Li Wei, Wang Jun, Tang Chao, Lv Xuan, Zhu Suijun
Department of Neurosurgery, First People's Hospital of Linping District, Hangzhou, People's Republic of China.
Department of Neurosurgery, Linping Campus, the Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, People's Republic of China.
Neuropsychiatr Dis Treat. 2024 Mar 29;20:737-753. doi: 10.2147/NDT.S455049. eCollection 2024.
Nucleotide-binding oligomerization domain-like receptor family pyrin domain-containing 1 (NLRP1) participates in neuroinflammation. This study aimed to identify serum NLRP as a potential prognostic biomarker of acute intracerebral hemorrhage (ICH).
This prospective cohort study enrolled 145 patients with supratentorial ICH and 51 healthy controls. Serum NLRP1 levels were quantified on admission of all 145 patients, on days 1, 3, 5, 7, and 10 after stroke in 51 of 145 patients and at entry into the study of controls. Poststroke 6-month modified Rankin Scale (mRS) scores of 3-6 signified a poor prognosis.
Compared to controls, patients had prominently increased serum NLRP1 levels until day 10 after ICH, with the highest levels at days 1 and 3. Serum NLRP1 levels were independently correlated with National Institutes of Health Stroke Scale (NIHSS) scores, hematoma volume and six-month mRS scores, and independently predicted six-month bad prognosis. A linear relationship was observed between serum NLRP1 levels and the risk of poor prognosis in a restricted cubic spline. Under the receiver operating characteristic (ROC) curve, serum NLRP levels efficiently discriminated poor prognosis. Serum NLRP1, NIHSS, and hematoma volume were merged into a prognosis prediction model, which was portrayed using a nomogram. Good performance of the model was verified using calibration curve, decision curve, and ROC curve.
Serum NLRP1 levels are elevated during the early period following ICH and are independently related to hemorrhagic severity and poor prognosis, suggesting that serum NLRP1 may represent a promising prognostic biomarker of ICH.
含吡啉结构域的核苷酸结合寡聚化结构域样受体家族成员1(NLRP1)参与神经炎症反应。本研究旨在确定血清NLRP1作为急性脑出血(ICH)潜在的预后生物标志物。
这项前瞻性队列研究纳入了145例幕上脑出血患者和51名健康对照者。对所有145例患者在入院时、145例患者中的51例在卒中后第1、3、5、7和10天以及对照者在进入研究时测定血清NLRP1水平。卒中后6个月改良Rankin量表(mRS)评分为3 - 6分表示预后不良。
与对照组相比,患者血清NLRP1水平在脑出血后第10天前显著升高,在第1天和第3天达到最高水平。血清NLRP1水平与美国国立卫生研究院卒中量表(NIHSS)评分、血肿体积和6个月mRS评分独立相关,并独立预测6个月不良预后。在限制立方样条图中观察到血清NLRP1水平与预后不良风险之间存在线性关系。在受试者工作特征(ROC)曲线下,血清NLRP水平能有效区分不良预后。将血清NLRP1、NIHSS和血肿体积纳入预后预测模型,并用列线图进行描述。使用校准曲线、决策曲线和ROC曲线验证了该模型的良好性能。
脑出血后早期血清NLRP1水平升高,且与出血严重程度和不良预后独立相关,提示血清NLRP1可能是脑出血有前景的预后生物标志物。