Literature DB >> 28019071

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

Michelle J Pena1, Dick de Zeeuw1, Dennis Andress2, John J Brennan2, Ricardo Correa-Rotter3, Blai Coll4, Donald E Kohan5, Hirofumi Makino6, Vlado Perkovic7, Giuseppe Remuzzi8,9, Sheldon W Tobe10, Robert Toto11, Hans-Henrik Parving12, Shoba Sharma13, Tom Corringham13, Kumar Sharma14, Hiddo J L Heerspink1.   

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, 4 of the 13 metabolites, quantified by gas-chromatography mass spectrometry, were below detectable levels, and 6 were reduced in patients with eGFR < 60 mL/min/1.73 m2 . After 12 weeks of atrasentan treatment in patients with eGFR < 60 mL/min/1.73 m2 , a single-value index of the metabolites changed by -0.31 (95%CI -0.60 to -0.02; P  = .035), -0.08 (-12 to 0.29; P  = .43) and 0.01 (-0.21 to 0.19; P  = .913) in placebo, atrasentan 0.75 and 1.25 mg/d, respectively. The metabolite index difference compared to placebo was 0.13 (-0.17 to 0.43; P  = .40) and 0.35 (0.05-0.65; P  = .02) for atrasentan 0.75 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 m2 , 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.
© 2016 John Wiley & Sons Ltd.

Entities:  

Keywords:  zzm321990eGFR decline; diabetic kidney disease; metabolomics

Mesh:

Substances:

Year:  2017        PMID: 28019071     DOI: 10.1111/dom.12864

Source DB:  PubMed          Journal:  Diabetes Obes Metab        ISSN: 1462-8902            Impact factor:   6.577


  5 in total

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Journal:  Nat Rev Nephrol       Date:  2019-06       Impact factor: 28.314

2.  A Targeted Multiomics Approach to Identify Biomarkers Associated with Rapid eGFR Decline in Type 1 Diabetes.

Authors:  Christine P Limonte; Erkka Valo; Daniel Montemayor; Farsad Afshinnia; Tarunveer S Ahluwalia; Tina Costacou; Manjula Darshi; Carol Forsblom; Andrew N Hoofnagle; Per-Henrik Groop; Rachel G Miller; Trevor J Orchard; Subramaniam Pennathur; Peter Rossing; Niina Sandholm; Janet K Snell-Bergeon; Hongping Ye; Jing Zhang; Loki Natarajan; Ian H de Boer; Kumar Sharma
Journal:  Am J Nephrol       Date:  2020-10-14       Impact factor: 3.754

Review 3.  Biomarkers of diabetic kidney disease.

Authors:  Helen M Colhoun; M Loredana Marcovecchio
Journal:  Diabetologia       Date:  2018-03-08       Impact factor: 10.122

Review 4.  Endothelin Receptor Antagonists as a Potential Treatment of Diabetic Nephropathy: A Systematic Review.

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Journal:  Cureus       Date:  2021-11-07

Review 5.  Podocyte Injury in Diabetic Kidney Disease: A Focus on Mitochondrial Dysfunction.

Authors:  Simeng Liu; Yanggang Yuan; Yi Xue; Changying Xing; Bo Zhang
Journal:  Front Cell Dev Biol       Date:  2022-03-07
  5 in total

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