Uraemic Toxins in Chronic Kidney Disease Paediatric Patients: Observational Study

NCT ID: NCT02624466

Last Updated: 2023-02-01

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 120 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2015-10-31
• Study Completion Date: 2019-02-28

Brief Summary

Children with chronic kidney disease (CKD) suffer from one of the most devastating diseases in childhood resulting in a lifelong need for health care, and a 3 times decreased life expectancy. In addition, they have important comorbidities that negatively impact on their quality of life and integration in society, jeopardizing their future even after a potential transplantation. Retention of uraemic toxins is accepted to play a major role in the pathogenesis of the comorbid conditions, but studies in children are lacking. Furthermore, there are currently no good tools to evaluate severity and monitor adequacy of treatment, resulting in suboptimal management.

The overall scientific objective of this four years UToPaed IWT-TBM project is to provide the clinician with new diagnostic and therapeutic tools for the management of children with CKD, based on the improved understanding of uraemic toxicity.

In this first part of UToPaed, the investigators will associate concentrations of a wide variety of uraemic toxins with different comorbidities in CKD children, i.e. growth, protein-energy wasting, quality of life, cardiovascular risk factors, circadian rhythm, sleep quality, and psychosocial and neurocognitive functioning (i.e. cross-sectional and longitudinal). The toxins of which concentrations are best correlated with comorbidities during the progress of CKD and eventually have representative kinetics (UToPaed - part 2: Kinetic analysis) will be selected as markers. These markers will be, together with the comorbidities, further tracked after interventions, i.e. starting on dialysis, transplantation, changes in dialysis strategy (UToPaed - part 3 - intervention study).

From the validated kinetic models (UToPaed - part 2 and 3), an open access user-friendly prediction simulator (PAEDSIM) based on patient characteristics and marker concentrations will be developed to optimise and individualise the dialysis therapy.

By providing clinicians with more advanced and appropriate tools to improve management of all children with CKD, i.e. better assessment of the degree of renal dysfunction, better determination of the ideal time to start renal replacement therapy, and more accurate monitoring of dialysis adequacy, the investigators aim to improve neurocognitive and psychosocial functioning (short term), growth, maturation into puberty, and social integration (median term) and survival (long term).

Detailed Description

This is a prospective observational multicenter study in children (≤ 18 years) with chronic kidney disease (CKD) stage 2 to 5D with or without renal replacement therapy. In this study, 60 children with CKD stage 2 - 5 (without renal replacement therapy)(GROUP 1), 30 children with CKD stage 5D treated with peritoneal dialysis (GROUP 2) and 30 children with CKD stage 5D treated with haemodialysis (GROUP 3) will be followed for a total duration of 24 months.

The study participants are evaluated on their standard visit at the outpatient clinic every 3 months. At this visit, a blood sample for uraemic toxin concentration is withdrawn and several co-morbidities (growth, protein-energy wasting, cardiovascular disease, quality of life, psychosocial functioning, sleep, attention and executive functions) are assessed. Anthropometric parameters, dietary assessment, stool evaluation, nail evaluation, office and 24 hours ambulatory blood pressure monitoring, echocardiography and questionnaires are used to map out the several co-morbidities.

Blood analyses are performed to get the concentrations of a wide variety of uraemic toxins: i.e. small water soluble solutes, middle molecules and protein-bound solutes. All blood analyses within this project are performed in the Ghent University Hospital: i.e. urea, creatinine, calcium, and phosphorus are determined in the routine laboratory of the Ghent University Hospital using standard methods, while all other uraemic toxins are determined in the laboratory of the Nephrology Section using ELISA and (in-house developed) HPLC/UPLC techniques. For the protein-bound solutes two runs are needed to distinguish between total and free fractions of the protein-bound solutes.

The following actions are performed prior to enrolment:

• Review medical history to determine eligibility based on inclusion/exclusion criteria
• Obtain document consent from participant (>12 years) and parent/representative on study consent form
• Schedule study visits for individuals who are eligible and available for the duration of the study
• Provide potential participants with instructions needed to prepare for first study visit

Baseline visit:

• Verify inclusion/exclusion criteria.
• Obtain and record general patient information: age, sex, medical history, underlying kidney disease, medication history, current medication chart, dialysis settings and demographic information
• Assessment of dietary assessment by a skilled dietician by means of 3-day diet diary or three 24-hours recall
• Perform clinical assessment including anthropometric parameters and office blood pressure
• Perform a body composition monitoring (BCM) in children > 10 kg
• Collection of blood sample (all groups; EDTA immediately on ice; serum 15-30 minutes rest and subsequently on ice), 24 hours urine sample (group 2; 24 hours prior to visit), intradialytic urine sample (group 3) and 24 hours dialysate collection (group 2; 24 hours prior to visit) for determination of uraemic toxin concentration

Intermediate visits:

