Zhao Nan, Chen Yi, Lu Zhongjiao, Han Lu, Song Yaying, Ding Jie, Zhu Desheng, Guan Yangtai
Department of Neurology, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200127, People's Republic of China.
Department of Neurology, Punan Hospital, Pudong New District, Shanghai, 200125, People's Republic of China.
J Inflamm Res. 2024 Dec 6;17:10557-10570. doi: 10.2147/JIR.S495788. eCollection 2024.
Both neutrophil gelatinase-associated lipocalin (NGAL) and fibrinogen are involved in the inflammation in acute ischemic stroke (AIS), but the interaction among them is unknown. Clarifying this issue will contribute to a better understanding of the mechanisms of injury in AIS. This study aimed to explore the association between NGAL, fibrinogen and neuronal damage in AIS.
This study is a cross-section study. One hundred ninety-six successively hospitalized AIS patients in Renji Hospital in China between January 1, 2023, and May 31, 2023, were included. Circulating NGAL and fibrinogen were measured, and neuron-specific enolase (NSE) was detected to evaluate central neuronal damage. All data were analyzed by linear curve fitting analysis, multiple linear regression analysis, and moderated mediation analysis, respectively.
There are linear relationships between log2-transformed NGAL, NSE, and fibrinogen, respectively. The β (95%) for the positive association between log2-transformed NGAL and NSE was 2.24 (1.15-3.32, < 0.01), between log2-transformed NGAL and fibrinogen was 0.37 (0.19-0.56, < 0.01), and between fibrinogen and NSE was 1.16 (0.48-1.85, < 0.01) adjusting for potential confounders. These associations remained consistent in sensitivity analysis and hierarchical analysis. Increased fibrinogen significantly ( < 0.01) mediated 14.28% of log2-transformed NGAL-associated increased NSE risk.
The NGAL levels were associated with NSE, and the NGAL-associated neuronal damage might be partially mediated by fibrinogen, suggesting that the inflammatory response among NGAL, fibrinogen, and NSE should be intervened to reduce neuronal damage after ischemic stroke. Further animal experiments are needed to clarify their specific mechanisms and precise relationships.
中性粒细胞明胶酶相关脂质运载蛋白(NGAL)和纤维蛋白原均参与急性缺血性卒中(AIS)的炎症反应,但它们之间的相互作用尚不清楚。阐明这一问题将有助于更好地理解AIS的损伤机制。本研究旨在探讨AIS中NGAL、纤维蛋白原与神经元损伤之间的关联。
本研究为横断面研究。纳入2023年1月1日至2023年5月31日期间在上海交通大学医学院附属仁济医院连续住院的196例AIS患者。检测循环中的NGAL和纤维蛋白原,并检测神经元特异性烯醇化酶(NSE)以评估中枢神经元损伤。所有数据分别采用线性曲线拟合分析、多元线性回归分析和调节中介分析。
经log2转换后的NGAL、NSE和纤维蛋白原之间分别存在线性关系。经log2转换后的NGAL与NSE之间正相关的β(95%)为2.24(1.15 - 3.32,P < 0.01),经log2转换后的NGAL与纤维蛋白原之间为0.37(0.19 - 0.56,P < 0.01),纤维蛋白原与NSE之间为1.16(0.48 - 1.85,P < 0.01),校正潜在混杂因素后。这些关联在敏感性分析和分层分析中保持一致。纤维蛋白原升高显著(P < 0.01)介导了经log2转换后的NGAL相关的NSE升高风险的14.28%。
NGAL水平与NSE相关,NGAL相关的神经元损伤可能部分由纤维蛋白原介导,提示应干预NGAL、纤维蛋白原和NSE之间的炎症反应以减少缺血性卒中后的神经元损伤。需要进一步的动物实验来阐明它们的具体机制和精确关系。