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1型糖尿病中的血脂异常:分子机制与治疗机遇

Dyslipidaemia in Type 1 Diabetes: Molecular Mechanisms and Therapeutic Opportunities.

作者信息

O'Brien Stephen T, Neylon Orla M, O'Brien Timothy

机构信息

Department of Paediatrics, University Hospital Limerick, V94 F858 Limerick, Ireland.

Department of Medicine, School of Medicine, National University of Ireland, H91 TK33 Galway, Ireland.

出版信息

Biomedicines. 2021 Jul 16;9(7):826. doi: 10.3390/biomedicines9070826.

Abstract

Cardiovascular disease (CVD) is the leading cause of death in Type 1 Diabetes (T1D). The molecular basis for atherosclerosis in T1D is heavily influenced by hyperglycaemia and its atherogenic effects on LDL. Ongoing research into the distinct pathophysiology of atherosclerosis in T1D offers exciting opportunities for novel approaches to calculate CVD risk in patients with T1D and to manage this risk appropriately. Currently, despite the increased risk of CVD in the T1D population, there are few tools available for estimating the risk of CVD in younger patients. This poses significant challenges for clinicians in selecting which patients might benefit from lipid-lowering therapies over the long term. The current best practice guidance for the management of dyslipidaemia in T1D is generally based on evidence from patients with T2D and the opinion of experts in the field. In this review article, we explore the unique pathophysiology of atherosclerosis in T1D, with a specific focus on hyperglycaemia-induced damage and atherogenic LDL modifications. We also discuss the current clinical situation of managing these patients across paediatric and adult populations, focusing on the difficulties posed by a lack of strong evidence and various barriers to treatment.

摘要

心血管疾病(CVD)是1型糖尿病(T1D)患者的主要死因。T1D患者动脉粥样硬化的分子基础受高血糖及其对低密度脂蛋白(LDL)的致动脉粥样硬化作用的严重影响。对T1D患者动脉粥样硬化独特病理生理学的持续研究为计算T1D患者心血管疾病风险及合理管理该风险的新方法提供了令人兴奋的机会。目前,尽管T1D人群患心血管疾病的风险增加,但用于评估年轻患者心血管疾病风险的工具很少。这给临床医生在选择哪些患者可能长期受益于降脂治疗方面带来了重大挑战。目前T1D患者血脂异常管理的最佳实践指南通常基于2型糖尿病患者的证据和该领域专家的意见。在这篇综述文章中,我们探讨了T1D患者动脉粥样硬化的独特病理生理学,特别关注高血糖诱导的损伤和致动脉粥样硬化的LDL修饰。我们还讨论了在儿科和成人人群中管理这些患者的当前临床情况,重点关注缺乏有力证据所带来的困难以及各种治疗障碍。

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