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The nuances of atherogenic dyslipidemia in diabetes: Focus on triglycerides and current management strategies

机译:糖尿病中动脉粥样硬化血脂异常的细微差别:关注甘油三酸酯和当前的治疗策略

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摘要

Diabetes mellitus (DM) is a pandemic disease and an important cardiovascular (CV) risk factor. The atherogenic dyslipidemia in diabetes (ADD) is characterized by high serum triglycerides, high small dense LDL levels, low HDL levels and postprandial lipemia. Insulin resistance is a primary cause for ADD. Though statins are highly effective for CVD prevention in DM but a significant residual CV risk remains even after optimal statin therapy. Fibrates, niacin and omega-3 fatty acids are used in addition to statin for treatment of ADD (specifically hypertriglyceridemia). All these drugs have some limitations and they are far from being ideal companions of statins. Many newer drugs are in pipeline for management of ADD. Dual PPAR α/γ agonists are in most advanced stage of clinical development and they have a rational approach as they control blood glucose levels (by reducing insulin resistance, a primary factor for ADD) in addition to modulating ADD. Availability of dual PPAR α/γ agnosits and other drugs for ADD management may improve CV outcomes and decrease morbidity and mortality in diabetic patients in future.
机译:糖尿病(DM)是一种大流行疾病,也是重要的心血管(CV)危险因素。糖尿病(ADD)的致动脉粥样硬化血脂异常的特征在于高血清甘油三酸酯,高的小致密LDL水平,低的HDL水平和餐后血脂。胰岛素抵抗是ADD的主要原因。尽管他汀类药物对于DM的CVD预防非常有效,但是即使经过最佳他汀类药物治疗,仍然存在显着的残留CV风险。除他汀类药物外,还使用贝特类,烟酸和omega-3脂肪酸治疗ADD(特别是高甘油三酯血症)。所有这些药物都有一定的局限性,远非他汀类药物的理想伴侣。许多新药正在管理ADD。 PPARα/γ双重激动剂处于临床开发的最高级阶段,它们除了控制ADD之外,还通过控制血糖水平(通过降低胰岛素抵抗(ADD的主要因素))来控制血糖水平。双重PPARα/γ不可知物和其他药物可用于ADD管理可能会改善糖尿病患者的CV结果并降低未来的发病率和死亡率。

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