原发性醛固酮增多症患者CYP11B2(醛固酮合成酶)的免疫组化分析及HISTALDO分类的评价。

IF 2.2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Mustafa Karadepe, Hande Yanar, Hülya Binokay, Şeyda Erdoğan, Gamze Akkus
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引用次数: 0

摘要

目的:原发性醛固酮增多症(PA)是继发性高血压最常见的病因。PA的免疫组织化学分析是基于针对CYP11B1和CYP11B2的特异性单克隆抗体,这两种酶负责肾上腺皮质醛固酮的产生。最近提出的HISTALDO分类引入了CYP11B2免疫组织化学来定义临床相关的诊断类别。我们的目的是通过对比库欣综合征(CS)患者,研究PA的临床特征与CYP11B2免疫组化的关系,并评估皮质醇生成细胞的染色情况。2015-2022年间,连续诊断为PA (n=21)和CS (n=20)的患者被纳入研究。所有患者均在我院三级中心行单侧肾上腺切除术。方法:病理标本经苏木精和伊红(H&E)染色后,对所有载玻片进行重新评估,并对CYP11B2进行免疫染色。对每位患者进行半定量h评分并比较染色强度。根据HISTALDO分类对PA患者进行分组和分类。结果:PA患者的平均腺瘤大小比CS患者小得多(p=0.001)。PA组免疫组化h评分较CS组升高(121.36±81.04 vs 73.94±57.70,p=0.045)。根据HISTALDO标准对PA患者进行比较,醛固酮产生性腺瘤(APA, n=10)患者的h评分为136.6±78.86,非APA组为86.81±85.3 (n=11, p=0.05)。此外,与非APA患者相比,APA患者的平均术前醛固酮水平(p=0.06)和醛固酮-肾素比值(ARR, p=0.03)更高。与非APA患者相比,APA患者对手术治疗的反应更有利。结论:CYP11B2是醛固酮合成的关键酶。通过免疫染色评估,CYP11B2的表达与临床特征、PA的严重程度和对治疗的反应有关。因此,CYP11B2的免疫组织化学分析应纳入常规临床检查,以更好地定位醛固酮产生细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunohistochemical Analysis of CYP11B2 (Aldosterone Synthase) and Evaluation of the HISTALDO Classification in Patients with Primary Aldosteronism.

Objective: Primary Aldosteronism (PA) is the most common cause of secondary hypertension. Immunohistochemical analysis of PA is based on specific monoclonal antibodies targeting CYP11B1 and CYP11B2, which are enzymes responsible for the aldosterone production in the adrenal cortex. The recently proposed HISTALDO classification introduced CYP11B2 immunohistochemistry to define clinically relevant diagnostic categories. We aimed to investigate the relationship between clinical characteristics and immunohistochemistry of CYP11B2 in PA and also evaluate staining in cortisol-producing cells by comparing patients with Cushing's Syndrome (CS). Consecutive patients diagnosed with PA (n=21) and CS (n=20) were included between 2015-2022. All of them underwent unilateral adrenalectomy in our tertiary center.

Methods: Following hematoxylin and eosin (H&E) staining of the pathological specimens, all slides were re-evaluated and immunostained for CYP11B2. A semiquantitative H-score was assessed for each patient and compared with staining intensity. Patients with PA were grouped and classified according to the HISTALDO classification.

Results: The mean size of adenoma in patients with PA was much smaller compared to patients with CS (p=0.001). An increase in the immunohistochemical H-score of the patients with PA (121.36 ±81.04 vs 73.94±57.70, p=0.045) was observed in comparison to the patients with CS. When comparing the patients with PA according to HISTALDO criteria, the H-score of the patients with Aldosterone Producing Adenoma (APA, n=10) was 136.6±78.86 compared to the non-APA group, which was 86.81±85.3 (n=11, p=0.05). Moreover, mean preoperative aldosterone levels (p=0.06) and aldosterone-to-renin ratio (ARR, p=0.03) were higher in patients with APA compared to non-APA patients. Response to surgical therapy was more favorable in patients with APA than the patients with non-APA.

Conclusion: CYP11B2 is a key enzyme responsible for the synthesis of aldosterone. CYP11B2 expression, as assessed by immunostaining, was associated with the clinical characteristics, severity of PA, and response to the treatment. Hence, immunohistochemical analysis of CYP11B2 should be incorporated into the routine clinical workup to better localize aldosterone-producing cells.

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来源期刊
Current molecular medicine
Current molecular medicine 医学-医学:研究与实验
CiteScore
5.00
自引率
4.00%
发文量
141
审稿时长
4-8 weeks
期刊介绍: Current Molecular Medicine is an interdisciplinary journal focused on providing the readership with current and comprehensive reviews/ mini-reviews, original research articles, short communications/letters and drug clinical trial studies on fundamental molecular mechanisms of disease pathogenesis, the development of molecular-diagnosis and/or novel approaches to rational treatment. The reviews should be of significant interest to basic researchers and clinical investigators in molecular medicine. Periodically the journal invites guest editors to devote an issue on a basic research area that shows promise to advance our understanding of the molecular mechanism(s) of a disease or has potential for clinical applications.
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