Clinical and Translational Neuroscience Unit, Department of Neurology, Feil Family Brain and Mind Research Institute, Weill Cornell Medicine, New York, NY, USA.
Department of Neurological Surgery, University of Texas Health Science Center, Houston, TX, USA.
Neurocrit Care. 2024 Apr;40(2):529-537. doi: 10.1007/s12028-023-01774-6. Epub 2023 Jun 22.
Serum neutrophil-lymphocyte ratio (NLR) is a surrogate marker for the inflammatory response after intracerebral hemorrhage (ICH) and is associated with perihematomal edema and long-term functional outcomes. Whether NLR is associated with short-term ICH complications is poorly understood. We hypothesized that NLR is associated with 30-day infection and thrombotic events after ICH.
We performed a post hoc exploratory analysis of the Clot Lysis: Evaluating Accelerated Resolution of Intraventricular Hemorrhage III trial. The study exposure was the serum NLR obtained at baseline and on days 3 and 5. The coprimary outcomes, ascertained at 30 days, were any infection and a thrombotic event, defined as composite of cerebral infarction, myocardial infarction, or venous thromboembolism; both infection and thrombotic event were determined through adjudicated adverse event reporting. Binary logistic regression was used to study the relationship between NLR and outcomes, after adjustment for demographics, ICH severity and location, and treatment randomization.
Among the 500 patients enrolled in the Clot Lysis: Evaluating Accelerated Resolution of Intraventricular Hemorrhage III trial, we included 303 (60.6%) without missing data on differential white blood cell counts at baseline. There were no differences in demographics, comorbidities, or ICH severity between patients with and without data on NLR. In adjusted logistic regression models, NLR ascertained at baseline (odds ratio [OR] 1.03; 95% confidence interval [CI] 1.01-1.07, p = 0.03) and NLR ascertained at day 3 were associated with infection (OR 1.15; 95% CI 1.05-1.20, p = 0.001) but not with thrombotic events. Conversely, NLR at day 5 was associated with thrombotic events (OR 1.07, 95% CI 1.01-1.13, p = 0.03) but not with infection (OR 1.13; 95% CI 0.76-1.70, p = 0.56). NLR at baseline was not associated with either outcome.
Serum NLR ascertained at baseline and on day 3 after randomization was associated with 30-day infection, whereas NLR obtained on day 5 was associated with thrombotic events after ICH, suggesting that NLR could be a potential early biomarker for ICH-related complications.
血清中性粒细胞与淋巴细胞比值(NLR)是脑出血(ICH)后炎症反应的替代标志物,与血肿周围水肿和长期功能结局相关。NLR 是否与 ICH 短期并发症相关尚不清楚。我们假设 NLR 与 ICH 后 30 天的感染和血栓事件相关。
我们对 Clot Lysis: Evaluating Accelerated Resolution of Intraventricular Hemorrhage III 试验进行了事后探索性分析。研究暴露因素为基线及第 3、5 天的血清 NLR。30 天的主要转归是任何感染和血栓事件,定义为脑梗死、心肌梗死或静脉血栓栓塞的复合事件;感染和血栓事件均通过不良事件报告进行裁定。二元逻辑回归用于研究 NLR 与结局之间的关系,调整了人口统计学、ICH 严重程度和部位以及治疗随机分组等因素。
在 Clot Lysis: Evaluating Accelerated Resolution of Intraventricular Hemorrhage III 试验中,共纳入了 500 名患者,其中 303 名(60.6%)无基线时白细胞分类计数缺失数据。在有无 NLR 数据的患者中,人口统计学特征、合并症或 ICH 严重程度均无差异。在调整后的逻辑回归模型中,基线时 NLR(比值比[OR]1.03;95%置信区间[CI]1.01-1.07,p=0.03)和第 3 天 NLR 与感染相关(OR 1.15;95% CI 1.05-1.20,p=0.001),但与血栓事件无关。相反,第 5 天的 NLR 与血栓事件相关(OR 1.07,95% CI 1.01-1.13,p=0.03),但与感染无关(OR 1.13;95% CI 0.76-1.70,p=0.56)。基线 NLR 与任何结局均无关。
随机分组后基线和第 3 天的血清 NLR 与 30 天的感染相关,而第 5 天的 NLR 与 ICH 后血栓事件相关,提示 NLR 可能是 ICH 相关并发症的潜在早期生物标志物。