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N-terminal Pro-B type Natriutetic Peptide is a significant Biochemical Predictor of Computed Tomograpic Angiography Evidence of Right Ventricular Dysfunction
전남대학교병원 순환기내과¹ , 방사선과²
이우석¹, 김계훈¹, 선현주², 윤현주¹ , 윤남식¹, 문재연¹, 홍영준¹, 박형욱¹, 김주한¹, 안영근¹, 김윤현², 정명호¹, 조정관¹, 박종춘¹, 강정채¹
Backgroud and Objectives Right ventricular (RV) dysfunction and some biochemical markers were used in the risk stratification of acute pulmonary thromboembolism (PTE). The aim of this study was to investigate the relation between computed tomographic angiographic (CTA) evidence of RV dysfunction and risk-related biochemical markers in patients with acute PTE. Methods A total of 82 patients with acute PTE were divided into two groups by CTA evidence of RV dysfunction; the patients with RV dysfunction (group I, n=49, 63.0±15.2 years, 32 females) versus the patients without RV dysfunction (group II, n=33, 65.8±14.0 years, 19 females). Biochemical markers such as N-terminal pro B type natriuretic peptide (NT-proBNP), cardiac enzymes, high sensitivity C-reactive protein (hsCRP), and D-dimer were measured and analyzed between the groups. Results The levels of biochemical markers were as follows; 3922.22±4192.86 pg/ml in NT-proBNP, 0.09±0.21 ng/mL in cardiac-specific troponin T (cTnt), 0.68±2.17 ng/mL in cardiac-specific troponin I (cTni), 119.91±131.20 U/L in creatine kinase (CK), 8.65±8.34 U/L in MB fraction of CK, 4.15±5.20 mg/dL in hsCRP, and 1.61±2.29 mg/L in D-dimer. The level of NT-proBNP was significantly higher in group I than in group II (5334.72±6867.46 vs 1685.19±4144.02 pg/mL, p= 0.015). However, the other biochemical markers were not different between the groups. By receiver operation curve analysis, the optimal cut-off value of NT-proBNP to predict CTA based RV dysfunction was 731.75 pg/mL (sensitivity: 80.6%, specificity: 76.2%). Conclusion The results of this study demonstrated that NT-proBNP is a strong biochemical predictor of RV dysfunction by CTA. NT-proBNP may be used as a simple and available biochemical marker in the risk stratification of acute PTE.


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