Department of Paediatrics and Endocrinology, Medical University of Warsaw, Warsaw, Poland.
Department of Laboratory Diagnostics and Clinical Immunology of Developmental Age, Medical University of Warsaw, Warsaw, Poland.
Front Endocrinol (Lausanne). 2022 Aug 19;13:963467. doi: 10.3389/fendo.2022.963467. eCollection 2022.
Childhood obesity contributes to the development of cardiovascular diseases. The molecular pathway - receptor activator of nuclear factor-κβ ligand (RANKL), its receptor RANK and osteoprotegerin (OPG) - takes part not only in bone metabolism but is also involved in the atherosclerosis process. RANKL stimulates osteogenic differentiation and calcification of vascular smooth cells. The associations between the OPG-sRANKL system and various cardiovascular risk factors were displayed. We aimed to evaluate the relationships between serum sRANKL (soluble RANKL) levels and the OPG/sRANKL ratio with cardiometabolic risk factors in overweight and obese children.
The study included 70 children with overweight and obesity (mean age 13.0 ± 2.8) and 35 age-matched normal weight, healthy peers as a control group. In all patients, anthropometric measurements and laboratory tests were performed. Additionally, an oral glucose tolerance test (OGTT) was made only in overweight and obese children. Atherogenic and insulin resistance indices were calculated.
Overweight and obese children had lower sRANKL levels compared to the control group (median 276.95 vs 325.90, p=0.011), and consequently a higher OPG/sRANKL ratio (0.02 vs 0.01, p = 0.013). The studied children in the lowest quartile of sRANKL levels had higher body weight, Body Mass Index, waist circumference and increased glucose and insulin levels 60 minutes after OGTT and higher uric acid values compared to children in the highest quartile. In multivariable linear regression analysis sRANKL negatively correlated only with uric acid (β = - 0.508, p = 0.041). No association was found for the OPG/sRANKL ratio.
Excess fat mass seems to alter the OPG/RANKL ratio mainly by reducing serum sRANKL levels. The correlation between sRANKL and uric acid may suggest a contribution of the OPG-sRANKL system in the cardiometabolic process, but that observation should be confirmed in future studies.
儿童肥胖会导致心血管疾病的发生。分子途径——核因子-κβ配体(RANKL)的受体激活物、其受体 RANK 和护骨素(OPG)——不仅参与骨代谢,还参与动脉粥样硬化过程。RANKL 刺激成骨细胞分化和血管平滑肌细胞钙化。显示了 OPG-sRANKL 系统与各种心血管危险因素之间的关联。我们旨在评估超重和肥胖儿童血清可溶性 RANKL(sRANKL)水平与 OPG/sRANKL 比值与心脏代谢危险因素之间的关系。
该研究纳入了 70 名超重和肥胖儿童(平均年龄 13.0±2.8 岁)和 35 名年龄匹配的健康正常体重儿童作为对照组。所有患者均进行了体格测量和实验室检查。此外,仅在超重和肥胖儿童中进行口服葡萄糖耐量试验(OGTT)。计算了致动脉粥样硬化和胰岛素抵抗指数。
与对照组相比,超重和肥胖儿童的 sRANKL 水平较低(中位数 276.95 比 325.90,p=0.011),因此 OPG/sRANKL 比值较高(0.02 比 0.01,p=0.013)。sRANKL 水平最低四分位数的研究儿童体重、体重指数、腰围较高,OGTT 后 60 分钟血糖和胰岛素水平升高,尿酸值较高,而最高四分位数的儿童则较低。多元线性回归分析显示,sRANKL 仅与尿酸呈负相关(β=-0.508,p=0.041)。OPG/sRANKL 比值无相关性。
过多的脂肪似乎主要通过降低血清 sRANKL 水平来改变 OPG/RANKL 比值。sRANKL 与尿酸之间的相关性可能表明 OPG-sRANKL 系统在心脏代谢过程中的作用,但这一观察结果需要在未来的研究中得到证实。