Uremic Toxin Concentrations are Related to Residual Kidney Function in the Pediatric Hemodialysis Population

Protein-bound uremic toxins (PBUTs) play a role in the multisystem disease that children on hemodialysis (HD) are facing, but little is known about their levels and protein binding (%PB). In this study, we evaluated the levels and %PB of six PBUTs cross-sectionally in a large pediatric HD cohort ( =...

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Published inToxins Vol. 11; no. 4; p. 235
Main Authors Snauwaert, Evelien, Holvoet, Els, Van Biesen, Wim, Raes, Ann, Glorieux, Griet, Vande Walle, Johan, Roels, Sanne, Vanholder, Raymond, Askiti, Varvara, Azukaitis, Karolis, Bayazit, Aysun, Canpolat, Nur, Fischbach, Michel, Godefroid, Nathalie, Krid, Saoussen, Litwin, Mieczyslaw, Obrycki, Lukasz, Paglialonga, Fabio, Ranchin, Bruno, Samaille, Charlotte, Schaefer, Franz, Schmitt, Claus Peter, Spasojevic, Brankica, Stefanidis, Constantinos J, Van Dyck, Maria, Van Hoeck, Koen, Collard, Laure, Eloot, Sunny, Shroff, Rukshana
Format Journal Article Web Resource
LanguageEnglish
Published Switzerland MDPI AG 24.04.2019
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Abstract Protein-bound uremic toxins (PBUTs) play a role in the multisystem disease that children on hemodialysis (HD) are facing, but little is known about their levels and protein binding (%PB). In this study, we evaluated the levels and %PB of six PBUTs cross-sectionally in a large pediatric HD cohort ( = 170) by comparing these with healthy and non-dialysis chronic kidney disease (CKD) stage 4-5 ( = 24) children. In parallel β2-microglobulin (β2M) and uric acid (UA) were evaluated. We then explored the impact of age and residual kidney function on uremic toxin levels and %PB using analysis of covariance and Spearman correlation coefficients ( ). We found higher levels of β2M, p-cresyl glucuronide (pCG), hippuric acid (HA), indole acetic acid (IAA), and indoxyl sulfate (IxS) in the HD compared to the CKD4-5 group. In the HD group, a positive correlation between age and pCG, HA, IxS, and pCS levels was shown. Residual urine volume was negatively correlated with levels of β2M, pCG, HA, IAA, IxS, and CMPF ( -0.2 to -0.5). In addition, we found overall lower %PB of PBUTs in HD versus the CKD4-5 group, and showed an age-dependent increase in %PB of IAA, IxS, and pCS. Furhtermore, residual kidney function was overall positively correlated with %PB of PBUTs. In conclusion, residual kidney function and age contribute to PBUT levels and %PB in the pediatric HD population.
AbstractList Protein-bound uremic toxins (PBUTs) play a role in the multisystem disease that children on hemodialysis (HD) are facing, but little is known about their levels and protein binding (%PB). In this study, we evaluated the levels and %PB of six PBUTs cross-sectionally in a large pediatric HD cohort (n = 170) by comparing these with healthy and non-dialysis chronic kidney disease (CKD) stage 4–5 (n = 24) children. In parallel β2-microglobulin (β2M) and uric acid (UA) were evaluated. We then explored the impact of age and residual kidney function on uremic toxin levels and %PB using analysis of covariance and Spearman correlation coefficients (rs). We found higher levels of β2M, p-cresyl glucuronide (pCG), hippuric acid (HA), indole acetic acid (IAA), and indoxyl sulfate (IxS) in the HD compared to the CKD4–5 group. In the HD group, a positive correlation between age and pCG, HA, IxS, and pCS levels was shown. Residual urine volume was negatively correlated with levels of β2M, pCG, HA, IAA, IxS, and CMPF (rs −0.2 to −0.5). In addition, we found overall lower %PB of PBUTs in HD versus the CKD4–5 group, and showed an age-dependent increase in %PB of IAA, IxS, and pCS. Furhtermore, residual kidney function was overall positively correlated with %PB of PBUTs. In conclusion, residual kidney function and age contribute to PBUT levels and %PB in the pediatric HD population.
