ARMC5 Alterations in Primary Macronodular Adrenal Hyperplasia (PMAH) and the Clinical State of Variant Carriers

Chika Kyo, Takeshi Usui, Rieko Kosugi, Mizuki Torii, Takako Yonemoto, Tatsuo Ogawa, Masato Kotani, Naohisa Tamura, Yutaro Yamamoto, Takuyuki Katabami, Isao Kurihara, Kohei Saito, Naotetsu Kanamoto, Hidenori Fukuoka, Norio Wada, Hiroyuki Murabe, Tatsuhide Inoue

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Context: Primary macronodular adrenal hyperplasia (PMAH) is a rare type of Cushing or subclinical Cushing syndrome and is associated with bilateral multinodular formation. ARMC5 is one of the responsible genes for PMAH. Objectives: This study was performed to identify the genotype-phenotype correlation of ARMC5 in a cohort of Japanese patients. Patients and Methods: Fourteen patients with clinically diagnosed PMAH and family members of selected patients were studied for ARMC5 gene alteration and clinical phenotype. The associated nonadrenal tumor tissues were also studied. Results: Of fourteen patients with PMAH, 10 had pathogenic or likely pathogenic variants of ARMC5. We found two variants. Five unrelated patients had identical variants (p.R619∗). In two patients, the variant was found in offspring with the asymptomatic or presymptomatic state. Six of ten patients who tested positive for the ARMC5 pathogenic or likely pathogenic variant carried nonadrenal tumors; however, no loss of heterozygosity (LOH) or second hit of the ARMC5 gene was evident. The ARMC5 variant-positive group showed a significantly higher basal cortisol level. Furthermore, age-dependent cortisol hypersecretion was seen in the ARMC5 variant-positive group. Conclusions: ARMC5 pathogenic variants are common (71%) in Japanese patients with PMAH. p.R619∗ might be a hot spot in Japanese patients with PMAH. Asymptomatic or presymptomatic pathogenic variant carriers were found among the family members of the patients. Although 50% of ARMC5 variant carriers had nonadrenal neoplastic lesions, no LOH or second hit of ARMC5 in the tumor tissues was evident. The ARMC5 variant-positive mutant group showed a higher basal cortisol level than the negative group.

Original languageEnglish
Pages (from-to)1837-1846
Number of pages10
JournalJournal of the Endocrine Society
Volume3
Issue number10
DOIs
Publication statusPublished - 2019 Oct

Keywords

  • ARMC5
  • PMAH
  • the second hit
  • variant carrier

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism

Fingerprint Dive into the research topics of 'ARMC5 Alterations in Primary Macronodular Adrenal Hyperplasia (PMAH) and the Clinical State of Variant Carriers'. Together they form a unique fingerprint.

  • Cite this

    Kyo, C., Usui, T., Kosugi, R., Torii, M., Yonemoto, T., Ogawa, T., Kotani, M., Tamura, N., Yamamoto, Y., Katabami, T., Kurihara, I., Saito, K., Kanamoto, N., Fukuoka, H., Wada, N., Murabe, H., & Inoue, T. (2019). ARMC5 Alterations in Primary Macronodular Adrenal Hyperplasia (PMAH) and the Clinical State of Variant Carriers. Journal of the Endocrine Society, 3(10), 1837-1846. https://doi.org/10.1210/js.2019-00210