4.6 Review

The Biology of Normal Zona Glomerulosa and Aldosterone-Producing Adenoma: Pathological Implications

Journal

ENDOCRINE REVIEWS
Volume 39, Issue 6, Pages 1029-1056

Publisher

ENDOCRINE SOC
DOI: 10.1210/er.2018-00060

Keywords

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Funding

  1. Ministry of Health [RF2011-02352318]
  2. University of Padova [DOR1625891/16, DOR1670784/16, BIRD163255/16]
  3. Foundation for Advanced Research in Arterial Hypertension and Cardiovascular Disease (FORICA)
  4. National Heart, Lung, and Blood Institute [R01 HL27255]
  5. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL027255] Funding Source: NIH RePORTER

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The identification of several germline and somatic ion channel mutations in aldosterone-producing adenomas (APAs) and detection of cell clusters that can be responsible for excess aldosterone production, as well as the isolation of autoantibodies activating the angiotensin II type 1 receptor, have rapidly advanced the understanding of the biology of primary aldosteronism (PA), particularly that of APA. Hence, the main purpose of this review is to discuss how discoveries of the last decade could affect histopathology analysis and clinical practice. The structural remodeling through development and aging of the human adrenal cortex, particularly of the zona glomerulosa, and the complex regulation of aldosterone, with emphasis on the concepts of zonation and channelopathies, will be addressed. Finally, the diagnostic workup for PA and its subtyping to optimize treatment are reviewed.

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