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Soluble Urokinase Plasminogen Activator Receptor Levels and Outcomes in Patients with Heart Failure.
Hayek, Salim S; Tahhan, Ayman Samman; Ko, Yi-An; Alkhoder, Ayman; Zheng, Shuai; Bhimani, Ravila; Hartsfield, Joy; Kim, Jonathan; Wilson, Peter; Shaw, Leslee; Wei, Changli; Reiser, Jochen; Quyyumi, Arshed A.
Afiliação
  • Hayek SS; Division of Cardiology, University of Michigan, Ann Arbor, MI. Electronic address: shayek@med.umich.edu.
  • Tahhan AS; Division of Cardiology, Emory University School of Medicine, Atlanta, GA.
  • Ko YA; Division of Cardiology, Emory University School of Medicine, Atlanta, GA.
  • Alkhoder A; Division of Cardiology, Emory University School of Medicine, Atlanta, GA.
  • Zheng S; Department of Biostatistics and Bioinformatics, Emory University, Atlanta, GA.
  • Bhimani R; Division of Cardiology, Emory University School of Medicine, Atlanta, GA.
  • Hartsfield J; Division of Cardiology, Emory University School of Medicine, Atlanta, GA.
  • Kim J; Division of Cardiology, Emory University School of Medicine, Atlanta, GA.
  • Wilson P; Division of Cardiology, Emory University School of Medicine, Atlanta, GA.
  • Shaw L; Division of Cardiology, Emory University School of Medicine, Atlanta, GA.
  • Wei C; Department of Medicine, Rush University, Chicago, IL.
  • Reiser J; Department of Medicine, Rush University, Chicago, IL.
  • Quyyumi AA; Division of Cardiology, Emory University School of Medicine, Atlanta, GA.
J Card Fail ; 29(2): 158-167, 2023 02.
Article em En | MEDLINE | ID: mdl-36122818
ABSTRACT

BACKGROUND:

Soluble urokinase-type plasminogen activator receptor (suPAR) is a marker of immune activation and pathogenic factor for kidney disease shown to predict cardiovascular outcomes including heart failure (HF) in various populations. We characterized suPAR levels in patients with HF and compared its ability to discriminate risk to that of B-type natriuretic peptide (BNP). METHODS AND

RESULTS:

We measured plasma suPAR and BNP levels in 3,437 patients undergoing coronary angiogram and followed for a median of 6.2 years. We performed survival analyses for the following

outcomes:

all-cause death, cardiovascular death, and hospitalization for HF. We then assessed suPAR's ability to discriminate risk for the aforementioned outcomes. We identified 1116 patients with HF (age 65±12, 67.2% male, 20.0% Black, 67% with reduced ejection fraction). The median suPAR level was higher in HF compared to those without HF (3370 [IQR 2610-4371] vs. 2880 [IQR 2270-3670] pg/mL, respectively, P<0.001). In patients with HF, suPAR levels (log-base 2) were associated with outcomes including all-cause death (adjusted hazard ratio aHR 2.30, 95%CI[1.90-2.77]), cardiovascular death (aHR 2.33 95%CI[1.81-2.99]) and HF hospitalization (aHR 1.96, 95%CI[1.06-1.25]) independently of clinical characteristics and BNP levels. The association persisted across subgroups and did not differ between patients with reduced or preserved ejection fraction, or those with ischemic or non-ischemic cardiomyopathy. Addition of suPAR to a model including BNP levels significantly improved the C-statistic for death (Δ0.027), cardiovascular death (Δ0.017) and hospitalization for HF (Δ0.017).

CONCLUSIONS:

SuPAR levels are higher in HF compared to non-HF, are strongly predictive of outcomes, and combined with BNP, significantly improved risk prediction.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Cardíaca / Nefropatias Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Cardíaca / Nefropatias Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article