How peritoneal dialysis transforms the peritoneum and vasculature in children with chronic kidney disease—what can we learn for future treatment?
Children with chronic kidney disease (CKD) suffer from inflammation and reactive metabolite-induced stress, which massively accelerates tissue and vascular aging. Peritoneal dialysis (PD) is the preferred dialysis mode in children, but currently used PD fluids contain far supraphysiological glucose...
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Published in | Molecular and cellular pediatrics Vol. 9; no. 1; p. 9 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Cham
Springer International Publishing
05.05.2022
Springer Nature B.V SpringerOpen |
Subjects | |
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Abstract | Children with chronic kidney disease (CKD) suffer from inflammation and reactive metabolite-induced stress, which massively accelerates tissue and vascular aging. Peritoneal dialysis (PD) is the preferred dialysis mode in children, but currently used PD fluids contain far supraphysiological glucose concentrations for fluid and toxin removal and glucose degradation products (GDP). While the peritoneal membrane of children with CKD G5 exhibits only minor alterations, PD fluids trigger numerous molecular cascades resulting in major peritoneal membrane inflammation, hypervascularization, and fibrosis, with distinct molecular and morphological patterns depending on the GDP content of the PD fluid used. PD further aggravates systemic vascular disease. The systemic vascular aging process is particularly pronounced when PD fluids with high GDP concentrations are used. GDP induce endothelial junction disintegration, apoptosis, fibrosis, and intima thickening. This review gives an overview on the molecular mechanisms of peritoneal and vascular transformation and strategies to improve peritoneal and vascular health in patients on PD. |
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AbstractList | Children with chronic kidney disease (CKD) suffer from inflammation and reactive metabolite-induced stress, which massively accelerates tissue and vascular aging. Peritoneal dialysis (PD) is the preferred dialysis mode in children, but currently used PD fluids contain far supraphysiological glucose concentrations for fluid and toxin removal and glucose degradation products (GDP). While the peritoneal membrane of children with CKD G5 exhibits only minor alterations, PD fluids trigger numerous molecular cascades resulting in major peritoneal membrane inflammation, hypervascularization, and fibrosis, with distinct molecular and morphological patterns depending on the GDP content of the PD fluid used. PD further aggravates systemic vascular disease. The systemic vascular aging process is particularly pronounced when PD fluids with high GDP concentrations are used. GDP induce endothelial junction disintegration, apoptosis, fibrosis, and intima thickening. This review gives an overview on the molecular mechanisms of peritoneal and vascular transformation and strategies to improve peritoneal and vascular health in patients on PD. Abstract Children with chronic kidney disease (CKD) suffer from inflammation and reactive metabolite-induced stress, which massively accelerates tissue and vascular aging. Peritoneal dialysis (PD) is the preferred dialysis mode in children, but currently used PD fluids contain far supraphysiological glucose concentrations for fluid and toxin removal and glucose degradation products (GDP). While the peritoneal membrane of children with CKD G5 exhibits only minor alterations, PD fluids trigger numerous molecular cascades resulting in major peritoneal membrane inflammation, hypervascularization, and fibrosis, with distinct molecular and morphological patterns depending on the GDP content of the PD fluid used. PD further aggravates systemic vascular disease. The systemic vascular aging process is particularly pronounced when PD fluids with high GDP concentrations are used. GDP induce endothelial junction disintegration, apoptosis, fibrosis, and intima thickening. This review gives an overview on the molecular mechanisms of peritoneal and vascular transformation and strategies to improve peritoneal and vascular health in patients on PD. Abstract Children with chronic kidney disease (CKD) suffer from inflammation and reactive metabolite-induced stress, which massively accelerates tissue and vascular aging. Peritoneal dialysis (PD) is the preferred dialysis mode in children, but currently used PD fluids contain far supraphysiological glucose concentrations for fluid and toxin removal and glucose degradation products (GDP). While the peritoneal membrane of children with CKD G5 exhibits only minor alterations, PD fluids trigger numerous molecular cascades resulting in major peritoneal membrane inflammation, hypervascularization, and fibrosis, with distinct molecular and morphological patterns depending on the GDP content of the PD fluid used. PD further aggravates systemic vascular disease. The systemic vascular aging process is particularly pronounced when PD fluids with high GDP concentrations are used. GDP induce endothelial junction disintegration, apoptosis, fibrosis, and intima thickening. This review gives an overview on the molecular mechanisms of peritoneal and vascular transformation and strategies to improve peritoneal and vascular health in patients on PD. |
