Our objective was to determine the effect of creatine monohydrate on
disease progression in patients with amyotrophic lateral sclerosis
(ALS). One hundred and seven patients with the diagnosis of probable or
definite ALS, of less than five years duration from symptom onset, were
randomized to either treatment with daily creatine monohydrate (5 g/d)
or placebo.
In this multicenter, double-blinded study we followed
changes in disease progression: using quantitative measures of strength
via maximal isometric voluntary contraction, forced vital capacity,
ALSFRS, quality of life, fatigue and survival. Patients were followed
for nine months. The results showed that creatine monohydrate did not
significantly improve motor, respiratory or functional capacity in this
patient population.
The drug was well tolerated and the study groups
well balanced, especially considering the absence of forced vital
capacity criteria for entrance into the study. There was a trend toward
improved survival in patients taking daily creatine monohydrate and this
was identical to the trend seen in another recently published report of
creatine in ALS patients 1.
In conclusion,creatine monohydrate (5 g/d)
did not have an obvious benefit on the multiple markers of disease
progression measured over nine months. We measured fatigue during
isometric contraction and found no significant improvement despite
anecdotal patient reports prior to and during the study. The trend
toward improved survival was also found in another recently completed
blinded trial using creatine monohydrate. Further investigation on the
possible survival benefit of creatine in this patient population is
ongoing.
Americans use more than 4 million kilograms of creatine each year.
Creatine is most commonly used for improving exercise performance and increasing muscle mass in athletes and older adults. There is some science supporting the use of creatine in improving the athletic performance of young, healthy people during brief high-intensity activity such as sprinting.
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