Probiotics-Supplemented Low-Protein Diet for Microbiota Modulation in Patients with Advanced Chronic Kidney Disease (ProLowCKD): Results from a Placebo-Controlled Randomized Trial.

Andreana De Mauri, Deborah Carrera, Marco Bagnati, Roberta Rolla, Matteo Vidali, Doriana Chiarinotti, Marco Pane, Angela Amoruso, Mario Del Piano

Journal: Nutrients 2022;14(8):1637

PMID: 35458199

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Chronic kidney disease (CKD) is characterized by the accumulation of a number of metabolites—referred to as uremic toxins—that cannot be excreted by failing kidneys. Dysbiotic microbiota is a feature of patients affected by CKD. The aim of this study was to evaluate whether the association of selected probiotics on top of a low protein diet (LPD) are able to reduce the burden of uremic, microbiota-derived, and proatherogenic toxins in patients with advanced renal failure who were not on dialysis. This study was a single-centre, double-blind, placebo-controlled, randomised study. Participants were prescribed LPD in addition to their ongoing pharmacological therapy; after 2 months (T2), they were randomized in a 1:1 ratio to receive, in addition to the LPD, either probiotics (probiotics group) or a placebo (placebo group). Results showed that a probiotics-supplemented LPD reduced traditional uremic, microbiota-derived and atherogenic uremic toxins, delayed the progression to end stage renal disease, allowed the reduction of loop diuretics and antihypertensive agent use, and improved quality of life. Authors conclude that a probiotics-supplemented LPD represents not only a holistic kidney-friendly approach but allows for ecological and planet-friendly management of renal disease.

Abstract

The probiotics-supplemented low-protein diet in chronic kidney disease (ProLowCKD) was a single-centre, double-blind, placebo-controlled, randomised trial that was conducted to investigate whether the association between a low protein diet (LPD) and a new formulation of probiotics ( and ) was effective at reducing traditional uremic, microbiota-derived, and proatherogenic toxins in sixty patients affected by advanced CKD. After 2 months of a LPD-a reduction in blood urea nitrogen (52 ± 17 vs. 46 ± 15 mg/dL, = 0.003), total cholesterol (185 ± 41 vs. 171 ± 34 mg/dL, = 0.001), and triglycerides (194 ± 148 vs. 161 ± 70 mg/dL, = 0.03) was observed; 57 subjects were then randomized to receive probiotics or a placebo for the subsequent 3 months. A total of 27 patients in the placebo group showed increased serum values of total cholesterol (169 ± 36 vs. 185 ± 40 mg/dL, = 0.01), LDL cholesterol (169 ± 36 vs. 185 ± 40 mg/dL, = 0.02), lipoprotein-associated phospholipase A (155.4 ± 39.3 vs. 167.5 ± 51.4 nmol/mL/min, = 0.006), and indoxyl-sulphate (30.1 ± 17.6 vs. 34.5 ± 20.2 μM, = 0.026), while the 24 subjects in the probiotics group showed a trend in the reduction of microbiota toxins. A reduction of antihypertensive and diuretic medications was possible in the probiotics group. This study shows that associating probiotics to LPD may have an additional beneficial effect on the control and modulation of microbiota-derived and proatherogenic toxins in CKD patients.

Address: Nephrology and Dialysis Unit, Maggiore della Carità University Hospital, 28100 Novara, Italy.; Dietetic and Clinical Nutrition, Maggiore della Carità University Hospital, 28100 Novara, Italy.; Clinical Chemistry Laboratory, Maggiore della Carità University Hospital, 28100 Novara, Italy.; Department of Health Sciences, Amedeo Avogadro University of Eastern Piedmont, 28100 Novara, Italy.; Clinical Chemistry Unit, Fondazione IRCCS Ca' Granda Maggiore Policlinico Hospital, 20122 Milano, Italy.; Research & Development, Probiotical Research Srl, 28100 Novara, Italy.; Past head of Clinical Research, Probiotical SpA, 28100 Novara, Italy.

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