Proteinuria Clinical Trial
The purpose of this study is to determine if the oral supplementation with curcumin reduces proteinuria, improves the redox and pro-inflammatory state in patients with chronic kidney disease associated to Diabetes mellitus.
Diabetic Kidney Disease (DKD) represents the fist cause of end-stage kidney disease in
Mexico and the world, and it is characterized by the presence of hyperfiltration, glomerular
hypertrophy, tubular albuminuria and mesangial matrix expansion, mainly by the oxidative
stress and the pro-inflammatory state.
Current treatments are limited on controlling proteinuria and delay progression of the
disease, but even with an optimal management, a significant number of patient progress to
end-stage renal disease.
Curcumin, found in the extracts of the rhizome of the plant Curcuma longa L., has a wide
spectrum of biological and pharmacological activities, such as anti-oxidant,
anti-inflammatory, anti-carcinogenic and anti-diabetic effects. It has the capacity to act
directly with highly reactive oxygen species, induce the expression of various
cytoprotective proteins through Keap1/Nrf2/ARE pathway and reducing inflammatory
transcription factors such as NF-κB and TNF-α.
Curcumin could be an adjuvant treatment in the management of DKC due to his pleiotropic
nature, low cost and few side effects.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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