Protein-bound uremic toxins (PBUTs) play a role in the multisystem disease that children on hemodialysis (HD) are facing, but little is known about their levels and protein binding (%PB). In this study, we evaluated the levels and %PB of six PBUTs cross-sectionally in a large pediatric HD cohort ( n = 170) by comparing these with healthy and non-dialysis chronic kidney disease (CKD) stage 4–5 ( n = 24) children. In parallel β2-microglobulin (β2M) and uric acid (UA) were evaluated. We then explored the impact of age and residual kidney function on uremic toxin levels and %PB using analysis of covariance and Spearman correlation coefficients ( r s ). We found higher levels of β2M, p-cresyl glucuronide (pCG), hippuric acid (HA), indole acetic acid (IAA), and indoxyl sulfate (IxS) in the HD compared to the CKD4–5 group. In the HD group, a positive correlation between age and pCG, HA, IxS, and pCS levels was shown. Residual urine volume was negatively correlated with levels of β2M, pCG, HA, IAA, IxS, and CMPF ( r s −0.2 to −0.5). In addition, we found overall lower %PB of PBUTs in HD versus the CKD4–5 group, and showed an age-dependent increase in %PB of IAA, IxS, and pCS. Furhtermore, residual kidney function was overall positively correlated with %PB of PBUTs. In conclusion, residual kidney function and age contribute to PBUT levels and %PB in the pediatric HD population.
Protein-bound uremic toxins (PBUTs) play a role in the multisystem disease that children on hemodialysis (HD) are facing, but little is known about their levels and protein binding (%PB). In this study, we evaluated the levels and %PB of six PBUTs cross-sectionally in a large pediatric HD cohort (n = 170) by comparing these with healthy and non-dialysis chronic kidney disease (CKD) stage 4-5 (n = 24) children. In parallel β2-microglobulin (β2M) and uric acid (UA) were evaluated. We then explored the impact of age and residual kidney function on uremic toxin levels and %PB using analysis of covariance and Spearman correlation coefficients (rs). We found higher levels of β2M, p-cresyl glucuronide (pCG), hippuric acid (HA), indole acetic acid (IAA), and indoxyl sulfate (IxS) in the HD compared to the CKD4-5 group. In the HD group, a positive correlation between age and pCG, HA, IxS, and pCS levels was shown. Residual urine volume was negatively correlated with levels of β2M, pCG, HA, IAA, IxS, and CMPF (rs -0.2 to -0.5). In addition, we found overall lower %PB of PBUTs in HD versus the CKD4-5 group, and showed an age-dependent increase in %PB of IAA, IxS, and pCS. Furhtermore, residual kidney function was overall positively correlated with %PB of PBUTs. In conclusion, residual kidney function and age contribute to PBUT levels and %PB in the pediatric HD population. © 2019 by the authors. Licensee MDPI, Basel, Switzerland.
Protein-bound uremic toxins (PBUTs) play a role in the multisystem disease that children on hemodialysis (HD) are facing, but little is known about their levels and protein binding (%PB). In this study, we evaluated the levels and %PB of six PBUTs cross-sectionally in a large pediatric HD cohort ( = 170) by comparing these with healthy and non-dialysis chronic kidney disease (CKD) stage 4-5 ( = 24) children. In parallel β2-microglobulin (β2M) and uric acid (UA) were evaluated. We then explored the impact of age and residual kidney function on uremic toxin levels and %PB using analysis of covariance and Spearman correlation coefficients ( ). We found higher levels of β2M, p-cresyl glucuronide (pCG), hippuric acid (HA), indole acetic acid (IAA), and indoxyl sulfate (IxS) in the HD compared to the CKD4-5 group. In the HD group, a positive correlation between age and pCG, HA, IxS, and pCS levels was shown. Residual urine volume was negatively correlated with levels of β2M, pCG, HA, IAA, IxS, and CMPF ( -0.2 to -0.5). In addition, we found overall lower %PB of PBUTs in HD versus the CKD4-5 group, and showed an age-dependent increase in %PB of IAA, IxS, and pCS. Furhtermore, residual kidney function was overall positively correlated with %PB of PBUTs. In conclusion, residual kidney function and age contribute to PBUT levels and %PB in the pediatric HD population.