• Obtain general patient information: medication chart, changes in medical situation and dialysis settings
• Assessment of dietary intake by a skilled dietician by means of 3-day diet diary or three 24-hours recall every 3 months
• Perform clinical assessment including anthropometric parameters and office blood pressure
• Perform BCM 3-monthly in children > 10 kg with renal replacement therapy (group 2 and 3) and 1-yearly in children > 10 kg without renal replacement therapy (group 1)
• Collection of blood sample (group 1 to 3; EDTA immediately on ice; serum 15-30 minutes rest and subsequently on ice), 24 hours urine sample (group 2 and 3; 24 hours prior to visit) and 24 hours dialysate collection (group 2; 24 hours prior to visit) every 3 months for determination of uraemic toxin concentration.
• Collection of stool sample for determination of microbiota and metabolome 1-yearly (only participants of Ghent University Hospital)
• Collection of nails for determination of carbamylation process every 6 months (only participants of Ghent University Hospital)
• Perform echocardiography by a skilled paediatric cardiologist every year (visit 2, 5)
• Withdraw questionnaires from the parent and/or child assessing quality of life, attention, sleep, executive function and parental functioning every 6 months (visit 2, 4, 6, 8)
• Perform 24 hours ambulatory blood pressure measurement in children > 6 years once a year (visit 2, 5)

Final Study Visit:

• Obtain general patient information: medication chart, changes in medical situation and dialysis settings (detailed overview appendix 2)
• Assessment of dietary assessment by a skilled dietician by means of 3-day diet diary or three 24-hours recall
• Perform clinical assessment including anthropometric parameters and office blood pressure
• Perform a body composition monitoring (BCM) in children > 10 kg
• Collection of blood sample (group 1 to 3; EDTA immediately on ice; serum 15-30 minutes rest and subsequently on ice), 24 hours urine sample (group 2 and 3; 24 hours prior to visit) and 24 hours dialysate collection (group 2; 24 hours prior to visit) for determination of uraemic toxin concentration
• Perform echocardiography by a skilled paediatric cardiologist
• Perform 24 hours ambulatory blood pressure measurement in children > 6 years

The following socio-demographic questionnaires are asked to be completed:

1. Assessment of quality of life (QoL)

• PedsQL for children (5-18 years)
• PedsQL for children, disease specific (8-12 years, 13-18 years)
• Parent Proxy Report by parents (2-4 years, 5-7 years, 8-12 years, 13-18 years)
• Parent Proxy Report, disease specific by parents (8-12 years, 13-18 years)

2. Assessment of psychological wellbeing

• YSR for children (> 11 years)
• CBCL/TRF by parent/teachers (1,5-5 years, 6-18 years)
• CBSK for children (8-12 years), CBSA for children (13-18 years)

3. Assessment of attention & executive functions

• DBDRS by parents, teachers (6-16 years)
• BRIEF by parents/teachers (5-18 years)

4. Assessment of sleep

• ESS questionnaire by parents
• CSHQ questionnaire by parents

5. Assessment of family functioning

• PIP by parents
• HADS by parents
• PSI-S by parents
• PPS by parents
• CVS by parents

Conditions

Chronic Kidney Disease

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

CKD - no dialysis

Follow-up of CKD progress by frequent assessment of: concentration of uraemic toxins in blood, anthropometry, cardio-vascular parameters, body composition monitoring, dietary assessment, psycho-social questionnaires, sleep disorders, stool, nails.

CKD progress

Intervention Type: OTHER

CKD progress

Patients on PD

Follow-up of CKD progress by frequent assessment of: concentration of uraemic toxins in blood, urine and PD fluid, anthropometry, cardio-vascular parameters, body composition monitoring, dietary assessment, psycho-social questionnaires, sleep disorders, stool, nails.

CKD progress

Intervention Type: OTHER

CKD progress

Patients on HD

Follow-up of CKD progress by frequent assessment of: concentration of uraemic toxins in blood, urine and spent dialysate, anthropometry, cardio-vascular parameters, body composition monitoring, dietary assessment, psycho-social questionnaires, sleep disorders, stool, nails.

CKD progress

Intervention Type: OTHER

CKD progress

Interventions

CKD progress

CKD progress

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Provide signed and dated informed consent form.
• Willing to comply with all study procedures and be available for the duration of the study
• Male or female, aged ≤ 18 years
• Diagnosed with chronic kidney disease stage 2 to 5D, according to the K/DOQI guidelines.

Exclusion Criteria

• Partially exclusion of children and/or parents who cannot fill in the questionnaires due to language barriers. They will be excluded only from the questionnaires; the other comorbidities will be followed.
• Partially exclusion of children who cannot fill in the questionnaires due to mental retardation. They will be excluded only from the questionnaires; the other comorbidities will be followed.

• Maximum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Ghent

OTHER

Sponsor Role: collaborator

Agentschap voor Innovatie door Wetenschap en Technologie

OTHER

Sponsor Role: collaborator

University Hospital, Ghent

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Sunny Eloot, Prof Dr

Role: PRINCIPAL_INVESTIGATOR

Ghent University Hospital - Nephrology

Johan Vande Walle, Prof Dr

Role: STUDY_CHAIR

Ghent University Hospital - Paediatric Nephrology

Ann Raes, Prof Dr

Role: STUDY_CHAIR

Ghent University Hospital - Paediatric Nephrology

Wim Van Biesen, Prof Dr

Role: STUDY_CHAIR

Ghent University Hospital - Nephrology

Evelien Snauwaert

Role: STUDY_CHAIR

Ghent University Hospital - Paediatric Nephrology

Locations

Ghent University Hospital - Nephrology

Ghent, , Belgium

Countries

Belgium

Other Identifiers

UGent_UToPaed_1

Identifier Type: -

Identifier Source: org_study_id