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

Authors :
Pena, Michelle J.
de Zeeuw, Dick
Andress, Dennis
Brennan, John J.
Correa‐Rotter, Ricardo
Coll, Blai
Kohan, Donald E.
Makino, Hirofumi
Perkovic, Vlado
Remuzzi, Giuseppe
Tobe, Sheldon W.
Toto, Robert
Parving, Hans‐Henrik
Sharma, Shoba
Corringham, Tom
Sharma, Kumar
Heerspink, Hiddo J. L.
Source :
Diabetes, Obesity & Metabolism; May2017, Vol. 19 Issue 5, p749-753, 5p
Publication Year :
2017

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 m<superscript>2</superscript>. After 12 weeks of atrasentan treatment in patients with eGFR < 60 mL/min/1.73 m<superscript>2</superscript>, 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 m<superscript>2</superscript>, 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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14628902
Volume :
19
Issue :
5
Database :
Complementary Index
Journal :
Diabetes, Obesity & Metabolism
Publication Type :
Academic Journal
Accession number :
122561372
Full Text :
https://doi.org/10.1111/dom.12864