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超重和肥胖儿童及青少年肿瘤坏死因子系统炎症标志物的改变。

Alterations in the inflammatory markers of the Tumor Necrosis Factor system in overweight and obese children and adolescents.

作者信息

Palhares Heloísa Marcelina da Cunha, da Silva Adriana Paula, Tomé Janaíne Machado, da Silva Marcos Vinícius, Rodrigues Júnior Virmondes, Ribeiro Flávia Alves, Oliveira Marília Matos, Fonseca Elvi Cristina Rojas, Valle Ianessa Arantes, Borges Maria de Fátima

机构信息

Department of Endocrinology and Metabology, Federal University of Triângulo Mineiro/ Clinical Hospital, Uberaba, Minas Gerais, Brazil.

Department of Microbiology, Immunology and Parasitology/ Federal University of Triângulo Mineiro/ Clinical Hospital, Uberaba, Minas Gerais, Brazil.

出版信息

PLoS One. 2025 May 13;20(5):e0319832. doi: 10.1371/journal.pone.0319832. eCollection 2025.

Abstract

OBJECTIVE

This study analyzed the association between cardiometabolic risk markers and the tumor necrosis factor system in overweight and obese children and adolescents.

METHODS

This cross-sectional study included 201 overweight (n =  65), obese (n =  96), and eutrophic (n =  40) children and adolescents aged 5 to 19 years. Clinical markers (body mass index, percentage of body fat, waist circumference, systolic and diastolic blood pressures) and laboratory parameters (glucose, insulin, total cholesterol and fractions, triglycerides, homeostasis assessment of insulin resistance index [HOMA-IR], leptin, tumor necrosis fator-α [TNF-α], soluble TNF receptors [sTNFR1 and sTNFR2], soluble Tumor necrosis factor-Related Apoptosis-Inducing Ligand [sTRAIL]) were evaluated.

RESULTS

Serum TNF-α levels did not differ significantly between the participant groups, while the serum concentrations of sTNFR1 were higher in the obesity group, compared with those in the eutrophic and overweight groups. Regarding sTNFR2, there was no significant difference between the three study groups. Serum sTRAIL concentrations were higher in the eutrophic group compared with those in the overweight and obesity groups. We observed a positive correlation between sTNFR1 and body mass index, waist circumference, triglycerides, glucose and leptin levels. There was also a negative correlation between sTRAIL and body mass index, waist circumference, LDL cholesterol, glucose and HOMA-IR levels.

CONCLUSIONS

Inflammatory changes involving the TNF system (sTNFR1, sTRAIL) that correlate with obesity are present since childhood, indicating the need for early intervention in order to avoid cardiometabolic complications in adulthood.

摘要

目的

本研究分析超重和肥胖儿童及青少年心脏代谢风险标志物与肿瘤坏死因子系统之间的关联。

方法

这项横断面研究纳入了201名5至19岁的超重(n = 65)、肥胖(n = 96)和营养正常(n = 40)的儿童及青少年。评估了临床标志物(体重指数、体脂百分比、腰围、收缩压和舒张压)和实验室参数(葡萄糖、胰岛素、总胆固醇及其组分、甘油三酯、胰岛素抵抗稳态评估指数 [HOMA-IR]、瘦素、肿瘤坏死因子-α [TNF-α]、可溶性TNF受体 [sTNFR1和sTNFR2]、可溶性肿瘤坏死因子相关凋亡诱导配体 [sTRAIL])。

结果

各参与组之间血清TNF-α水平无显著差异,而肥胖组血清sTNFR1浓度高于营养正常组和超重组。关于sTNFR2,三个研究组之间无显著差异。营养正常组血清sTRAIL浓度高于超重组和肥胖组。我们观察到sTNFR1与体重指数、腰围甘油三酯、葡萄糖和瘦素水平呈正相关。sTRAIL与体重指数、腰围、低密度脂蛋白胆固醇、葡萄糖和HOMA-IR水平也呈负相关。

结论

涉及TNF系统(sTNFR1、sTRAIL)的与肥胖相关的炎症变化自幼就存在,这表明需要早期干预以避免成年期出现心脏代谢并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/515d/12074418/878b09478541/pone.0319832.g001.jpg

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