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Clinical Chemistry 49: 2020-2026, 2003. First published November 13, 2003; 10.1373/clinchem.2003.021311
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Right arrow Proteomics and Protein Markers
(Clinical Chemistry. 2003;49:2020-2026.)
© 2003 American Association for Clinical Chemistry, Inc.


Proteomics and Protein Markers

Prognostic Value of Combination of Cardiac Troponin T and B-Type Natriuretic Peptide after Initiation of Treatment in Patients with Chronic Heart Failure

Junnichi Ishii1,a, Wei Cui2, Fumihiko Kitagawa3, Takahiro Kuno3, Yuu Nakamura2, Hiroyuki Naruse2, Yoshihisa Mori2, Takashi Ishikawa3, Youichi Nagamura4, Takeshi Kondo2, Hisaji Oshima3, Masanori Nomura2, Kouji Ezaki2 and Hitoshi Hishida2

1 Division of Critical Care, Fujita Health University Graduate School of Health Sciences, 2 Department of Internal Medicine, Fujita Health University School of Medicine, 3 Department of Joint Research Laboratory of Clinical Medicine, Fujita Health University Hospital, and 4 Department of Clinical Chemistry, Fujita Health University School of Health Sciences, Toyoake 470-1192, Japan.

aAddress correspondence to this author at: Division of Critical Care, Fujita Health University Graduate School of Health Sciences, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake 470-1192, Japan. Fax 81-562-93-2315; e-mail jishii{at}fujita-hu.ac.jp.

Background: Recent studies have suggested that cardiac troponin T (cTnT) and troponin I may detect ongoing myocardial damage involved in the progression of chronic heart failure (CHF). This study was prospectively designed to examine whether the combination of cTnT, a marker for ongoing myocardial damage, and B-type natriuretic peptide (BNP), a marker for left ventricular overload, would effectively stratify patients with CHF after initiation of treatment.

Methods: We measured serum cTnT, plasma BNP, and left ventricular ejection fraction (LVEF) on admission for worsening CHF [New York Heart Association (NYHA) functional class III to IV] and 2 months after initiation of treatment to stabilize CHF (n = 100; mean age, 68 years).

Results: Mean (SD) concentrations of cTnT [0.023 (0.066) vs 0.063 (0.20) µg/L] and BNP [249 (276) vs 753 (598) ng/L], percentage increased cTnT (>0.01 µg/L; 35% vs 60%), NYHA functional class [2.5 (0.6) vs 3.5 (5)], and LVEF [43 (13)% vs 36 (12)%] were significantly (P <0.01) improved 2 months after treatment compared with admission. During a mean follow-up of 391 days, there were 44 cardiac events, including 12 cardiac deaths and 32 readmissions for worsening CHF. On a stepwise Cox regression analysis, increased cTnT and BNP were independent predictors of cardiac events (P <0.001). cTnT >0.01 µg/L and/or BNP >160 ng/L 2 months after initiation of treatment were associated with increased cardiac mortality and morbidity rates.

Conclusion: The combination of cTnT and BNP measurements after initiation of treatment may be highly effective for risk stratification in patients with CHF.




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