Kang Eugene Yu-Chuan, Kang Chunya, Wu Wei-Chi, Sun Chi-Chin, Chen Kuan-Jen, Lai Chi-Chun, Chen Tien-Hsing, Hwang Yih-Shiou
Department of Ophthalmology, Chang Gung Memorial Hospital, Linkou Medical Center, Taoyuan 333, Taiwan.
College of Medicine, Chang Gung University, Taoyuan 333, Taiwan.
J Clin Med. 2021 Jun 28;10(13):2871. doi: 10.3390/jcm10132871.
This study aimed to investigate the association of add-on dipeptidyl peptidase-4 inhibitor (DPP4i) therapy and the progression of diabetic retinopathy (DR). In this retrospective population-based cohort study, we examined Taiwanese patients with type 2 diabetes, preexisting DR, and aged ≥40 years from 2009 to 2013. Prescription of DPP4i was defined as a medication possession ratio of ≥80% during the first 6 months. The outcomes included vitreous hemorrhage (VH), tractional retinal detachment, macular edema, and interventions including retinal laser therapy, intravitreal injection (IVI), and vitrectomy. Of 1,767,640 patients, 62,824 were eligible for analysis. After matching, the DPP4i and non-DPP4i groups each contained 20,444 patients. The risks of VH ( = 0.013) and macular edema ( = 0.035) were higher in the DPP4i group. The DPP4i group also had higher risks of receiving surgical interventions (retinal laser therapy ( < 0.001), IVI ( = 0.049), vitrectomy ( < 0.001), and any surgical intervention ( < 0.001)). More patients in the DPP4i group received retinal laser therapy ( < 0.001) and IVI ( = 0.001) than in the non-DPP4i group. No between-group differences in cardiovascular outcomes were noted. In the real-world database study, add-on DPP4i therapy may be associated with the progression of DR in patients with type 2 diabetes. No additional cardiovascular risks were found. The early progression of DR in rapid glycemic control was inconclusive in our study. The possible effect of add-on DPP4i therapy in the progression of DR in patients with type 2 diabetes requires further research.
本研究旨在探讨加用二肽基肽酶-4抑制剂(DPP4i)治疗与糖尿病视网膜病变(DR)进展之间的关联。在这项基于人群的回顾性队列研究中,我们调查了2009年至2013年期间年龄≥40岁、患有2型糖尿病且已存在DR的台湾患者。DPP4i的处方定义为前6个月内药物持有率≥80%。研究结局包括玻璃体积血(VH)、牵拉性视网膜脱离、黄斑水肿以及包括视网膜激光治疗、玻璃体腔内注射(IVI)和玻璃体切除术在内的干预措施。在1767640例患者中,62824例符合分析条件。匹配后,DPP4i组和非DPP4i组各有20444例患者。DPP4i组发生VH( = 0.013)和黄斑水肿( = 0.035)的风险更高。DPP4i组接受手术干预的风险也更高(视网膜激光治疗( < 0.001)、IVI( = 0.049)、玻璃体切除术( < 0.001)以及任何手术干预( < 0.001))。与非DPP4i组相比,DPP4i组接受视网膜激光治疗( < 0.001)和IVI( = 0.001)的患者更多。未观察到两组在心血管结局方面的差异。在这项真实世界数据库研究中,加用DPP4i治疗可能与2型糖尿病患者DR的进展相关。未发现额外的心血管风险。在我们的研究中,血糖快速控制时DR的早期进展尚无定论。加用DPP4i治疗对2型糖尿病患者DR进展的可能影响需要进一步研究。