Wrenn Sean M, Vaidya Anand, Lubitz Carrie C
Department of General Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Department of General Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Gland Surg. 2020 Feb;9(1):14-24. doi: 10.21037/gs.2019.10.23.
Primary aldosteronism (PA) is a common cause of secondary hypertension caused by excessive and inappropriate secretion of the hormone aldosterone from one or both adrenal glands. The prevalence of PA ranges from 10% in the general hypertensive population to 20% in resistant hypertension, yet only a small fraction of patients is diagnosed. Disease and symptom recognition, screening in indicated populations, multidisciplinary communication, and appropriate imaging and biochemical workup can identify patients who might benefit from effective and targeted treatment modalities. Effective treatments available include both surgical and medical approaches, usually dependent on the subtype of PA present. Our collective understanding of the pathophysiology of PA is expanded by recent developments in molecular biology and genetics, including understanding the specific somatic and germline mutations involved in pathogenesis. We review the pathophysiology, diagnostic workup, and treatment considerations for this disease process.
原发性醛固酮增多症(PA)是继发性高血压的常见病因,由一侧或双侧肾上腺分泌过多且不适当的醛固酮激素所致。PA在普通高血压人群中的患病率为10%,在难治性高血压患者中为20%,但仅有一小部分患者得到诊断。疾病及症状识别、在特定人群中进行筛查、多学科沟通以及适当的影像学和生化检查,能够识别出可能从有效且有针对性的治疗方式中获益的患者。现有的有效治疗方法包括手术和药物治疗,通常取决于所患PA的亚型。分子生物学和遗传学的最新进展拓展了我们对PA病理生理学的总体认识,包括对发病机制中涉及的特定体细胞和种系突变的了解。我们综述了该疾病过程的病理生理学、诊断检查及治疗注意事项。