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本文引用的文献

1
International Histopathology Consensus for Unilateral Primary Aldosteronism.国际单侧原发性醛固酮增多症组织病理学共识。
J Clin Endocrinol Metab. 2021 Jan 1;106(1):42-54. doi: 10.1210/clinem/dgaa484.
2
Precise Mapping of Intra-Adrenal Aldosterone Activities Provides a Novel Surgical Strategy for Primary Aldosteronism.精准定位肾上腺醛固酮活性为原发性醛固酮增多症提供了新的手术策略。
Hypertension. 2020 Sep;76(3):976-984. doi: 10.1161/HYPERTENSIONAHA.119.14341. Epub 2020 Jun 15.
3
The Potential Role of Aldosterone-Producing Cell Clusters in Adrenal Disease.醛固酮分泌细胞簇在肾上腺疾病中的潜在作用。
Horm Metab Res. 2020 Jun;52(6):427-434. doi: 10.1055/a-1128-0421. Epub 2020 Mar 30.
4
Prevalence, diagnosis and outcomes of treatment for primary aldosteronism.原发性醛固酮增多症的患病率、诊断和治疗结果。
Best Pract Res Clin Endocrinol Metab. 2020 Mar;34(2):101365. doi: 10.1016/j.beem.2019.101365. Epub 2019 Dec 5.
5
Primary Aldosteronism: JACC State-of-the-Art Review.原发性醛固酮增多症:JACC 现状述评。
J Am Coll Cardiol. 2019 Dec 3;74(22):2799-2811. doi: 10.1016/j.jacc.2019.09.057.
6
Tandem Mass Spectrometry Imaging Reveals Distinct Accumulation Patterns of Steroid Structural Isomers in Human Adrenal Glands.串联质谱成像揭示了人类肾上腺中类固醇结构异构体的不同积累模式。
Anal Chem. 2019 Jul 16;91(14):8918-8925. doi: 10.1021/acs.analchem.9b00619. Epub 2019 Jun 26.
7
Aldosterone and 18-Oxocortisol Coaccumulation in Aldosterone-Producing Lesions.醛固酮和 18-氧皮质醇在醛固酮瘤中的共同积聚。
Hypertension. 2018 Dec;72(6):1345-1354. doi: 10.1161/HYPERTENSIONAHA.118.11243.
8
Cellular and Genetic Causes of Idiopathic Hyperaldosteronism.特发性醛固酮增多症的细胞和遗传病因。
Hypertension. 2018 Oct;72(4):874-880. doi: 10.1161/HYPERTENSIONAHA.118.11086.
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Molecular genetics of Conn adenomas in the era of exome analysis.外显子组分析时代Conn腺瘤的分子遗传学
Presse Med. 2018 Jul-Aug;47(7-8 Pt 2):e151-e158. doi: 10.1016/j.lpm.2018.07.006. Epub 2018 Jul 30.
10
Impact of aldosterone-producing cell clusters on diagnostic discrepancies in primary aldosteronism.醛固酮生成细胞团对原发性醛固酮增多症诊断差异的影响。
Oncotarget. 2018 May 25;9(40):26007-26018. doi: 10.18632/oncotarget.25418.

醛固酮分泌细胞簇在原发性醛固酮增多症和年龄相关性高血压中的功能特征及意义。

Functional Characteristic and Significance of Aldosterone-Producing Cell Clusters in Primary Aldosteronism and Age-Related Hypertension.

机构信息

Department of Medicine, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre, Cheras, Malaysia.

出版信息

Front Endocrinol (Lausanne). 2021 Mar 3;12:631848. doi: 10.3389/fendo.2021.631848. eCollection 2021.

DOI:10.3389/fendo.2021.631848
PMID:33763031
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7982842/
Abstract

Primary aldosteronism (PA) is one of the most frequent curable forms of secondary hypertension. It can be caused by the overproduction of aldosterone in one or both adrenal glands. The most common subtypes of PA are unilateral aldosterone over-production due to aldosterone-producing adenomas (APA) or bilateral aldosterone over-production due to bilateral hyperaldosteronism (BHA). Utilizing the immunohistochemical (IHC) detection of aldosterone synthase (CYP11B2) has allowed the identification of aldosterone-producing cell clusters (APCCs) with unique focal localization positive for CYP11B2 expression in the subcapsular portion of the human adult adrenal cortex. The presence of CYP11B2 supports that synthesis of aldosterone can occur in these cell clusters and therefore might contribute to hyperaldosteronism. However, the significance of the steroidogenic properties of APCCs especially in regards to PA remains unclear. Herein, we review the available evidence on the presence of APCCs in normal adrenals and adrenal tissues adjacent to APAs, their aldosterone-stimulating somatic gene mutations, and their accumulation during the ageing process; raising the possibility that APCCs may play a role in the development of PA and age-related hypertension.

摘要

原醛症(PA)是继发性高血压最常见的可治愈形式之一。它可能是由于一个或两个肾上腺过度产生醛固酮引起的。PA 最常见的亚型是单侧醛固酮过度产生,原因是醛固酮瘤(APA)或双侧醛固酮过度产生,原因是双侧高醛固酮血症(BHA)。利用醛固酮合酶(CYP11B2)的免疫组织化学(IHC)检测,可以识别醛固酮产生细胞簇(APCCs),其在人类成年肾上腺皮质的包膜下部分具有独特的局灶性 CYP11B2 表达阳性。CYP11B2 的存在支持在这些细胞簇中可以发生醛固酮的合成,因此可能导致高醛固酮血症。然而,APCCs 的甾体生成特性,特别是在 PA 方面的意义尚不清楚。在此,我们回顾了关于正常肾上腺和 APA 附近肾上腺组织中 APCCs 的存在、它们的醛固酮刺激体细胞基因突变以及它们在衰老过程中的积累的现有证据;提出了 APCCs 可能在 PA 和与年龄相关的高血压的发展中发挥作用的可能性。