Publication Cover
Journal of Dual Diagnosis
research and practice in substance abuse comorbidity
Volume 11, 2015 - Issue 3-4
467
Views
27
CrossRef citations to date
0
Altmetric
PSYCHOPHARMACOLOGY & NEUROBIOLOGY

Creatine as a Novel Treatment for Depression in Females Using Methamphetamine: A Pilot Study

, PhD RN, , MD, , PhD, , Mstat DSW, , PhD CNM FACNM, , RN, , MA, , RN MPH, , PhD & , MD PhD MBA show all
 

Abstract

Objective: Depression among methamphetamine users is more prevalent in females than males, but gender-specific treatment options for this comorbidity have not been described. Reduced brain phosphocreatine levels have been shown to be lower in female methamphetamine users compared to males, and, of relevance, studies have demonstrated an association between treatment-resistant depression and reduced brain phosphocreatine concentrations. The nutritional supplement creatine monohydrate has been reported to reduce symptoms of depression in female adolescents and adults taking antidepressants, as well as to increase brain phosphocreatine in healthy volunteers. Therefore, the purpose of this pilot study was to investigate creatine monohydrate as a treatment for depression in female methamphetamine users. Methods: Fourteen females with depression and comorbid methamphetamine dependence were enrolled in an 8-week open label trial of 5 g of daily creatine monohydrate and of these 14, 11 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. Results: 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. Conclusions: 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).

ACKNOWLEDGMENTS

We would like to acknowledge AlzChem AG for supplying Creapure® for this study.

DISCLOSURES

Dr. Perry Renshaw serves as a consultant to Kyowa Hakko, Tal Medical, and Ridge Diagnostics. He has received research support from GlaxoSmithKline and Roche. Dr. Perry Renshaw is an inventor on a patent application that has been assigned to the University of Utah, which describes the use of creatine as a treatment for depressive disorders. All other authors declare that they have no conflicts of interest.

FUNDING

Funding for this study was provided by NIDA grant 1R36DA036767-01 awarded to Dr. Tracy Hellem and by NIDA grant 1K05DA031247-01 awarded to Dr. Perry Renshaw.

Notes

1

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.