Sodium Deposition in Soft Tissues of Patients With Kidney Disease

Sponsor
Chris McIntyre (Other)
Overall Status
Recruiting
CT.gov ID
NCT03004547
Collaborator
(none)
400
1
44.9
8.9

Study Details

Study Description

Brief Summary

Sodium (Na+) hemostasis is abnormal in CKD patients, and this element can be deposited in the skin, muscle, and skeleton - to cope with long term sodium loading. It is known that sodium stored in this non-osmotically active way, is profoundly inflammatory. Furthermore, inflammation has been associated with several uremic symptoms. The investigators will use novel Na+ MRI imaging to examine the Na+ deposition in the skin, muscle, and skeleton of five groups:1) chronic in-center hemodialysis patients, 2) chronic peritoneal dialysis patients, 3) adult and paediatric patients with CKD stage 1-5 and 4) heart failure patients with and without renal dysfunction 5) sex and age-matched healthy adult and paediatric controls. Additionally, they will investigate the association between sodium deposition in these tissues with uremic symptomatology and biochemical markers of metabolism.

Condition or Disease Intervention/Treatment Phase
  • Other: Measuring sodium content

Detailed Description

Kidneys have a key role in sodium hemostasis through their excretory function. In patients with chronic kidney disease (CKD), kidney function is impaired; thus, suggesting that sodium handling is abnormal in this setting with long-term sodium loading (from oral intake) and lack of adequate urinary excretion. Yet, sodium concentration needs to stay relatively constant to prevent fatal intra-cellular accumulation, which would result in cell injury and death. In hemodialysis patients, at least a part of this extra sodium is non-osmotically active and deposited in the skin, muscle, and skeleton.

Furthermore, it has become increasingly recognized that sodium (once accumulated in tissues) is directly pro-inflammatory, affecting the innate immune system by regulating the activity of macrophages in skin. This linkage between sodium and inflammation indicates a potential link between sodium deposition and uremic symptoms experienced by patients.

There have been no studies to date examining the sodium deposition in the skin, muscle, and skeleton of patients with different kidney function and renal replacement therapy.

This is a pilot study involving a single center recruiting patients from the prevalent maintenance hemodialysis, peritoneal dialysis , CKD stage 1-5, and heart failure populations of London, Ontario, compared to healthy controls. Once recruited, participants will undergo one study visit with the potential of up to two follow-up visits (on a non-dialysis day for hemodialysis patients). Participants will be followed for up to two years after the first study visit. Each session will include symptom questionnaires, the five times sit to stand and 60-second chair stand test (excluding all children), blood pressure and heart rate measurements, blood work (excluding healthy children and adolescents), urine sampling (excluding those on dialysis), an echocardiogram (excluding healthy controls), and an MRI scan of the lower leg detecting sodium content.

Study Design

Study Type:
Observational
Anticipated Enrollment :
400 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Evaluation of Sodium Deposition in Soft Tissues of Patients With Kidney Disease and Its Association With Patient Symptomatology
Actual Study Start Date :
Mar 5, 2018
Anticipated Primary Completion Date :
Dec 1, 2021
Anticipated Study Completion Date :
Dec 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Chronic hemodialysis patients

Patients on standard in-centre 3 times a week hemodialysis

Other: Measuring sodium content
Sodium MRI measurement of sodium content in the tissues of all participants

Peritoneal dialysis patients

Patients on peritoneal dialysis

Other: Measuring sodium content
Sodium MRI measurement of sodium content in the tissues of all participants

Adult and paediatric patients with CKD stage 1-5

Patients with chronic kidney disease stage 1-5 (not dialysis dependent)

Other: Measuring sodium content
Sodium MRI measurement of sodium content in the tissues of all participants

Healthy adult and paediatric controls

Subjects without kidney disease

Other: Measuring sodium content
Sodium MRI measurement of sodium content in the tissues of all participants

Heart failure patients with and without renal dysfunction

Heart failure patients (atrial fibrillation etc ...) with and without renal dysfunction

Other: Measuring sodium content
Sodium MRI measurement of sodium content in the tissues of all participants

Outcome Measures

Primary Outcome Measures

  1. Na content in the skin, muscle and skeleton of five cohorts [2 years]

Secondary Outcome Measures

  1. Inflammatory Marker: CRP levels [2 years]

  2. Uremic symptom scores among the different groups [2 years]

  3. Liver function markers [2 years]

  4. Liver damage markers (liver enzymes) [2 years]

  5. cardiac markers (troponin) [2 years]

  6. bone markers (ALP, vitamin D levels) [2 years]

  7. Uremic toxin levels [3-4 years]

  8. Endotoxin levels [5 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Age greater than or equal to 6 years

  • For patients on maintenance hemodialysis or peritoneal dialysis: more than 3 months duration of therapy

  • For patients with CKD stage 1-5: CKD stage 1-5 and no indications to start dialysis

  • For heart failure patients: with or without renal dysfunction

  • For healthy controls: lack of kidney disease, heart failure, liver cirrhosis, and peripheral edema

For subsequent visits (must meet 1 of the below indicators):
  • Change in dialysis prescription

  • Change in renal replacement therapy modality

  • Change in medication

  • Parathyroidectomy

  • Intervention added to or removed from dialysis (i.e. such as but not limited exercise, cooling, and ischemic preconditioning)

Exclusion Criteria:
  • Pregnant, breastfeeding or intending pregnancy

  • Unable to give consent or understand written information

  • Contraindication to MRI study

Contacts and Locations

Locations

Site City State Country Postal Code
1 LHSC Regional Renal Care Program London Ontario Canada

Sponsors and Collaborators

  • Chris McIntyre

Investigators

  • Principal Investigator: Christopher W McIntyre, PhD, MD, University of Western Ontario, Canada

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Chris McIntyre, Professor of Medicine, UWO, Lawson Health Research Institute
ClinicalTrials.gov Identifier:
NCT03004547
Other Study ID Numbers:
  • 108765
First Posted:
Dec 29, 2016
Last Update Posted:
Apr 1, 2021
Last Verified:
Mar 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by Chris McIntyre, Professor of Medicine, UWO, Lawson Health Research Institute
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 1, 2021