Caveolin-1 rs4730751 single-nucleotide polymorphism may not influence kidney transplant allograft survival.
Mehdi MaanaouiRémi LenainAghilès HamrounCynthia Van der HauwaertBenjamin LopezJean-Baptiste GibierMarie FrimatGrégoire SavaryBenjamin HennartRomain LarrueNicolas PottierFranck BrolyFrançois ProvôtMarc HazzanFrançois GlowackiChristelle CauffiezPublished in: Scientific reports (2019)
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.
Keyphrases
- kidney transplantation
- genome wide
- free survival
- high density
- genetic diversity
- copy number
- single cell
- type diabetes
- gene expression
- cross sectional
- high throughput
- ultrasound guided
- mass spectrometry
- bone marrow
- cell therapy
- case control
- mesenchymal stem cells
- transcription factor
- liver fibrosis
- weight loss
- binding protein