Li Jie, Zhang Ping, Chen Hong, Wang Yanfen, Han Yangyun, Wang Chun, Yi Xingyang
Department of Neurology, Deyang People's Hospital, Deyang, China.
Sichuan Clinical Research Center for Neurological Diseases, Deyang, China.
Front Neurol. 2024 Nov 20;15:1492224. doi: 10.3389/fneur.2024.1492224. eCollection 2024.
Patients with minor ischemic stroke (MIS) have substantial disability rates at 90 days. Our study aimed to explore the association between the systemic inflammation response index (SIRI) and 3-month functional outcomes in patients with MIS.
We conducted a prospective observational study in patients with MIS [defined as a National Institutes of Health Stroke Scale (NIHSS) score of 0-3] admitted within 24 h from symptoms onset. Blood samples for the SIRI measurement were collected on admission. The primary outcome measure was poor outcomes at 90 days (defined as a modified Rankin Scale score of 2-6). Univariate and multivariate logistic analyses were performed to assess the association between the SIRI and the risk of 3-month poor outcomes.
A total of 152 patients with MIS were enrolled, of which 24 cases (15.8%) had poor outcomes at 90 days. The median SIRI level was 1.27 [interquartile range (IQR), 0.77-1.92, ×10^9 /L] on admission. MIS patients with poor outcomes had higher levels of the SIRI than patients with good outcomes (poor outcomes: median, 1.93, IQR: 1.17-3.28, ×10^9 /L; good outcomes: median, 1.21, IQR: 0.71-1.80, ×10^9 /L; = 0.003). The high SIRI level group (SIRI >1.27 × 10^9 /L) had significantly higher rates of poor outcomes at 90 days (22.4% vs. 9.2%, = 0.026). After adjusting for age, baseline NIHSS score, prehospital delay, Trial of Org 10,172 in Acute Stroke Treatment (TOAST) classification, and other confounders in multivariate analyses, an elevated SIRI level remained independently associated with an increased risk of poor outcomes in patients with MIS [odds ratio (OR): 1.57, 95% confidence interval (CI): 1.12-2.20; = 0.010]. Meanwhile, a high level of the SIRI (>1.27 × 10^9/L) was still an independent risk factor for 3-month poor outcomes (OR: 4.80, 95%CI: 1.51-15.29; = 0.008) in MIS patients.
Disability at 90 days was common in patients with MIS. An elevated SIRI was associated with poor outcomes in MIS patients. The SIRI might be a promising biomarker candidate that can help identify high-risk MIS patients with poor outcomes for reaching individual therapeutic decisions in clinical trials.
轻度缺血性卒中(MIS)患者在90天时存在较高的致残率。我们的研究旨在探讨全身炎症反应指数(SIRI)与MIS患者3个月功能结局之间的关联。
我们对症状发作后24小时内入院的MIS患者[定义为美国国立卫生研究院卒中量表(NIHSS)评分为0 - 3分]进行了一项前瞻性观察性研究。入院时采集用于测量SIRI的血样。主要结局指标为90天时预后不良(定义为改良Rankin量表评分为2 - 6分)。进行单因素和多因素逻辑分析以评估SIRI与3个月预后不良风险之间的关联。
共纳入152例MIS患者,其中24例(15.8%)在90天时预后不良。入院时SIRI水平的中位数为1.27[四分位数间距(IQR),0.77 - 1.92,×10^9 /L]。预后不良的MIS患者的SIRI水平高于预后良好的患者(预后不良:中位数,1.93,IQR:1.17 - 3.28,×10^9 /L;预后良好:中位数,1.21,IQR:0.71 - 1.80,×10^9 /L;P = 0.003)。高SIRI水平组(SIRI >1.27×10^9 /L)在90天时预后不良的发生率显著更高(22.4%对9.2%,P = 0.026)。在多因素分析中对年龄、基线NIHSS评分、院前延误、急性卒中治疗中组织纤溶酶原激活剂-10172试验(TOAST)分类及其他混杂因素进行校正后,SIRI水平升高仍与MIS患者预后不良风险增加独立相关[比值比(OR):1.57,95%置信区间(CI):1.12 - 2.20;P = 0.010]。同时,SIRI高水平(>1.27×10^9/L)仍是MIS患者3个月预后不良的独立危险因素(OR:4.80,95%CI:1.51 - 15.29;P = 0.008)。
MIS患者在90天时出现残疾很常见。SIRI升高与MIS患者预后不良相关。SIRI可能是一个有前景的生物标志物候选指标,有助于识别预后不良的高危MIS患者,以便在临床试验中做出个体化治疗决策。