Fourteen females with depression and comorbid methamphetamine
dependence were enrolled in an 8-week open label trial of 5 grams of daily creatine
monohydrate and of these 14, eleven females completed the study. Depression was
measured using the Hamilton Depression Rating Scale (HAMD) and brain phosphocreatine
levels were measured using phosphorus magnetic resonance spectroscopy pre- and post-creatine
treatment. Secondary outcome measures included anxiety symptoms, measured with the
Beck Anxiety Inventory (BAI), as well as methamphetamine use, monitored by twice
weekly urine drug screens and self-reported use.
The results of a linear mixed effects repeated measures model
showed significantly reduced HAMD and BAI scores as early as week 2 when compared
to baseline scores. This improvement was maintained through study completion. Brain
phosphocreatine concentrations were higher at the second phosphorus magnetic resonance
spectroscopy scan compared to the baseline scan; Mbaseline = 0.223 (SD = 0.013) vs.Mpost-treatment = 0.233 (SD = 0.009), t(9)
= 2.905, p < .01,
suggesting that creatine increased phosphocreatine levels. Also, a reduction in
methamphetamine positive urine drug screens of greater than 50% was observed by
week 6. Finally, creatine was well tolerated and adverse events that were related
to gastrointestinal symptoms and muscle cramping were determined as possibly related
to creatine.
The current study suggests
that creatine treatment may be a promising therapeutic approach for females with
depression and comorbid methamphetamine dependence. This study is registered on
clinicaltrials.gov (NCT01514630).
Purchase full article at: http://goo.gl/ENb1i8
By: Tracy L. Hellem PhD, RNab*, Young-Hoon Sung MDa*, Xian-Feng Shi PhDac*, Marjorie A. Pett Mstat, DSWb*, Gwen LatendressePhD, CNM, FACNMb*, Jubel Morgan RNac*, Rebekah S. HuberMAa*, Danielle Kuykendalla*, Kelly J. Lundbergc* & Perry F. Renshawacd*
- a The Brain Institute, University of Utah, Salt Lake City, UT, USA
- b The College of Nursing, University of Utah, Salt Lake City, UT, USA
- c The Department of Psychiatry, University of Utah, Salt Lake City, UT, USA
- d VISN 19 MIRECC, Salt Lake City, UT, USA
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