CreatinerctRCT2020

Does Creatine Supplementation Affect Renal Function in Patients with Peripheral Artery Disease? A Randomized, Double Blind, Placebo-controlled, Clinical Trial.

Annals of vascular surgery

confidence

Key findings

8 weeks of creatine supplementation did not compromise renal function (serum creatinine, creatinine excretion rate, or creatinine clearance) in patients with peripheral arterial disease.

View source on PubMed (PMID 31563660) ↗

Sample size
29 (Cr n=14, PLA n=15)
Population
Patients with symptomatic peripheral arterial disease
Dosing
20 g/day for 1 week (loading), then 5 g/day for 7 weeks (maintenance)
Duration
8 weeks
Route
oral
Blinding
double_blind
Controls
placebo
Drug class
supplement

Measured endpoints

  • Serum creatinineNo changerenal
    not_significanteffect: Cr: pre 1.00 ± 0.15 vs post 1.07 ± 0.16; PLA: pre 1.30 ± 0.53 vs post 1.36 ± 0.47
  • Creatinine excretion rateNo changerenal
    not_significanteffect: Cr: pre 81.73 ± 43.80 vs post 102.92 ± 59.57; PLA: pre 74.37 ± 38.90 vs post 86.22 ± 39.94
  • Creatinine clearanceNo changerenal
    not_significanteffect: Cr: pre 108 ± 59 vs post 117 ± 52; PLA: pre 88 ± 49 vs post 82 ± 47
Full abstract

Case studies and reviews have shown that creatine supplementation can affect kidney function. The objective of this study is to verify the effects of 8 weeks of creatine supplementation on renal function (creatinine clearance: primary outcome) in patients with symptomatic peripheral arterial disease. 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 20 g/day for 1 week divided into 4 equal doses (loading phase), followed by single daily doses of 5 g in the subsequent 7 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. 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/1.73 m2 vs. post 117 ± 52 mL/min/1.73 m2; PLA: pre 88 ± 49 mL/min/1.73 m2 vs. post 82 ± 47 mL/min/1.73 m2, P = 0.366). Eight weeks of creatine supplementation is safe and does not compromise the renal function of patients with peripheral arterial disease.

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