Modulation of Tissue Sodium in Hemodialysis Patients

Sponsor
University of Erlangen-Nürnberg Medical School (Other)
Overall Status
Recruiting
CT.gov ID
NCT03525223
Collaborator
(none)
40
1
2
43.6
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Study Details

Study Description

Brief Summary

Salt (NaCl) intake is implicated in causing hypertension and cardiovascular disease, the commonest cause of death worldwide. The investigators recently established that Na+ is stored in tissues, bound to glycosaminoglycans (GAGs) in skin and muscle. The resulting local hypertonicity leads to immune cell-driven induction of local tissue electrolyte clearance via modulation of cutaneous lymph capillary density. To visualize these complex processes in man directly, the investigators established Na+ magnetic resonance imaging (23Na-MRI) and investigated Na+ stores in hemodialysis (HD) patients. Hemodialysis patients were sodium-"overloaded" and HD treatment lowered tissue Na+ stores in this study. The observed effects were highly variable and independent of Na+ or water removal from the body during a dialysis session. Tissue Na+ mobilization correlated with circulating vascular endothelial growth factor-C (VEGF-C). The investigators believe that excessive Na+ storage is a reversible condition and therefore susceptible for therapeutic interventions. The investigators hypothesize that lowering dialysate Na+ concentration may favorably affect accelerated tissue Na+ accumulation in hemodialysis patients. Besides, improved tissue Na+ storage, osmostress-induced as well as pro-inflammatory immune cell response should be affected by such a revised dialysis management.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Change of dialysate [Na+]
N/A

Detailed Description

To evaluate effects of moderate reduction of dialysate Na+ concentration on tissue Na+ content the investigators intend to recruit 40 hemodialysis patients, who will be offered a therapeutic change of their dialysate Na+ concentration. After detection of tissue Na+ content using 23Na-MRI technique, the applied dialysate [Na+] will be initially increased stepwise by 2 mmol/l per week from 138 to 142 mmol/l and maintained for a period of 5 weeks. After another 23Na-MRI measurement, dialysate [Na+] will then be lowered stepwise by 1-2 mmol/l per week to a minimum of 135 mmol/l, which will be also maintained for a period of 5 weeks followed by a final 23Na-MRI assessment.

Hypothesis: Reduction of dialysate Na+ concentration will decrease tissue sodium storage.

Additionally, the investigators will assess changes in body fluid distribution by bioimpedance spectroscopy. Furthermore, vascular compliance in response to the modulation of dialysate [Na+] and its correlation with tissue Na+ will be assessed. To investigate the immune response to tissue Na+ accumulation, the osmostress-induced as well as pro-inflammatory immune cell response of isolated monocytes will be quantified.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Non-Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Impact of Changes in Dialysis Sodium Concentration on Tissue Sodium Storage in Hemodialysis Patients
Actual Study Start Date :
May 15, 2018
Anticipated Primary Completion Date :
Jul 31, 2021
Anticipated Study Completion Date :
Dec 31, 2021

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: dialysate [Na+] 138 mmol/l

Intervention: Change of dialysate [Na+] from 138 mmol/l to 142 mmol/l The dialysate [Na+] will be increased by 2 mmol/l per week and kept constant for 5 weeks (altogether 6 weeks). Before and after intervention tissue [Na+] will be determined by sodium MRI. Additionally body fluid distribution (by bioimpedance spectroscopy) and central arterial pressure wave form, pulse wave velocity as well as flow-mediated vasodilatation will be assessed.

Procedure: Change of dialysate [Na+]
Stepwise modulation of dialysate sodium concentration by 1-2 mmo/l per week

Active Comparator: dialysate [Na+] 142 mmol/l

Intervention: Change of dialysate [Na+] from 142 mmol/l to 135 mmol/l The dialysate [Na+] will be decreased by 2 mmol/l per week for 3 weeks and by 1mmol/l for 1 further week. Afterwards the dialysate [Na+] will be kept constant for 5 weeks (altogether 8 weeks). Before and after intervention tissue [Na+] will be determined by sodium MRI. Additionally body fluid distribution (by bioimpedance spectroscopy) and central arterial pressure wave form, pulse wave velocity as well as flow-mediated vasodilatation will be assessed.

Procedure: Change of dialysate [Na+]
Stepwise modulation of dialysate sodium concentration by 1-2 mmo/l per week

Outcome Measures

Primary Outcome Measures

  1. Tissue sodium content [14 weeks]

    Tissue sodium content measured by 23Na MRI

Secondary Outcome Measures

  1. Lymphangiogenic profile [14 weeks]

    Serum VEGF-C and sFLT4 levels will be determined

  2. Body fluid distribution (extracellular and intracellular water) [14 weeks]

    Change in body fluid distribution will be assessed by body composition monitor (bioimpedance spectroscopy)

  3. Pulse wave analysis and pulse wave velocity [14 weeks]

    Change in central arterial pressure wave form and pulse wave velocity will be analyzed by SphygmoCor

  4. Flow-mediated vasodilatation (FMD) [14 weeks]

    Measurement of vasodilatation and thereby arterial stiffness by a semi-automated ultrasound System (UNEXEF)

  5. Immune response to tissue Na+ accumulation [14 weeks]

    Blood monocytes will be isolated and their osmotic and inflammatory response will be determined

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Chronic Kidney Disease Stage 5D, hemodialysis performed for at least 6 months, three times hemodialysis per week, signed informed consent
Exclusion Criteria:
  • Pregnancy, severe heart failure (NYHA III - IV), severe liver disease (CHILD C), acute infection, pacemaker or other non-MRI suitable conditions, hyponatremia < 132 mmol/l

Contacts and Locations

Locations

Site City State Country Postal Code
1 Nephrology Department, University Hospital Erlangen Erlangen Bavaria Germany 91054

Sponsors and Collaborators

  • University of Erlangen-Nürnberg Medical School

Investigators

  • Principal Investigator: Christoph Kopp, MD, Nephrology Department, University Erlangen, Germany

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University of Erlangen-Nürnberg Medical School
ClinicalTrials.gov Identifier:
NCT03525223
Other Study ID Numbers:
  • DNa
First Posted:
May 15, 2018
Last Update Posted:
Dec 1, 2020
Last Verified:
Nov 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Erlangen-Nürnberg Medical School
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 1, 2020