Center for Thrombosis and Hemostasis (CTH), University Medical Center Mainz, Johannes Gutenberg University of Mainz, Germany; Department of Cardiology and Pulmonology, Heart Center of the Georg August University of Göttingen, Germany.
Thromb Res. 2013 Nov;132(5):543-7. doi: 10.1016/j.thromres.2013.09.022. Epub 2013 Sep 24.
Heart-type fatty acid-binding protein (H-FABP) is a useful biomarker for risk stratification of patients with pulmonary embolism (PE). In patients with acute myocardial infarction, H-FABP plasma concentrations rise after 30 minutes and return to normal within 20-24 hours. We tested whether the predictive value of H-FABP is affected by the duration of symptoms prior to diagnosis in patients with PE.
We prospectively studied 257 consecutive normotensive patients with confirmed symptomatic PE.
Patients with acute (<24 hours; n=150) symptom onset presented more often with syncope (28.7% vs. 6.5%; p<0.001) compared to patients with symptoms ≥ 24 hours (n=107); other baseline characteristics, comorbidities, and risk factors were distributed equally. Patients with an adverse 30-day outcome (6.6%) had higher H-FABP levels (11.84 [3.57-19.62] ng/ml) compared to patients with a favorable course (3.42 [1.92-5.42] ng/ml; p<0.001). However, the proportion of patients with H-FABP levels ≥ 6 ng/ml did not differ among patients with acute symptom onset and late presentation (p=0.104). Only tachycardia and elevation of H-FABP were associated with an increased risk of an adverse 30-day outcome both in patients with acute symptom onset (H-FABP: OR, 5.8; 95% CI, 1.4-24.5; p=0.016; tachycardia: 7.0 [1.4-36.0]; p=0.018) and late presentation (H-FABP: 9.3 [2.0-43.2]; p=0.004 and tachycardia: 12.3 [1.5-103.6]; p=0.021). The prognostic value could further be improved by the use of a simple H-FABP-based clinical prediction score.
Our findings indicate that H-FABP is a useful biomarker for risk stratification of normotensive patients with PE regardless of symptom duration prior to diagnosis.
心脏型脂肪酸结合蛋白(H-FABP)是一种有用的生物标志物,可用于肺栓塞(PE)患者的风险分层。在急性心肌梗死患者中,H-FABP 血浆浓度在 30 分钟后升高,并在 20-24 小时内恢复正常。我们检测了 H-FABP 的预测价值是否受 PE 患者诊断前症状持续时间的影响。
我们前瞻性研究了 257 例连续确诊的有症状的 PE 患者。
急性(<24 小时;n=150)症状发作的患者更常出现晕厥(28.7%比 6.5%;p<0.001),而症状持续时间≥24 小时(n=107)的患者则较少出现晕厥;其他基线特征、合并症和危险因素分布均匀。30 天不良预后(6.6%)的患者 H-FABP 水平较高(11.84[3.57-19.62]ng/ml),而预后良好的患者 H-FABP 水平较低(3.42[1.92-5.42]ng/ml;p<0.001)。然而,急性症状发作和晚期表现患者中 H-FABP 水平≥6ng/ml 的患者比例无差异(p=0.104)。只有心动过速和 H-FABP 升高与急性症状发作(H-FABP:OR,5.8;95%CI,1.4-24.5;p=0.016;心动过速:7.0[1.4-36.0];p=0.018)和晚期表现(H-FABP:9.3[2.0-43.2];p=0.004 和心动过速:12.3[1.5-103.6];p=0.021)的 30 天不良预后风险增加相关。通过使用简单的基于 H-FABP 的临床预测评分,可以进一步提高预后价值。
无论诊断前症状持续时间如何,H-FABP 都是一种有用的生物标志物,可用于对 PE 血压正常患者进行风险分层。