Biomarkers of Thromboelastography Platelet Mapping Predict Hematoma Expansion After Spontaneous Intracerebral Hemorrhage.

IF 8.9 1区 医学 Q1 CLINICAL NEUROLOGY
Stroke Pub Date : 2025-10-01 Epub Date: 2025-07-18 DOI:10.1161/STROKEAHA.125.051447
Kaleigh M Copenhaver, Juliana Silva Pinheiro do Nascimiento, Rajeev K Garg, Fernando D Goldenberg, Harish Shownkeen, Matthew B Potts, Babak S Jahromi, Paul F Lindholm, Andrew M Naidech
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Abstract

Background: Hematoma expansion (HE) is a preventable cause of disability and death in patients with acute intracerebral hemorrhage (ICH). Platelet activity is essential for coagulation, and antiplatelet medications (eg, aspirin, clopidogrel) increase HE risk. General markers of platelet activity are associated with later HE, but specific biomarkers of platelet activity could enhance our understanding. We hypothesized that hemostatic biomarkers of platelet activity would correlate with later HE.

Methods: We conducted a tri-center observational cohort study of spontaneous ICH patients with multiple imaging scans for HE calculation. The thromboelastography 6s Platelet Mapping assay assessed platelet activity with 3 biomarkers: (1) adenosine diphosphate receptor-induced platelet activation, (2) platelet-fibrin network clot strength measured by heparinized kaolin with heparinase, and (3) fibrinogen-only clot strength measured by activator F (ActF). Spearman rank measured the correlation between HE and platelet activity. A linear regression model predicted HE from ActF. We tested whether the relationship between ActF and HE interacted with pre-ICH antiplatelet medication.

Results: Thirty-five patients were included. Eleven (35.48%) took pre-ICH antiplatelet medication. Heparinized kaolin with heparinase negatively correlated with HE (ρ=-0.34, P=0.02), indicating that stronger platelet-fibrin clots were associated with less subsequent HE. ActF's association with HE depended on pre-ICH antiplatelet medication use (interaction P=0.005). More ActF (fibrinogen) was associated with less HE in patients who did not take pre-ICH antiplatelet medication.

Conclusions: Hemostatic biomarkers from the thromboelastography 6s Platelet Mapping assay predicted subsequent HE and may aid in determining neurosurgical need. Strengthening platelet-mediated coagulation may be a target for reducing HE and improving ICH outcomes.

血栓弹性成像血小板定位的生物标志物预测自发性脑出血后血肿扩张。
背景:血肿扩张(HE)是急性脑出血(ICH)患者致残和死亡的可预防原因。血小板活性对凝血至关重要,抗血小板药物(如阿司匹林、氯吡格雷)会增加HE风险。血小板活性的一般标记物与晚期HE相关,但血小板活性的特定生物标记物可以增强我们的认识。我们假设血小板活性的止血生物标志物与晚期HE相关。方法:我们对自发性脑出血患者进行了三中心观察队列研究,并进行了多次影像学扫描以计算HE。血小板弹性描记法通过3种生物标志物评估血小板活性:(1)二磷酸腺苷受体诱导的血小板活化,(2)用肝素酶测定的肝素化高土测定的血小板-纤维蛋白网络凝块强度,(3)用激活剂F (ActF)测定的仅纤维蛋白原凝块强度。Spearman rank测定HE与血小板活性的相关性。用线性回归模型预测了ActF对HE的影响。我们测试了ActF和HE之间的关系是否与ich前抗血小板药物相互作用。结果:纳入35例患者。11例(35.48%)患者接受脑出血前抗血小板药物治疗。肝素酶化高岭土与HE呈负相关(ρ=-0.34, P=0.02),表明血小板-纤维蛋白凝块越强,随后HE越少。ActF与HE的关联依赖于ich前抗血小板药物的使用(相互作用P=0.005)。在未服用脑出血前抗血小板药物的患者中,更多的ActF(纤维蛋白原)与较少的HE相关。结论:血栓弹性图中的止血生物标志物可以预测随后的HE,并可能有助于确定神经外科手术的需要。加强血小板介导的凝血可能是降低HE和改善ICH结果的目标。
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来源期刊
Stroke
Stroke 医学-临床神经学
CiteScore
13.40
自引率
6.00%
发文量
2021
审稿时长
3 months
期刊介绍: Stroke is a monthly publication that collates reports of clinical and basic investigation of any aspect of the cerebral circulation and its diseases. The publication covers a wide range of disciplines including anesthesiology, critical care medicine, epidemiology, internal medicine, neurology, neuro-ophthalmology, neuropathology, neuropsychology, neurosurgery, nuclear medicine, nursing, radiology, rehabilitation, speech pathology, vascular physiology, and vascular surgery. The audience of Stroke includes neurologists, basic scientists, cardiologists, vascular surgeons, internists, interventionalists, neurosurgeons, nurses, and physiatrists. Stroke is indexed in Biological Abstracts, BIOSIS, CAB Abstracts, Chemical Abstracts, CINAHL, Current Contents, Embase, MEDLINE, and Science Citation Index Expanded.
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