Elian Viviana, Dorita Alina, Stegaru Daniela, Vinereanu Dragos
Diabetes, Nutrition and Metabolic Disease Unit, University of Medicine and Pharmacy Carol Davila, 5-7 Ion Movila Street, 0202475 Bucharest, Romania.
Diabetes, Nutrition and Metabolic Disease Unit, National Institute of Diabetes, Nutrition and Metabolic Disease Prof. N. C. Paulescu, 020475 Bucharest, Romania.
Int J Mol Sci. 2025 Sep 3;26(17):8558. doi: 10.3390/ijms26178558.
Type 1 diabetes (T1D) is a chronic condition with an increasing prevalence worldwide and a significant improvement in life expectancy in the last decades. T1D confers an increased risk of cardiovascular events, driven by elevated LDL cholesterol (LDL-C) and qualitative lipoprotein abnormalities, such as dysfunctional HDL and smaller, denser LDL-C. Lipid-lowering outcome trials have overwhelmingly focused on type 2 diabetes or the general population, resulting in very limited T1D-specific evidence. Recommendations from major medical associations (ADA, ESC/EAS, ACC/AHA, ISPAD) create additional ambiguity regarding the treatment of dyslipidemia in T1D. This review synthesizes the available evidence on dyslipidemia management in T1D, including published observational cohorts, randomized controlled trials, and international guideline recommendations from January 2000 to June 2025. LDL-C remains the primary modifiable risk factor. Each 1 mmol/L increase is associated with 35-50% greater cardiovascular (CV) risk in T1D cohorts. Statin therapy reduces CV risk by up to 25% in patients with diabetes; however, evidence remains limited in patients with T1D. Ezetimibe provides an additional 18% LDL-C lowering and a 14% event reduction in mixed-diabetes trials, while PCSK9 inhibitors offer a potent 40-60% LDL-C reduction and an 18% MACE reduction. The uptake of statins in eligible adults with T1D remains below 50%. Statins remain the cornerstone of dyslipidemia management in T1D, with emerging evidence supporting ezetimibe and PCSK9 inhibitors. The heterogeneity across international guidelines and the scarcity of T1D-specific outcome data underscore the need for targeted research and evidence-based strategies.
1型糖尿病(T1D)是一种慢性疾病,在全球范围内患病率不断上升,并且在过去几十年中预期寿命有了显著提高。T1D会增加心血管事件的风险,这是由低密度脂蛋白胆固醇(LDL-C)升高和定性脂蛋白异常(如功能失调的高密度脂蛋白和更小、更致密的LDL-C)驱动的。降脂结局试验绝大多数都集中在2型糖尿病或普通人群上,导致T1D特异性证据非常有限。主要医学协会(美国糖尿病协会、欧洲心脏病学会/欧洲动脉粥样硬化学会、美国心脏病学会/美国心脏协会、国际儿童和青少年糖尿病学会)的建议在T1D血脂异常治疗方面造成了更多的模糊性。本综述综合了2000年1月至2025年6月期间关于T1D血脂异常管理的现有证据,包括已发表的观察性队列研究、随机对照试验和国际指南建议。LDL-C仍然是主要的可改变风险因素。在T1D队列中,每增加1 mmol/L与心血管(CV)风险增加35%至50%相关。他汀类药物治疗可使糖尿病患者的CV风险降低多达25%;然而,在T1D患者中的证据仍然有限。依折麦布在混合糖尿病试验中可使LDL-C额外降低18%,事件减少14%,而前蛋白转化酶枯草溶菌素9(PCSK9)抑制剂可使LDL-C有效降低40%至60%,主要不良心血管事件(MACE)减少18%。符合条件的T1D成年患者中他汀类药物的使用率仍低于50%。他汀类药物仍然是T1D血脂异常管理的基石,新出现的证据支持依折麦布和PCSK9抑制剂。国际指南之间的异质性以及T1D特异性结局数据的稀缺凸显了针对性研究和循证策略的必要性。