Department of Neurology and Sagol Neuroscience Center, Stroke Center, Sheba Medical Center, Tel Hashomer, Israel.
Institute of Clinical Chemistry and Laboratory Medicine, Johannes Gutenberg Universität Mainz Klinikum, Mainz, Germany.
Eur J Neurol. 2020 Aug;27(8):1604-1611. doi: 10.1111/ene.14279. Epub 2020 May 25.
Myeloperoxidase (MPO) is an important oxidative enzyme participating in different stages of cardiovascular disease and predicts prognosis. Little is known about its role in acute cerebrovascular events and carotid plaque vulnerability. In this study, the aim was to assess plasma MPO levels in acute stroke patients and their correlation to stroke severity and stroke outcome.
Plasma MPO levels were assessed in patients presenting with acute brain ischaemia within 36 h of symptom onset (n = 144, mean age 64.7 ± 11.6 years, 67% men) and in patients with moderate-to-severe carotid stenosis undergoing carotid artery stenting (n = 51, mean age 66.3 ± 8.4 years, 75% men). Patients presenting with acute brain ischaemia were assessed serially for stroke severity and disability.
Plasma MPO concentrations (ng/ml) were associated with interleukin-6 (r = 0.38, P < 0.0001) and gender (median interquartile range) of 68.6 (49.8-107.0) vs. 59.7 (42.7-85.5) in women vs. men (P = 0.02). In acute brain ischaemia, MPO concentrations were associated with non-lacunar subtype (bottom, middle and top tertiles 37.5%, 71.7% and 71.7% respectively; P = 0.001), with stroke severity (baseline National Institutes of Health Stroke Scale score > 10, bottom, middle and top tertiles 6.3%, vs. 41.7% and 31.3%, respectively; P < 0.006) as well as with stroke severity at days 1-2, days 4-5 and at discharge (P < 0.05 for all), but less with disability at discharge (modified Rankin Scale score ≥ 2, 41.7% vs. 60.4% and 58.7% for the bottom, middle and top tertiles, respectively; P = 0.096).
Amongst patients with acute brain ischaemia, plasma MPO concentrations were associated with stroke severity and non-lacunar subtype, but not with long-term functional disability.
髓过氧化物酶(MPO)是一种重要的氧化酶,参与心血管疾病的不同阶段,并可预测预后。但其在急性脑血管事件和颈动脉斑块易损性中的作用知之甚少。本研究旨在评估急性脑卒中患者的血浆 MPO 水平及其与卒中严重程度和预后的相关性。
在症状发作后 36 小时内,评估 144 名急性脑缺血患者(平均年龄 64.7±11.6 岁,67%为男性)和 51 名接受颈动脉支架置入术的中重度颈动脉狭窄患者(平均年龄 66.3±8.4 岁,75%为男性)的血浆 MPO 水平。对急性脑缺血患者进行卒中严重程度和残疾的连续评估。
血浆 MPO 浓度(ng/ml)与白细胞介素-6(r=0.38,P<0.0001)和性别(中位数四分位数范围)相关,女性为 68.6(49.8-107.0),男性为 59.7(42.7-85.5)(P=0.02)。在急性脑缺血中,MPO 浓度与非腔隙性亚型相关(底、中、顶三分位数分别为 37.5%、71.7%和 71.7%;P=0.001),与卒中严重程度相关(基线 NIHSS 评分>10,底、中、顶三分位数分别为 6.3%、41.7%和 31.3%;P<0.006),与 1-2 天、4-5 天和出院时的卒中严重程度相关(P<0.05),与出院时的残疾程度相关性较低(改良 Rankin 量表评分≥2,底、中、顶三分位数分别为 41.7%、60.4%和 58.7%;P=0.096)。
在急性脑缺血患者中,血浆 MPO 浓度与卒中严重程度和非腔隙性亚型相关,但与长期功能残疾无关。