Abstract
Constitutive activation of the Wnt pathway/β-catenin signaling may be important in aldosterone-producing adenoma (APA). However, significant gaps remain in our understanding of the prevalence and clinical outcomes after adrenalectomy in APA patients harboring CTNNB1 mutations. The molecular expression of CYP11B2 and gonadal receptors in adenomas were also explored. Adenomas from 219 APA patients (95 men; 44.2%; aged 50.5 ± 11.9 years) showed a high rate of somatic mutations (n = 128, 58.4%). The majority of them harbored KCNJ5 mutations (n = 116, 52.9%); 8 patients (3.7%, 6 women) had CTNNB1 mutations. Patients with APAs harboring CTNNB1 mutations were older and had shorter duration of hypertension. After adrenalectomy, CTNNB1 mutation carriers had a higher possibility (87.5%) of residual hypertension than other APA patients. APAs harboring CTNNB1 mutations have heterogeneous staining of β-catenin and variable expression of gonadal receptors and both CYP11B1 and CYP11B2. This suggests that CTNNB1 mutations may be more related to tumorigenesis rather than excessive aldosterone production.
Highlights
Targeted sequencing for the reported mutations in aldosterone-producing adenoma (APA) of KCNJ5, CACNA1D, ATP1A1, ATP2B3 and CTNNB1 exons was performed from the adenomas
About 3.7% (8 adenomas) of our 219 APA patients were found to harbor somatic CTNNB1 mutations, and their molecular expressions and clinical outcomes were reported. This low prevalence is similar to the 5.1% (10/189) reported in APAs29, but much lower than those reported in 15–26.9% of various types of adrenal adenomas and up to 30.8% of adrenocortical carcinomas[30,31]
We found that patients who harbor CTNNB1 mutations had a higher likelihood of residual hypertension after adrenalectomy, when compared with wild-type APA patients or KNCJ5 mutation carriers
Summary
The aim of this study was to determine the prevalence of the CTNNB1 mutations in APA patients and to correlate the mutation status with clinical outcomes in order to determine the outcomes on patients who harbor these mutations
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