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
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

15541

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Auteurs

Mehdi Maanaoui (M)

Service de Néphrologie, CHU Lille, F-59000, Lille, France.

Rémi Lenain (R)

Service de Néphrologie, CHU Lille, F-59000, Lille, France.

Aghilès Hamroun (A)

Service de Néphrologie, CHU Lille, F-59000, Lille, France.

Cynthia Van der Hauwaert (C)

University Lille, EA4483, F-59000, Lille, France.
Département de la Recherche en Santé, CHU Lille, F-59000, Lille, France.

Benjamin Lopez (B)

Service d'Immunologie, CHU Lille, F-59000, Lille, France.

Jean-Baptiste Gibier (JB)

Institut de Pathologie, CHU Lille, F-59000, Lille, France.
University Lille, INSERM UMR1172, F-59000, Lille, France.

Marie Frimat (M)

Service de Néphrologie, CHU Lille, F-59000, Lille, France.
University Lille, INSERM UMR995, F-59000, Lille, France.

Grégoire Savary (G)

University Lille, EA4483, F-59000, Lille, France.

Benjamin Hennart (B)

Service de Toxicologie et Génopathies, CHU Lille, 59000, Lille, France.

Romain Larrue (R)

Service de Toxicologie et Génopathies, CHU Lille, 59000, Lille, France.

Nicolas Pottier (N)

University Lille, EA4483, F-59000, Lille, France.
Service de Toxicologie et Génopathies, CHU Lille, 59000, Lille, France.

Franck Broly (F)

Service de Toxicologie et Génopathies, CHU Lille, 59000, Lille, France.

François Provôt (F)

Service de Néphrologie, CHU Lille, F-59000, Lille, France.

Marc Hazzan (M)

Service de Néphrologie, CHU Lille, F-59000, Lille, France.

François Glowacki (F)

Service de Néphrologie, CHU Lille, F-59000, Lille, France. francois.glowacki@chru-lille.fr.
University Lille, EA4483, F-59000, Lille, France. francois.glowacki@chru-lille.fr.

Christelle Cauffiez (C)

University Lille, EA4483, F-59000, Lille, France.

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