Benson Eve-Marie A, Tibuakuu Martin, Zhao Di, Akinkuolie Akintunde O, Otvos James D, Duprez Daniel A, Jacobs David R, Mora Samia, Michos Erin D
Ciccarone Center for Prevention of Cardiovascular Disease, Johns Hopkins School of Medicine, Baltimore, Maryland.
Department of Medicine, St. Luke's Hospital, Chesterfield, Missouri.
Clin Cardiol. 2018 Nov;41(11):1439-1445. doi: 10.1002/clc.23069. Epub 2018 Nov 19.
Unhealthy lifestyles and inflammation contribute to cardiovascular disease (CVD). GlycA is a novel biomarker of systemic inflammation representing post-translational glycosylation of acute phase reactants and associated with increased clinical CVD risk.
We hypothesized that ideal cardiovascular health (CVH), as assessed by (higher) Life's Simple 7 (LS7) scores, would be associated with lower GlycA levels among individuals free of CVD in a multiethnic community-based population.
This was a cross-sectional study of 6479 Multi-Ethnic Study of Atherosclerosis participants [53% women; mean age 62 ± 10 years] with GlycA levels measured at baseline by nuclear magnetic resonance spectroscopy. The LS7 metrics (smoking, physical activity, diet, body mass index, blood pressure, cholesterol, and glucose) were each scored as ideal (2), moderate (1), or poor (0). Total scores were summed and categorized as optimal (12-14), average (8-11), and inadequate (0-7). Linear regression assessed percent difference in GlycA by LS7 scores, after adjusting for age, sex, ethnicity, education, income, family history of CVD, and other inflammatory biomarkers.
GlycA levels were 403.4 ± 63.1, 374.4 ± 59.2, and 350.3 ± 56.2 micromoles per liter (μmol/L) for inadequate, average, and optimal CVH, respectively (P-trend <0.001). After multivariable adjustment, GlycA remained independently and inversely associated with CVH categories, with a lower mean GlycA level of 5 μmol/L (95% confidence interval 4.5-5.8) for each one unit increment in LS7 score.
Among this group of ethnically diverse individuals without CVD, suboptimal CVH is associated with higher GlycA levels, independent of traditional inflammatory biomarkers. Strategies aimed at improving CVH might reduce GlycA, which could be a marker of reduced risk of future CVD events.
不健康的生活方式和炎症会导致心血管疾病(CVD)。糖化终产物(GlycA)是一种全身性炎症的新型生物标志物,代表急性期反应物的翻译后糖基化,并与临床CVD风险增加相关。
我们假设,在一个基于社区的多民族人群中,通过(更高的)简单生活7项指标(LS7)评分评估的理想心血管健康状况(CVH)与无CVD个体的较低GlycA水平相关。
这是一项对6479名动脉粥样硬化多民族研究参与者的横断面研究[53%为女性;平均年龄62±10岁],在基线时通过核磁共振波谱法测量GlycA水平。LS7指标(吸烟、身体活动、饮食、体重指数、血压、胆固醇和血糖)每项的评分分别为理想(2分)、中等(1分)或差(0分)。将总分相加并分为最佳(12 - 14分)、平均(8 - 11分)和不足(0 - 7分)。在调整年龄、性别、种族、教育程度、收入、CVD家族史和其他炎症生物标志物后,采用线性回归评估GlycA水平随LS7评分的百分比差异。
CVH不足、平均和最佳的GlycA水平分别为403.4±63.1、374.4±59.2和350.3±56.2微摩尔每升(μmol/L)(P趋势<0.001)。经过多变量调整后,GlycA仍与CVH类别独立且呈负相关,LS7评分每增加一个单位,GlycA的平均水平降低5μmol/L(95%置信区间4.5 - 5.8)。
在这组无CVD的不同种族个体中,次优的CVH与较高的GlycA水平相关,独立于传统炎症生物标志物。旨在改善CVH的策略可能会降低GlycA水平,这可能是未来CVD事件风险降低的一个标志。