Carré Julie, Demont Yohann, Mouton Christine, Vayne Caroline, Guéry Eve-Anne, Voyer Annelise, Garçon Loïc, Le Guyader Maïlys, Demagny Julien
Service d'Hématologie Biologique, CHU Amiens-Picardie, Amiens, France.
Laboratoire d'Hématologie, Hôpital Haut-Lévêque, CHU Bordeaux, Bordeaux, France.
Br J Haematol. 2025 Feb;206(2):666-674. doi: 10.1111/bjh.19945. Epub 2024 Dec 10.
Heparin-induced thrombocytopenia (HIT) is an adverse reaction characterized by anti-PF4-heparin antibody generation and hypercoagulability. Imaging flow cytometry (IFC) provides a detailed morphological analysis of platelets, which change upon activation. We evaluated IFC-derived morphometric features to detect platelet activation and developed a functional assay for HIT diagnosis. We analysed blood samples from 42 patients with suspected HIT and extracted platelet size, shape and texture features using IFC. The morphological features were compared with CD62P expression, light transmission aggregometry (LTA) and a serotonin release assay (SRA) in terms of their ability to predict a HIT diagnosis. Five IFC-derived morphological features (area, circularity, contrast, diameter and major axis) significantly distinguished resting from activated platelets. The major axis feature performed best for HIT diagnosis, with a sensitivity of 89.3% and a specificity of 92.9% versus functional assays (LTA/SRA); this diagnostic performance was similar to that of CD62P expression on the same platelet donors. The area and diameter had similar specificity (92.9%) and a slightly lower sensitivity (85.7%). The morphological features associated with platelet activation might be effective markers for the diagnosis of HIT, matching platelet CD62P expression assay performance. The high-throughput IFC exploration of platelet activation offers new perspectives in label-free analysis and time-saving.
肝素诱导的血小板减少症(HIT)是一种以抗PF4-肝素抗体产生和高凝性为特征的不良反应。成像流式细胞术(IFC)可对激活时发生变化的血小板进行详细的形态学分析。我们评估了源自IFC的形态计量学特征以检测血小板激活,并开发了一种用于HIT诊断的功能测定方法。我们分析了42例疑似HIT患者的血样,并使用IFC提取了血小板的大小、形状和纹理特征。在预测HIT诊断的能力方面,将这些形态学特征与CD62P表达、透光聚集试验(LTA)和5-羟色胺释放试验(SRA)进行了比较。源自IFC的五个形态学特征(面积、圆形度、对比度、直径和长轴)显著区分了静息血小板和激活血小板。长轴特征在HIT诊断中表现最佳,与功能测定(LTA/SRA)相比,灵敏度为89.3%,特异性为92.9%;这种诊断性能与同一血小板供体上的CD62P表达相似。面积和直径具有相似的特异性(92.9%),灵敏度略低(85.7%)。与血小板激活相关的形态学特征可能是诊断HIT的有效标志物,与血小板CD62P表达测定性能相当。对血小板激活进行高通量IFC探索为无标记分析和节省时间提供了新的视角。