Author Azukaitis, Karolis
Schaefer, Franz
Snauwaert, Evelien
Roels, Sanne
Ranchin, Bruno
Collard, Laure
Glorieux, Griet
Spasojevic, Brankica
Obrycki, Lukasz
Vande Walle, Johan
Askiti, Varvara
Shroff, Rukshana
Vanholder, Raymond
Schmitt, Claus Peter
Bayazit, Aysun
Holvoet, Els
Paglialonga, Fabio
Stefanidis, Constantinos J
Eloot, Sunny
Litwin, Mieczyslaw
Van Dyck, Maria
Godefroid, Nathalie
Samaille, Charlotte
Van Biesen, Wim
Canpolat, Nur
Krid, Saoussen
Raes, Ann
Fischbach, Michel
Van Hoeck, Koen
AuthorAffiliation 3 A & P Kyriakou Children’s Hospital, 11527 Athens, Greece; vaskiti@gmail.com (V.A.); cjstefanidis@gmail.com (C.J.S.)
11 Pediatric Nephrology Dialysis and Transplant Unit, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy; fabio.paglialonga@policlinico.mi.it
18 Department of Pediatric Nephrology, CHU Liège, 4000 Liège, Belgium; laure.collard@chc.be
17 Department of Pediatric Nephrology, Antwerp University, 2650 Antwerp, Belgium; koen.vanhoeck@uza.be
1 Ghent University Hospital, 9000 Ghent, Belgium; els.holvoet@uzgent.be (E.H.); wim.vanbiesen@ugent.be (W.V.B.); ann.raes@ugent.be (A.R.); griet.glorieux@ugent.be (G.G.); johan.vandewalle@uzgent.be (J.V.W.); Raymond.vanholder@ugent.be (R.V.); sunny.eloot@ugent.be (S.E.)
5 Department of Pediatric Nephrology, Cukurova University, 01330 Adana, Turkey; ayskar@cu.edu.tr
14 Center for Pediatrics and Adolescent Medicine, 69120 Heidelberg, Germany; franz.schaefer@med.uni-heidelberg.de (F.S.); clauspeter.schmitt@med.uni-heidelb
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10.1002/bdd.1834
10.1097/01.ASN.0000135053.98172.D6
10.1681/ASN.V12102158
10.3390/toxins7103933
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2019 by the authors. 2019
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Keywords hemodialysis
chronic kidney disease
end-stage kidney disease
uremic toxins
residual kidney function
child
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Snippet Protein-bound uremic toxins (PBUTs) play a role in the multisystem disease that children on hemodialysis (HD) are facing, but little is known about their...
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StartPage 235
SubjectTerms Acetic acid
Acids
Adolescent
Adults
Age
Child
Child, Preschool
Children
Chronic kidney disease
Correlation coefficient
Correlation coefficients
Dialysis
End-stage kidney disease
Female
Hemodialysis
Hippuric acid
Human health sciences
Humans
Indoleacetic acid
Kidney - metabolism
Kidney - physiopathology
Kidney diseases
Kidneys
Male
Mortality
Patients
Pediatrics
Plasma
Population
Protein Binding
Proteins
Pédiatrie
Quality of life
Renal Dialysis
Renal Insufficiency, Chronic - metabolism
Renal Insufficiency, Chronic - physiopathology
Residual kidney function
Sciences de la santé humaine
Toxins
Toxins, Biological - blood
Toxins, Biological - metabolism
Uremia
Uremic toxins
Uric acid
Urine
Urologie & néphrologie
Urology & nephrology
β2 Microglobulin
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Title Uremic Toxin Concentrations are Related to Residual Kidney Function in the Pediatric Hemodialysis Population
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