Wang Yu, Li Bohong, Jiang Yong, Zhang Runhua, Meng Xia, Zhao Xingquan, Wang Yongjun, Zhao Xihai, Liu Gaifen
Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Department of Rehabilitation Medicine, The People's Hospital of Xiangzhou District, Zhuhai, China.
Front Neurol. 2021 Feb 17;12:622869. doi: 10.3389/fneur.2021.622869. eCollection 2021.
YKL-40, an inflammatory biomarker, has been reported to be involved in the process and progression of atherosclerosis. Several studies have investigated the association between YKL-40 and plaque and suggested YKL-40 might be a potential biomarker for plaque instability. This study aimed to investigate the association between YKL-40 and carotid plaque instability. Based on a community-based study in Beijing from February 2014 to May 2016, 1,132 participants with carotid plaques were enrolled in this study. Data on demographics and medical history were collected through face-to-face interviews, and fasting blood samples were collected and stored. We used ultrasound to evaluate the presence of carotid plaque and its instability. The level of YKL-40 was measured by enzyme-linked immunosorbent assay (ELISA). Multivariate logistic regression analysis was performed to investigate the association between YKL-40 level and carotid atherosclerotic plaque instability. The mean age of the 1,132 participants was 58.0 (52.0-64.0) years, and 560 (49.5%) were male. Unstable plaques were detected in 855 (75.53%) participants. YKL-40 level was classified into four groups according to its quartile: quartile 1: <25.47 ng/mL, quartile 2: 25.47-39.53 ng/mL, quartile 3: 39.53-70.55 ng/mL, quartile 4: ≥70.55 ng/mL. After adjusting for age, sex, smoking, alcohol drinking, medical history, triglycerides, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, homocysteine, high-sensitivity C-reactive protein, and plaque thickness, the top quartiles of YKL-40 level were significantly associated with unstable plaque (quartile 3: OR 2.10, 95% CI 1.29-3.40; quartile 4: OR 1.70, 95% CI 1.04-2.80). This study found that YKL-40 was associated with carotid plaque instability determined by ultrasound. Individuals with high YKL-40 may have a higher risk of unstable carotid plaque.
YKL-40是一种炎症生物标志物,据报道其参与动脉粥样硬化的发生发展过程。多项研究调查了YKL-40与斑块之间的关联,并提示YKL-40可能是斑块不稳定的潜在生物标志物。本研究旨在探讨YKL-40与颈动脉斑块不稳定之间的关联。基于2014年2月至2016年5月在北京开展的一项社区研究,本研究纳入了1132例有颈动脉斑块的参与者。通过面对面访谈收集人口统计学和病史数据,并采集空腹血样进行保存。我们使用超声评估颈动脉斑块的存在及其不稳定性。采用酶联免疫吸附测定法(ELISA)检测YKL-40水平。进行多因素逻辑回归分析以探讨YKL-40水平与颈动脉粥样硬化斑块不稳定之间的关联。1132例参与者的平均年龄为58.0(52.0 - 64.0)岁,其中560例(49.5%)为男性。855例(75.53%)参与者检测到不稳定斑块。YKL-40水平根据四分位数分为四组:四分位数1:<25.47 ng/mL,四分位数2:25.47 - 39.53 ng/mL,四分位数3:39.53 - 70.55 ng/mL,四分位数4:≥70.55 ng/mL。在调整年龄、性别、吸烟、饮酒、病史、甘油三酯、低密度脂蛋白胆固醇、高密度脂蛋白胆固醇、同型半胱氨酸、高敏C反应蛋白和斑块厚度后,YKL-40水平的最高四分位数与不稳定斑块显著相关(四分位数3:比值比2.10,95%置信区间1.29 - 3.40;四分位数4:比值比1.70,95%置信区间1.04 - 2.80)。本研究发现,YKL-40与超声测定的颈动脉斑块不稳定相关。YKL-40水平高的个体可能有更高的颈动脉不稳定斑块风险。