Hauser Christoph, Lona Giulia, Köchli Sabrina, Streese Lukas, Infanger Denis, Faude Oliver, Hanssen Henner
Department of Sport, Exercise and Health, Medical Faculty, University of Basel, Basel, Switzerland.
Front Physiol. 2024 Jul 19;15:1371618. doi: 10.3389/fphys.2024.1371618. eCollection 2024.
Skin-derived advanced glycation end products (sAGEs) have been associated with cardiovascular (CV) risk and mortality in adults. We hypothesize that cardiorespiratory fitness (CRF), body mass index (BMI) and vascular health are associated with development of sAGEs during childhood.
In our prospective cohort study, 1171 children aged 6-8 years were screened for sAGEs, BMI, retinal arteriolar diameters (CRAE) and pulse wave velocity (PWV), using standardized procedures. To determine CRF a 20 m shuttle run was performed. After four 4 years, all parameters were assessed in 675 children using the same protocols.
Higher initial CRF levels were significantly associated with lower sAGEs (β [95 CI] -0.02 [-0.03 to -0.002] au, = 0.022) levels at follow-up, although they showed a greater change from baseline to follow-up (β [95 CI] 0.02 [0.002 to 0.03] au, = 0.027). Moreover, individuals with higher sAGEs at baseline showed narrower CRAE (β [95% CI] -5.42 [-8.76 to -2.08] μm, = 0.001) at follow-up and showed a greater change in CRAE (β [95% CI] -3.99 [-7.03 to -0.96] μm, = 0.010) from baseline to follow-up.
Exercise and higher CRF may help mitigate the formation of AGEs during childhood, thereby reducing the risk for development of CV disease associated with AGEs-induced damage. Preventive strategies may need to target CRF early in life to achieve improvement of CV risk factors and may counteract the development of CV disease later in life.
皮肤衍生的晚期糖基化终产物(sAGEs)与成人的心血管(CV)风险和死亡率相关。我们假设心肺适能(CRF)、体重指数(BMI)和血管健康与儿童期sAGEs的发生有关。
在我们的前瞻性队列研究中,使用标准化程序对1171名6 - 8岁儿童进行了sAGEs、BMI、视网膜小动脉直径(CRAE)和脉搏波速度(PWV)的筛查。为了确定CRF,进行了20米穿梭跑测试。4年后,使用相同方案对675名儿童的所有参数进行了评估。
较高的初始CRF水平与随访时较低的sAGEs水平(β[95%可信区间]-0.02[-0.03至-0.002]au,P = 0.022)显著相关,尽管从基线到随访其变化更大(β[95%可信区间]0.02[0.002至0.03]au,P = 0.027)。此外,基线时sAGEs较高的个体在随访时CRAE较窄(β[95%可信区间]-5.42[-8.76至-2.08]μm,P = 0.