Different Somatic Mutations in Multinodular Adrenals With Aldosterone-Producing Adenoma

被引:52
作者
Fernandes-Rosa, Fabio Luiz [1 ,2 ,3 ]
Giscos-Douriez, Isabelle [1 ,2 ]
Amar, Laurence [1 ,2 ,4 ]
Gomez-Sanchez, Celso E. [6 ,7 ]
Meatchi, Tchao [1 ,2 ,5 ]
Boulkroun, Sheerazed [1 ,2 ]
Zennaro, Maria-Christina [1 ,2 ,3 ]
机构
[1] Paris Cardiovasc Res Ctr, INSERM, UMRS 970, Paris, France
[2] Univ Paris 05, Sorbonne Paris Cite, Paris, France
[3] Hop Europeen Georges Pompidou, Serv Genet, AP HP, Paris, France
[4] Hop Europeen Georges Pompidou, Unite Hypertens Arterielle, AP HP, Paris, France
[5] Hop Europeen Georges Pompidou, Serv Anat Pathol, AP HP, Paris, France
[6] GV Sonny Montgomery VA Med Ctr, Div Endocrinol, Jackson, MS USA
[7] Univ Mississippi, Med Ctr, Jackson, MS 39216 USA
关键词
adrenal cortex; aldosterone; hyperaldosteronism; mineralocorticoids; mutation; potassium channels; CHANNEL MUTATIONS; HYPERPLASIA; KCNJ5; PREVALENCE; EXPRESSION; DIAGNOSIS; CORTEX;
D O I
10.1161/HYPERTENSIONAHA.115.05993
中图分类号
R6 [外科学];
学科分类号
100210 [外科学];
摘要
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.
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收藏
页码:1014 / 1022
页数:9
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