Validation of a novel scoring tool for assessment of the severity of coronary disease and ischaemia burden to predict major adverse cardiac events at 5 years in the 3V-FFR FRIENDS population.
Mohamed Kira, Hussein Bashar, Lavinia Gabara, Mohamed Aboulassad, Ahmed Elserwey, Pamela S Douglas, Nicholas Ng, Sang-Hyeon Park, Bon-Kwon Koo, Nick Curzen
{"title":"Validation of a novel scoring tool for assessment of the severity of coronary disease and ischaemia burden to predict major adverse cardiac events at 5 years in the 3V-FFR FRIENDS population.","authors":"Mohamed Kira, Hussein Bashar, Lavinia Gabara, Mohamed Aboulassad, Ahmed Elserwey, Pamela S Douglas, Nicholas Ng, Sang-Hyeon Park, Bon-Kwon Koo, Nick Curzen","doi":"10.1016/j.carrev.2025.05.030","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Ischaemic heart disease is the most prevalent form of cardiovascular disease (CVD) worldwide and imposes a substantial burden on healthcare systems. Identification of patients at high risk of events in a tailored primary prevention strategy is hindered by relatively blunt risk assessment tools. A novel scoring model that allows for rapid calculation of atheroma and ischaemia burden may facilitate earlier identification of high risk individuals. Our aim was to validate the ability of a novel candidate scoring model (Functional FFR Score 2, FFS2) to predict adverse clinical events, as a proof of concept, by applying it in a cohort of patients in whom coronary artery disease was assessed by means of invasive coronary angiography (ICA) and intracoronary pressure wire.</p><p><strong>Methods: </strong>We retrospectively applied the novel FFS2 to a population of patients in whom there was comprehensive anatomical and physiological data from ICA plus intracoronary measurement of fractional flow reserve (FFR), the 3V-FFR FRIENDS study. The FFS2 includes an anatomical and physiological component, each used to score severity. Receiver operating characteristics (ROC) analysis and area under curve (AUC) were performed for the total FFS2 score, and for its components. The best cut-off value was then used to classify patients into high and low score groups to assess association with updated 5-year major adverse cardiac events (MACE).</p><p><strong>Results: </strong>The FFS2 was applied on 616 patients from the 3V-FFR FRIENDS population, and was associated with MACE up to 5-years follow up (4.9 % Ischaemia-driven revascularisation, 1.6 % myocardial infarction (MI), and 1.3 % cardiac death), when patients were classified into \"high\" and \"low\" risk groups according to the best cut-off value of 11.5 following the initial ROC analysis of the total FFS2 score. The calculated hazard ratio (HR) was 2.87 (95 % CI 1.50-5.49, P = 0.002) for MACE and 3.75 (95 % CI 1.79-7.89, P < 0.001) for the ischaemia-driven revascularisation in the high risk group of patients.</p><p><strong>Conclusion: </strong>The novel FFS2 score, incorporating an assessment of total atheroma and ischaemia burden, is associated with the rate of MACE and ischaemia-driven revascularisation. Further testing of this scoring tool to primary prevention populations is now warranted.</p>","PeriodicalId":47657,"journal":{"name":"Cardiovascular Revascularization Medicine","volume":" ","pages":""},"PeriodicalIF":1.6000,"publicationDate":"2025-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cardiovascular Revascularization Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.carrev.2025.05.030","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Ischaemic heart disease is the most prevalent form of cardiovascular disease (CVD) worldwide and imposes a substantial burden on healthcare systems. Identification of patients at high risk of events in a tailored primary prevention strategy is hindered by relatively blunt risk assessment tools. A novel scoring model that allows for rapid calculation of atheroma and ischaemia burden may facilitate earlier identification of high risk individuals. Our aim was to validate the ability of a novel candidate scoring model (Functional FFR Score 2, FFS2) to predict adverse clinical events, as a proof of concept, by applying it in a cohort of patients in whom coronary artery disease was assessed by means of invasive coronary angiography (ICA) and intracoronary pressure wire.
