Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
China National Clinical Research Center for Neurological Diseases, Capital Medical University, Beijing, China.
CNS Neurosci Ther. 2022 Oct;28(10):1637-1647. doi: 10.1111/cns.13909. Epub 2022 Jul 4.
Gamma-glutamyl transferase (GGT) is considered a marker of oxidative stress in vivo. In this study, we aimed to examine the association of serum GGT levels with 3-month and 1-year stroke recurrence in patients with acute ischemic stroke or transient ischemic attack (TIA).
We conducted a large and multicenter cohort study. Participants with ischemic stroke or TIA who had a baseline GGT measurement were enrolled in the China National Stroke Registry-3 study from August 2015 to March 2018. They were divided into four groups according to sex-specific quartiles of GGT levels. The effect of GGT on stroke recurrence and other vascular events was examined during the 1-year follow-up period. Multivariate Cox regression models were performed to evaluate the association. Discrimination tests were used to examine the degree to which incorporating GGT into the conventional model predicted stroke adverse outcomes.
A total of 12,504 patients were enrolled. At both the 3-month and 1-year follow-ups, patients in the highest quartile group of GGT levels exhibited a higher risk of stroke recurrence [HR 1.32 (95% CI 1.07-1.63), HR 1.34 (95% CI 1.13-1.60)], ischemic stroke [HR 1.37 (95% CI 1.10-1.71), HR 1.37 (95% CI 1.14-1.64)], and combined vascular events [HR 1.34 (95% CI 1.09-1.65), HR 1.34 (95% CI 1.13-1.59)] than those in the lowest quartile group. Moreover, the Kaplan-Meier curves revealed that the incidence rates of stroke adverse outcomes were quite different in the four groups. The highest quartile group showed the highest cumulative incidence, while the lowest quartile group showed the lowest cumulative incidence. After applying discrimination tests, adding GGT into the conventional model resulted in slight improvements in predicting stroke adverse outcomes (NRI: 10%-14%).
This study demonstrated that elevated GGT levels were positively associated with an increased risk of stroke adverse outcomes, namely, recurrence, ischemic stroke, and combined vascular events.
γ-谷氨酰转移酶(GGT)被认为是体内氧化应激的标志物。本研究旨在探讨急性缺血性卒中和短暂性脑缺血发作(TIA)患者血清 GGT 水平与 3 个月和 1 年卒中复发的关系。
我们进行了一项大型多中心队列研究。2015 年 8 月至 2018 年 3 月,在中国国家卒中登记研究-3 中纳入基线 GGT 检测的缺血性卒中和 TIA 患者。根据 GGT 水平的性别特异性四分位区间,将患者分为四组。在 1 年随访期间,检查 GGT 对卒中复发和其他血管事件的影响。采用多变量 Cox 回归模型评估相关性。采用判别试验评估将 GGT 纳入常规模型预测卒中不良结局的程度。
共纳入 12504 例患者。在 3 个月和 1 年随访时,GGT 水平最高四分位组患者卒中复发[风险比(HR)1.32(95%可信区间 1.07-1.63),HR 1.34(95%可信区间 1.13-1.60)]、缺血性卒中[HR 1.37(95%可信区间 1.10-1.71),HR 1.37(95%可信区间 1.14-1.64)]和复合血管事件[HR 1.34(95%可信区间 1.09-1.65),HR 1.34(95%可信区间 1.13-1.59)]的风险高于最低四分位组。此外,Kaplan-Meier 曲线显示,四组患者卒中不良结局的发生率差异较大。四分位最高组累积发生率最高,四分位最低组累积发生率最低。应用判别试验后,将 GGT 纳入常规模型可轻微改善预测卒中不良结局的能力(NRI:10%-14%)。
本研究表明,GGT 水平升高与卒中不良结局(即复发、缺血性卒中和复合血管事件)的风险增加呈正相关。