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The effect of paricalcitolon dialysate protein loss in peritoneal dialysis patients

dc.contributor.authorJerĂłnimo, Teresa
dc.contributor.authordel Peso, Gloria
dc.contributor.authorGayo, Lucia
dc.contributor.authorGuedes, A. Malho
dc.contributor.authorSilva, Ana P.
dc.contributor.authorNeves, Pedro L.
dc.contributor.authorSelgas, Rafael
dc.contributor.authorBajo, Maria A.
dc.date.accessioned2017-04-07T15:56:41Z
dc.date.available2017-04-07T15:56:41Z
dc.date.issued2016-05
dc.description.abstractEver since peritoneal dialysis (PD) has been used in the treatment of chronic kidney disease (CKD), high peritoneal protein loss has been observed on each PD exchange. In adult patients, the loss has been estimated at 6 to 13 g daily. Paricalcitol, a selective activator of vitamin D receptors (VDR), is successfully used as a treatment of hyperparathyroidism secondary to CKD. In addition, it has been proposed for reducing proteinuria in patients with CKD. Nonetheless, little is known about its effect on peritoneal protein loss (PPL) in patients on PD, namely after the identification of VDRon the peritoneal membrane. The aim of this study wasto examine the effect of paricalcitol on PPL in PD patients.
dc.identifier.issn0931-0509
dc.identifier.urihttp://hdl.handle.net/10400.1/9498
dc.language.isoeng
dc.peerreviewedyes
dc.publisherOxford University Press (OUP)- European Renal Association - European Dialysis and Transplant Association (ERA-EDTA)
dc.relation.isbasedonWOS:000376653802283
dc.titleThe effect of paricalcitolon dialysate protein loss in peritoneal dialysis patients
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceVienna, Austria
oaire.citation.endPage1508
oaire.citation.titleNephrology Dialysis Transplantation
oaire.citation.volume31
person.familyNameMalho Guedes
person.givenNameAnabela
person.identifier.orcid0000-0002-9627-908X
person.identifier.scopus-author-id37087078200
rcaap.rightsopenAccess
rcaap.typearticle
relation.isAuthorOfPublication316db235-e120-46dc-8ec6-518d8ff314c2
relation.isAuthorOfPublication.latestForDiscovery316db235-e120-46dc-8ec6-518d8ff314c2

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