Synbiotics Easing Renal Failure by Improving Gut Microbiology (SYNERGY): A Randomized Trial

被引:276
作者
Rossi, Megan [1 ,5 ,6 ]
Johnson, David W. [1 ,5 ,6 ]
Morrison, Mark [2 ,5 ]
Pascoe, Elaine M. [1 ]
Coombes, Jeff S. [3 ]
Forbes, Josephine M. [1 ,4 ,5 ]
Szeto, Cheuk-Chun [7 ]
McWhinney, Brett C. [8 ]
Ungerer, Jacobus P. J. [8 ]
Campbell, Katrina L. [1 ,5 ,6 ]
机构
[1] Univ Queensland, Sch Med, Brisbane, Qld, Australia
[2] Univ Queensland, Diamantina Inst, Brisbane, Qld, Australia
[3] Univ Queensland, Human Movement & Nutr Sci, Brisbane, Qld, Australia
[4] Univ Queensland, Mater Res Inst, Brisbane, Qld, Australia
[5] Translat Res Inst, Brisbane, Qld, Australia
[6] Princess Alexandra Hosp, Dept Nephrol, Level 2,ARTS Bldg,Ipswich Rd, Brisbane, Qld 4102, Australia
[7] Chinese Univ Hong Kong, Prince Wales Hosp, Hong Kong, Hong Kong, Peoples R China
[8] Pathol Queensland, Dept Chem Pathol, Brisbane, Qld, Australia
来源
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2016年 / 11卷 / 02期
关键词
CHRONIC KIDNEY-DISEASE; P-CRESYL SULFATE; CARDIOVASCULAR RISK; INDOXYL SULFATE; UREMIC TOXINS; PRO;
D O I
10.2215/CJN.05240515
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background and objectives The generation of key uremic nephrovascular toxins, indoxyl sulfate (IS), and p-cresyl sulfate (PCS), is attributed to the dysbiotic gut microbiota in CKD. The aim of our study was to evaluate whether synbiotic (pre- and probiotic) therapy alters the gut microbiota and reduces serum concentrations of microbiome-generated uremic toxins, IS and PCS, in patients with CKD. Design, setting, participants, & measurements Predialysis adult participants with CKD (eGFR=10-30 ml/min per 1.73 m(2)) were recruited between January 5, 2013 and November 12, 2013 to a randomized, double-blind, placebo-controlled, crossover trial of synbiotic therapy over 6 weeks (4-week washout). The primary outcome was serum IS. Secondary outcomes included serum PCS, stool microbiota profile, eGFR, proteinuria-albuminuria, urinary kidney injury molecule-1, serum inflammatory biomarkers (IL-1 beta, IL-6, IL-10, and TNF-alpha), serum oxidative stress biomarkers (F-2-isoprostanes and glutathione peroxidase), serum LPS, patient-reported health, Gastrointestinal Symptom Score, and dietary intake. A prespecified subgroup analysis explored the effect of antibiotic use on treatment effect. Results Of 37 individuals randomized (age =69 +/- 10 years old; 57% men; eGFR=24 +/- 8 ml/min per 1.73 m(2)), 31 completed the study. Synbiotic therapy did not significantly reduce serum IS (-2 mu mol/L; 95% confidence interval [95% CI], -5 to 1 mu mol/L) but did significantly reduce serum PCS (-14 mu mol/L; 95% CI, -27 to -2 mu mol/L). Decreases in both PCS and IS concentrations were more pronounced in patients who did not receive antibiotics during the study (n=21; serum PCS, -25 mu mol/L; 95% CI,-38 to-12 mu mol/L; serum IS, -5 mu mol/L; 95% CI,-8 to-1 mu mol/L). Synbiotics also altered the stool microbiome, particularly with enrichment of Bifidobacterium and depletion of Ruminococcaceae. Except for an increase in albuminuria of 38 mg/24 h (P=0.03) in the synbiotic arm, no changes were observed in the other secondary outcomes. Conclusion In patients with CKD, synbiotics did not significantly reduce serum IS but did decrease serum PCS and favorably modified the stool microbiome. Large-scale clinical trials are justified.
引用
收藏
页码:223 / 231
页数:9
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