Publication:
Biocompatible Dialysis Solutions Preserve Peritoneal Mesothelial Cell and Vessel Wall Integrity. A Case-Control Study on Human Biopsies.

dc.contributor.authordel Peso, Gloria
dc.contributor.authorJiménez-Heffernan, José Antonio
dc.contributor.authorSelgas, Rafael
dc.contributor.authorRemón, César
dc.contributor.authorOssorio, Marta
dc.contributor.authorFernández-Perpén, Antonio
dc.contributor.authorSánchez-Tomero, José Antonio
dc.contributor.authorCirugeda, Antonio
dc.contributor.authorde Sousa, Erika
dc.contributor.authorSandoval, Pilar
dc.contributor.authorDíaz, Raquel
dc.contributor.authorLópez-Cabrera, Manuel
dc.contributor.authorBajo, María Auxiliadora
dc.date.accessioned2023-01-25T08:36:21Z
dc.date.available2023-01-25T08:36:21Z
dc.date.issued2015-10-16
dc.description.abstract♦ Chronic exposure to conventional peritoneal dialysis (PD) solutions has been related to peritoneal function alterations in PD patients, and associated with mesothelial cell loss, submesothelial fibrosis, vasculopathy, and angiogenesis. In vitro and ex vivo analyses, as well as studies with animal models, have demonstrated that biocompatible PD solutions attenuate these morphological alterations. Our aim was to confirm the morphological benefits of biocompatible solutions in PD patients. ♦ We analyzed biopsies from 23 patients treated with biocompatible solutions (study group, SG), and compared them with a control group (n = 23) treated with conventional solutions (CG), matched for time on PD. ♦ A total of 56.5% of SG patients showed total or partial preservation of mesothelial cells monolayer, in contrast with 26.1% of patients in CG (p = 0.036). Peritoneal fibrosis was not significantly less frequent in SG patients (47.8% SG vs 69.6% CG; p = 0.13). In patients without previous peritonitis, a significantly lower prevalence of fibrosis was present in SG patients (41.7% SG vs 77.8% CG; p = 0.04). Hyalinizing vasculopathy (HV) was significantly lower in SG (4.3% SG vs 30.4% CG; p = 0.02). Cytokeratin-positive fibroblast-like cells were detected in 10 patients (22%), but the prevalence was not significantly lower in SG. In the univariate regression analysis, the use of biocompatible solutions was associated with mesothelial monolayer integrity (p = 0.04) and an absence of vasculopathy (p = 0.04). ♦ The present study demonstrates in vivo in human biopsies that biocompatible solutions are better tolerated by the peritoneum in the medium and long term than conventional solutions.
dc.identifier.doi10.3747/pdi.2014.00038
dc.identifier.essn1718-4304
dc.identifier.pmcPMC4803356
dc.identifier.pmid26475848
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4803356/pdf
dc.identifier.unpaywallURLhttps://europepmc.org/articles/pmc4803356?pdf=render
dc.identifier.urihttp://hdl.handle.net/10668/10427
dc.issue.number2
dc.journal.titlePeritoneal dialysis international : journal of the International Society for Peritoneal Dialysis
dc.journal.titleabbreviationPerit Dial Int
dc.language.isoen
dc.organizationHospital Universitario de Puerto Real
dc.page.number129-34
dc.pubmedtypeComparative Study
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rights.accessRightsopen access
dc.subjectPeritoneal biopsy
dc.subjectbiocompatible dialysis solutions
dc.subjecthyalinizing vasculopathy
dc.subjectmesothelial cell integrity
dc.subjectsubmesothelial fibrosis
dc.subject.meshAdult
dc.subject.meshBiocompatible Materials
dc.subject.meshBiopsy
dc.subject.meshBlood Vessels
dc.subject.meshCase-Control Studies
dc.subject.meshDialysis Solutions
dc.subject.meshEpithelial Cells
dc.subject.meshEpithelial-Mesenchymal Transition
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshKeratins
dc.subject.meshLogistic Models
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshPeritoneal Dialysis
dc.subject.meshPeritoneum
dc.titleBiocompatible Dialysis Solutions Preserve Peritoneal Mesothelial Cell and Vessel Wall Integrity. A Case-Control Study on Human Biopsies.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number36
dspace.entity.typePublication

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