Puder Jardena J, Schindler Christian, Zahner Lukas, Kriemler Susi
Service of Endocrinology, Diabetes and Metabolism, University of Lausanne, Lausanne, Switzerland.
Int J Pediatr Obes. 2011 Jun;6(2-2):e297-306. doi: 10.3109/17477166.2010.533774. Epub 2010 Nov 22.
To better understand the early development of cardiovascular disease, we examined the association of adiposity measures and cardiorespiratory fitness (CRF) with baseline values and changes in low-grade chronic inflammation and insulin resistance (IR) in school children.
Eighty-three 1(st) and 5(th) grade children from a randomly selected control group of a physical activity intervention study (KISS) were prospectively studied during one academic year. Outcome variables included highly sensitive C-reactive protein (hs-CRP) and homeostasis assessment of IR (HOMA-IR). Adiposity measures included body mass index (BMI), waist circumference and the sum of skinfold thickness at four sites. CRF was assessed by the 20 m shuttle run test. All models were adjusted for age group, sex and pubertal group and included children who had a complete valid dataset for all variables.
Baseline metabolic markers correlated positively with measures of adiposity and inversely with CRF (all p ≤ 0.02). On average, longitudinal changes in hs-CRP concentration increased with high baseline BMI in boys and skinfold thickness in both genders (both p < 0.01). Increases in adiposity had an additional effect on these changes (adjusted R(2) of the models including baseline and change in adiposity 0.49-0.53, p < 0.001). On the other hand, longitudinal changes in HOMA-IR were positively related to changes in BMI and waist circumference (p ≤ 0.03). Increases in HOMA-IR, but not in hs-CRP concentrations, were associated with low baseline CRF (p = 0.01).
The relationship of baseline adiposity and CRF with increases in metabolic risk markers may have relevant implications for long-term cardiovascular risk. International Standard Randomised Controlled Trial Number (ISRCTN):
isrctn.org 15360785.
为了更好地了解心血管疾病的早期发展,我们研究了肥胖指标和心肺适能(CRF)与学童低度慢性炎症和胰岛素抵抗(IR)的基线值及变化之间的关联。
在一个学年期间,对来自一项体育活动干预研究(KISS)随机选择的对照组中的83名一年级和五年级儿童进行了前瞻性研究。结果变量包括高敏C反应蛋白(hs-CRP)和IR的稳态评估(HOMA-IR)。肥胖指标包括体重指数(BMI)、腰围和四个部位皮褶厚度之和。通过20米穿梭跑测试评估CRF。所有模型均根据年龄组、性别和青春期组进行了调整,纳入了所有变量均有完整有效数据集的儿童。
基线代谢标志物与肥胖指标呈正相关,与CRF呈负相关(所有p≤0.02)。平均而言,hs-CRP浓度的纵向变化在男孩中随高基线BMI增加,在男女两性中随皮褶厚度增加(均p<0.01)。肥胖增加对这些变化有额外影响(包括基线和肥胖变化的模型调整R²为0.49 - 0.53,p<0.001)。另一方面,HOMA-IR的纵向变化与BMI和腰围变化呈正相关(p≤0.03)。HOMA-IR的增加而非hs-CRP浓度的增加与低基线CRF相关(p = 0.01)。
基线肥胖和CRF与代谢风险标志物增加之间的关系可能对长期心血管风险具有重要意义。国际标准随机对照试验编号(ISRCTN):
isrctn.org 15360785。