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儿科代谢综合征:我们有可靠的定义吗?系统综述。

The metabolic syndrome in pediatrics: do we have a reliable definition? A systematic review.

机构信息

Department of Human Pathology of Adulthood and Childhood, Unit of Pediatrics, University of Messina, Messina, Italy.

出版信息

Eur J Endocrinol. 2021 Jul 1;185(2):265-278. doi: 10.1530/EJE-21-0238.

Abstract

OBJECTIVE

Metabolic syndrome is a cluster of cardio-metabolic risk factors associated with an increased risk of cardiovascular disease and type 2 diabetes. In the last two decades, several definitions of metabolic syndrome have been proposed for the pediatric population; all of them agree on the defining components but differ in the suggested criteria for diagnosis. This review aims to analyze the current diagnostic criteria of metabolic syndrome in pediatrics with reference to their feasibility and reliability in clinical practice.

METHODS

The systematic research was conducted from January 2003 to June 2020 through MEDLINE via PubMed, Cochrane Library and EMBASE databases.

RESULTS

After the selection phase, a total of 15 studies (182 screened) met the inclusion criteria and are reported in the present review. Twelve studies were cross-sectional, two were longitudinal and one was a consensus report. The sample population consisted of multiethnic group or single ethnic group, including Turkish, European, Asian and Hispanic subjects.

CONCLUSIONS

To date, there is not a univocal, internationally accepted pediatric definition of metabolic syndrome, which guarantees a high sensitivity and stability of the diagnosis. The definition proposed by IDF results the most straightforward and easy to use in clinical practice, having the unquestionable advantage of requiring measurements quickly accessible in clinical practice, without the adoption of multiple reference tables. Further research is needed to validate a new version of such definition which includes the diagnostic cut-off points recently suggested by published guidelines.

摘要

目的

代谢综合征是一组与心血管疾病和 2 型糖尿病风险增加相关的心血管代谢危险因素。在过去的二十年中,已经为儿科人群提出了几种代谢综合征的定义;它们都同意定义成分,但在诊断的建议标准上有所不同。本综述旨在分析儿科代谢综合征的现行诊断标准,并参考其在临床实践中的可行性和可靠性。

方法

系统研究于 2003 年 1 月至 2020 年 6 月通过 MEDLINE 在 PubMed、Cochrane 图书馆和 EMBASE 数据库中进行。

结果

经过筛选阶段,共有 15 项研究(筛选出的 182 项研究)符合纳入标准,并在本综述中报告。其中 12 项为横断面研究,2 项为纵向研究,1 项为共识报告。样本人群包括多民族群体或单一民族群体,包括土耳其人、欧洲人、亚洲人和西班牙裔。

结论

迄今为止,还没有一个统一的、国际上公认的儿科代谢综合征定义,该定义能保证诊断的高灵敏度和稳定性。IDF 提出的定义在临床实践中最简单易用,具有无可置疑的优势,只需测量在临床实践中快速获得的指标,而无需采用多个参考表。需要进一步的研究来验证这样一个新定义的新版本,该版本包括最近发表的指南中建议的诊断截止值。

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