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Cardiovascular Outcomes of KCNJ5 Mutated Aldosterone-Producing Adenoma: A Systematic Review.
Kato, Hajime; Kitamoto, Takumi; Kimura, Soichiro; Sunouchi, Takashi; Hoshino, Yoshitomo; Hidaka, Naoko; Tsurutani, Yuya; Ito, Nobuaki; Makita, Noriko; Nishikawa, Tetsuo; Nangaku, Masaomi; Inoue, Kosuke.
Afiliação
  • Kato H; Division of Nephrology and Endocrinology, The University of Tokyo Hospital, Tokyo, Japan. Electronic address: hajkatoh@gmail.com.
  • Kitamoto T; Department of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine, Chiba, Japan.
  • Kimura S; Division of Nephrology and Endocrinology, The University of Tokyo Hospital, Tokyo, Japan.
  • Sunouchi T; Division of Nephrology and Endocrinology, The University of Tokyo Hospital, Tokyo, Japan.
  • Hoshino Y; Division of Nephrology and Endocrinology, The University of Tokyo Hospital, Tokyo, Japan.
  • Hidaka N; Division of Nephrology and Endocrinology, The University of Tokyo Hospital, Tokyo, Japan.
  • Tsurutani Y; Endocrinology and Diabetes Center, Yokohama Rosai Hospital, Yokohama, Japan.
  • Ito N; Division of Nephrology and Endocrinology, The University of Tokyo Hospital, Tokyo, Japan.
  • Makita N; Division of Nephrology and Endocrinology, The University of Tokyo Hospital, Tokyo, Japan.
  • Nishikawa T; Endocrinology and Diabetes Center, Yokohama Rosai Hospital, Yokohama, Japan.
  • Nangaku M; Division of Nephrology and Endocrinology, The University of Tokyo Hospital, Tokyo, Japan.
  • Inoue K; Department of Social Epidemiology, Graduate School of Medicine, Kyoto University, Kyoto, Japan; Hakubi Center, Kyoto University, Kyoto, Japan.
Endocr Pract ; 30(7): 670-678, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38657793
ABSTRACT

BACKGROUND:

While clinical features of KCNJ5-mutated aldosterone-producing adenoma (APA) have been reported, evidence of its clinical outcomes is lacking. We aimed to synthesize available literature about the associations between KCNJ5 mutation with cardiovascular and metabolic outcomes among patients with APA.

METHODS:

In this systematic review of observational studies, MEDLINE and Embase were searched through August 2022. Two independent authors screened the search results and extracted data from eligible observational studies investigating cardiovascular or metabolic outcomes between KCNJ5-mutated APAs and KCNJ5-non-mutated APAs. Risk of Bias In Non-randomized Studies of Interventions was used to assess the quality of the included studies.

RESULTS:

A total of 573 titles/abstracts were screened and after the expert opinion of the literature, full text was read in 20 titles/abstracts, of which 12 studies were included. Across 3 studies comparing the baseline or change in the cardiac function between KCNJ5-mutated APAs and KCNJ5-non-mutated APAs, all studies reported the association between impaired cardiac functions and KCNJ5 mutation status. Among 6 studies evaluating the cure of hypertension after surgery, all studies showed that KCNJ5 mutation was significantly associated with the cure of hypertension. In quality assessment, 7 studies were at serious risk of bias, while the remaining studies were at moderate risk of bias.

CONCLUSIONS:

This systematic review provided evidence of the significant association between KCNJ5 mutation and unfavorable cardiovascular outcomes in patients with primary aldosteronism. Further research is needed to improve the quality of evidence on this topic and elucidate the underlying mechanisms of the potential burden of KCNJ5 mutation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aldosterona / Canais de Potássio Corretores do Fluxo de Internalização Acoplados a Proteínas G / Mutação Limite: Humans Idioma: En Revista: Endocr Pract Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aldosterona / Canais de Potássio Corretores do Fluxo de Internalização Acoplados a Proteínas G / Mutação Limite: Humans Idioma: En Revista: Endocr Pract Ano de publicação: 2024 Tipo de documento: Article