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晚期糖基化终产物受体能否被视为肥胖儿童的心血管风险标志物?

Could receptors for advanced glycation end products be considered cardiovascular risk markers in obese children?

机构信息

Department of Pediatrics, University of Chieti, Chieti, Italy.

出版信息

Antioxid Redox Signal. 2012 Jul 15;17(2):187-91. doi: 10.1089/ars.2012.4525. Epub 2012 Mar 14.

Abstract

Early development of increased cardiovascular risk in obese children and the possible related cardiovascular diseases into adulthood have been shown; however, the underling pathogenetic mechanisms implicated are not yet completely defined. Receptors for advanced glycation end products (RAGE) pathway play a pivotal role in the genesis of abnormality of arterial wall. However, whether obese prepubertal children present impaired levels of endogenous and soluble secretory receptor for advanced glycation end products (esRAGE/sRAGE) and whether an association exists between RAGE levels and carotid intima media thickness (cIMT) are not yet evaluated in this age group. We note that esRAGE and sRAGE were significantly lower in obese children than controls and were independently related to cIMT. Our findings lead to the hypothesis that RAGE system seems to be related to the development of atherosclerosis even in obese prepubertal children.

摘要

肥胖儿童的心血管风险早期增加以及可能相关的成年后心血管疾病已经得到证实;然而,涉及的潜在发病机制尚未完全确定。晚期糖基化终产物(RAGE)途径的受体在动脉壁异常的发生中起着关键作用。然而,肥胖青春期前儿童是否存在内源性和可溶性分泌型晚期糖基化终产物受体(esRAGE/sRAGE)水平受损,以及 RAGE 水平与颈动脉内膜中层厚度(cIMT)之间是否存在关联,在该年龄组尚未得到评估。我们注意到,肥胖儿童的 esRAGE 和 sRAGE 明显低于对照组,并且与 cIMT 独立相关。我们的研究结果表明,RAGE 系统似乎与动脉粥样硬化的发展有关,即使在肥胖青春期前儿童中也是如此。

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