Primary aldosteronism
Primary aldosteronism (PA) is a common cause of secondary hypertension caused by excessive and inappropriate secretion of the hormone aldosterone from one or both adrenal glands. The prevalence of PA ranges from 10% in the general hypertensive population to 20% in resistant hypertension, yet only a...
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Published in: | Gland surgery Vol. 9; no. 1; pp. 14 - 24 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
China (Republic : 1949- )
AME Publishing Company
01-02-2020
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Subjects: | |
Online Access: | Get full text |
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Summary: | Primary aldosteronism (PA) is a common cause of secondary hypertension caused by excessive and inappropriate secretion of the hormone aldosterone from one or both adrenal glands. The prevalence of PA ranges from 10% in the general hypertensive population to 20% in resistant hypertension, yet only a small fraction of patients is diagnosed. Disease and symptom recognition, screening in indicated populations, multidisciplinary communication, and appropriate imaging and biochemical workup can identify patients who might benefit from effective and targeted treatment modalities. Effective treatments available include both surgical and medical approaches, usually dependent on the subtype of PA present. Our collective understanding of the pathophysiology of PA is expanded by recent developments in molecular biology and genetics, including understanding the specific somatic and germline mutations involved in pathogenesis. We review the pathophysiology, diagnostic workup, and treatment considerations for this disease process. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 Contributions: (I) Conception and design: SM Wrenn; (II) Administrative support: SM Wrenn, CC Lubitz; (III) Provision of study materials or patients: All authors; (IV) Collection and assembly of data: SM Wrenn; (V) Data analysis and interpretation: All authors; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors. |
ISSN: | 2227-684X 2227-8575 |
DOI: | 10.21037/gs.2019.10.23 |