Department of Cerebrovascular Diseases, The Fifth Affiliated Hospital of Sun Yat-Sen University, Zhuhai, 528406, China.
Curr Neurovasc Res. 2024;21(3):310-319. doi: 10.2174/0115672026332171240624100802.
END (Early Neurologic Deterioration) significantly elevates the risk of morbidity and mortality. While numerous studies have investigated END following hemorrhagic transformation post-thrombolysis in acute cerebral infarction research on END without hemorrhagic transformations in patients with acute cerebral infarction due to non-cardiogenic embolism remains scarce.
This study aimed to elucidate the impact of PCSK9 inhibitors on early neurological deterioration (END) in patients with acute non-cardioembolism cerebral infarction without hemorrhagic transformation post-intravenous thrombolysis. Additionally it aimed to identify risk factors associated with END in patients suffering from this type of stroke.
The objective of this study is to investigate the effect of PCSK9 inhibitors on early neurologic deterioration (END) in patients with acute non-cardiogenic cerebral infarction without hemorrhagic transformation after intravenous thrombolysis and identify associated risk factors for END in this patient population.
In this retrospective case-control study the data of consecutive patients who underwent intravenous thrombolysis after AIS (acute ischemic stroke) without hemorrhagic transformation during hospitalization at the Stroke Center of The Fifth Affiliated Hospital of Sun Yat-sen University between January 2018 to February 2023 were retrieved and assessed. An increase of >2 in the National Institutes of Health Stroke Scale (NIHSS) within 7 days after admission was defined as END.
This study included 250 patients (56 males 22.4%) they were 63.344±12.901 years old. There were 41 patients in the END group and 209 in the non-END group. The usage rate of PCSK9 inhibitors was significantly different between the END group and non-END group (29.268% vs 58.852% P<0.001). The White blood cell count (WBC) and homocysteine levels showed a significant difference between the two groups (all P<0.05). Patients not using PCSK9 inhibitors (OR=0.282 95%CI: 0.127-0.593) and white blood cell count (OR=1.197, 95%CI: 1.085-1.325) were independently associated with END. Receiver-operating characteristic curve analysis suggested that the sensitivity specificity and area under the curve for PCSK9 inhibitors used for END were 88.9%, 80.7% and 0.648 respectively.
The use of PCSK9 inhibitors can reduce the incidence of early neurological deterioration in patients with acute non-cardioembolism and non-hemorrhagic transformation after intravenous thrombolysis.
早期神经功能恶化(END)显著增加了发病率和死亡率。虽然有许多研究探讨了急性脑梗死溶栓后出血转化后的 END,但对于非心源性栓塞性急性脑梗死患者无出血转化的 END 研究仍然很少。
本研究旨在阐明 PCSK9 抑制剂对急性非心源性脑梗死患者静脉溶栓后无出血转化的早期神经功能恶化(END)的影响。此外,还旨在确定此类卒中患者 END 的相关危险因素。
本研究旨在探讨 PCSK9 抑制剂对急性非心源性脑梗死患者静脉溶栓后无出血转化的早期神经功能恶化(END)的影响,并确定该患者人群中 END 的相关危险因素。
在这项回顾性病例对照研究中,检索了 2018 年 1 月至 2023 年 2 月期间在中山大学第五附属医院卒中中心住院期间发生急性缺血性卒中(AIS)且无出血转化的连续患者的数据,并进行了评估。入院后 7 天内 NIHSS 评分增加>2 定义为 END。
本研究纳入了 250 例患者(56 例男性,22.4%),年龄为 63.344±12.901 岁。END 组 41 例,非 END 组 209 例。END 组和非 END 组 PCSK9 抑制剂的使用率差异有统计学意义(29.268% vs 58.852%,P<0.001)。两组间白细胞计数(WBC)和同型半胱氨酸水平差异有统计学意义(均 P<0.05)。未使用 PCSK9 抑制剂的患者(OR=0.282,95%CI:0.127-0.593)和白细胞计数(OR=1.197,95%CI:1.085-1.325)与 END 独立相关。受试者工作特征曲线分析表明,PCSK9 抑制剂用于 END 的灵敏度、特异度和曲线下面积分别为 88.9%、80.7%和 0.648。
PCSK9 抑制剂的使用可降低急性非心源性和非出血性转化患者静脉溶栓后早期神经功能恶化的发生率。