Long-term allograft function in kidney transplant recipients (KTRs) remain suboptimal, and graft failure causes significant morbidity and mortality, with cardiovascular disease being the leading cause of death in KTRs and the most common cause of death with a functioning graft. Sodium-glucose cotransporter 2 (SGLT2) inhibitors safely lower cardiovascular and kidney disease risk in the non-transplant population, yet data in KTRs are lacking. This clinical trial seeks to establish the efficacy and safety of dapagliflozin, a SGLT2 inhibitor, for improving cardiovascular and kidney graft function in adult KTRs with type 2 diabetes and post-transplant diabetes, and to leverage innovate translational methods to define the underlying mechanisms of action.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
80
Dapagliflozin 10mg orally daily
Placebo one tablet orally daily
University of Colorado Anschutz Medical Campus
Aurora, Colorado, United States
RECRUITINGAlbuminuria
Measured by urine albumin to creatinine ratio
Time frame: Change from baseline to 12 months
Kidney fibrosis
Measured by Magnetic Resonance Imaging (MRI) and kidney biopsy tissue
Time frame: Change from baseline to 12 months
Kidney oxygenation
Measured by MRI
Time frame: Change from baseline to 12 months
Arterial stiffness
Measured by aortic pulse wave velocity
Time frame: Change from baseline to 12 months
Left ventricular mass
measured by cardiac MRI
Time frame: Change from baseline to 12 months
estimated glomerular filtration rate
estimated by CKD epi equation
Time frame: Change from baseline to 12 months
Kidney morphometry, metabolomics from paired kidney biopsies
measured by single cell RNA sequencing from paired kidney biopsies
Time frame: Change from baseline to 12 months
safety and tolerability
assessed on basis of adverse events
Time frame: baseline, 6 and 12 months
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