Familial Aggregation and Heritability of Aldosteronism with Cardiovascular Events

Author:

Wu Vin-Cent1ORCID,Chueh Jeff S2,Hsieh Mei-Yun3,Hu Ya-Hui4,Huang Kuo-How5,Lin Yen-Hung1,Yang Shao-Yu1,Chu Tzong-Shinn1,Kuo Chang-Fu3

Affiliation:

1. Division of Nephrology and Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan

2. Cleveland Clinic Lerner College of Medicine and Glickman Urological and Kidney Institute, Cleveland Clinic, Cleveland, Ohio

3. Division of Rheumatology, Allergy and Immunology, Chang Gung Memorial Hospital, Taoyuan, Taiwan

4. Division of Endocrinology and Metabolism, Department of Internal Medicine, Taipei Tzu Chi Hospital, The Buddhist Medical Foundation, Taipei, Taiwan

5. Division of Urology, National Taiwan University Hospital, Taipei, Taiwan

Abstract

Abstract Context To date, the effect of positive family history as a risk factor of primary aldosteronism (PA) is largely unknown. Studies have failed to distinguish the heritability of PA as well as the associations between positive family history of PA and clinical outcomes. Objectives We quantified the prevalence, the extent of familial aggregation, the heritability of PA among family members of patients with PA, and the association between positive PA family history and major cardiovascular events (MACE). Design and Settings Using the Taiwan National Health Insurance Database, 30 245 077 National Health Insurance beneficiaries (both alive and those deceased between January 1, 1999, and December 31, 2015) were identified. Results We identified 7902 PA patients. Forty-four had PA (0.3%) among 10 234 individuals with affected parents, 2298 with affected offspring, 1924 with affected siblings, and 22 with affected twins. A positive family history was associated with the adjusted relative risk (RR) (95% confidence interval [CI]) of 11.60 (7.63–17.63) for PA in people with an affected first-degree relative. In subgroup analysis, the risk for PA across all relationships (parent, siblings, offspring, and spouse) showed highly significant differences to PA without family history. The accountability for phenotypic variance of PA was 51.0% for genetic factors, 24.9% for shared environmental factors, and 24.1% for nonshared environmental factors. PA patients with an affected first-degree relative were associated with an increased risk for composite major cardiovascular events (RR 1.31; 95% CI 1.24–1.40, P < .001) compared with PA patients without family history. Conclusion Familial clustering of PA exists among a population-based study, supporting a genetic susceptibility leading to PA. There is increased coaggregation of MACE in first-degree relatives of PA patients. Our findings suggest a strong genetic component in the susceptibility of PA, involving different kinships.

Funder

Center for Big Data Analytics and Statistics

Chang Gung Memorial Hospital

Applied Health Research Data Integration Service

National Health Insurance Administration

Taiwan National Science Council

National Taiwan University Hospital

Ministry of Science and Technology

Republic of China

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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