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The effects of atrasentan on urinary metabolites in patients with type 2 diabetes and nephropathy

Michelle J Pena, Dick de Zeeuw, Dennis Andress, John J Brennan, Ricardo Correa-Rotter, Blai Coll, Donald E Kohan, Hirofumi Makino, Vlado Perkovic, Giuseppe Remuzzi, Sheldon W Tobe, Robert Toto, Hans-Henrik Parving, Shoba Sharma, Tom Corringham, Kumar Sharma, Hiddo Jl Heerspink

    23 Citations (Scopus)

    Abstract

    We assessed the effect of atrasentan therapy on a pre-specified panel of 13 urinary metabolites known to reflect mitochondrial function in patients with diabetic kidney disease. This post-hoc analysis was performed using urine samples collected during the RADAR study which was a randomized, double-blind, placebo-controlled trial that tested the effects of atrasentan on albuminuria reduction in patients with type 2 diabetes and nephropathy. At baseline, four of the 13 metabolites, quantified by gas-chromatography mass spectrometry, were below detectable levels, and six were reduced in patients with eGFR <60 ml/min/1.73 m(2) . After 12-weeks of atrasentan treatment in patients with eGFR <60 ml/min/1.73 m(2) , a single-value index of the metabolites changed by -0.31 (95%CI -0.60 to -0.02; p = 0.035), -0.08 (-12 to 0.29; p = 0.43) and 0.01 (-0.21 to 0.19; p = 0.913) in placebo, atrasentan 0.75 mg/d and 1.25 mg/d, respectively. The metabolite index difference compared to placebo was 0.13 (-0.17 to 0.43; p = 0.40) and 0.35 (0.05 to 0.65; p = 0.02) for atrasentan 0.75 mg/d and 1.25 mg/d, respectively. These data corroborate previous findings of mitochondrial dysfunction in patients with type 2 diabetes, nephropathy, and eGFR <60 ml/min/1.73 m(2) , suggesting that atrasentan may prevent the progression of mitochondrial dysfunction common to this specific patient population. Future studies of longer treatment duration with atrasentan are indicated.

    Original languageEnglish
    JournalDiabetes, Obesity and Metabolism Online
    Volume19
    Issue number5
    Pages (from-to)749-753
    ISSN1463-1326
    DOIs
    Publication statusPublished - 2017

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