Risk Stratification of Chronic Heart Failure Patients by Multiple Biomarkers Implications of BNP, H-FABP, and PTX3
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- Ishino Mitsunori
- Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine
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- Takeishi Yasuchika
- First Department of Internal Medicine, Fukushima Medical University
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- Niizeki Takeshi
- Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine
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- Watanabe Tetsu
- Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine
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- Nitobe Joji
- Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine
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- Miyamoto Takuya
- Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine
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- Miyashita Takehiko
- Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine
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- Kitahara Tatsuro
- Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine
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- Suzuki Satoshi
- Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine
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- Sasaki Toshiki
- Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine
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- Bilim Olga
- Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine
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- Kubota Isao
- Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine
書誌事項
- タイトル別名
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- Implications of BNP, H-FABP, and PTX3
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Background B-type natriuretic peptide (BNP), heart-type fatty acid-binding protein (H-FABP), and pentraxin 3 (PTX3) each predict adverse cardiac events in chronic heart failure (CHF) patients. For prognostic evaluation from different aspects, the utility of combined measurement of the 3 biomarkers in patients with CHF was examined in the present study. Methods and Results Levels of BNP (associated with left ventricular dysfunction, positive if >200 pg/ml), H-FABP (marker of myocardial damage, positive if >4.1 ng/ml), and PTX3 (marker of inflammation, positive if >4.0 ng/ml) were measured in 164 consecutive CHF patients, and patients were prospectively followed with endpoints of cardiac death or rehospitalization. When patients were categorized on the basis of the number of elevated biomarkers, patients with 1, 2, and 3 elevated biomarkers had a 5.4-fold (not significant), 11.2-old (p<0.05), and 34.6-fold increase (p<0.01), respectively, in the risk of adverse cardiac events compared with those without elevated biomarkers. Kaplan-Meier analysis revealed that patients with 3 elevated biomarkers had a significantly higher cardiac event rate than patients with a lower number of elevated biomarkers. Conclusion The combination of these 3 biomarkers could reliably risk-stratify CHF patients for prediction of cardiac events. (Circ J 2008; 72: 1800 - 1805)<br>
収録刊行物
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- Circulation Journal
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Circulation Journal 72 (11), 1800-1805, 2008
一般社団法人 日本循環器学会
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詳細情報 詳細情報について
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- CRID
- 1390001205103188480
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- NII論文ID
- 110006975572
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- NII書誌ID
- AA11591968
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- ISSN
- 13474820
- 13469843
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- 本文言語コード
- en
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- データソース種別
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- JaLC
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