Caveolin-1 rs4730751 single-nucleotide polymorphism may not influence kidney transplant allograft survival

Author:

Maanaoui Mehdi,Lenain Rémi,Hamroun AghilèsORCID,Van der Hauwaert Cynthia,Lopez Benjamin,Gibier Jean-Baptiste,Frimat Marie,Savary Grégoire,Hennart Benjamin,Larrue Romain,Pottier Nicolas,Broly Franck,Provôt François,Hazzan Marc,Glowacki François,Cauffiez Christelle

Abstract

Abstract Caveolin-1 is a protein (encoded by the CAV1 gene) supposedly harboring a protective effect against fibrosis. CAV1 rs4730751 single nucleotide polymorphism (SNP) AA genotype was initially associated with lower graft survival compared to non-AA. However, subsequent studies could not find the same effect. CAV1 rs4730751 SNP was investigated on 918 kidney donors. Multivariate Cox-model analyses were performed to evaluate risk factors for graft loss. Longitudinal changes on long-term estimated glomerular filtration rate (eGFRs) were evaluated with a linear mixed model. Histopathological findings from protocolled biopsies after 3 months post transplantation were also analyzed. Donor CAV1 rs4730751 genotyping proportions were 7.1% for AA, 41.6% for AC and 51.3% for CC. The AA genotype, compared to non-AA, was not associated with lower graft survival censored or not for death (multivariate analysis: HR = 1.23 [0.74–2.05] and HR = 1.27 [0.84–1.92]). Linear mixed model on long-term eGFRs revealed also no significant difference according to the genotype, yet we observed a trend. AA genotype was also not associated with a higher degree of fibrosis index on protocolled kidney biopsies at 3 months. To conclude, donor CAV1 rs4730751 SNP may impact on kidney transplantation outcomes, but this study could not confirm this hypothesis.

Funder

Santelys Association

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

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