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Cited 13 time in webofscience Cited 11 time in scopus
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Time-Dependent Risk of Atrial Fibrillation in Patients With Primary Aldosteronism After Medical or Surgical Treatment Initiation

Authors
Kim, Kyoung JinHong, NamkiYu, Min HeuiLee, HokyouLee, SeunghyunLim, Jung SooRhee, Yumie
Issue Date
Jun-2021
Publisher
Lippincott Williams & Wilkins Ltd.
Keywords
adrenalectomy; atrial fibrillation; cardiovascular diseases; hypertension; hyperaldosteronism; stroke
Citation
Hypertension, v.77, no.6, pp 1964 - 1973
Pages
10
Indexed
SCIE
SCOPUS
Journal Title
Hypertension
Volume
77
Number
6
Start Page
1964
End Page
1973
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/53473
DOI
10.1161/HYPERTENSIONAHA.120.16909
ISSN
0194-911X
1524-4563
Abstract
Increased risk of atrial fibrillation was reported in patients with primary aldosteronism. However, data are limited regarding the time-dependent risk of atrial fibrillation in surgically or medically treated primary aldosteronism. From the National Health Insurance Claim database in Korea (2003-2017), a total of 1418 patients with primary aldosteronism (adrenalectomy [ADX], n=755, mineralocorticoid receptor antagonist n=663) were age- and sex-matched at a 1:5 ratios to patients with essential hypertension (n=7090). Crude incidence of new onset atrial fibrillation was 2.96% in primary aldosteronism and 1.97% in essential hypertension. Because of nonproportional hazard observed in new onset atrial fibrillation, analysis time was split at 3 years. Compared with essential hypertension, risk of new onset atrial fibrillation peaked at 1 year gradually declined but remained elevated up to 3 years in overall treated primary aldosteronism (adjusted hazard ratio [aHR] 3.02; P<0.001) as well as in both ADX (aHR, 3.54; P<0.001) and mineralocorticoid receptor antagonist groups (aHR 2.27; P=0.031), which became comparable to essential hypertension afterward in both groups (ADX aHR, 0.38; P=0.102; mineralocorticoid receptor antagonist aHR, 0.60; P=0.214). Nonetheless, mineralocorticoid receptor antagonist group was associated with increased risk of nonfatal stroke (aHR, 1.21; P=0.031) compared with essential hypertension, whereas ADX was not (aHR, 1.26; P=0.288). Our results suggest the risk of new-onset atrial fibrillation remained elevated up to 3 years in treated primary aldosteronism compared with essential hypertension, which declined to comparable risk in essential hypertension thereafter. Monitoring for atrial fibrillation up to 3 years after treatment, particularly ADX, might be warranted.
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Kim, Kyoung Jin
Anam Hospital (Department of Endocrinology and Metabolism, Anam Hospital)
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