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Does creatine supplementation affect renal function in patients with peripheral artery disease? A randomized, double blind, placebo-controlled, clinical trial

W. R. Domingues, R. Ritti-Dias, G. Cucato, N. Wolosker, A. Zerati, P. Puech-Leão, P. M. Nunhes, André Alberto Moliterno et al.

Annals of Vascular Surgery, 2020

15 participants · 10 citations

Abstract

BACKGROUND

Case studies and reviews have shown that creatine supplementation can affect kidney function.

OBJECTIVE

The objective of this study was to verify the effects of eight weeks of creatine supplementation on renal function (creatinine clearance - primary outcome) in patients with symptomatic peripheral arterial disease.

METHODS

Twenty-nine patients, of both genders, were randomized (1:1) in a double-blind manner for administration of Placebo (PLA, n=15) or creatine monohydrate (Cr, n = 14). The supplementation protocol consisted of 20g/day for one week divided into four equal doses (loading phase), followed by single daily doses of 5g in the subsequent seven weeks (maintenance phase). Before and after the supplementation period, markers of renal function, serum creatinine, creatinine excretion rate, and creatinine clearance were evaluated. The Generalized Estimation Equation Model was used for comparison between groups. The level of significance was P <0.05.

RESULTS

No significant differences were found between groups before and after the intervention for serum creatinine (Cr - pre 1.00 ± 0.15 ml/dl vs. post 1.07 ± 0.16 ml/dl; PLA pre 1.30 ± 0.53 ml/dl vs. post 1.36 ± 0.47 ml/dl, p = 0.590), creatinine excretion rate (Cr - pre 81.73 ± 43.80 mg/dl vs. post 102.92 ± 59.57 mg/dl; PLA pre 74.37 ± 38.90 mg/dl vs. post 86.22 ± 39.94 mg/dl, p = 0.560), or creatinine clearance (Cr pre 108 ± 59 ml.min-1.1.73 m-2 vs. post 117 ± 52 ml.min-1.1.73 m-2; PLA pre 88 ± 49…

How strong is the evidence?

Evidence Hub reads this as a randomized trial, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence. Reported size: 15 participants or records.

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