急性缺血性脑卒中患者中性粒细胞与脂蛋白 A1 比值的预测价值

Chao Chen, Shengqi Li, Fangyue Sun, Yiqun Chen, H. Qiu, Jiaqi Huang, Yining Jin, Jiexi Huang, Jiahan Xu, Zerui Jiang, Kun Li, Yanchu Wang, Hai Lin
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摘要

中性粒细胞与脂蛋白 A1 的比值(NAR)已成为不同病症的可能预后生物标志物。然而,NAR 在确定接受静脉溶栓治疗的急性缺血性脑卒中(AIS)患者 3 个月预后方面的预测潜力尚未得到充分认可。本研究纳入了196名接受重组组织浆细胞酶原激活剂(r-tPA)治疗的AIS患者和133名健康对照者。同时,我们还纳入了386名非溶栓AIS患者。根据 NAR 的四分位数将使用 r-tPA 的 AIS 患者分为四组。通过单变量和多变量回归分析评估了 NAR 与 3 个月预后之间的关系。此外,还进行了亚组分析,以研究 NAR 在不同患者群体中的预测价值。不良后果的定义是改良Rankin量表(mRS)评分为3-6分。研究结果显示,NAR水平升高与AIS患者预后不良之间存在显著关联。在 NAR 水平最高的四分位数(Q4)中,在控制了年龄、性别、入院时美国国立卫生研究院卒中量表评分、血尿素氮和卒中亚型后,3 个月后出现不良预后的几率比(OR)为 13.314(95% CI:2.878-61.596,p = 0.001)。研究发现,无论是否接受r-tPA治疗,NAR值升高都与AIS患者的不良预后有关。将 NAR 纳入传统模型的新模型在统计学上显著提高了对接受 r-tPA 治疗的 AIS 患者 3 个月不良预后的判别能力和风险再分类能力。新模型的分类净再分类指数 (NRI) (p = 0.035) 为 12.9%,综合判别改进 (IDI) (p = 0.013) 为 5.2%。亚组分析表明,NAR 的预测价值因中风亚型而异。NAR 是预测 AIS 患者预后的潜在生物标志物。我们的研究结果具有重要的临床意义,因为早期识别和干预高危患者可以改善他们的预后。然而,还需要进一步的研究来验证我们的结果,并阐明 NAR 与 AIS 患者不良预后之间关联的内在机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predictive value of neutrophil to apolipoprotein A1 ratio in patients with acute ischemic stroke
The neutrophil-to-apolipoprotein A1 ratio (NAR) has emerged as a possible prognostic biomarker in different medical conditions. Nonetheless, the predictive potential of NAR in determining the 3-month prognosis of acute ischemic stroke (AIS) patients who undergo intravenous thrombolysis has yet to be fully acknowledged. In this study, 196 AIS patients with recombinant tissue plasminogen activator (r-tPA) and 133 healthy controls were included. Meanwhile, we incorporated a total of 386 non-thrombolytic AIS patients. The AIS patients with r-tPA were divided into four groups based on quartiles of NAR. The association between NAR and the 3-month prognosis was evaluated through univariate and multivariate regression analyses. Additionally, subgroup analyses were conducted to investigate the predictive value of NAR in different patient populations. Adverse outcomes were defined as a modified Rankin Scale (mRS) score of 3-6. The study findings revealed a significant association between elevated NAR levels and poor prognosis in AIS patients. In the highest quartile of NAR levels (Q4), after controlling for age, gender, admission The National Institutes of Health Stroke Scale score, blood urea nitrogen, and stroke subtypes, the odds ratio (OR) for adverse outcomes at 3-months was 13.314 (95% CI: 2.878-61.596, p = 0.001). An elevated NAR value was found to be associated with a poor prognosis in AIS patients, regardless of whether they received r-tPA treatment or not. The new model, which incorporating NAR into the conventional model, demonstrated a statistically significant improvement in discriminatory power and risk reclassification for 3-month poor outcomes in AIS patients treated with r-tPA. The new model exhibited a categorical Net Reclassification Index (NRI) (p = 0.035) of 12.9% and an Integrated Discrimination Improvement (IDI) (p = 0.013) of 5.2%. Subgroup analyses indicated that the predictive value of NAR differed across stroke subtypes. NAR is a potential biomarker for predicting the prognosis of AIS patients. The clinical implications of our findings are significant, as early identification and intervention in high-risk patients can improve their outcomes. However, further studies are required to validate our results and elucidate the underlying mechanisms of the association between NAR and poor prognosis in AIS patients.
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