Kempel Mia Klinkvort, Winding Trine Nøhr, Lynggaard Vibeke, Brantlov Steven, Andersen Johan Hviid, Böttcher Morten
Department of Occupational Medicine - University Research Clinic Danish Ramazzini Centre Regional Hospital West Jutland Herning Denmark.
Cardiovascular Research Unit Department of Cardiology Gødstrup Hospital Herning Denmark.
Obes Sci Pract. 2021 Jun 1;7(6):727-737. doi: 10.1002/osp4.528. eCollection 2021 Dec.
Cardiometabolic risk increases with increasing body mass index (BMI). The exact mechanism is poorly understood, and traditional risk assessment of young adults with obesity has shown to be ineffective. Greater knowledge about potential new effective biomarkers and the use of advanced cardiac imaging for risk assessment in young adults is, therefore, necessary.
This study aims to explore traditional and novel cardiometabolic risk markers across strata of BMI in young adults.
Participants ( = 264, 50% women, age 28-30 years) were invited from an ongoing cohort study, based on BMI and sex. BMI-strata were: BMI <25, 25-30, >30 kg/m, representing normal weight (NW), overweight (OW), and obesity (OB). Participants underwent cardiac computed tomography to detect coronary artery calcification, measures of body composition, blood pressure measurements, and a comprehensive panel of circulating cardiometabolic risk markers.
No significant coronary artery calcifications were detected in this study. Minor differences in median levels of traditional risk markers were detected across BMI-strata, for example, total cholesterol (men- NW: 4.7 (4.3-5.1) and OB: 4.8 (4.2-5.6) mmol/L, = 0.58; women- NW: 4.3 (3.9-4.8) and OB: 4.7 (4.2-5.3) mmol/L, = 0.016), whereas substantial differences were seen in markers of inflammation and glucose metabolism, for example, high sensitive CRP (men- NW: 0.6 (0.3-1.1) and OB: 2.8 (1.5-4.0) mg/L, < 0.001; women- NW: 0.7 (0.3-1.7) and OB: 4.0 (2.2-7.8) mg/L, < 0.001) and insulin (men- NW: 47.0 (35.0-59.0) and OB: 113.5 (72.0-151.0) pmol/L, < 0.001; women- NW: 44.0 (35.0-60.0) and OB: 84.5 (60.0-126.0) pmol/L, < 0.001).
In young adults, obesity is associated with an early onset insulin resistance and inflammatory response prior to development of coronary artery calcification and deterioration of lipid profiles.
心血管代谢风险随体重指数(BMI)的增加而升高。其确切机制尚不清楚,而且对肥胖的年轻成年人进行传统风险评估已证明效果不佳。因此,有必要更深入了解潜在的新型有效生物标志物以及利用先进的心脏成像技术对年轻成年人进行风险评估。
本研究旨在探索年轻成年人中不同BMI分层的传统和新型心血管代谢风险标志物。
根据BMI和性别,从一项正在进行的队列研究中邀请参与者(n = 264,50%为女性,年龄28 - 30岁)。BMI分层为:BMI <25、25 - 30、>30 kg/m²,分别代表正常体重(NW)、超重(OW)和肥胖(OB)。参与者接受心脏计算机断层扫描以检测冠状动脉钙化、身体成分测量、血压测量以及一组全面的循环心血管代谢风险标志物检测。
本研究中未检测到显著的冠状动脉钙化。在不同BMI分层中,传统风险标志物的中位数水平存在微小差异,例如总胆固醇(男性 - NW:4.7(4.3 - 5.1)和OB:4.8(4.2 - 5.6)mmol/L,P = 0.58;女性 - NW:4.3(3.9 - 4.8)和OB:4.7(4.2 - 5.3)mmol/L,P = 0.016),而炎症和葡萄糖代谢标志物存在显著差异,例如高敏CRP(男性 - NW:0.6(0.3 - 1.1)和OB:2.8(1.5 - 4.0)mg/L,P < 0.001;女性 - NW:0.7(0.3 - 1.7)和OB:4.0(2.2 - 7.8)mg/L,P < 0.001)和胰岛素(男性 - NW:47.0(35.0 - 59.0)和OB:113.5(72.0 - 151.0)pmol/L,P < 0.001;女性 - NW:44.0(35.0 - 60.0)和OB:84.5(60.0 - 126.0)pmol/L,P < 0.001)。
在年轻成年人中,肥胖与冠状动脉钙化发生和血脂异常恶化之前的早期胰岛素抵抗及炎症反应相关。