Riggs Kayla A, Joshi Parag H, Khera Amit, Otvos James D, Greenland Philip, Ayers Colby R, Rohatgi Anand
The University of Texas Southwestern Medical Center and the Donald W. Reynolds Cardiovascular Clinical Research Center, Dallas, TX, USA.
Laboratory Corporation of America Holdings (LabCorp), Morrisville, NC, USA.
Am J Prev Cardiol. 2022 Aug 22;12:100373. doi: 10.1016/j.ajpc.2022.100373. eCollection 2022 Dec.
Inflammatory markers are associated with cardiovascular disease (CVD); however, the ability to specifically predict myocardial infarction (MI) as well as ischemic stroke remains unknown. There has not been a direct comparison of the associations between GlycA and hsCRP and MI and ischemic stroke in a multi-ethnic pooled cohort.
Multi-center, multi-ethnic, population-based community prospective pooled cohort of the Dallas Heart Study (DHS) and Multi-Ethnic Study of Atherosclerosis (MESA). 9,785 participants without baseline CVD enrolled with median follow-up of 13.4 years. Fatal/nonfatal MI and fatal/nonfatal ischemic stroke were assessed separately and then combined.
GlycA was moderately associated with hsCRP (R=0.58 in DHS and R=0.55 in MESA). In adjusted Cox proportional hazards models with competing risk adjusted for both inflammatory markers, GlycA was directly associated with MI (HR Q4 vs. Q1 1.90, 95% CI 1.39 to 2.58), whereas hsCRP was not (HR Q4 vs. Q1 0.92, 95% CI 0.70 to 1.21). Conversely, hsCRP was directly associated with ischemic stroke (HR Q4 vs. Q1 1.73, 95% CI 1.15 to 2.59), but GlycA was not (HR Q4 vs. Q1 1.21, 95% CI 0.77 to 1.90). GlycA improved net reclassification for MI and hsCRP did so for ischemic stroke.
Although both GlycA and hsCRP were associated with incident CVD, GlycA more strongly predicted incident MI, and hsCRP more strongly predicted ischemic stroke.
炎症标志物与心血管疾病(CVD)相关;然而,其特异性预测心肌梗死(MI)以及缺血性中风的能力尚不清楚。在多民族合并队列中,尚未对糖化白蛋白(GlycA)和高敏C反应蛋白(hsCRP)与MI及缺血性中风之间的关联进行直接比较。
达拉斯心脏研究(DHS)和动脉粥样硬化多民族研究(MESA)的多中心、多民族、基于人群的社区前瞻性合并队列。9785名无基线CVD的参与者入组,中位随访时间为13.4年。分别评估致命性/非致命性MI和致命性/非致命性缺血性中风,然后合并。
GlycA与hsCRP中度相关(DHS中R = 0.58,MESA中R = 0.55)。在针对两种炎症标志物进行竞争风险调整的校正Cox比例风险模型中,GlycA与MI直接相关(四分位间距4组与1组相比,HR为1.90,95%CI为1.39至2.58),而hsCRP则不然(四分位间距4组与1组相比,HR为0.92,95%CI为0.70至1.21)。相反,hsCRP与缺血性中风直接相关(四分位间距4组与1组相比,HR为1.73,95%CI为1.15至2.59),但GlycA则不然(四分位间距4组与1组相比,HR为1.21,95%CI为0.77至1.90)。GlycA改善了MI的净重新分类,hsCRP改善了缺血性中风的净重新分类。
尽管GlycA和hsCRP均与新发CVD相关,但GlycA对新发MI的预测更强,hsCRP对缺血性中风的预测更强。