Prostacyclin Analogues and Diabetic Retinopathy Outcomes in Pulmonary Hypertension Patients: A Cohort Analysis
Purpose: To evaluate the association between prostacyclin analogue (PCA) therapy and the long-term incidence of diabetic retinopathy (DR) in patients with diabetes and pulmonary arterial hypertension. Methods: In this retrospective, real-world cohort study, we utilized 1:1 propensity score matching within the TriNetX Global Collaborative Network to compare patients receiving dual therapy including PCAs versus matched controls treated with endothelin receptor antagonists, phosphodiesterase-5 inhibitors, or soluble guanylate cyclase stimulators without PCAs. Patients with a prior DR diagnosis were excluded. The incidence of non-proliferative DR (NPDR), proliferative DR (PDR), and diabetes with ophthalmic complications was assessed over a 5-year period using Cox proportional hazards models and Kaplan-Meier survival analyses. Results: Among matched cohorts, PCA therapy was associated with a significantly lower incidence of NPDR (24 vs. 42 events; hazard ratio [HR] = 0.59; 95% confidence interval [CI], 0.35-0.97; p = 0.0345) and diabetes with ophthalmic complications (65 vs. 99 events; HR = 0.67; 95% CI, 0.49-0.91; p = 0.0105). No statistically significant difference was observed in PDR incidence (10 vs. 15 events; HR = 0.63; 95% CI, 0.27-1.43; p = 0.2617). Conclusions: PCA therapy may be associated with a reduced risk of developing diabetic retinopathy, suggesting potential systemic microvascular protective effects. Further prospective studies are warranted to explore the therapeutic role of PCAs in diabetes-related retinal disease.
Authors
- Natan Lishinsky-Fischer (ORCID: https://orcid.org/0009-0008-5695-9954)
- Jaime Levy
Institutions
- Hebrew University of Jerusalem (IL)
- Hadassah Medical Center (IL)
Publication Details
- Journal
- Retina
- Published
- 2026-03-02
- DOI
- https://doi.org/10.1097/iae.0000000000004821
- Primary Topic
- Retinal Diseases and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00