Department of Medical Sciences, Cardiology, Uppsala University, Uppsala, Sweden; Uppsala Clinical Research Center, Uppsala University, Uppsala, Sweden.
Uppsala Clinical Research Center, Uppsala University, Uppsala, Sweden.
J Am Coll Cardiol. 2017 Aug 15;70(7):813-826. doi: 10.1016/j.jacc.2017.06.030.
Currently, there is no generally accepted model to predict outcomes in stable coronary heart disease (CHD).
This study evaluated and compared the prognostic value of biomarkers and clinical variables to develop a biomarker-based prediction model in patients with stable CHD.
In a prospective, randomized trial cohort of 13,164 patients with stable CHD, we analyzed several candidate biomarkers and clinical variables and used multivariable Cox regression to develop a clinical prediction model based on the most important markers. The primary outcome was cardiovascular (CV) death, but model performance was also explored for other key outcomes. It was internally bootstrap validated, and externally validated in 1,547 patients in another study.
During a median follow-up of 3.7 years, there were 591 cases of CV death. The 3 most important biomarkers were N-terminal pro-B-type natriuretic peptide (NT-proBNP), high-sensitivity cardiac troponin T (hs-cTnT), and low-density lipoprotein cholesterol, where NT-proBNP and hs-cTnT had greater prognostic value than any other biomarker or clinical variable. The final prediction model included age (A), biomarkers (B) (NT-proBNP, hs-cTnT, and low-density lipoprotein cholesterol), and clinical variables (C) (smoking, diabetes mellitus, and peripheral arterial disease). This "ABC-CHD" model had high discriminatory ability for CV death (c-index 0.81 in derivation cohort, 0.78 in validation cohort), with adequate calibration in both cohorts.
This model provided a robust tool for the prediction of CV death in patients with stable CHD. As it is based on a small number of readily available biomarkers and clinical factors, it can be widely employed to complement clinical assessment and guide management based on CV risk. (The Stabilization of Atherosclerotic Plaque by Initiation of Darapladib Therapy Trial [STABILITY]; NCT00799903).
目前,尚无普遍接受的模型来预测稳定性冠心病(CHD)患者的结局。
本研究评估和比较了生物标志物和临床变量的预后价值,以建立一种基于生物标志物的稳定性 CHD 患者预测模型。
在一项前瞻性、随机临床试验队列中,纳入了 13164 例稳定性 CHD 患者,我们分析了多个候选生物标志物和临床变量,并使用多变量 Cox 回归来基于最重要的标志物建立临床预测模型。主要结局是心血管(CV)死亡,但也对其他关键结局探索了模型性能。对其进行了内部 bootstrap 验证,并在另一项研究的 1547 例患者中进行了外部验证。
在中位随访 3.7 年期间,有 591 例发生 CV 死亡。3 个最重要的生物标志物是 N 末端 pro-B 型利钠肽(NT-proBNP)、高敏心肌肌钙蛋白 T(hs-cTnT)和低密度脂蛋白胆固醇,其中 NT-proBNP 和 hs-cTnT 比任何其他生物标志物或临床变量都具有更大的预后价值。最终的预测模型包括年龄(A)、生物标志物(B)(NT-proBNP、hs-cTnT 和低密度脂蛋白胆固醇)和临床变量(C)(吸烟、糖尿病和外周动脉疾病)。这种“ABC-CHD”模型对 CV 死亡具有较高的区分能力(推导队列中的 c 指数为 0.81,验证队列中的 c 指数为 0.78),并且在两个队列中都具有良好的校准。
该模型为稳定性 CHD 患者 CV 死亡的预测提供了一种可靠的工具。由于它基于少数易于获得的生物标志物和临床因素,因此可以广泛用于补充临床评估,并根据 CV 风险指导管理。(起始用达拉帕利治疗稳定动脉粥样硬化斑块试验[STABILITY];NCT00799903)。