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Evidence summaries

Creatine for Amyotrophic Lateral Sclerosis

Creatine appears not to improve survival or slow progression in amyotrophic lateral sclerosis. Level of evidence: "B"

A Cochrane review [Abstract] 1 included 3 RCTs with a total of 386 patients with amyotrophic lateral sclerosis (ALS). The patients were randomized to either creatine 5 to 10 g per day or placebo. There was no statistical difference in survival between the creatine and placebo groups across all 3 studies (Chi2 = 0.09, p = 0.76). In addition, there was no statistical difference in ALS functional rating revised scores (ALSFRS-R) slopes between the groups in any studies (slope difference of +0.03 ALSFRS-R/month in the creatine group; p = 0.76). Interestingly, there was a trend towards slightly worsened forced vital capacity (FVC) slope in the creatine group (slope difference of -0.63 FVC/month in the creatine group) in 2 studies which included FVC as an outcome, but this difference was not statistically significant (p = 0.054). Creatine was well-tolerated in all studies, with no evidence of renal failure or serious adverse events specifically attributable to creatine.

Comment: The quality of the evidence is downgraded by indirectness of evidence (differences in studied patients).

References

  • Pastula DM, Moore DH, Bedlack RS. Creatine for amyotrophic lateral sclerosis/motor neuron disease. Cochrane Database Syst Rev 2012;12:CD005225. [PubMed].

Primary/Secondary Keywords