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Usefulness of S100A12 as a prognostic biomarker for adverse events in patients with heart failure.
He, Yun-Yun; Yan, Wei; Liu, Chun-Lei; Li, Xin; Li, Rui-Jun; Mu, Yang; Jia, Qian; Wu, Fen-Fen; Wang, Li-Li; He, Kun-Lun.
Afiliação
  • He YY; Department of Cardiology, Chinese PLA General Hospital, Beijing China; School of Medicine, Nankai University, Tianjin China.
  • Yan W; Department of Cardiology, Chinese PLA General Hospital, Beijing China.
  • Liu CL; Department of Cardiology, Chinese PLA General Hospital, Beijing China.
  • Li X; Department of Cardiology, Chinese PLA General Hospital, Beijing China.
  • Li RJ; Department of Cardiology, Chinese PLA General Hospital, Beijing China.
  • Mu Y; Department of Cardiology, Chinese PLA General Hospital, Beijing China; School of Medicine, Nankai University, Tianjin China.
  • Jia Q; Department of Cardiology, Chinese PLA General Hospital, Beijing China; School of Medicine, Nankai University, Tianjin China.
  • Wu FF; Department of Cardiology, Chinese PLA General Hospital, Beijing China.
  • Wang LL; Beijing Institute of Pharmacology and Toxicology, Beijing China. Electronic address: wangll63@126.com.
  • He KL; Department of Cardiology, Chinese PLA General Hospital, Beijing China. Electronic address: hekl301@aliyun.com.
Clin Biochem ; 48(4-5): 329-33, 2015 Mar.
Article em En | MEDLINE | ID: mdl-25438075
ABSTRACT

OBJECTIVES:

S100A12 has been proposed as a novel pivotal factor in inflammation produced by granulocytes. The purpose of this study was to investigate the relationship between S100A12 and chronic heart failure (CHF). DESIGN AND

METHODS:

One hundred and seventy-seven patients with CHF and 66 subjects without CHF were included in this study. Plasma levels of S100A12 and high-sensitivity C-reactive protein (hs-CRP) were measured in all participants. After a follow-up period of 18months for CHF patients, major cardiovascular events (MCE), including cardiac death and rehospitalization for heart failure, were recorded.

RESULTS:

Plasma levels of S100A12 were significantly higher in CHF patients than in control subjects (P<0.001) and positively correlated with hs-CRP (r=0.316, P<0.001). S100A12 levels were also higher in MCE patients than in MCE-free patients. The occurrence of MCE increased with advancing plasma S100A12 levels by stratification according to quartiles (Q4 vs Q1, P=0.015). Cox proportional hazards regression analysis revealed that S100A12 was an independent risk factor for MCE in CHF patients (P=0.009).

CONCLUSIONS:

S100A12 is a potential biomarker of CHF that may provide important information regarding the prediction of MCE in patients with CHF.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína S100A12 / Insuficiência Cardíaca Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína S100A12 / Insuficiência Cardíaca Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article