Ma. Tarnopolsky et al., A RANDOMIZED, CONTROLLED TRIAL OF CREATINE MONOHYDRATE IN PATIENTS WITH MITOCHONDRIAL CYTOPATHIES, Muscle & nerve, 20(12), 1997, pp. 1502-1509
Fatigue in patients with mitochondrial cytopathies is associated with
decreased basal and postactivity muscle phosphocreatine (PCr). Creatin
e monohydrate supplementation has been shown to increase muscle PCr an
d high-intensity power output in healthy subjects. We studied the effe
cts of creatine monohydrate administration (5 g PO b.i.d. x 14 days --
> 2 g PO b.i.d, x 7 days) in 9 mitochondrial cytopathy patients using
a randomized, crossover design. Measurements included: activities of d
aily living (visual analog scale); ischemic isometric handgrip strengt
h (1 min); basal and postischemic exercise lactate; evoked and volunta
ry contraction strength oi the dorsiflexors; nonischemic, isometric, d
orsiflexion torque (NIDFT, 2 min); and aerobic cycle ergometry with pr
e-and post-lactate measurements. Creatine treatment resulted in signif
icantly (P < 0.05) increased handgrip strength, NIDFT, and postexercis
e lactate, with no changes in the other measured variables. We conclud
ed that creatine monohydrate increased the strength of high-intensity
anaerobic and aerobic type activities in patients with mitochondrial c
ytopathies but had no apparent effects upon lower intensity aerobic ac
tivities. (C) 1997 John Wiley & Sons, Inc.