Wu Hao, He Hongbo, Han Tong, Tian Xiaoyu, Zhu Zhiming
Department of Hypertension and Endocrinology, Center for Hypertension and Metabolic Diseases, Daping Hospital, Army Medical University, Chongqing Institute of Hypertension, Chongqing, China.
School of Biomedical Sciences, Heart, and Vascular Institute, The Chinese University of Hong Kong, Hong Kong.
Trends Endocrinol Metab. 2025 Sep;36(9):789-801. doi: 10.1016/j.tem.2024.12.001. Epub 2025 Jan 6.
Primary aldosteronism (PA) is a common, salt-sensitive form of endocrine hypertension. Compared with essential hypertension (EH), PA is more susceptible to cardiorenal complications and metabolic risks. However, PA has a low screening rate and a poor response to mineralocorticoid receptor antagonists (MRAs). In addition to somatic ion channel mutations and epigenetic alterations, which contribute to excessive production of aldosterone, cholesterol, as a crucial precursor for aldosterone biosynthesis, may be involved in PA pathogenesis. Abnormal adrenal cholesterol uptake and steroidogenesis have been found in patients with PA. Therefore, we propose that a statin-based therapeutic strategy may be pivotal for antagonizing PA-related comorbidities by targeting cholesterol-dependent adrenal steroidogenesis.
原发性醛固酮增多症(PA)是一种常见的、盐敏感型的内分泌性高血压。与原发性高血压(EH)相比,PA更容易引发心肾并发症和代谢风险。然而,PA的筛查率较低,且对盐皮质激素受体拮抗剂(MRAs)反应不佳。除了导致醛固酮过度产生的体细胞离子通道突变和表观遗传改变外,胆固醇作为醛固酮生物合成的关键前体,可能参与PA的发病机制。在PA患者中已发现肾上腺胆固醇摄取和类固醇生成异常。因此,我们提出基于他汀类药物的治疗策略可能通过靶向胆固醇依赖性肾上腺类固醇生成来对抗PA相关的合并症起着关键作用。