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Published on: April 28, 2013
Glomerular Neovascularization in Nondiabetic Renal Allograft Is Associated with Calcineurin Inhibitor Toxicity
Anri Sawada1,2, Masayoshi Okumi3, Shigeru Horita4
1Department of Analytic Human Pathology, Nippon Medical School, Tokyo, Japan, anri-sawada@nms.ac.jp.
Introduction:
Extra efferent arterioles, also known as polar vasculosis (PV), are often observed in the glomerular vascular pole and are associated with glomerular hypertrophy, indicating early recurrent diabetic kidney disease (DKD) in renal allografts. However, its significance in patients without diabetes remains uncertain.
Methods:
A total of 9,004 renal allograft biopsy specimens obtained between January 2007 and December 2017 at Tokyo Women's Medical University were retrospectively analyzed to examine the clinical and pathological significance of PV in renal allografts. PV was identified in 186 biopsy specimens obtained from 165 patients. The PV group comprised 46 patients; 35 patients without DKD and 11 patients with DKD as the initial cause of ESRD, whose clinical information was available and treated with the calcineurin inhibitor (CNI) tacrolimus. The non-PV group comprising patients with renal allografts matched for age and postoperative day included 93 patients without DKD and 16 patients with DKD as the initial cause of ESRD.
Results:
In patients with nondiabetic renal allografts, systolic blood pressure was significantly higher in the PV group than in the non-PV group. The trough tacrolimus levels during the overall study period and at 2 weeks, 1 month, and 2 years after transplantation were significantly higher in the PV group compared with the non-PV group. Glomerulomegaly was significantly more common. Moreover, ah and aah scores in Banff score were significantly higher in the PV group than in the non-PV group. In those with diabetic renal allografts, although the clinical parameters and tacrolimus trough levels in all time periods were not significantly different between the PV and non-PV groups, the ah score was significantly higher in the PV group.
Conclusion:
PV was associated with CNI toxicity in nondiabetic but not in diabetic renal allografts. The pathogenesis of PV in renal allografts is considered to be multifactorial.
Insights
Extra efferent arterioles (polar vasculosis) in kidney transplants are linked to calcineurin inhibitor toxicity in non-diabetic patients. This finding highlights potential risks in specific transplant populations.
Area of Science:
- Nephrology
- Transplantation Immunology
- Pathology
Background:
- Extra efferent arterioles, termed polar vasculosis (PV), are observed in renal allografts and linked to glomerular hypertrophy, suggesting early diabetic kidney disease (DKD).
- The clinical significance of PV in non-diabetic patients with renal allografts remains unclear.
Purpose of the Study:
- To investigate the clinical and pathological significance of polar vasculosis (PV) in renal allografts.
- To determine the association between PV and calcineurin inhibitor (CNI) toxicity in diabetic and non-diabetic kidney transplant recipients.
Main Methods:
- Retrospective analysis of 9,004 renal allograft biopsy specimens.
- Comparison of clinical and pathological parameters between patients with and without PV, stratified by diabetes status.
- Assessment of tacrolimus trough levels and Banff scoring criteria (ah, aah).
Main Results:
- In non-diabetic allografts, PV was associated with higher systolic blood pressure, elevated tacrolimus trough levels, and increased glomerulomegaly, ah, and aah scores.
- In diabetic allografts, only the ah score was significantly higher in the PV group.
- PV correlated with calcineurin inhibitor (CNI) toxicity in non-diabetic allografts but not in diabetic allografts.
Conclusions:
- Polar vasculosis (PV) is associated with calcineurin inhibitor (CNI) toxicity in non-diabetic renal allografts.
- The pathogenesis of PV in renal allografts is likely multifactorial.
- Further research is needed to elucidate the precise mechanisms and implications of PV in kidney transplantation.
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