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Published on: September 27, 2024
Glucocorticoid Receptor Polymorphisms and Avascular Osteonecrosis After Kidney Transplantation
Jalal Etemadi, Mohammad Reza Jafari Nakhjavani, Saber Sepehri
1Kidney Research Center, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran. sepide.zununi@gmail.com.
Introduction:
Glucocorticoids (GCs) are commonly prescribed as immunosuppressive agents after kidney transplantation and their most common non-traumatic adverse effect is Avascular Necrosis (AVN) of the femoral head. In this regard, this study aimed to evaluate the glucocorticoid receptor (GR) polymorphisms among kidney transplant recipients and their potential role as a risk factor for the incidence of AVN.
Methods:
In this study, 99 renal transplant recipients were evaluated for the correlations of GR polymorphisms including N363S (rs6195), BclI (rs41423247), ER22/23EK (rs6189/rs6190), and A3669G (rs6198) with AVN after renal transplantation.
Results:
Results showed that none of the renal-transplanted patients neither with GC hypersensitive polymorphisms (N363S and BclI) nor with GC-resistant polymorphisms (A3669G and ER22/23EK) developed AVN (P > .05). In addition, the medications of the renal recipients with AVN were significantly different from the nonAVN patients (P < .001).
Conclusion:
The study results indicate that the GR polymorphisms have no critical roles in the susceptibility to AVN after renal transplantation. However, further studies to confirm the results are recommended. DOI: 10.52547/ijkd.7221.
Insights
Glucocorticoid receptor (GR) gene variations do not appear to increase the risk of avascular necrosis (AVN) in kidney transplant recipients. Further research is recommended to confirm these findings regarding AVN incidence.
Area of Science:
- Nephrology
- Pharmacogenomics
- Immunosuppression
Background:
- Glucocorticoids (GCs) are vital immunosuppressants post-kidney transplant.
- Avascular Necrosis (AVN) of the femoral head is a significant non-traumatic adverse effect of GCs.
- Understanding genetic predispositions to GC-related side effects is crucial.
Purpose of the Study:
- To investigate the association between glucocorticoid receptor (GR) gene polymorphisms and AVN risk in kidney transplant recipients.
- To evaluate specific GR polymorphisms (N363S, BclI, ER22/23EK, A3669G) as potential risk factors for AVN.
Main Methods:
- A cohort of 99 renal transplant recipients was analyzed.
- Genotyping was performed for four key GR polymorphisms: N363S (rs6195), BclI (rs41423247), ER22/23EK (rs6189/rs6190), and A3669G (rs6198).
- Correlations between these polymorphisms and the incidence of AVN were assessed.
Main Results:
- No statistically significant association was found between any of the tested GR polymorphisms (GC-sensitive or GC-resistant) and the development of AVN (P > .05).
- Medication profiles differed significantly between patients with and without AVN (P < .001), suggesting other factors influence AVN development.
Conclusions:
- Glucocorticoid receptor gene polymorphisms do not appear to play a critical role in the susceptibility to AVN after kidney transplantation.
- The findings suggest that factors other than GR genetics are more influential in AVN development post-transplant.
- Further studies are warranted to validate these results and explore alternative risk factors for AVN.
Related Concept Videos
Kidney Transplant I: Introduction
Kidney Transplant II: Surgical Procedure
Acute Kidney Injury II: Pathophysiology
Kidney Transplant III: Nursing Management
Acute Kidney Injury IV: Diagnostic Studies and Prevention
Chronic Kidney Disease II: Clinical Manifestations

