Time-Dependent Risk of Atrial Fibrillation in Patients With Primary Aldosteronism After Medical or Surgical Treatment Initiation

Author:

Kim Kyoung Jin1ORCID,Hong Namki2ORCID,Yu Min Heui3ORCID,Lee Hokyou24ORCID,Lee Seunghyun2ORCID,Lim Jung Soo5ORCID,Rhee Yumie2ORCID

Affiliation:

1. Department of Internal Medicine, Korea University College of Medicine, Seoul (K.J.K.).

2. Department of Internal Medicine (N.H., H.L., S.L., Y.R.), Yonsei University College of Medicine, Seoul.

3. SENTINEL team, Division of Endocrinology, Department of Internal Medicine (M.H.Y.), Yonsei University College of Medicine, Seoul.

4. Department of Preventive Medicine (H.L.), Yonsei University College of Medicine, Seoul.

5. Department of Internal Medicine, Wonju Severance Christian Hospital, Yonsei University Wonju College of Medicine, South Korea (J.S.L.).

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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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