Małyszczak Artur, Przeździecka-Dołyk Joanna, Szydełko-Paśko Urszula, Misiuk-Hojło Marta
Department and Clinic of Ophthalmology, Wroclaw Medical University, 50-367 Wroclaw, Poland.
Ophthalmology Clinical Center SPEKTRUM, Research and Development Center CREO, 53-334 Wroclaw, Poland.
J Clin Med. 2024 Mar 20;13(6):1797. doi: 10.3390/jcm13061797.
: The aim of this study is to compare the effect of sodium-glucose cotransporter-2 inhibitors (SGLT-2i), glucagon-like peptide-1 receptor agonists (GLP-1RA), and dipeptidyl peptidase-4 inhibitors (DPP-4i) on the risk of diabetic retinopathy (DR) in patients with type 2 diabetes (DM2). We systematically searched the databases Pubmed, Embase, and Clinicaltrials up to October 2, 2023, for randomized clinical trials (RCTs) of drugs from the GLP-1RA, SGLT-2i, and DPP-4i groups, with at least 24 weeks duration, including adult patients with DM2 and reported ocular complications. A pairwise meta-analysis was performed to calculate the odds ratio (OR) of DR incidents. Our study included 61 RCTs with a total of 188,463 patients and 2773 DR events. Pairwise meta-analysis showed that included drug groups did not differ in the risk of DR events: GLP1-RA vs. placebo (OR 1.08; CI 95% 0.94, 1.23), DPP-4i vs. placebo (OR 1.10; CI 95% 0.84, 1.42), SGLT2i vs. placebo (OR 1.02; CI 95% 0.76, 1.37). Empagliflozin may be associated with a lower risk of DR, but this sub-analysis included only three RCTs (OR 0.38; 95% CI 0.17, 0.88, = 0.02). Based on currently available knowledge, it is challenging to conclude that the new antidiabetic drugs significantly differ in their effect on DR complications.
本研究的目的是比较钠-葡萄糖协同转运蛋白2抑制剂(SGLT-2i)、胰高血糖素样肽-1受体激动剂(GLP-1RA)和二肽基肽酶-4抑制剂(DPP-4i)对2型糖尿病(DM2)患者糖尿病视网膜病变(DR)风险的影响。我们系统检索了截至2023年10月2日的数据库PubMed、Embase和Clinicaltrials,以查找GLP-1RA、SGLT-2i和DPP-4i组药物的随机临床试验(RCT),试验持续时间至少24周,纳入成年DM2患者并报告眼部并发症。进行了成对荟萃分析以计算DR事件的比值比(OR)。我们的研究纳入了61项RCT,共188463例患者和2773例DR事件。成对荟萃分析表明,各药物组在DR事件风险方面无差异:GLP-1RA与安慰剂相比(OR 1.08;95%CI 0.94,1.23),DPP-4i与安慰剂相比(OR 1.10;95%CI 0.84,1.42),SGLT-2i与安慰剂相比(OR 1.02;95%CI 0.76,1.37)。恩格列净可能与较低的DR风险相关,但该亚组分析仅包括三项RCT(OR 0.38;95%CI 0.17,0.88,P = 0.02)。基于目前可得的知识,很难得出结论认为新型抗糖尿病药物对DR并发症的影响存在显著差异。