Effect of fructooligosaccharide on endothelial function in CKD patients: a randomized controlled trial

医学 动脉硬化 脉冲波速 低聚果糖 肾功能 内科学 肾脏疾病 安慰剂 内皮功能障碍 氧化三甲胺 胃肠病学 纳帕 泌尿系统 泌尿科 内分泌学 血压 病理 生物化学 替代医学 三甲胺 化学
作者
Rachel Gatti Armani,Aluízio Barbosa Carvalho,Christiane Ishikawa Ramos,Valéria Costa‐Hong,Luiz Aparecido Bortolotto,José Luiz Cassiolato,Natacha Oliveira,Zuzana Cieslarová,Claudimir Lúcio do Lago,Aline Klassen,Lílian Cuppari,Dominic S. Raj,Maria Eugênia Fernandes Canziani
出处
期刊:Nephrology Dialysis Transplantation [Oxford University Press]
卷期号:37 (1): 85-91 被引量:24
标识
DOI:10.1093/ndt/gfaa335
摘要

Abstract Background Microbiota-derived uremic toxins have been associated with inflammation that could corroborate with endothelial dysfunction (ED) and increase cardiovascular risk in patients with chronic kidney disease (CKD). This trial aimed to evaluate the effect of the prebiotic fructooligosaccharide (FOS) on endothelial function and arterial stiffness in nondialysis CKD patients. Methods In a double-blind controlled trial, 46 nondiabetic CKD patients were randomized to receive 12 g/day of FOS or placebo (maltodextrin) for 3 months. Total p-cresyl sulfate (PCS) and indoxyl sulfate by high-performance liquid chromatography, urinary trimethylamine N-oxide by mass spectrometry, C-reactive protein, interleukin-6 (IL-6), serum nitric oxide and stroma-derived factor-1 alfa were measured at baseline and at the end of follow-up; endothelial function was assessed through flow-mediated dilatation (FMD) and arterial stiffness by pulse wave velocity (PWV). Results The mean (± standard deviation) age of the study participants was 57.6 ± 14.4 years, with an estimated glomerular filtration rate of 21.3 ± 7.3 mL/min/1.73 m2. During the follow-up, regarding the inflammatory markers and uremic toxins, there was a significant decrease in IL-6 levels (3.4 ± 2.1 pg/mL versus 2.6 ± 1.4 pg/mL; P = 0.04) and a trend toward PCS reduction (55.4 ± 38.1 mg/L versus 43.1 ± 32.4 mg/L, P = 0.07) only in the prebiotic group. Comparing both groups, there was no difference in FMD and PWV. In an exploratory analysis, including a less severe ED group of patients (FMD ≥2.2% at baseline), FMD remained stable in the prebiotic group, while it decreased in the placebo group (group effect P = 0.135; time effect P = 0.012; interaction P = 0.002). Conclusions The prebiotic FOS lowered circulating levels of IL-6 in CKD patients and preserved endothelial function only in those with less damaged endothelium. No effect of FOS in arterial stiffness was observed.
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