Microvascular Disease After Renal Transplantation
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Updated: Mar 30, 2026

Murine Kidney Transplant Technique
Published on: October 20, 2015
Qi Lun Ooi1, Foong Kien Newk-Fon Hey Tow, Raj Deva
1The University of Melbourne, Department of Medicine (Northern Health), Epping, Australia.
Insights
Kidney transplant recipients and patients with end-stage kidney disease (CKD5) show similar rates and severity of microvascular disease. This suggests microvascular changes may persist post-transplantation, potentially increasing cardiac event risk.
Area of Science:
- Nephrology
- Ophthalmology
- Vascular Biology
Background:
- End-stage kidney disease (CKD5) confers a high risk of vascular events.
- This risk persists even after successful renal transplantation.
- Microvascular disease is a key contributor to vascular complications.
Purpose of the Study:
- To compare the prevalence and severity of microvascular disease in renal transplant recipients versus patients with CKD5.
- To assess retinal microvascular changes in these two patient groups.
Main Methods:
- Retinal photography was performed on 92 transplant recipients and 70 CKD5 patients.
- Images were analyzed for hypertensive/microvascular retinopathy using the Wong and Mitchell classification.
- Vessel caliber was measured using a computer-assisted method.
Main Results:
- No significant difference in moderate-severe retinopathy prevalence between transplant recipients (50%) and CKD5 patients (54%).
- Mean arteriole and venular calibers were similar between the two groups.
- Vessel caliber remained unchanged before and after transplantation in a subset of patients.
Conclusions:
- Hypertensive/microvascular disease is equally prevalent and severe in transplant recipients and CKD5 patients.
- Microvascular disease may be a significant factor contributing to cardiac events post-renal transplantation.
Background/Aims:
Individuals who reach end-stage kidney disease (CKD5) have a high risk of vascular events that persists even after renal transplantation. This study compared the prevalence and severity of microvascular disease in transplant recipients and patients with CKD5.
Methods:
Individuals with a renal transplant or CKD5 were recruited consecutively from renal clinics, and underwent bilateral retinal photography (Canon CR5-45, Canon). Their retinal images were deidentified and reviewed for hypertensive/microvascular signs by an ophthalmologist and a trained grader (Wong and Mitchell classification), and for vessel caliber at a grading centre using a computer-assisted method and Knudtson's modification of the Parr-Hubbard formula.
Results:
Ninety-two transplant recipients (median duration 6.4 years, range 0.8 to 28.8) and 70 subjects with CKD5 were studied. Transplant recipients were younger (p<0.001), with a higher eGFR (p< 0.001), but were just as likely to have a moderate-severe hypertensive/microvascular retinopathy (46/92, 50%) as subjects with CKD5 (38/70, 54%; OR 0.84, CI 0.45 to 1.57, p=0.64), and had similar mean arteriole and venular calibres (135.1 ± 7.5 µm and 137.9 ± 14.9 µm, p=0.12; and 199.1 ± 17.8 µm and 202.4 ± 27.8 µm, p=0.36, respectively). Arteriole and venular caliber were not different in nine patients examined before and after transplantation (p=0.62 and p=0.11, respectively).
Conclusions:
Hypertensive/microvascular disease occurred just as often and was generally as severe in transplant recipients and subjects with CKD5. Microvascular disease potentially contributes to increased cardiac events post-transplantation.
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