 December 2005
Nature Clinical Practice Endocrinology & Metabolism volume 1, pages 62–63 (2005)Cite this article
- 139 Accesses
- 14 Citations
- Metrics details
Thomas Addison, who first described “the constitutional and local effects of disease of the suprarenal capsules” in 1849, said he feared the disease was irremediable.1 In the 21st century, we assume that mortality in patients treated for autoimmune Addison's disease is not increased when compared to the general population, and the death rate of patients with hypopituitarism treated for secondary hypoadrenalism does not differ from those without adrenocorticotropic hormone deficiency.2 Mortality rates, however, are not the whole story. Many patients perceive that their health is impaired, and report fatigue and reduced vitality compared with the general population.3 As we understand more about the physiology of glucocorticoid production, it becomes clear that current treatment regimens do not reproduce normal physiology, so perhaps it is unsurprising that patients report an impaired quality of life. The data challenge us to respond and translate this knowledge into improved patient care.
Historically, patients with hypoadrenalism have received high daily doses of glucocorticoids, equivalent to 30 mg hydrocortisone or more. In two studies using different experimental methods,4,5 the normal daily cortisol production rate was found to be lower than previously thought, at approximately 10 mg (5.7 mg/m2), suggesting that many patients were receiving chronic over-replacement. The multiple adverse effects of long-term treatment with high, pharmacologic doses of glucocorticoid are well recognized. We know much less about whether similar problems are associated with minor over-replacement, because data have been gleaned from studies examining the effect of different replacement regimens on osteoporosis and cardiovascular disease in small populations assessing surrogate markers of these outcomes.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 12 print issues and online access
$189.00 per year
only $15.75 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to the full article PDF.
USD 39.95
Prices may be subject to local taxes which are calculated during checkout
Additional access options:
References
- Addison T (1945) On the constitutional and local effects of disease of the supra-renal capsule. In Classic Descriptions of Disease, edn 3, 290–294 (Ed. Major R) Springfield: Charles C Thomas
Google Scholar - Tomlinson J et al. (2001) Association between premature mortality and hypopituitarism. Lancet 357: 425–431
Article CAS Google Scholar - Lovas K et al. (2002) Subjective health status in Norwegian patients with Addison's disease. Clin Endocrinol 56: 581–588
Article Google Scholar - Esteban N et al. (1991) Daily cortisol production rate in man determined by stable isotope dilution/mass spectrometry. J Clin Endocrinol Metab 71: 39–45
Article Google Scholar - Kerrigan J et al. (1993) Estimation of daily cortisol production and clearance rates in normal pubertal males by deconvolution analysis. J Clin Endocrinol Metab 76: 1505–1510
CAS PubMed Google Scholar - Crown A and Lightman S (2005) Why is the management of glucocorticoid deficiency still controversial? Clin Endocrinol [10.1111/j.1365-2265.2005.02320.x]
- Seckl J and Walker B (2004) 11β-hydroxysteroid dehydrogenase type 1 as a modulator of glucocorticoid action: from metabolism to memory. Trends Endocrinol Metab 15: 418–424
Article CAS Google Scholar - Windle R et al. (1998) Ultradian rhythm of basal corticosterone release in the female rat: dynamic interaction with the response to acute stress. Endocrinology 139: 443–450
Article CAS Google Scholar - Young E et al. (2004) Cortisol pulsatility and its role in stress regulation and health. Front Neuroendocrinol 25: 69–76
Article CAS Google Scholar - Weise M et al. (2004) Stress dose of hydrocortisone is not beneficial in patients with classic congenital adrenal hyperplasia undergoing short-term, high-intensity exercise. J Clin Endocrinol Metabolism 89: 3679–3684
Article CAS Google Scholar
Author information
Authors and Affiliations
- University of Bristol and a Specialist Registrar in Endocrinology and Diabetes,
Anna Crown & Stafford Lightman - University of Bristol and the Director of the Henry Wellcome Laboratories for Integrative Neuroscience and Endocrinology, Bristol, UK
Anna Crown & Stafford Lightman
Authors
- Anna Crown
- Stafford Lightman
Corresponding author
Correspondence toStafford Lightman.
Ethics declarations
Competing interests
The authors declare no competing financial interests.
Rights and permissions
About this article
Cite this article
Crown, A., Lightman, S. Management of patients with glucocorticoid deficiency.Nat Rev Endocrinol 1, 62–63 (2005). https://doi.org/10.1038/ncpendmet0051
- Received: 15 July 2005
- Accepted: 17 October 2005
- Issue date: 01 December 2005
- DOI: https://doi.org/10.1038/ncpendmet0051