Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine.
Biomedical Instrument Institute, School of Biomedical Engineering, Shanghai Jiao Tong University.
Circ J. 2024 Oct 25;88(11):1809-1818. doi: 10.1253/circj.CJ-24-0480. Epub 2024 Sep 21.
Proprotein convertase subtilisin/kexin type 9 inhibitors stabilize vulnerable plaque, reducing cardiovascular events. However, manual optical coherence tomography (OCT) analysis of drug efficacy is challenging because of signal attenuation within lipid plaques.
Twenty-four patients with thin-cap fibroatheroma were prospectively enrolled and randomized to receive alirocumab (75 mg every 2 weeks) plus rosuvastatin (10 mg/day) or rosuvastatin (10 mg/day) alone. OCT images at baseline and 36 weeks were analyzed manually and with artificial intelligence (AI)-aided software. AI-aided OCT analysis showed significantly greater percentage changes in the alirocumab+rosuvastatin vs. rosuvastatin-alone group in fibrous cap thickness (FCT; median [interquartile range] 212.3% [140.5-253.5%] vs. 88.6% [63.0-119.6%]; P=0.006) and lipid volume (median [interquartile range] -30.8% [-51.8%, -16.6%] vs. -2.1% [-21.6%, 4.3%]; P=0.015). Interobserver reproducibility for changes in minimum FCT and lipid index was relatively low for manual analysis (interobserver intraclass correlation coefficient [ICC] 0.780 and 0.499, respectively), but high for AI-aided analysis (interobserver ICC 0.999 and 1.000, respectively). Agreements between manual and AI-aided OCT analyses of FCT and the lipid index were acceptable (concordance correlation coefficients 0.859 and 0.833, respectively).
AI-aided OCT analysis objectively showed greater plaque stabilization of adding alirocumab to rosuvastatin. Our results highlight the benefits of a fully automated AI-assisted approach for assessing drug efficacy, offering greater objectivity in evaluating serial changes in plaque stability vs. conventional OCT assessment.
前蛋白转化酶枯草溶菌素/克那霉 9 抑制剂可稳定易损斑块,减少心血管事件。然而,由于脂质斑块内信号衰减,药物疗效的手动光学相干断层扫描(OCT)分析具有挑战性。
前瞻性纳入 24 例薄帽纤维粥样瘤患者,并随机分为接受阿利西尤单抗(每 2 周 75mg)加瑞舒伐他汀(10mg/天)或瑞舒伐他汀(10mg/天)单药治疗。基线和 36 周时行手动和人工智能(AI)辅助 OCT 分析。AI 辅助 OCT 分析显示,与瑞舒伐他汀单药组相比,阿利西尤单抗+瑞舒伐他汀组纤维帽厚度(FCT)的百分比变化显著更大(中位数[四分位距]:212.3%[140.5-253.5%] vs. 88.6%[63.0-119.6%];P=0.006)和脂质体积(中位数[四分位距]:-30.8%[-51.8%,-16.6%] vs. -2.1%[-21.6%,4.3%];P=0.015)。手动分析时,最小 FCT 和脂质指数变化的观察者间可重复性相对较低(观察者内组内相关系数分别为 0.780 和 0.499),但 AI 辅助分析时较高(观察者内 ICC 分别为 0.999 和 1.000)。FCT 和脂质指数的手动和 AI-OCT 分析之间的一致性较好(一致性相关系数分别为 0.859 和 0.833)。
AI 辅助 OCT 分析客观地显示,在瑞舒伐他汀基础上加用阿利西尤单抗可更好地稳定斑块。我们的结果强调了完全自动化 AI 辅助方法在评估药物疗效方面的优势,与传统 OCT 评估相比,该方法在评估斑块稳定性的连续变化方面提供了更大的客观性。