Abstract
Adrenal disorders causing hypertension can be related to the dysfunction of either the adrenal cortex or the adrenal medulla. These disorders, including congenital adrenal hyperplasia (CAH), owing to 11β-hydroxylase deficiency and to 17α-hydroxylase deficiency; apparent mineralocorticoid excess; familial hyperaldosteronism type I; primary aldosteronism; Cushing’s syndrome; and familial glucocorticoid resistance, primarily affect the adrenal cortex and cause low-renin hypertension. The classic disorder of the adrenal medulla resulting in hypertension is pheochromocytoma, although hypertension in obesity might also be associated with catecholamine secretion. In this review, we discuss these etiologies and the most recent advances in our knowledge of their pathophysiology, diagnosis, and treatment.
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References and Recommended Reading
Speiser PW, New MI: Hormonal hypertension. In Manual of Endocrinology and Metabolism, edn 3. Edited by Lavin N. Philadelphia: Lippincott Williams & Wilkins; 2002:163–179. This chapter summarizes remarkably the main causes of low-renin hypertension and the recent advances in their management.
Newman KD, Ponsky T: The diagnosis and management of endocrine tumors causing hypertension in children. Ann NY Acad Sci 2002, 970:155–158.
New MI: Hypertension in congenital adrenal hyperplasia and apparent mineralocorticoid excess. Ann NY Acad Sci 2002, 970:145–154. This paper gives a clear and complete account of the causes of hormonal hypertension in children.
Peter M: Congenital adrenal hyperplasia: 11b-hydroxylase deficiency. Semin Reprod Med 2002, 20:249–254.
White PC, Dupont J, New MI, et al.: A mutation in CYP11B1 (Arg-448-His) associated with steroid 11b-hydroxylase deficiency in Jews of Moroccan origin. J Clin Invest 1991, 87:1664–1667.
Cerame B, Newfield RS, Pascoe L, et al.: Prenatal diagnosis and treatment of 11b-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia. J Clin Endocrinol Metab 1999, 84:3129–3134.
New MI: Male pseudohermaphroditism due to 17a hydroxylase deficiency. J Clin Invest 1970, 49:1930–1941.
New MI: Diagnosis and management of congenital adrenal hyperplasia. Ann Rev Med 1998, 49:311–328.
Fan YS, Sasi R, Lee C, et al.: Localization of the human CYP-17 gene (cytochrome P45017a) to 10q24.3 by fluorescence in situ binding and simultaneous chromosome banding. Genomics 1992, 14:1110–1111.
New MI, Levine LS, Biglieri EG, et al.: Evidence for an unindentified ACTH-induced steroid hormone causing hypertension. J Clin Endocrinol Metab 1977, 44:924–933.
Wilson RC, Harbison MD, Krozowski ZS, et al.: Several homozygous mutations in the gene for 11-beta hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess. J Clin Endocrinol Metab 1995, 80:3145–3150.
Tannin GM, Agarwal AK, Monder C, et al.: The human gene for 11beta-hydroxysteroid dehydrogenase: structure, distribution and chromosomal localization. J Biol Chem (United States) 1991, 266:16653–16658.
Dave-Sharma S, Wilson RC, Harbison MD, et al.: Extensive personal experience: examination of genotype and phenotype relationships in 14 patients with apparent-mineralocorticoid excess. J Clin Endocrinol Metab 1998, 83:2244–2254.
Wilson RC, Dave-Sharma S, Wei J, et al.: A genetic defect resulting in mild low-renin hypertension. Proc Natl Acad Sci U S A 1998, 95:10200–10205.
Dluhy RG, Lifton RP: Glucocorticoid-remediable aldosteronism. J Clin Endocrinol Metab 1999, 84:4341–4344. This concise and clear review is a precise reference on FH-I.
Lifton RP, Dluhy RG, Powers M, et al.: A chimeric 11b-hydroxylase aldosterone synthase gene causes glucocorticoid remediable aldosteronism and human hypertension. Nature 1992, 355:262–265.
Young WF Jr: Minireview: Primary aldosteronism, changing concepts in diagnosis and treatment. Endocrinology 2003, 144:2208–2213. This article covers the most recent advances in the diagnosis and treatment of primary aldosteronism.
Auchus RJ: Aldo is back: recent advances and unresolved controversies in hyperaldosteronism. Curr Opin Nephrol Hypertens 2003, 12:153–159.
Nieman LK: Diagnostic test for Cushing’s syndrome. Ann NY Acad Sci 2002, 970:112–118. This article gives a clear and complete account of the diagnostic tests in Cushing’s syndrome.
Morris D, Grossman A: The medical management of Cushing’s syndrome. Ann NY Acad Sci 2002, 970:119–133. This paper offers a complete overview of the medical treatments in Cushing’s syndrome.
Miller WL: The adrenal cortex. In Pediatric Endocrinology, edn 2. Edited by Sperling MA. Philadelphia: WB Saunders; 2002:419–438.
Kino T, Vottero A, Charmandari E, Chrousos GP: Familial/ sporadic glucocorticoid resistance syndrome and hypertension. Ann NY Acad Sci 2002, 970:101–111. This article offers a complete and clear overview of this rare disorder.
Fonseca V, Bouloux P: Phaeochromocytoma and paraganglioma. Baillere’s Clin Endocrinol Metab 1993, 7:509–544.
Dubois R, Chappuis J: Pheochromcytoma: pediatric features. Arch Pediatr 1997, 4:1217–1225.
Bravo EL: Pheochromocytoma: an approach to antihypertensive management. Ann NY Acad Sci 2002, 970:1–10. This article summarizes the interesting findings on the contribution of sympathetic nervous sytem dysfunction to pheochromocytomainduced hypertension.
McClellan MW: New therapeutic and surgical approaches for sporadic and hereditary pheochromocytoma. Ann NY Acad Sci 2002, 970:41–53. This article offers a complete and clear account of the current treatments of pheochromocytoma and provides a clear and concise overview of the hereditary causes of the disease.
Lenders JWM, Pacak K, Eisenhofer G: New advances in the biochemical diagnosis of pheochromocytoma. Ann NY Acad Sci 2002, 970:29–40.
Opocher G, Schiavi F, Conton P, et al.: Clinical and genetic aspects of phaeochromocytoma. Horm Res 2003, 59(Suppl1):56–61.
Rahmouni K, Hayes W: Leptin and the central neural mechanisms of obesity hypertension. Drugs Today 2002, 38:807–817.
Shibuya I, Utsunomya K, Toyohira Y, et al.: Regulation of catecholamine synthesis by leptin. Ann NY Acad Sci 2002, 971:522–527. This article, by providing in vitro evidence of leptin’s action on catecholamine secretion, opens the discussion of a possible contribution of the adrenals to obesity hypertension.
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Chemaitilly, W., Wilson, R.C. & New, M.I. Hypertension and adrenal disorders. Current Science Inc 5, 498–504 (2003). https://doi.org/10.1007/s11906-003-0058-1
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DOI: https://doi.org/10.1007/s11906-003-0058-1