Methods: We retrospectively applied the novel FFS2 to a population of patients in whom there was comprehensive anatomical and physiological data from ICA plus intracoronary measurement of fractional flow reserve (FFR), the 3V-FFR FRIENDS study. The FFS2 includes an anatomical and physiological component, each used to score severity. Receiver operating characteristics (ROC) analysis and area under curve (AUC) were performed for the total FFS2 score, and for its components. The best cut-off value was then used to classify patients into high and low score groups to assess association with updated 5-year major adverse cardiac events (MACE).
Results: The FFS2 was applied on 616 patients from the 3V-FFR FRIENDS population, and was associated with MACE up to 5-years follow up (4.9 % Ischaemia-driven revascularisation, 1.6 % myocardial infarction (MI), and 1.3 % cardiac death), when patients were classified into "high" and "low" risk groups according to the best cut-off value of 11.5 following the initial ROC analysis of the total FFS2 score. The calculated hazard ratio (HR) was 2.87 (95 % CI 1.50-5.49, P = 0.002) for MACE and 3.75 (95 % CI 1.79-7.89, P < 0.001) for the ischaemia-driven revascularisation in the high risk group of patients.
Conclusion: The novel FFS2 score, incorporating an assessment of total atheroma and ischaemia burden, is associated with the rate of MACE and ischaemia-driven revascularisation. Further testing of this scoring tool to primary prevention populations is now warranted.
背景:缺血性心脏病是世界范围内最常见的心血管疾病(CVD),对卫生保健系统造成了沉重的负担。相对迟钝的风险评估工具阻碍了在量身定制的一级预防策略中识别高危事件患者。一种新的评分模型,允许快速计算动脉粥样硬化和缺血负担可能有助于早期识别高风险个体。我们的目的是验证一种新的候选评分模型(功能性FFR评分2,FFS2)预测不良临床事件的能力,作为概念证明,通过将其应用于通过侵入性冠状动脉造影(ICA)和冠状动脉内压力线评估冠状动脉疾病的患者队列。方法:在3V-FFR FRIENDS研究中,我们回顾性地将新型FFS2应用于具有ICA和冠状动脉内分数血流储备(FFR)测量综合解剖和生理数据的患者群体。FFS2包括解剖学和生理学两部分,分别用于严重程度评分。对FFS2总分及其组成部分进行受试者工作特征(ROC)分析和曲线下面积(AUC)分析。然后使用最佳临界值将患者分为高分组和低分组,以评估与更新的5年主要不良心脏事件(MACE)的关联。结果:FFS2应用于来自3V-FFR FRIENDS人群的616例患者,并与MACE相关长达5年的随访(4.9%缺血驱动的血血重建,1.6%心肌梗死(MI)和1.3%心源性死亡),根据初始FFS2总评分的最佳临界值11.5将患者分为“高”和“低”风险组。计算的MACE风险比(HR)为2.87 (95% CI 1.50-5.49, P = 0.002), 3.75 (95% CI 1.79-7.89), P结论:新的FFS2评分,包括对总动脉粥样硬化和缺血负担的评估,与MACE发生率和缺血驱动的血运重建相关。现在有必要对初级预防人群进一步测试这一评分工具。
期刊介绍:
Cardiovascular Revascularization Medicine (CRM) is an international and multidisciplinary journal that publishes original laboratory and clinical investigations related to revascularization therapies in cardiovascular medicine. Cardiovascular Revascularization Medicine publishes articles related to preclinical work and molecular interventions, including angiogenesis, cell therapy, pharmacological interventions, restenosis management, and prevention, including experiments conducted in human subjects, in laboratory animals, and in vitro. Specific areas of interest include percutaneous angioplasty in coronary and peripheral arteries, intervention in structural heart disease, cardiovascular surgery, etc.