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Increased placental growth factor (PlGF) concentrations in children and adolescents with obesity and the metabolic syndrome

机译:肥胖和代谢综合征儿童和青少年的胎盘生长因子(PlGF)浓度升高

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OBJECTIVE: Childhood obesity and the Metabolic Syndrome (MetS) are associated with an increased risk for early onset endothelial dysfunction and atherosclerosis. Placental growth factor (PlGF), a member of the vascular endothelial growth factor family, plays an important role in atherosclerosis by stimulating angiogenesis and atherogenic migration of monocytes/macrophages into the arterial wall. The aim of this study was to investigate differences in circulating PlGF concentrations between children with obesity/metabolic syndrome and non-obese children. We have previously shown increased high-sensitivity troponin (hs-TnT) concentrations in children with MetS from the same cohort. DESIGN: Fifty-seven obese (49 without and 8 with MetS) and 25 non-obese children (controls) were assessed at the Childhood Obesity Clinic of our Department. Obesity was defined using the IOTF criteria. MetS was defined based on the IDF criteria. PlGF was measured using electrochemiluminescence methodology. RESULTS: Mean PIGF concentrations of obese children were significantly higher (p=0.048) compared with those of the controls. Analysis of the three groups, the οbese (without MetS), the MetS and the control, demonstrated a significant difference in PlGF concentrations (p=0.035). Subgroup analysis revealed increased PlGF concentrations in children with the MetS compared to the controls (p=0.009). Troponin had a significant positive correlation with PlGF overall (p=0.003) and in the obese group (p=0.046). CONCLUSIONS: Increased serum concentrations of PlGF, a biomarker of angiogenesis, are found in obese children with the MetS compared to non-obese controls, whereas PlGF correlated positively with troponin. Longitudinal studies may reveal the prognostic role of this biomarker in the progression of atherosclerosis in obese children with the MetS.
机译:目的:儿童肥胖和代谢综合征(MetS)与早期发作的内皮功能障碍和动脉粥样硬化的风险增加有关。胎盘生长因子(PlGF)是血管内皮生长因子家族的成员,通过刺激单核细胞/巨噬细胞向血管壁的血管生成和动脉粥样硬化迁移,​​在动脉粥样硬化中起重要作用。这项研究的目的是调查肥胖/代谢综合征儿童与非肥胖儿童之间循环中PlGF浓度的差异。我们先前已经显示,来自同一队列的MetS儿童的高敏感性肌钙蛋白(hs-TnT)浓度增加。设计:我们部门的儿童肥胖诊所评估了57名肥胖症患者(49名无肥胖症,8名MetS肥胖)和25名非肥胖儿童(对照)。肥胖症是根据IOTF标准定义的。 MetS是根据IDF标准定义的。使用电化学发光方法测量PlGF。结果:与对照组相比,肥胖儿童的平均PIGF浓度显着更高(p = 0.048)。对三个组(肥胖(无MetS),MetS和对照)的分析表明,PlGF浓度存在显着差异(p = 0.035)。亚组分析显示,与对照组相比,患有MetS的儿童的PlGF浓度升高(p = 0.009)。肌钙蛋白与整体PlGF(p = 0.003)和肥胖组(p = 0.046)呈显着正相关。结论:与非肥胖对照组相比,MetS肥胖儿童的血清PlGF浓度升高是血管生成的生物标志物,而PlGF与肌钙蛋白呈正相关。纵向研究可能揭示这种生物标志物在肥胖儿童MetS的动脉粥样硬化进展中的预后作用。

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