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  1. NTU Scholars
  2. 醫學院
  3. 醫學系
Please use this identifier to cite or link to this item: https://scholars.lib.ntu.edu.tw/handle/123456789/514968
Title: Atrial Fibrillation in Primary Aldosteronism
Authors: CHIEN-TING PAN 
CHENG-HSUAN TSAI 
ZHENG-WEI CHEN 
Chang Y.-Y.
VIN-CENT WU 
Chen Z.-W.
YEN-HUNG LIN 
Hung C.-S.
Hung C.-S.
Lin Y.-H.
Lin Y.-H.
Issue Date: 2020
Publisher: Georg Thieme Verlag
Journal Volume: 52
Journal Issue: 6
Start page/Pages: 357-365
Source: Hormone and Metabolic Research
Abstract: 
Primary aldosteronism (PA) is the most common cause of secondary hypertension. Increasing evidence has demonstrated an increased cardiovascular risk in patients with PA compared to those with essential hypertension (EH), including atrial fibrillation (AF), the most prevalent arrhythmia among adults that is associated with an elevated risk of subsequent cerebro-cardiovascular adverse events. The mechanisms of increased prevalence of AF in PA patients are complex. Excessive aldosterone production is regarded to be a key component in the pathogenesis of AF, in addition to arterial hypertension and electrolyte imbalance. In addition, several translational and clinical studies have reported that structural remodeling with atrial fibrosis and electrical remodeling with arrhythmogenicity induced by an excess of aldosterone also play major roles in AF genesis. Clinical studies from several registries and meta-analysis have reported an increased prevalence and risk of AF in PA patients compared to EH patients. Recent trials have further demonstrated a reduction in the risk of new-onset atrial fibrillation (NOAF) after adrenalectomy, while the results of medical treatment with mineralocorticoid receptor antagonists (MRAs) have been inconsistent. This review outlines the current evidence of the relationship between PA and AF, and highlights recent progress in the management of PA with regards to the development of AF. ? 2020 Georg Thieme Verlag KG Stuttgart New York.
URI: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85086681442&doi=10.1055%2fa-1141-5989&partnerID=40&md5=532546421876b80f8794ab6ff28d9147
https://scholars.lib.ntu.edu.tw/handle/123456789/514968
ISSN: 0018-5043
DOI: 10.1055/a-1141-5989
SDG/Keyword: antihypertensive agent; cs 3150; eplerenone; esaxerenone; finerenone; mineralocorticoid antagonist; osilodrostat; potassium; spironolactone; adrenalectomy; antihypertensive therapy; arrhythmogenesis; atrial fibrillation; autonomic dysfunction; Cushing syndrome; disease association; echocardiography; gene; heart atrium function; heart atrium remodeling; heart electrophysiology; heart left atrium; heart left ventricle function; heart left ventricle mass; heart ventricle remodeling; human; hypertension; hypokalemia; incidence; kcnj5 gene; nonhuman; pathophysiology; primary hyperaldosteronism; priority journal; radiofrequency ablation; Review; somatic mutation; x-ray computed tomography; adult; atrial fibrillation; complication; hyperaldosteronism; hypertension; risk factor; Adrenalectomy; Adult; Atrial Fibrillation; Humans; Hyperaldosteronism; Hypertension; Mineralocorticoid Receptor Antagonists; Risk Factors
[SDGs]SDG3
Appears in Collections:醫學系

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