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Soluble fibrin monomer complex is associated with cardio- and cerebrovascular events in patients with heart failure.
Yoshihisa, Akiomi; Sato, Yu; Kimishima, Yusuke; Ichijo, Yasuhiro; Yokokawa, Tetsuro; Misaka, Tomofumi; Sato, Takamasa; Oikawa, Masayoshi; Kobayashi, Atsushi; Nakazato, Kazuhiko; Takeishi, Yasuchika.
Afiliação
  • Yoshihisa A; Department of Cardiovascular Medicine, Fukushima Medical University, Fukushima, Japan.
  • Sato Y; Department of Cardiovascular Medicine, Fukushima Medical University, Fukushima, Japan.
  • Kimishima Y; Department of Cardiovascular Medicine, Fukushima Medical University, Fukushima, Japan.
  • Ichijo Y; Department of Cardiovascular Medicine, Fukushima Medical University, Fukushima, Japan.
  • Yokokawa T; Department of Cardiovascular Medicine, Fukushima Medical University, Fukushima, Japan.
  • Misaka T; Department of Cardiovascular Medicine, Fukushima Medical University, Fukushima, Japan.
  • Sato T; Department of Cardiovascular Medicine, Fukushima Medical University, Fukushima, Japan.
  • Oikawa M; Department of Cardiovascular Medicine, Fukushima Medical University, Fukushima, Japan.
  • Kobayashi A; Department of Cardiovascular Medicine, Fukushima Medical University, Fukushima, Japan.
  • Nakazato K; Department of Cardiovascular Medicine, Fukushima Medical University, Fukushima, Japan.
  • Takeishi Y; Department of Cardiovascular Medicine, Fukushima Medical University, Fukushima, Japan.
Int J Cardiol Heart Vasc ; 32: 100697, 2021 Feb.
Article em En | MEDLINE | ID: mdl-33392385
ABSTRACT

BACKGROUND:

A biomarker of fibrin formation, the soluble fibrin monomer complex (SFMC), is abnormally elevated in a variety of clinical situations of hypercoagulability. The aim of the present study was to examine the prognostic impact of SFMC, with regard to increased risk of major cardio- and cerebrovascular events (MACCE) and all-cause mortality, on patients with heart failure (HF). METHODS AND

RESULTS:

We conducted a prospective observational study where we analyzed data of 723 hospitalized patients with decompensated HF who were discharged alive and whose SFMC had been measured in a stable condition prior to discharge. The patients were divided into tertiles based on SFMC levels the first (SFMC < 1.7 µg/ml, n = 250), second (≤1.8 SFMC < 2.9 µg/ml, n = 233), and third (3.0 µg/ml ≤ SFMC, n = 240) tertiles. The prevalence of chronic kidney disease and anemia was significantly higher in the third tertile than in the first and second tertiles. In contrast, age, sex, CHADS2-Vasc score, left ventricular ejection fraction, and prevalence of hypertension, diabetes and atrial fibrillation did not differ among the tertiles. In the Kaplan-Meier analysis, accumulated event rates of both MACCE and all-cause mortality progressively increased from the first to third tertiles (log-rank P < 0.05, respectively). In the multivariate Cox proportional hazard analysis, the third tertile was found to be an independent predictor of MACCE (HR 2.014, P = 0.046) and all-cause mortality (HR 1.792, P = 0.036).

CONCLUSION:

SFMC is an independent predictor of adverse prognosis in patients with HF.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article