ArticleNumber | 9 |
Author | Bartosova, Maria Zarogiannis, Sotirios G. Schmitt, Claus Peter |
Author_xml | – sequence: 1 givenname: Maria surname: Bartosova fullname: Bartosova, Maria organization: Center for Pediatric and Adolescent Medicine, University of Heidelberg – sequence: 2 givenname: Sotirios G. surname: Zarogiannis fullname: Zarogiannis, Sotirios G. organization: Center for Pediatric and Adolescent Medicine, University of Heidelberg, Department of Physiology, Faculty of Medicine, University of Thessaly – sequence: 3 givenname: Claus Peter surname: Schmitt fullname: Schmitt, Claus Peter email: clauspeter.schmitt@med.uni-heidelberg.de organization: Center for Pediatric and Adolescent Medicine, University of Heidelberg |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35513740$$D View this record in MEDLINE/PubMed |
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Copyright | The Author(s) 2022 2022. The Author(s). The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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Keywords | Vascular disease Mesothelial Endothelial Chronic kidney disease Peritoneal membrane Glucose degradation products Peritoneal dialysis |
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385 van de Luijtgaarden, Jager, Segelmark, Pascual, Collart, Hemke, Remon, Metcalfe, Miguel, Kramar, Aasarod, Abu Hanna, Krediet, Schon, Ravani, Caskey, Couchoud, Palsson, Wanner, Finne, Noordzij (CR2) 2016; 31 González-Mateo, Aroeira, López-Cabrera, Ruiz-Ortega, Ortiz, Selgas (CR17) 2012; 27 Zareie, van Lambalgen, ter Wee, Hekking, Keuning, Schadee-Eestermans, Faict, Degréve, Tangelder, Beelen, van den Born (CR37) 2005; 25 CR27 Buchel, Bartosova, Eich, Wittenberger, Klein-Hitpass, Steppan, Hackert, Schaefer, Passlick-Deetjen, Schmitt (CR36) 2015; 35 Fang, Mullan, Shah, Mujais, Bargman, Oreopoulos (CR46) 2008; 28 Ni, Verbavatz, Rippe, Boisde, Moulin, Rippe, Verkman, Devuyst (CR60) 2006; 69 Oh, Wunsch, Turzer, Bahner, Raggi, Querfeld, Mehls, Schaefer (CR4) 2002; 106 Nakayama, Miyazaki, Honda, Kasai, Tomo, Nakamoto, Kawanishi (CR48) 2014; 34 CR62 Bammens, Evenepoel, Verbeke, Vanrenterghem (CR6) 2003; 64 M Vila Cuenca (141_CR12) 2020; 35 MW van de Luijtgaarden (141_CR2) 2016; 31 B Schaefer (141_CR9) 2018; 94 ATN van Diepen (141_CR24) 2020; 5 CP Schmitt (141_CR35) 2011; 26 K Goossen (141_CR30) 2020; 75 J Morelle (141_CR8) 2015; 26 141_CR34 KE Manera (141_CR3) 2020; 75 M Litwin (141_CR10) 2005; 16 M Vila Cuenca (141_CR19) 2018; 50 G Eich (141_CR29) 2017; 12 J Ni (141_CR60) 2006; 69 J Oh (141_CR4) 2002; 106 DA Chistiakov (141_CR41) 2015; 6 141_CR52 M Bartosova (141_CR20) 2019; 10 W Fang (141_CR46) 2008; 28 R Mehrotra (141_CR59) 2021; 100 CP Schmitt (141_CR28) 2013; 8 MS Balzer (141_CR18) 2020; 75 GT González-Mateo (141_CR17) 2012; 27 C Freise (141_CR13) 2019; 9 C Hamada (141_CR31) 2015; 18 B Canaud (141_CR51) 2022; 35 G Del Peso (141_CR26) 2016; 36 S Mortier (141_CR15) 2004; 66 M Bonomini (141_CR55) 2013; 62 B Bammens (141_CR6) 2003; 64 141_CR62 CP Schmitt (141_CR39) 2007; 22 M Tawada (141_CR45) 2019; 23 M Zareie (141_CR37) 2005; 25 NA Flavahan (141_CR42) 2017; 69 M Bonomini (141_CR33) 2021; 34 J Buchel (141_CR36) 2015; 35 R Shroff (141_CR50) 2019; 30 M Zeier (141_CR40) 2003; 63 141_CR58 141_CR57 J Lowenstein (141_CR7) 2016; 310 MG Betjes (141_CR47) 2017; 37 K Kawanishi (141_CR25) 2013; 33 T Mihara (141_CR53) 2017; 79 BA Warady (141_CR1) 2020; 40 A Vychytil (141_CR56) 2018; 94 DH Endemann (141_CR11) 2004; 15 B Schaefer (141_CR5) 2016; 6 141_CR32 141_CR27 A Garcia-Ponce (141_CR43) 2015; 113 EH Elphick (141_CR21) 2018; 13 M Nakayama (141_CR48) 2014; 34 J Morelle (141_CR61) 2021; 385 DW Johnson (141_CR23) 2012; 23 E Gaggiotti (141_CR54) 2005; 28 M Bartosova (141_CR44) 2018; 29 AS De Vriese (141_CR16) 2003; 14 JD Williams (141_CR14) 2002; 13 H Htay (141_CR49) 2018; 10 DW Johnson (141_CR22) 2012; 32 HL Tjiong (141_CR38) 2007; 2007 |
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Snippet | Children with chronic kidney disease (CKD) suffer from inflammation and reactive metabolite-induced stress, which massively accelerates tissue and vascular... Abstract Children with chronic kidney disease (CKD) suffer from inflammation and reactive metabolite-induced stress, which massively accelerates tissue and... Abstract Children with chronic kidney disease (CKD) suffer from inflammation and reactive metabolite-induced stress, which massively accelerates tissue and... |
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SubjectTerms | Aging Apoptosis Children Chronic kidney disease Degradation products Diabetes Endocrinology Endothelial Fibrosis Glucose degradation products Inflammation Kidney diseases Mechanism of kidney disease development and CKD associated morbidities Medicine Medicine & Public Health Molecular modelling Oncology Pediatrics Peritoneal dialysis Peritoneal membrane Peritoneum Review Vascular disease Vascular diseases |
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Title | How peritoneal dialysis transforms the peritoneum and vasculature in children with chronic kidney disease—what can we learn for future treatment? |
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