Suppr超能文献

髓过氧化物酶是青春期前肥胖儿童炎症和心血管风险的早期生物标志物。

Myeloperoxidase is an early biomarker of inflammation and cardiovascular risk in prepubertal obese children.

机构信息

Department of Biochemistry and Molecular Biology II, Institute of Nutrition and Food Technology, Center for Biomedical Research, University of Granada, Granada, Spain.

出版信息

Diabetes Care. 2012 Nov;35(11):2373-6. doi: 10.2337/dc12-0614. Epub 2012 Aug 21.

Abstract

OBJECTIVE

Obesity is associated with a state of chronic low-grade inflammation. Myeloperoxidase (MPO) plays an important role in the initiation and progression of acute and chronic inflammatory diseases, such as cardiovascular disease (CVD). The objectives of the current study were to evaluate plasma MPO levels in prepubertal obese children and to determine whether MPO could be an early biomarker of inflammation and CVD risk.

RESEARCH DESIGN AND METHODS

In a prospective multicenter case-control study paired by age and sex of 446 Caucasian prepubertal children ages 6-12 years, 223 normal-weight and 223 obese children were recruited. Blood pressure, waist circumference, weight, and height were measured. In addition to MPO, glucose, insulin, metabolic lipid parameters, oxidized low-density lipoproteins, adiponectin, leptin, resistin, C-reactive protein (CRP), interleukin 6, tumor necrosis factor α, matrix metalloproteinase-9 (MMP-9), and plasminogen activator inhibitor 1 were determined.

RESULTS

We found that MPO was elevated in prepubertal obese children and that this enzyme was associated with such proinflammatory and cardiovascular risk biomarkers as CRP, MMP-9, and resistin. Insulin resistance calculated by the homeostatic assessment model was the best predictor of MPO.

CONCLUSIONS

MPO is an early biomarker of inflammation associated with CVD risk in obese children at the prepubertal age.

摘要

目的

肥胖与慢性低度炎症状态有关。髓过氧化物酶(MPO)在急性和慢性炎症性疾病(如心血管疾病(CVD))的发生和进展中起着重要作用。本研究的目的是评估青春期前肥胖儿童的血浆 MPO 水平,并确定 MPO 是否可以作为炎症和 CVD 风险的早期生物标志物。

研究设计和方法

在一项前瞻性、多中心病例对照研究中,对 446 名 6-12 岁的白种人青春期前儿童按年龄和性别进行配对,其中 223 名体重正常,223 名肥胖。测量血压、腰围、体重和身高。除 MPO 外,还测定了葡萄糖、胰岛素、代谢脂质参数、氧化型低密度脂蛋白、脂联素、瘦素、抵抗素、C 反应蛋白(CRP)、白细胞介素 6、肿瘤坏死因子-α、基质金属蛋白酶-9(MMP-9)和纤溶酶原激活物抑制剂 1。

结果

我们发现青春期前肥胖儿童的 MPO 升高,这种酶与 CRP、MMP-9 和抵抗素等促炎和心血管风险生物标志物相关。稳态评估模型计算的胰岛素抵抗是 MPO 的最佳预测因子。

结论

MPO 是青春期前肥胖儿童与 CVD 风险相关的炎症的早期生物标志物。

相似文献

3
Waist-to-height ratio, inflammation and CVD risk in obese children.肥胖儿童的腰高比、炎症与心血管疾病风险
Public Health Nutr. 2014 Oct;17(10):2378-85. doi: 10.1017/S1368980013003285. Epub 2014 Jan 2.
6
Waist circumference is related to low-grade inflammation in youth.腰围与年轻人的低度炎症有关。
Int J Pediatr Obes. 2010 Aug;5(4):313-9. doi: 10.3109/17477160903497035.

引用本文的文献

3
Skeletal muscle disorders as risk factors for type 2 diabetes.骨骼肌疾病作为2型糖尿病的风险因素。
Mol Cell Endocrinol. 2025 Apr 1;599:112466. doi: 10.1016/j.mce.2025.112466. Epub 2025 Jan 21.
4
Effect of Diet on HDL in Obesity.饮食对肥胖症患者高密度脂蛋白的影响。
Molecules. 2024 Dec 17;29(24):5955. doi: 10.3390/molecules29245955.

本文引用的文献

2
Elevated plasma myeloperoxidase concentration in adults with obesity.肥胖成年人血浆髓过氧化物酶浓度升高。
Clin Chim Acta. 2011 Sep 18;412(19-20):1891-2. doi: 10.1016/j.cca.2011.06.010. Epub 2011 Jun 15.
3
Inflammatory mechanisms in obesity.肥胖中的炎症机制。
Annu Rev Immunol. 2011;29:415-45. doi: 10.1146/annurev-immunol-031210-101322.
4
Assessment of endothelial dysfunction.内皮功能障碍的评估。
Expert Rev Cardiovasc Ther. 2010 Apr;8(4):557-71. doi: 10.1586/erc.09.184.
6
TNF-alpha and obesity.肿瘤坏死因子-α与肥胖
Curr Dir Autoimmun. 2010;11:145-56. doi: 10.1159/000289203. Epub 2010 Feb 18.
7
Assessment and management of hypertension in children and adolescents.儿童和青少年高血压的评估和管理。
Nat Rev Cardiol. 2010 Mar;7(3):155-63. doi: 10.1038/nrcardio.2009.231. Epub 2010 Jan 12.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验