A Pilot Trial of Nicotinamide Riboside and Coenzyme Q10 on Inflammation and Oxidative Stress in Chronic Kidney Disease

氧化应激 医学 辅酶Q10 内科学 内分泌学 肾脏疾病 炎症 脂质代谢 安慰剂 肾功能 病理 替代医学
作者
Armin Ahmadi,Ana P. Valencia,Gwénaëlle Begue,Jennifer Norman,Sili Fan,Blythe Durbin‐Johnson,Bradley N. Jenner,Matthew D. Campbell,Gustavo A. Reyes,Pankaj Kapahi,Jonathan Himmelfarb,Ian H. de Boer,David J. Marcinek,Bryan Kestenbaum,Jorge Gamboa,Baback Roshanravan
出处
期刊:Clinical Journal of The American Society of Nephrology [Lippincott Williams & Wilkins]
标识
DOI:10.2215/cjn.0000000624
摘要

Background: Mitochondria-driven oxidative/redox stress and inflammation play a major role in chronic kidney disease (CKD) pathophysiology. Compounds targeting mitochondrial metabolism may improve mitochondrial function, inflammation, and redox stress; however, there is limited evidence of their efficacy in CKD. Methods: We conducted a pilot randomized, double-blind, placebo-controlled crossover trial comparing the effects of 1200 mg/day of coenzyme Q10 (CoQ10) or 1000 mg/day of nicotinamide riboside (NR) supplementation to placebo in 25 people with moderate-to-severe CKD (estimated glomerular filtration rate [eGFR] <60mL/min/1.73m 2 ). We assessed changes in the blood transcriptome using 3'-Tag-Seq gene expression profiling and changes in pre-specified secondary outcomes of inflammatory and oxidative stress biomarkers. For a subsample of participants (N=14), we assessed lymphocyte and monocyte bioenergetics using an extracellular flux analyzer. Results: The (mean±SD) age, eGFR, and body mass index of the participants were 61±11 years, 37±9 mL/min/1.73m 2 , and 28±5 kg/m 2 respectively. Of the participants, 16% had diabetes and 40% were female. Compared to placebo, NR-mediated transcriptomic changes were enriched in gene ontology (GO) terms associated with carbohydrate/lipid metabolism and immune signaling while, CoQ10 changes were enriched in immune/stress response and lipid metabolism GO terms. NR increased plasma IL-2 (estimated difference, 0.32, 95% CI of 0.14 to 0.49 pg/mL), and CoQ10 decreased both IL-13 (estimated difference, -0.12, 95% CI of -0.24 to -0.01 pg/mL) and CRP (estimated difference, -0.11, 95% CI of -0.22 to 0.00 mg/dL) compared to placebo. Both NR and CoQ10 reduced 5 series F2-Isoprostanes (estimated difference, -0.16 and -0.11 pg/mL, respectively; P<0.05 for both). NR, but not CoQ10, increased the bioenergetic health index (BHI) (estimated difference, 0.29, 95% CI of 0.06 to 0.53) and spare respiratory capacity (estimated difference, 3.52, 95% CI of 0.04 to 7 pmol/min/10,000 cells) in monocytes. Conclusion: Six weeks of NR and CoQ10 improved markers of oxidative stress, inflammation, and cell bioenergetics in persons with moderate to severe CKD.

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