Cardiovascular Biochemistry, Biomedical Research Institute Sant Pau (IIB-Sant Pau), Barcelona, Spain.
Department of Biochemistry and Molecular Biology, Faculty of Medicine, Building M, Universitat Autònoma de Barcelona (UAB), Cerdanyola del Vallès, Barcelona, Spain.
Transl Stroke Res. 2022 Oct;13(5):745-756. doi: 10.1007/s12975-022-01002-x. Epub 2022 Mar 2.
F-fluorodeoxyglucose positron emission tomography (F-FDG PET) identifies carotid plaque inflammation and predicts stroke recurrence in patients with atherothrombotic stroke. The aim of the study was to identify plasma inflammatory biomarkers associated with plaque inflammation according to F-FDG uptake. We conducted a prospective study of consecutive adult patients with a recent (< 7 days) anterior circulation ischemic stroke and at least one atherosclerotic plaque in the ipsilateral internal carotid artery. We included 64 patients, 57.8% of whom showed a carotid stenosis ≥ 50%. All patients underwent an early (< 15 days from inclusion) F-FDG PET, and a blood sample was obtained at days 7 ± 1 from the stroke. The plasma concentration of 16 inflammation-related molecules was analyzed in a Luminex using xMAP technology. Multivariable linear regression was used to assess the association between plasma biomarkers and the standardized uptake value (SUV) of F-FDG uptake. Soluble intercellular adhesion molecule-1 (sICAM-1), soluble vascular adhesion molecule-1 (sVCAM-1), and fractalkine (FKN) were independently associated with plaque inflammation (β = 0.121, 95% CI 0.061-0.181, p < 0.001; β = 0.144, 95% CI 0.012-0.276, p = 0.033; β = 0.136, 95% CI 0.037-0.235, p = 0.008). In a multivariable logistic regression analysis, sICAM-1 was associated with SUVmax ≥ 2.85 (OR = 1.02, 95% CI 1.00-1.03, p = 0.020). Multivariable Cox regression was used to assess the association between biomarkers and stroke recurrence. sICAM-1 was associated with stroke recurrence (HR = 1.03, 95% CI 1.00-1.05, p = 0.002). In summary, elevated concentrations of sICAM-1 were associated with carotid plaque inflammation and an increased risk of stroke recurrence in patients with recent ischemic stroke and carotid atherosclerosis.
正电子发射断层扫描(F-FDG PET)可识别颈动脉斑块炎症,并预测动脉粥样硬化性血栓性脑卒中患者的卒中复发。本研究旨在根据 F-FDG 摄取情况,确定与斑块炎症相关的血浆炎症生物标志物。
我们进行了一项前瞻性研究,纳入了近期(<7 天)前循环缺血性脑卒中且同侧颈内动脉至少有一处动脉粥样硬化斑块的连续成年患者。共纳入 64 例患者,57.8%的患者存在颈动脉狭窄≥50%。所有患者均在入组后 15 天内进行了早期(<15 天)F-FDG PET,且在卒中后第 7 天±1 天采集了血液样本。采用 Luminex 技术的 xMAP 技术分析了 16 种炎症相关分子的血浆浓度。多变量线性回归用于评估血浆生物标志物与 F-FDG 摄取标准化摄取值(SUV)之间的关系。
可溶性细胞间黏附分子-1(sICAM-1)、可溶性血管细胞黏附分子-1(sVCAM-1)和 fractalkine(FKN)与斑块炎症独立相关(β=0.121,95%CI 0.061-0.181,p<0.001;β=0.144,95%CI 0.012-0.276,p=0.033;β=0.136,95%CI 0.037-0.235,p=0.008)。在多变量逻辑回归分析中,sICAM-1 与 SUVmax≥2.85 相关(OR=1.02,95%CI 1.00-1.03,p=0.020)。采用多变量 Cox 回归评估生物标志物与卒中复发的关系。sICAM-1 与卒中复发相关(HR=1.03,95%CI 1.00-1.05,p=0.002)。
综上所述,在近期发生缺血性卒中和颈动脉粥样硬化的患者中,sICAM-1 浓度升高与颈动脉斑块炎症及卒中复发风险增加相关。