Association of Diuretics With Change in Extracellular Volume, Natriuretic Peptides, Symptoms, and Cardiovascular Outcomes in CKD
- Conditions
- Chronic Kidney Disease
- Interventions
- Drug: Diuretic initiation or augmentation
- Registration Number
- NCT04192110
- Lead Sponsor
- VA Office of Research and Development
- Brief Summary
Almost 15% of Americans have chronic kidney disease (CKD), with an even higher rate in Veterans due to common risk factors such as high blood pressure and diabetes. People with CKD have a high risk of cardiovascular (CV) diseases, such as heart attacks, heart failure, and strokes. Extra fluid in the body, called volume overload, may lead to CV disease in people with CKD. It is unknown if volume overload develops in the earliest stages of CKD, when treating it with common, inexpensive medicines called diuretics may improve long-term CV outcomes. This study will lay important groundwork to answer this question in Veterans with early CKD by comparing two ways to measure volume overload and studying the change in common symptoms like fatigue and short-term CV function after treatment with diuretic medicines.
- Detailed Description
The investigators previously showed that brain natriuretic peptide (BNP) and N-terminal-pro-BNP (NT-pro-BNP), measures of ventricular stretch, are associated with death and cardiovascular (CV) outcomes in chronic kidney disease (CKD) stages 1-3 patients, and the investigators' preliminary pilot results suggest that these natriuretic peptides may correlate with objective measures of excess extracellular volume (ECV) and with symptoms common in CKD. The overarching objective is to determine if initiation of diuretic treatment or increase in dose is associated with changes in BNP and NT-pro-BNP, patient-reported symptom burden, and short-term hemodynamic parameters in patients with CKD stages 1-3 and elevated blood pressure, and whether these changes correlate with changes in ECV. The central hypothesis is that the change in ECV after starting or increasing diuretics in Veterans with stages 1-3 CKD is associated with changes in 1) natriuretic peptides, 2) patient-level factors, and 3) CV physiology.
The investigators will compare the changes in natriuretic peptides, symptoms, and CV parameters with the change in ECV after diuretic initiation or dose increase. The primary aim is to determine if initiation of diuretic treatment or increase in diuretic dose is associated with changes in natriuretic peptides. Secondary aims are to determine the effect of diuretic change on patient-reported symptom burden, and CV physiology.
This clinical trial will include 46 outpatients with CKD stages 1-3 and blood pressure \>140/90 mmHg. At the first visit, I will initiate or increase the dose of a thiazide or loop diuretic. Study measures other than echocardiogram will be repeated 4 weeks after the intervention to determine changes in these parameters. ECV will be measured by whole-body multifrequency bioimpedance spectroscopy (BIS), which is a validated, non-invasive, painless measure of ECV. Plasma BNP and NT-pro-BNP will be measured, and patient-reported fatigue, depression, and quality of life will be quantified using validated questionnaires. Hemodynamic parameters include blood pressure, pulse pressure, total peripheral resistance index (TPRI), and cardiac index measured by Non-Invasive Cardiac Output Monitoring. A transthoracic echocardiogram will measure left ventricular mass index, valvular disease, and diastolic dysfunction.
Variables will be compared within participants between baseline and Visit 2 using paired Wilcoxon Signed Rank tests or paired Student's t tests, depending on variable distributions. Correlations between change in ECV/total body weight and all continuous outcome measures will be analyzed using Spearman or Pearson correlations, applying appropriate transformations. Linear regression analysis will control for clinically relevant variables. The relationship between ECV/total body weight and natriuretic peptides from both visits will be evaluated using a mixed effects model to account for the change in these measures between baseline and Visit 2.
This study is minimal risk to human subjects. Participants may benefit from improved control of their blood pressure. The knowledge to be gained may also benefit others in the future.
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- All
- Target Recruitment
- Not specified
-
The presence of CKD stages 1, 2, or 3, as defined below by National Kidney Foundation guidelines, for a period of at least 3 months.
- Stage 1: eGFR 90 mL/min/1.73 m2 and spot urine albumin-to-creatinine ratio 30 mg/g.
- Stage 2: eGFR 60-89 mL/min/1.73 m2 and spot urine albumin-to-creatinine ratio 30 mg/g.
- Stage 3: eGFR 30-59 mL/min/1.73 m2.
-
Measured blood pressure either >140 mmHg systolic or >90 mmHg diastolic at the two most recent clinic visits.
- Rationale: The investigators' unpublished preliminary data show that blood pressure correlates with both BNP and NT-pro-BNP more strongly in those with CKD than those without CKD. Thus, selecting hypertensive individuals is more likely to identify those with elevated natriuretic peptides in the CKD group.
- Furthermore, starting or increasing a diuretic medication is part of standard of care to treat blood pressures >140/90 mmHg, so the study intervention will be consistent with appropriate care for the Veteran and avoid hypotension.
-
Able to understand and sign informed consent after the nature of the study has been fully explained.
- Unable to understand or provide informed consent.
- Unwilling or unable to participate in the protocol or comply with any of its components.
- CKD stages 4-5, defined as eGFR <30 mL/min/1.73 m2.
- Receiving chronic hemodialysis or peritoneal dialysis.
- Recipient of a kidney transplant.
- Serum potassium <3.5 mg/dL at baseline.
- Known left ventricular ejection fraction <40% on visual estimate based on chart review of available echocardiogram data.
- Known hepatic cirrhosis.
- Major limb amputation.
- Known pregnancy.
- Presence of a pacemaker or defibrillator.
- Presence of metal prostheses.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Diuretic initiation or augmentation Diuretic initiation or augmentation Participants will either initiate or increase the dose of a loop or thiazide-type diuretic
- Primary Outcome Measures
Name Time Method NT-pro-BNP 4 weeks Change from baseline to 4 weeks in NT-pro-BNP
Total peripheral resistance index 4 weeks The change from baseline to 4 weeks in total peripheral resistance index will be measured using Non-Invasive Cardiac Output Monitoring (Cheetah)
- Secondary Outcome Measures
Name Time Method Pulse pressure 4 weeks The change in pulse pressure from baseline to 4 weeks
BNP 4 weeks Change from baseline to 4 weeks in BNP
Fatigue 4 weeks The change in fatigue from baseline to 4 weeks, measured by the Functional Assessment of Chronic Illness Therapy - Fatigue, a validated measure of patient-reported fatigue
Depression 4 weeks The change in depressive symptoms from baseline to 4 weeks, measured by the Quick Inventory of Depressive Symptomatology, a validated measure of patient-reported depression
Quality of Life - Kidney Disease Quality of Life (KDQOL) 4 weeks The change in quality of life from baseline to 4 weeks, measured by the KDQOL, a validated measure of patient-reported quality of life
Hospitalizations 6 months Hospitalizations as quantified by review of the medical record and telephone contact with the participant
Systolic blood pressure 4 weeks The change in systolic blood pressure from baseline to 4 weeks
Diastolic blood pressure 4 weeks The change in diastolic blood pressure from baseline to 4 weeks
Mean arterial blood pressure 4 weeks The change in mean arterial blood pressure from baseline to 4 weeks
Cardiac index 4 weeks The change from baseline to 4 weeks in cardiac index will be measured using Non-Invasive Cardiac Output Monitoring (Cheetah)
Trial Locations
- Locations (1)
VA North Texas Health Care System Dallas VA Medical Center, Dallas, TX
🇺🇸Dallas, Texas, United States