Department of Nutrition, Food Sciences and Physiology, University of Navarra, Pamplona, Spain.
IdiSNA (Navarra Institute for Health Research), Pamplona, Spain.
Pediatr Diabetes. 2018 Mar;19(2):217-222. doi: 10.1111/pedi.12561. Epub 2017 Jul 27.
Inflammation related molecules such as tumor necrosis factor-α (TNF-α), interleukin 6 (IL-6), and cardiotrophin-1 (CT-1) are highly expressed in obese individuals and could partly explain some comorbidities associated to obesity. In obese children, lifestyle interventions are able to lower inflammation and reduce cardiovascular risk factors associated with obesity. The aim of the present work was to study changes in inflammation-related molecules serum and peripheral blood mononuclear cells (PBMC) transcript levels after a 10-week lifestyle intervention in obese children and asses their potential association with glucose metabolism.
Twenty-three obese children (mean age 11.5 years; 48% males) underwent a 10-week lifestyle not controlled intervention trial. Anthropometric and biochemical measurements were analyzed. Transcript analysis for CT-1, IL-6, and TNF-α in PBMC were performed by RT-PCR. Serum cytokine levels were also measured at baseline and after 10-weeks.
Participants achieved a significant reduction in body adiposity (0.34 decrease in body mass index-standard deviation), total cholesterol, and glucose levels after 10-weeks. A Significant decrease in serum TNF-α and C reactive protein (CRP) were observed. CT-1 transcript levels were significantly reduced (P = .005) after lifestyle intervention, and these changes were significantly correlated with changes in serum CT-1 levels (r = 0.451; P = .031). In multiple regression analysis baseline CT-1 transcript levels were positively associated with final insulin (R = 0.506; P = .035) and HOMA-IR values (R = 0.473; P = .034).
We reported that serum CRP, TNF-α, as well as PBMC CT-1 transcript levels were reduced after lifestyle intervention in obese children. More studies are needed to clarify the role of inflammation-related molecules in glucose metabolism.
在肥胖个体中,炎症相关分子如肿瘤坏死因子-α(TNF-α)、白细胞介素 6(IL-6)和心营养素-1(CT-1)表达水平升高,这在一定程度上可以解释肥胖相关的一些合并症。在肥胖儿童中,生活方式干预能够降低炎症并减少与肥胖相关的心血管危险因素。本研究旨在探讨肥胖儿童生活方式干预 10 周后血清和外周血单个核细胞(PBMC)中炎症相关分子的转录水平变化,并评估其与葡萄糖代谢的潜在相关性。
23 名肥胖儿童(平均年龄 11.5 岁,48%为男性)接受了为期 10 周的生活方式非对照干预试验。分析了人体测量学和生化指标。采用 RT-PCR 法检测 PBMC 中 CT-1、IL-6 和 TNF-α的转录水平。基线和 10 周后测量血清细胞因子水平。
参与者在 10 周后体脂显著减少(体重指数标准差降低 0.34),总胆固醇和血糖水平也显著降低。血清 TNF-α和 C 反应蛋白(CRP)水平显著下降。生活方式干预后 CT-1 转录水平显著降低(P=0.005),且这些变化与血清 CT-1 水平的变化显著相关(r=0.451,P=0.031)。多元回归分析显示,基线 CT-1 转录水平与最终胰岛素(R=0.506,P=0.035)和 HOMA-IR 值(R=0.473,P=0.034)呈正相关。
我们报道了肥胖儿童生活方式干预后血清 CRP、TNF-α和 PBMC CT-1 转录水平降低。需要进一步研究来阐明炎症相关分子在葡萄糖代谢中的作用。