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原发性醛固酮增多症中CYP11B2表达紊乱

Disordered CYP11B2 Expression in Primary Aldosteronism.

作者信息

Gomez-Sanchez Celso E, Kuppusamy Maniselvan, Reincke Martin, Williams Tracy Ann

机构信息

Endocrine Section, G. V. (Sonny) Montgomery VA Medical Center, Jackson, MS, USA.

University of Mississippi Medical Center, Jackson, MS, USA.

出版信息

Horm Metab Res. 2017 Dec;49(12):957-962. doi: 10.1055/s-0043-122238. Epub 2017 Dec 4.

Abstract

Primary aldosteronism is the most common type of secondary hypertension affecting 6-10% of patients with primary hypertension. PA is mainly caused by unilateral hyperaldosteronism due to an aldosterone-producing adenoma, unilateral hyperplasia with or without micronodules or bilateral zona glomerulosa hyperplasias with or without macro or micronodules. The development of antibodies against the terminal enzyme of aldosterone biosynthesis (CYP11B2) has permitted the further characterization of normal adrenals and resected adrenals from patients with primary aldosteronism. Normal adrenals exhibit two different patterns of cellular expression of CYP11B2: young individuals display a relatively uniform expression of the enzyme throughout the zona glomerulosa while the adrenals of older individuals have dispersed CYP11B2-expressing cells but have more groups of cells called aldosterone-producing cell clusters (APCC). APAs exhibit different patterns of CYP11B2 staining that vary from uniform to homogeneous. There are also a proportion of cells within the APA that co-express different enzymes that are not normally co-expressed in normal individuals. Approximately 30% of patients with unilateral hyperaldosteronism do not have an APA, but either have an increased number of CYP11B2 expressing micronodules or hyperplasia of the zona glomerulosa. In summary, the studies reported in this review are shedding new light on the pathophysiology of primary aldosteronism. The wide variation in histopathological features of the adenomas and concurrent presence of APCCs raises the possibility that most cases of unilateral production of aldosterone actually might represent bilateral asymmetric hyperplasia with nodules frequently due to the development of somatic aldosterone-driving mutations.

摘要

原发性醛固酮增多症是继发性高血压最常见的类型,影响6% - 10%的原发性高血压患者。原发性醛固酮增多症主要由醛固酮分泌腺瘤导致的单侧醛固酮增多、伴有或不伴有微结节的单侧增生或伴有或不伴有大结节或微结节的双侧球状带增生引起。针对醛固酮生物合成末端酶(CYP11B2)的抗体的研发,使得对原发性醛固酮增多症患者的正常肾上腺和切除的肾上腺有了进一步的特征描述。正常肾上腺呈现出CYP11B2两种不同的细胞表达模式:年轻个体在整个球状带中该酶表达相对均匀,而老年个体的肾上腺中有分散的CYP11B2表达细胞,但有更多称为醛固酮分泌细胞簇(APCC)的细胞群。醛固酮分泌腺瘤呈现出不同的CYP11B2染色模式,从均匀到同质不等。醛固酮分泌腺瘤内也有一定比例的细胞共同表达正常个体中通常不共同表达的不同酶。大约30%的单侧醛固酮增多症患者没有醛固酮分泌腺瘤,而是有表达CYP11B2的微结节数量增加或球状带增生。总之,本综述中报道的研究为原发性醛固酮增多症的病理生理学带来了新的认识。腺瘤组织病理学特征的广泛差异以及醛固酮分泌细胞簇的同时存在,增加了一种可能性,即大多数单侧醛固酮分泌病例实际上可能代表双侧不对称增生伴结节,这通常是由于体细胞醛固酮驱动突变的发生。

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