Department of Medicine, Kristiansund Hospital, Møre og Romsdal Hospital Trust, Kristiansund, Norway; Department of Neuromedicine and Movement Science, Faculty of Medicine and Health Science, Norwegian University of Science and Technology, Trondheim, Norway.
Department of Neuromedicine and Movement Science, Faculty of Medicine and Health Science, Norwegian University of Science and Technology, Trondheim, Norway; Department of Geriatric Medicine, Clinic of Medicine, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.
Brain Behav Immun. 2024 May;118:167-177. doi: 10.1016/j.bbi.2024.02.030. Epub 2024 Feb 28.
We have previously shown that systemic inflammation was associated with post-stroke cognitive impairment (PSCI). Because neopterin, kynurenine pathway (KP) metabolites, and B6 vitamers are linked to inflammation, in our study we investigated whether those biomarkers were associated with PSCI.
The Norwegian Cognitive Impairment After Stroke study is a prospective multicenter cohort study of patients with acute stroke recruited from May 2015 through March 2017. Plasma samples of 422 participants (59 % male) with ischemic stroke from the index hospital stay and 3 months post-stroke were available for analyses of neopterin, KP metabolites, and B6 vitamers using liquid chromatography-tandem mass spectrometry. Mixed linear regression analyses adjusted for age, sex, and creatinine, were used to assess whether there were associations between those biomarkers and cognitive outcomes, measured by the Montreal Cognitive Assessment scale (MoCA) at 3-, 18-, and 36-month follow-up.
Participants had a mean (SD) age of 72 (12) years, with a mean (SD) National Institutes of HealthStroke Scale score of 2.7 (3.6) at Day 1. Higher baseline values of quinolinic acid, PAr (i.e., an inflammatory marker based on vitamin B6 metabolites), and HKr (i.e., a marker of functional vitamin B6 status based on selected KP metabolites) were associated with lower MoCA score at 3, 18, and 36 months post-stroke (p < 0.01). Higher baseline concentrations of neopterin and 3-hydroxykynurenine were associated with lower MoCA scores at 18 and 36 months, and higher concentrations of xanthurenic acid were associated with higher MoCA score at 36 months (p < 0.01). At 3 months post-stroke, higher concentrations of neopterin and lower values of pyridoxal 5́-phosphate were associated with lower MoCA scores at 18- and 36-month follow-up, while lower concentrations of picolinic acid were associated with a lower MoCA score at 36 months (p < 0.01).
Biomarkers and metabolites of systemic inflammation, including biomarkers of cellular immune activation, indexes of vitamin B6 homeostasis, and several neuroactive metabolites of the KP pathway, were associated with PSCI.
ClinicalTrials.gov: NCT02650531.
我们之前的研究表明,全身炎症与卒中后认知障碍(PSCI)有关。由于新蝶呤、犬尿氨酸途径(KP)代谢物和 B6 维生素与炎症有关,因此在本研究中,我们研究了这些生物标志物是否与 PSCI 有关。
挪威急性卒中后认知障碍研究是一项前瞻性多中心队列研究,于 2015 年 5 月至 2017 年 3 月期间从指数住院期间和卒中后 3 个月的缺血性卒中患者中招募。使用液相色谱-串联质谱法分析 422 名参与者(59%为男性)的血浆样本中的新蝶呤、KP 代谢物和 B6 维生素,以评估那些生物标志物与认知结果之间是否存在关联,认知结果通过 3 个月、18 个月和 36 个月的蒙特利尔认知评估量表(MoCA)进行测量。采用混合线性回归分析调整年龄、性别和肌酐,以评估那些生物标志物与认知结果之间是否存在关联。
参与者的平均(SD)年龄为 72(12)岁,第 1 天的平均(SD)国立卫生研究院卒中量表评分为 2.7(3.6)。较高的基线值喹啉酸、PAr(即基于维生素 B6 代谢物的炎症标志物)和 HKr(即基于选定 KP 代谢物的功能性维生素 B6 状态标志物)与卒中后 3、18 和 36 个月时较低的 MoCA 评分相关(p<0.01)。较高的新蝶呤和 3-羟基犬尿氨酸基线浓度与 18 个月和 36 个月时的 MoCA 评分较低相关,而较高的黄尿酸浓度与 36 个月时的 MoCA 评分较高相关(p<0.01)。卒中后 3 个月,较高的新蝶呤浓度和较低的吡哆醛 5′-磷酸浓度与 18 个月和 36 个月时的 MoCA 评分较低相关,而较低的吡啶酸浓度与 36 个月时的 MoCA 评分较低相关(p<0.01)。
全身炎症的生物标志物和代谢物,包括细胞免疫激活的生物标志物、维生素 B6 内稳态的指标以及 KP 途径的几种神经活性代谢物,与 PSCI 有关。
ClinicalTrials.gov:NCT02650531。