Caveolin-1 rs4730751 single-nucleotide polymorphism may not influence kidney transplant allograft survival.
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
29 10 2019
29 10 2019
Historique:
received:
10
06
2019
accepted:
11
10
2019
entrez:
31
10
2019
pubmed:
31
10
2019
medline:
29
10
2020
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 31664124
doi: 10.1038/s41598-019-52079-8
pii: 10.1038/s41598-019-52079-8
pmc: PMC6820546
doi:
Substances chimiques
CAV1 protein, human
0
Caveolin 1
0
Types de publication
Journal Article
Observational Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
15541Références
Gene. 2018 Jul 20;664:44-49
pubmed: 29678659
Transplantation. 2016 Aug;100(8):1723-31
pubmed: 27306529
Cardiovasc Res. 2010 May 1;86(2):219-25
pubmed: 20202978
Fibrogenesis Tissue Repair. 2015 May 05;8:8
pubmed: 25945124
Clin Pharmacokinet. 2017 Aug;56(8):963-975
pubmed: 28050888
Am J Physiol Renal Physiol. 2010 Feb;298(2):F357-64
pubmed: 19906947
Semin Nephrol. 2017 Nov;37(6):530-537
pubmed: 29110760
Curr Opin Nephrol Hypertens. 2014 Nov;23(6):605-10
pubmed: 25188274
JAMA. 2010 Apr 7;303(13):1282-7
pubmed: 20371787
Front Pharmacol. 2017 Aug 24;8:567
pubmed: 28970796
Transplantation. 2017 Apr;101(4):713-726
pubmed: 27941433
PLoS One. 2013 Jul 19;8(7):e69022
pubmed: 23894397
J Virol. 2007 Aug;81(16):8552-62
pubmed: 17553887
Biochem Biophys Res Commun. 2007 Jul 27;359(2):385-90
pubmed: 17543885
Ther Drug Monit. 2010 Dec;32(6):708-14
pubmed: 20864901
Pharmacogenomics. 2014 Dec;15(16):2011-24
pubmed: 25521359
Am J Transplant. 2015 May;15(5):1392-9
pubmed: 25787790
Pediatr Nephrol. 2014 Sep;29(9):1485-92
pubmed: 23748364
Nephrol Dial Transplant. 2016 Jul;31(7):1140-4
pubmed: 26433014
Kidney Int. 2015 Sep;88(3):584-92
pubmed: 25853335
Pharmacogenomics. 2017 Nov;18(16):1503-1513
pubmed: 28952408
Pharmacogenomics. 2017 Nov;18(16):1473-1480
pubmed: 29095105
Biomarkers. 2014 Dec;19(8):652-9
pubmed: 25271040
Am J Transplant. 2017 Jan;17(1):28-41
pubmed: 27862883
J Clin Pathol. 2011 Jun;64(6):504-9
pubmed: 21450752
Clin Pharmacokinet. 2011 Jul;50(7):451-9
pubmed: 21528942
PLoS One. 2015 Jun 12;10(6):e0128771
pubmed: 26066055
Pharmacogenomics J. 2015 Feb;15(1):38-48
pubmed: 25201288