降低 1 型糖尿病儿童和青少年颈动脉内膜厚度的干预措施:系统回顾与元分析》。

Frontiers in clinical diabetes and healthcare Pub Date : 2022-07-04 eCollection Date: 2022-01-01 DOI:10.3389/fcdhc.2022.882504
Adina Mihaela Epure, Daniela Anker, Stefano Di Bernardo, Bruno R da Costa, Nicole Sekarski, Arnaud Chiolero
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引用次数: 0

摘要

导言:高血糖与较高的心血管风险有关,患有糖尿病的青少年颈动脉内膜厚度(CIMT)增加就是证明。我们进行了一项系统综述和荟萃分析,以评估药物或非药物干预对糖尿病前期或糖尿病儿童和青少年颈动脉内膜厚度的影响:我们对 MEDLINE、EMBASE 和 CENTRAL 进行了系统检索,并对截至 2019 年 9 月完成的试验登记和其他来源的研究进行了补充检索。考虑纳入评估糖尿病前期或糖尿病儿童和青少年超声CIMT的干预性研究。在适当的情况下,采用随机效应荟萃分析法对各项研究的数据进行汇总。研究质量采用 Cochrane 协作组织的偏倚风险工具和 CIMT 可靠性工具进行评估:共纳入六项研究,涉及 644 名 1 型糖尿病患儿。没有研究涉及糖尿病前期或 2 型糖尿病儿童。三项随机对照试验(RCT)评估了二甲双胍、奎那普利和阿托伐他汀的效果。三项采用前后对比设计的非随机研究评估了体育锻炼和持续皮下注射胰岛素(CSII)的效果。基线时的平均 CIMT 为 0.40 至 0.51 毫米。二甲双胍与安慰剂相比,CIMT 的汇总差异为-0.01 毫米(95% CI:-0.04 至 0.01)(2 项研究;135 名参与者;I2:0%)。与安慰剂相比,喹那普利的 CIMT 差异为-0.01 毫米(95% CI:-0.03 至 0.01)(1 项研究;406 名参与者)。体育锻炼后,CIMT 与基线相比的平均变化为-0.03 毫米(95% CI:-0.14 至 0.08)(1 项研究;7 名参与者)。关于 CSII 或阿托伐他汀的报告结果不一致。有 3 项研究(50%)的 CIMT 测量在所有可靠性方面都被评为较高质量。由于研究性临床试验的数量少、样本量小,以及前后对比研究的偏倚风险高,因此对结果的可信度受到了限制:结论:一些药物干预可降低1型糖尿病儿童的CIMT。结论:一些药物干预可降低 1 型糖尿病患儿的 CIMT,但其效果还存在很大的不确定性,因此无法得出有力的结论。需要通过更大规模的 RCT 研究进一步证明这一点:prospero,CRD42017075169。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Interventions to Decrease Carotid-Intima Media Thickness in Children and Adolescents With Type 1 Diabetes: A Systematic Review and Meta-Analysis.

Interventions to Decrease Carotid-Intima Media Thickness in Children and Adolescents With Type 1 Diabetes: A Systematic Review and Meta-Analysis.

Interventions to Decrease Carotid-Intima Media Thickness in Children and Adolescents With Type 1 Diabetes: A Systematic Review and Meta-Analysis.

Interventions to Decrease Carotid-Intima Media Thickness in Children and Adolescents With Type 1 Diabetes: A Systematic Review and Meta-Analysis.

Introduction: Hyperglycemia is associated with a higher cardiovascular risk, as evidenced by increased carotid-intima media thickness (CIMT) in youth with diabetes. We conducted a systematic review and meta-analysis to assess the effect of pharmacological or non-pharmacological interventions on CIMT in children and adolescents with prediabetes or diabetes.

Methods: We conducted systematic searches of MEDLINE, EMBASE, and CENTRAL, together with supplementary searches in trial registers and other sources for studies completed up to September 2019. Interventional studies assessing ultrasound CIMT in children and adolescents with prediabetes or diabetes were considered for inclusion. Where appropriate, data were pooled across studies using random-effect meta-analysis. Quality was assessed using The Cochrane Collaboration's risk-of-bias tool and a CIMT reliability tool.

Results: Six studies involving 644 children with type 1 diabetes mellitus were included. No study involved children with prediabetes or type 2 diabetes. Three randomized controlled trials (RCTs) evaluated the effects of metformin, quinapril, and atorvastatin. Three non-randomized studies, with a before-and-after design, evaluated the effects of physical exercise and continuous subcutaneous insulin infusion (CSII). The mean CIMT at baseline ranged from 0.40 to 0.51 mm. The pooled difference in CIMT was -0.01 mm (95% CI: -0.04 to 0.01) for metformin compared to placebo (2 studies; 135 participants; I2: 0%). The difference in CIMT was -0.01 mm (95% CI: -0.03 to 0.01) for quinapril compared to placebo (1 study; 406 participants). The mean change from baseline in CIMT was -0.03 mm (95% CI: -0.14 to 0.08) after physical exercise (1 study; 7 participants). Inconsistent results were reported for CSII or for atorvastatin. CIMT measurement was rated at a higher quality on all reliability domains in 3 (50%) studies. The confidence in results is limited by the low number of RCTs and their small sample sizes, as well as the high risk of bias in before-and-after studies.

Conclusions: Some pharmacological interventions may decrease CIMT in children with type 1 diabetes. However, there is great uncertainty with respect to their effects and no strong conclusions can be drawn. Further evidence from larger RCTs is required.

Systematic review registration: PROSPERO, CRD42017075169.

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