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首页> 外文期刊>Hypertension: An Official Journal of the American Heart Association >Different Somatic Mutations in Multinodular Adrenals With Aldosterone-Producing AdenomaNovelty and Significance
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Different Somatic Mutations in Multinodular Adrenals With Aldosterone-Producing AdenomaNovelty and Significance

机译:多结节性肾上腺与醛固酮产生腺瘤的不同体细胞突变的意义和意义

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Primary aldosteronism is the most common form of secondary hypertension. Somatic mutations in KCNJ5 , ATP1A1 , ATP2B3 , and CACNA1D are found in aldosterone-producing adenoma. In addition, adrenals with aldosterone-producing adenomas show cortical remodeling and frequently multiple secondary nodules. Our aim was to investigate whether different aldosterone-producing nodules from the same adrenal share the same mutational status. Aldosterone synthase expression was assessed in multinodular adrenals from 27 patients. DNA of 37 aldosterone-producing secondary nodules was extracted from formalin-fixed paraffin-embedded tissues and genotyped for KCNJ5 , ATP1A1 , ATP2B3 , and CACNA1D mutations. Among 17 adrenals with a somatic mutation in the principal nodule, 4 showed the same mutation in a secondary nodule, whereas 10 had no mutation in any of the known genes. In 1 adrenal harboring the KCNJ5 p.Gly151Arg mutation in the principal nodule, the same mutation was present in 2 secondary nodules, but no mutation was found in a third nodule. Finally, in 2 adrenals with a CACNA1D mutation in the principal nodule, a KCNJ5 mutation was identified in the secondary nodule. Among 10 adrenals without mutations in the principal nodule, 1 carried a KCNJ5 mutation in the secondary nodule. No mutations were detected in 7 aldosterone-producing cell clusters from 6 adrenals. No association was observed between the presence of mutations in secondary nodules and clinical parameters. In conclusion, different mutations are found in different aldosterone-producing nodules from the same adrenal, suggesting that somatic mutations are independent events triggered by mechanisms that remain to be identified.# Novelty and Significance {#article-title-29}
机译:原发性醛固酮增多症是继发性高血压最常见的形式。在产生醛固酮的腺瘤中发现了KCNJ5,ATP1A1,ATP2B3和CACNA1D的体细胞突变。此外,具有产生醛固酮的腺瘤的肾上腺表现出皮质重塑,并经常有多个继发性结节。我们的目的是调查来自同一肾上腺的不同醛固酮生产结节是否具有相同的突变状态。在来自27位患者的多结节肾上腺中评估了醛固酮合酶的表达。从福尔马林固定石蜡包埋的组织中提取37个产生醛固酮的次级结节的DNA,并对KCNJ5,ATP1A1,ATP2B3和CACNA1D突变进行基因分型。在主结节发生体细胞突变的17个肾上腺中,有4个在次生结节中显示相同的突变,而10个在任何已知基因中均没有突变。在1个在主结节中携带KCNJ5 p.Gly151Arg突变的肾上腺中,在2个继发结节中存在相同的突变,但在第三个结节中未发现任何突变。最后,在2个在主要结节中具有CACNA1D突变的肾上腺中,在次要结节中发现了KCNJ5突变。在主结节无突变的10个肾上腺中,有1个在继发结节中携带KCNJ5突变。在来自6个肾上腺的7个醛固酮生成细胞簇中未检测到突变。在继发性结节中突变的存在与临床参数之间未发现关联。总之,在同一肾上腺的不同醛固酮生产结节中发现了不同的突变,表明体细胞突变是由尚待确定的机制触发的独立事件。#新奇和意义{#article-title-29}

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