©The Author(s) 2025.
World J Diabetes. Oct 15, 2025; 16(10): 110138
Published online Oct 15, 2025. doi: 10.4239/wjd.v16.i10.110138
Published online Oct 15, 2025. doi: 10.4239/wjd.v16.i10.110138
Table 2 The ten most significantly affected biological pathways and molecules related to diabetic retinopathy identified through ingenuity pathway analysis
| Ingenuity canonical pathways | -log (P value) | Molecules |
| Assembly of RNA polymerase I complex | 2.57 | TAF1C |
| Rap1 signalling | 2.48 | PRKG1 |
| BMAL1: CLOCK, NPAS2 activates circadian gene expression | 2.26 | KLF15 |
| SIRT1 negatively regulates rRNA expression | 2.22 | TAF1C |
| Oxytocin in spinal neurons signaling pathway | 2.14 | PRKG1 |
| Netrin-1 signaling | 1.99 | SLIT3 |
| RNA polymerase I transcription | 1.99 | TAF1C |
| B-WICH complex positively regulates rRNA expression | 1.97 | TAF1C |
| Platelet homeostasis | 1.75 | PRKG1 |
| Beta-catenin independent Wnt signaling | 1.68 | PRKG1 |
- Citation: Huang YC, Liao WL, Lin HJ, Huang YT, Chang YW, Yang JS, Weng AL, Tsai FJ. Polygenic risk score for predicting diabetic retinopathy in patients with type 2 diabetes: A twenty-year follow-up study. World J Diabetes 2025; 16(10): 110138
- URL: https://www.wjgnet.com/1948-9358/full/v16/i10/110138.htm
- DOI: https://dx.doi.org/10.4239/wjd.v16.i10.110138