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dc.contributor.authorSuchai Sritippayawanen_US
dc.contributor.authorWararat Chiangjongen_US
dc.contributor.authorTheptida Semangoenen_US
dc.contributor.authorNipa Aiyasanonen_US
dc.contributor.authorParnthip Jaetanawanitchen_US
dc.contributor.authorSupachok Sinchaikulen_US
dc.contributor.authorShui Tein Chenen_US
dc.contributor.authorSomkiat Vasuvattakulen_US
dc.contributor.authorVisith Thongboonkerden_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherAcademia Sinica Taiwanen_US
dc.contributor.otherNational Taiwan Universityen_US
dc.date.accessioned2018-08-24T01:39:48Z-
dc.date.available2018-08-24T01:39:48Z-
dc.date.issued2007-11-01en_US
dc.identifier.citationJournal of Proteome Research. Vol.6, No.11 (2007), 4356-4362en_US
dc.identifier.issn15353893en_US
dc.identifier.other2-s2.0-36348985603en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=36348985603&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/24095-
dc.description.abstractEfficacy of peritoneal dialysis is determined by solute transport through peritoneal membranes. With the use of the peritoneal equilibration test (PET), peritoneal membranes can be classified as high (H), high average (HA), low average (LA), and low (L) transporters, based on the removal or transport rate of solutes, which are small molecules. Whether there is any difference in macromolecules (i.e., proteins) removed by different types of peritoneal membranes remains unclear. We performed a gel-based differential proteomics study of peritoneal dialysate effluents (PDE) obtained from chronic peritoneal dialysis (CPD) patients with H, HA, LA, and L transport rates (n = 5 for each group; total n = 20). Quantitative analysis and ANOVA with Tukey's posthoc multiple comparisons revealed five proteins whose abundance in PDE significantly differed among groups. These proteins were successfully identified by matrix-assisted laser desorption ionization quadrupole time-of-flight (MALDI-Q-TOF) mass spectrometry (MS) and tandem mass spectrometry (MS/MS) analyses, including serum albumin in a complex with myristic acid and triiodobenzoic acid, α1-antitrypsin, complement component C4A, immunoglobulin κ light chain, and apolipoprotein A-I. The differences among groups in PDE levels of C4A and immunoglobulin κ were clearly confirmed in a validation set of the other 24 patients (n = 6 for each group) using ELISA. These data may lead to better understanding of the physiology of peritoneal membrane transport in CPD patients. Extending the study to a larger number of patients with subgroup analyses may yield additional information of the peritoneal dialysate proteins in association with dialysis adequacy, residual renal function, nutritional status, and risk of peritoneal infection. © 2007 American Chemical Society.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=36348985603&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.titleProteomic analysis of peritoneal dialysate fluid in patients with different types of peritoneal membranesen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1021/pr0702969en_US
Appears in Collections:Scopus 2006-2010

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