REVIEW Dietary ber effects in chronic kidney disease: a systematic review and meta-analysis of controlled feeding trials L Chiavaroli 1,2 , A Mirrahimi 2,3 , JL Sievenpiper 1,4,5,7 , DJA Jenkins 1,4,6,7 and PB Darling 1,2,4 BACKGROUND/OBJECTIVES: Chronic kidney disease (CKD) is a major health concern associated with increased risk of cardiovascular disease, morbidity and mortality. Current CKD practice guidelines overlook dietary ber, which is chronically low in the renal diet. However, increasing dietary ber has been proposed to ameliorate the progress of CKD. We therefore conducted a systematic review and meta-analysis on the effect of dietary ber intake on serum urea and creatinine as classical markers of renal health in individuals with CKD. SUBJECTS/METHODS: We searched MEDLINE, EMBASE, CINHAL and the Cochrane Library for relevant clinical trials with a follow-up 7 days. Data were pooled by the generic inverse variance method using random-effects models and expressed as mean difference (MD) with 95% condence intervals (95% CIs). Heterogeneity was assessed by the Cochran Q statistic and quantied by I 2 . RESULTS: A total of 14 trials involving 143 participants met the eligibility criteria. Dietary ber supplementation signicantly reduced serum urea and creatinine levels in the primary pooled analyses (MD, - 1.76 mmol/l (95% CI, - 3.00, - 0.51), P o0.01 and MD, - 22.83 mmol/l (95% CI, - 42.63, - 3.02), P = 0.02, respectively) with signicant evidence of interstudy heterogeneity only in the analysis of serum urea. CONCLUSIONS: This is the rst study to summarize the potential benecial effects of dietary ber in the CKD population demonstrating a reduction in serum urea and creatinine, as well as highlighting the lack of clinical trials on harder end points. Larger, longer, higher-quality clinical trials measuring a greater variety of uremic toxins in CKD are required (NCT01844882). European Journal of Clinical Nutrition advance online publication, 12 November 2014; doi:10.1038/ejcn.2014.237 INTRODUCTION Despite the accumulating evidence on the benecial effects of dietary ber in ameliorating uremic environments, guidelines make little or no reference to dietary ber intake for chronic kidney disease (CKD). 16 In fact, the renal diet has chronically been decient in dietary ber due to concerns over increased potassium and phosphorus intake. As a result, the benets of ber including adequate laxation are often overlooked in those with CKD. Stephen and Cummings 7 in the early 1980s were among the rst to show that dietary ber consumption increased fecal bacterial mass and nitrogen excretion. Their ndings for dietary ber intake have since been validated by others and support the notion of a lower uremic toxin production by bacterial degradation of dietary and secretory proteins of the gastrointest- inal tract, 811 as well as improved cardiovascular disease (CVD) risk factor prole and oxidative stress status. 12 A recent cohort study 13 concluded that participants with the highest dietary cereal ber intake, compared with those with the lowest, had a 50% reduced risk for incidence of moderate CKD. Furthermore, in the recent Prevención con Dieta Mediterránea study, a signicant association was found between greater ber intake and reduced risk of CKD. 14 Unfortunately, according to NHANES III data, the average dietary ber intake in the CKD population is about 15.4 g/day, which is much lower than the recommended 2530 g/day intake for the general population. 15 Considering the potential benets of dietary ber and the very low average intake of this nutrient in the CKD population, we have conducted a systematic review and meta- analysis of controlled feeding trials to assess the effect of dietary ber on serum urea and creatinine as clinical markers of uremia in individuals with CKD. SUBJECTS AND METHODS We conducted a systematic review and meta-analysis following the Cochrane Handbook for Systematic Reviews of Interventions 16 and have reported our ndings according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. 17,18 The protocol is registered at Clinical- trials.gov (NCT01844882). Study selection We searched MEDLINE, EMBASE, CINAHL and the Cochrane Library through 1 September 2014 using the search terms '(dietary ber OR ber$ OR bre$ OR polysaccharides OR psyllium$ OR metamucil OR polymers OR carbohydrate$ OR dietary carbohy- drate OR fermentable OR fructans OR Asteraceae OR fructooligo- saccharide$ OR oligofructose$ OR chicory root$ OR jerusalem artichoke$ OR inulin OR Beneber OR Uniber OR lactulose) AND 1 Department of Nutritional Sciences, University of Toronto, Toronto, Ontario, Canada; 2 Clinical Nutrition and Risk Factor Modication Centre, St. Michael's Hospital, Toronto, Ontario, Canada; 3 School of Medicine, Faculty of Health Sciences, Queens University, Kingston, Ontario, Canada; 4 Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Ontario, Canada; 5 Department of Pathology and Molecular Medicine, Faculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada; 6 Department of Medicine, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada and 7 Division of Endocrinology, Department of Medicine, St. Michael's Hospital, Toronto, Ontario, Canada. Correspondence: Dr PB Darling, Li Ka Shing Knowledge Institute, St Michael's Hospital, 209 Victoria Street, 3rd oor, Toronto, M5B 1W8 Ontario, Canada. E-mail: pauline.darling@utoronto.ca This study was presented in part at the Canadian Nutrition Society conference, St. Johns Newfoundland, 57 June 2014. Received 25 June 2014; revised 11 September 2014; accepted 21 September 2014 European Journal of Clinical Nutrition (2014), 1 8 © 2014 Macmillan Publishers Limited All rights reserved 0954-3007/14 www.nature.com/ejcn