已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

Diagnosis and treatment of primary aldosteronism.

医学 原发性醛固酮增多症 醛固酮增多症 内科学 醛固酮 泌尿科
作者
Martin Reincke,Irina Bancos,Paolo Mulatero,Ute I Scholl,Michael Stowasser,Tracy Ann Williams
出处
期刊:The Lancet Diabetes & Endocrinology [Elsevier BV]
卷期号:9 (12): 876-892 被引量:3
标识
DOI:10.1016/s2213-8587(21)00210-2
摘要

Primary aldosteronism is a common cause of secondary hypertension associated with excess cardiovascular morbidities. Primary aldosteronism is underdiagnosed because it does not have a specific, easily identifiable feature and clinicians can be poorly aware of the disease. The diagnostic investigation is a multistep process of screening, confirmatory testing, and subtype differentiation of unilateral from bilateral forms for therapeutic management. Adrenal venous sampling is key for reliable subtype identification, but can be bypassed in patients with specific characteristics. For unilateral disease, surgery offers the possibility of cure, with total laparoscopic unilateral adrenalectomy being the treatment of choice. Bilateral forms are treated mainly with mineralocorticoid receptor antagonists. The goals of treatment are to normalise both blood pressure and excessive aldosterone production, and the primary aims are to reduce associated comorbidities, improve quality of life, and reduce mortality. Prompt diagnosis of primary aldosteronism and the use of targeted treatment strategies mitigate aldosterone-specific target organ damage and with appropriate patient management outcomes can be excellent. Advances in molecular histopathology challenge the traditional concept of primary aldosteronism as a binary disease, caused by either a unilateral aldosterone-producing adenoma or bilateral adrenal hyperplasia. Somatic mutations drive autonomous aldosterone production in most adenomas. Many of these same mutations have been identified in nodular lesions adjacent to an aldosterone-producing adenoma and in patients with bilateral disease. In addition, germline mutations cause rare familial forms of aldosteronism (familial hyperaldosteronism types 1-4). Genetic testing for inherited forms in suspected cases of familial hyperaldosteronism avoids the burdensome diagnostic investigation in positive patients. In this Review, we discuss advances and future management approaches in the diagnosis of primary aldosteronism.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Lou关注了科研通微信公众号
刚刚
huishoushen完成签到 ,获得积分10
1秒前
David发布了新的文献求助10
1秒前
激动的翅膀完成签到,获得积分10
2秒前
菠萝完成签到 ,获得积分0
3秒前
4秒前
chandangfo应助ssy采纳,获得10
4秒前
6秒前
闪闪发布了新的文献求助10
12秒前
12秒前
小贵完成签到,获得积分10
14秒前
jjay完成签到 ,获得积分10
15秒前
脑洞疼应助我要发顶刊采纳,获得10
16秒前
17秒前
钟山完成签到,获得积分10
17秒前
17秒前
汪洋发布了新的文献求助10
17秒前
小马甲应助多味花生采纳,获得10
19秒前
完美世界应助给好评采纳,获得10
21秒前
28秒前
Jackson_Cheng发布了新的文献求助30
30秒前
时间煮雨我煮鱼完成签到,获得积分10
30秒前
Zora完成签到 ,获得积分10
31秒前
幸福铸海完成签到 ,获得积分10
32秒前
chamberlain完成签到,获得积分10
32秒前
32秒前
多味花生发布了新的文献求助10
34秒前
moon完成签到,获得积分10
35秒前
35秒前
菲菲完成签到 ,获得积分10
37秒前
37秒前
慕青应助矮小的断秋采纳,获得10
39秒前
美好问枫发布了新的文献求助10
39秒前
不爱睡觉完成签到 ,获得积分10
41秒前
41秒前
多味花生完成签到,获得积分10
41秒前
jiandan完成签到,获得积分10
43秒前
搜集达人应助空空采纳,获得10
45秒前
amazeman111发布了新的文献求助10
46秒前
收下那个我完成签到,获得积分10
48秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Les Mantodea de Guyane Insecta, Polyneoptera 2000
Quality by Design - An Indispensable Approach to Accelerate Biopharmaceutical Product Development 800
Pulse width control of a 3-phase inverter with non sinusoidal phase voltages 777
Signals, Systems, and Signal Processing 610
Research Methods for Applied Linguistics: A Practical Guide 600
Research Methods for Applied Linguistics 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6404116
求助须知:如何正确求助?哪些是违规求助? 8223361
关于积分的说明 17428820
捐赠科研通 5456467
什么是DOI,文献DOI怎么找? 2883501
邀请新用户注册赠送积分活动 1859814
关于科研通互助平台的介绍 1701219