Tissue Advanced Glycation End Product Deposition after Kidney Transplantation
Abstract
Background: Tissue advanced glycation end products (AGEs) accumulate in chronic kidney disease (CKD) and are a measure of cumulative metabolic stress. Measurement of tissue AGEs by skin autofluorescence (SAF) correlates well with cardiovascular outcomes in dialysis patients. SAF levels in transplant recipients relative to CKD and dialysis patients have not been previously studied, and the impact of transplantation on SAF levels in dialysis patients is unknown. Methods: SAF was measured using an AGE reader in 66 patients who had received a kidney transplant. Values were compared to those obtained in 1,707 patients with CKD stage 3 and in 115 patients on dialysis. Results: Mean SAF in transplant recipients [2.81 ± 0.64 arbitrary units (AU)] was significantly lower than in patients on haemodialysis (3.73 ± 0.88 AU) and peritoneal dialysis (3.57 ± 0.75 AU; p < 0.001), but was no different from CKD stage 3 (2.79 ± 0.66 AU; p = 0.42). In the transplant group, SAF correlated most strongly with age (r = 0.316). There was no correlation between SAF and estimated glomerular filtration rate or renal replacement therapy vintage. A small cohort of patients with SAF recorded on dialysis and following transplantation showed a drop in SAF over a mean time of 16 months after transplantation. Discussion: Tissue AGE values in kidney transplant recipients are significantly lower than in patients receiving dialysis and similar to those in patients with CKD stage 3. Our data suggest that transplantation may be associated with a reduction in tissue AGEs, and this might be an important component of the observed reduction in cardiovascular risk in transplant recipients compared to patients on dialysis.
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Acute/chronic kidney disease and end-stage renal failure can reduce AGE clearance, leading to accelerated progression and/or exacerbation of kidney malfunction and nephropathy.
“On the other hand, acute/chronic kidney disease and end-stage renal failure can reduce AGE clearance. Consequently, glomerular and tubular cells are exposed to potentially harmful AGEs for extended periods of time owing to the lower rates of glomerular filtration. These changes lead to accelerated progression and/or exacerbation of kidney malfunction and nephropathy along with greater amounts of”
From Advanced glycation end products (AGEs) and other adducts in aging-related diseases and alcohol-mediated tissue injury (2021) · cites this paper as [68]
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- Authors
- Crowley, L. E., Johnson, C. P., McIntyre, N., Fluck, R. J., McIntyre, C. W., Taal, M. W., & Leung, J. C. H.
- Affiliations
- Royal Derby Hospital (GB)
- University of Nottingham (GB)
- Venue
- Nephron Clinical Practice
- Publisher
- S. Karger AG
- Published
- 2013-10-15
- Volume
- 124
- Issue
- 1-2
- Pages
- 54-59
- ISSN
- 1660-2110 (ISSN-L)
- OpenAlex
- W2081246062
- Cited by
- 36
- References
- 25
- Citations by year
- 2024: 6 · 2023: 1 · 2022: 3 · 2021: 4 · 2020: 2 · 2019: 3 · 2018: 3 · 2017: 4 · 2016: 1 · 2015: 4 · 2014: 5
- FWCI
- 2.20
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Nephron Clinical Practice (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Advanced Glycation End Products research
- Health Sciences › Medicine › Nephrology › Dialysis and Renal Disease Management
- Health Sciences › Medicine › Nephrology › Chronic Kidney Disease and Diabetes
- Keywords
- advanced glycation end products, skin autofluorescence, kidney transplantation, dialysis, chronic kidney disease, metabolic stress, cardiovascular risk, hemodialysis, peritoneal dialysis
- MeSH terms
- Aged, Female, Renal Dialysis, Humans, Male, Middle Aged, Sensitivity and Specificity, Skin, Reproducibility of Results, Kidney Transplantation, Glycation End Products, Advanced, Advanced Cardiac Life Support, Renal Insufficiency, Chronic
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