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Creatine monohydrate treatment alleviates muscle cramps associated with haemodialysis

Chiz-Tzung Chang1, Chin-Herng Wu, Chih-Wei Yang

  • 1Department of Nephrology, Chang Gung Memorial Hospital, Taipei, Taiwan.

Insights

Creatine monohydrate supplementation significantly reduced the frequency of muscle cramps in patients undergoing hemodialysis (HAMC). This effect was reversible after stopping treatment, indicating creatine monohydrate is a safe option for managing HAMC.

Area of Science:

  • Nephrology
  • Clinical Nutrition
  • Exercise Physiology

Background:

  • Muscle cramps are a frequent complication of hemodialysis, with unclear underlying mechanisms.
  • Disturbances in muscle energy metabolism are a potential cause of hemodialysis-associated muscle cramps (HAMC).
  • Creatine monohydrate is known to enhance muscle metabolism.

Purpose of the Study:

  • To investigate the clinical efficacy of creatine monohydrate in reducing HAMC.
  • To assess the safety and tolerability of creatine monohydrate in this patient population.

Main Methods:

  • A double-blind, placebo-controlled study involving ten patients with frequent HAMC.
  • Patients received either 12 mg of creatine monohydrate or a placebo before each dialysis session for 4 weeks.
  • Incidence of muscle cramps, dialysis adequacy, hemodynamics, and side effects were monitored during treatment and a subsequent 4-week washout period.

Main Results:

  • Creatine monohydrate treatment led to a 60% decrease in symptomatic muscle cramps (P<0.05).
  • The reduction in cramp incidence was not observed in the placebo group.
  • The beneficial effect of creatine monohydrate on cramps diminished during the washout period.
  • No significant changes in hematocrit, Kt/V, serum albumin, or hemodynamics were noted. Serum creatinine showed a slight increase (P<0.05).
  • No adverse effects were reported in either group.

Conclusions:

  • Creatine monohydrate effectively reduces the incidence of hemodialysis-associated muscle cramps.
  • Creatine monohydrate appears to be a safe therapeutic agent for managing HAMC.
Abstract

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