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.

Abstract

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.

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