Emerging association between KCNJ5 mutations and vascular failure in primary aldosteronism

被引:2
|
作者
Jojima, Kota [1 ]
Tanaka, Atsushi [1 ]
Node, Koichi [1 ]
机构
[1] Saga Univ, Dept Cardiovasc Med, Saga, Japan
关键词
Primary aldosteronism; Aldosterone-producing adenoma; KCNJ5; Endothelial function; Vascular failure; ADENOMA;
D O I
10.1038/s41440-023-01428-2
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
引用
收藏
页码:2547 / 2550
页数:4
相关论文
共 50 条
  • [31] Double CYP11B1/CYP11B2 Immunohistochemistry and Detection of KCNJ5 Mutations in Primary Aldosteronism
    Caroccia, Brasilina
    Lenzini, Livia
    Ceolotto, Giulio
    Gioco, Francesca
    Benetti, Andrea
    Giannella, Alessandra
    Ajjour, Hala
    Galuppini, Francesca
    Pennelli, Gianmaria
    Seccia, Teresa Maria
    Gomez-Sanchez, Celso
    Rossi, Gian Paolo
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2024, 109 (10): : 2433 - 2443
  • [32] NEW GERM-LINE MUTATIONS AND A RARE CODING SNP WITHIN KCNJ5 IN "APPARENTLY SPORADIC" PRIMARY ALDOSTERONISM: A POSSIBLE ROLE IN PATHOGENESIS
    Xu, S.
    Murthy, M.
    Massimo, G.
    Wolley, M.
    Gordon, R. D.
    Stowasser, M.
    O'Shaughnessy, K.
    HYPERTENSION, 2014, 63 (06) : E142 - E143
  • [33] NP-59 Adrenal Scintigraphy as an Imaging Biomarker to Predict KCNJ5 Mutation in Primary Aldosteronism Patients
    Lu, Ching-Chu
    Yen, Ruoh-Fang
    Peng, Kang-Yung
    Huang, Jei-Yie
    Wu, Kwan-Dun
    Chueh, Jeff S.
    Lin, Wan-Yu
    FRONTIERS IN ENDOCRINOLOGY, 2021, 12
  • [34] DISCOVERY OF A NEW DRUG FOR PRIMARY ALDOSTERONISM TARGETING THE CYP11B2 AND KCNJ5 MUTANTS
    Otsubo, Yuri
    Shimada, Hiroki
    Nakamura, Yasuhiro
    Yokoyama, Atsushi
    Sugawara, Akira
    JOURNAL OF HYPERTENSION, 2023, 41 : E177 - E177
  • [35] Role for Germline Mutations and a Rare Coding Single Nucleotide Polymorphism Within the KCNJ5 Potassium Channel in a Large Cohort of Sporadic Cases of Primary Aldosteronism
    Murthy, Meena
    Xu, Shengxin
    Massimo, Gianmichele
    Wolley, Martin
    Gordon, Richard D.
    Stowasser, Michael
    O'Shaughnessy, Kevin M.
    HYPERTENSION, 2014, 63 (04) : 783 - 789
  • [36] Functional characterization of two novel germline mutations of the KCNJ5 gene in hypertensive patients without primary aldosteronism but with ACTH-dependent aldosterone hypersecretion
    Sertedaki, Amalia
    Markou, Athina
    Vlachakis, Dimitrios
    Kossida, Sophia
    Campanac, Emilie
    Hoffman, Dax A.
    Sierra, Maria De La Luz
    Xekouki, Paraskevi
    Stratakis, Constantine A.
    Kaltsas, Gregory
    Piaditis, George P.
    Chrousos, George P.
    Charmandari, Evangelia
    CLINICAL ENDOCRINOLOGY, 2016, 85 (06) : 845 - 851
  • [37] KCNJ5 gene somatic mutations affect cardiac remodelling but do not preclude cure of high blood pressure and regression of left ventricular hypertrophy in primary aldosteronism
    Rossi, Gian Paolo
    Cesari, Maurizio
    Letizia, Claudio
    Seccia, Teresa M.
    Cicala, Maria Verena
    Zinnamosca, Laura
    Kuppusamy, Maniselvan
    Mareso, Sara
    Sciomer, Susanna
    Iacobone, Maurizio
    Mantero, Franco
    Pessina, Achille C.
    JOURNAL OF HYPERTENSION, 2014, 32 (07) : 1514 - 1522
  • [38] PHEOCHROMOCYTOMA WITH HYPERALDOSTERONISM-LINKED MUTATIONS IN THE POTASSIUM CHANNEL KCNJ5
    Mai, Xurong
    Kometani, Mitsuhiro
    Kato, Toshiaki
    Mori, Shunsuke
    Aono, Daisuke
    Konishi, Seigo
    Karashima, Shigehiro
    Takeda, Yoshiyu
    Yoneda, Mau
    Furukawa, Kenji
    Yoneda, Takashi
    JOURNAL OF HYPERTENSION, 2023, 41 : E345 - E345
  • [39] Characteristics of Japanese aldosterone-producing adenomas with KCNJ5 mutations
    Okamura, Takashi
    Nakajima, Yasuyo
    Katano-Toki, Akiko
    Horiguchi, Kazuhiko
    Matsumoto, Shunichi
    Yoshino, Satoshi
    Yamada, Eijiro
    Tomaru, Takuya
    Ishii, Sumiyasu
    Saito, Tsugumichi
    Ozawa, Atsushi
    Shibusawa, Nobuyuki
    Satoh, Tetsurou
    Okada, Shuichi
    Nagaoka, Rin
    Takada, Daisuke
    Horiguchi, Jun
    Oyama, Tetsunari
    Yamada, Masanobu
    ENDOCRINE JOURNAL, 2017, 64 (01) : 39 - 47
  • [40] KCNJ5 Mutations in European Families With Nonglucocorticoid Remediable Familial Hyperaldosteronism
    Mulatero, Paolo
    Tauber, Philipp
    Zennaro, Maria-Christina
    Monticone, Silvia
    Lang, Katharina
    Beuschlein, Felix
    Fischer, Evelyn
    Tizzani, Davide
    Pallauf, Anna
    Viola, Andrea
    Amar, Laurence
    Williams, Tracy Ann
    Strom, Tim M.
    Graf, Elisabeth
    Bandulik, Sascha
    Penton, David
    Plouin, Pierre-Francois
    Warth, Richard
    Allolio, Bruno
    Jeunemaitre, Xavier
    Veglio, Franco
    Reincke, Martin
    HYPERTENSION, 2012, 59 (02) : 235 - +