Horii Takeshi, Kawaguchi Marina, Ikegami Yuichi, Oikawa Yoichi, Shimada Akira, Mihara Kiyoshi
Department of Pharmacy, Faculty of Pharmacy, Musashino University, Tokyo, Japan.
Department of Endocrinology and Diabetes, School of Medicine, Saitama Medical University, Saitama, Japan.
Sci Rep. 2025 Jun 3;15(1):19358. doi: 10.1038/s41598-025-03797-9.
Diabetic foot lesions are becoming increasingly prevalent due to increases in type 2 diabetes (T2D), aging populations, and atherosclerotic diseases. Individuals with T2D with comorbid lower extremity artery disease (LEAD) are particularly susceptible. Although pharmacological therapies are often combined with risk management strategies, like exercise and smoking cessation, their roles in preventing LEAD progression are unclear. Herein, we investigated factors suppressing LEAD progression in T2D. Using data from the DeSC database, this retrospective cross-sectional study defined severe LEAD as a diagnosis requiring revascularization (Revasc). Logistic regression analysis was used to calculate odds ratios (ORs) for associated factors. The analysis included 243,606 patients with T2D divided into two groups; those with (n = 890) and without (n = 242,716) Revasc. Subgroup analysis of patients with LEAD (n = 27,258) with (n = 890) and without (n = 26,368) Revasc was also conducted. Sodium-glucose cotransporter 2 inhibitors (SGLT2is) (OR 0.50), metformin (OR 0.78), and fibrates (OR 0.75) were associated with a significant reduction in severe LEAD in the primary and subgroup analyses. In conclusion, the active use of SGLT2 inhibitors, metformin, and fibrates may help prevent LEAD progression. However, these medications are associated with adverse events, making it essential to manage patients individually to optimize benefits while minimizing risks.
由于2型糖尿病(T2D)、人口老龄化以及动脉粥样硬化疾病的增加,糖尿病足病变正变得越来越普遍。患有T2D合并下肢动脉疾病(LEAD)的个体尤其易感。尽管药物治疗通常与运动和戒烟等风险管理策略相结合,但其在预防LEAD进展中的作用尚不清楚。在此,我们研究了抑制T2D中LEAD进展的因素。利用来自DeSC数据库的数据,这项回顾性横断面研究将严重LEAD定义为需要血管重建(Revasc)的诊断。采用逻辑回归分析计算相关因素的比值比(OR)。分析纳入了243,606例T2D患者,分为两组;有血管重建(n = 890)和无血管重建(n = 242,716)的患者。还对有(n = 890)和无(n = 26,368)血管重建的LEAD患者(n = 27,258)进行了亚组分析。在主要分析和亚组分析中,钠-葡萄糖协同转运蛋白2抑制剂(SGLT2is)(OR 0.50)、二甲双胍(OR 0.78)和贝特类药物(OR 0.75)与严重LEAD的显著降低相关。总之,积极使用SGLT2抑制剂、二甲双胍和贝特类药物可能有助于预防LEAD进展。然而,这些药物与不良事件相关,因此必须对患者进行个体化管理,以在将风险降至最低的同时优化获益。