# A Randomized Double-Blind Controlled Trial of Creatine in Female Methamphetamine Users

> **NIH NIH R01** · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · 2021 · $488,953

## Abstract

PROJECT SUMMARY
 Methamphetamine (MA) causes devastating harm to individuals, yet there are no approved treatments for
MA use disorders. Female MA users have increased rates of depression, and more severe depressive
symptoms than males. Depression may contribute to the risk of relapse because negative mood is associated
MA craving. Our previous neuroimaging study found that female MA users have decreased frontal lobe
phosphocreatine (PCr) levels, compared with both male MA users and female healthy controls. Following up
on this key translational finding, preliminary data collected at our site suggests that when administered to
female MA users, creatine monohydrate supplementation is associated with increased brain PCr, N-acetyl
aspartate (NAA, a marker for neuronal health) and gamma-aminobutyric acid (GABA, the major inhibitory
neurotransmitter of the brain). PCr is the substrate reservoir for the creatine kinase reaction, which reversibly
converts PCr into adenosine triphosphate (ATP), the brain's major energy supply, and creatine. Clinically,
creatine administration was associated with decreased depression and anxiety symptoms. It may also reduce
MA use, measured by urine drug screens. This proposal follows expert recommendations to target cognitive
enhancement, and neuronal repair, in developing pharmacotherapies for stimulant addiction. The long-term
goal of this research program is to define the alterations in brain chemistry that underlie MA use disorders, and
to utilize translational MRS neuroimaging to identify rational brain-based treatment targets. Once a hypothesis-
driven intervention is identified, MRS can then be further employed in treatment studies, to verify that "target
engagement" is achieved.
 In women with MA use disorders, creatine is a hypothesis-generated intervention aimed at restoring
neurochemistry, reducing depression and anxiety symptoms, and improving cognitive function. Over a 5-year
period, the project will enroll 76 women between the ages of 18 and 55 with MA use disorders and randomize
them to 8 weeks of treatment with either creatine or placebo. Neuroimaging and cognitive testing of MA users
will be performed at baseline, and repeated after 8 weeks of treatment. As outcome measures, multi-level
assessments will be performed for brain chemistry, cognitive function, and clinical symptoms. It will be
determined in female MA users whether creatine supplementation, compared to placebo, will 1) repair MA-
induced neurochemical toxicity in the frontal brain regions, which will be assessed using phosphorus-31 and
proton-1 multinuclear magnetic resonance spectroscopy (MRS), 2) improve depression and anxiety, which will
be assessed using Hamilton Depression Rating Scale and Beck Anxiety Inventory tests, and 3) restore
cognitive deficits associated with MA toxicity, which will be assessed using Wisconsin Card Sorting Task, the
Stroop Color-Word Test, and the Wechsler Memory Scale. Additionally, urine drug testing results w...

## Key facts

- **NIH application ID:** 10227185
- **Project number:** 5R01DA043248-05
- **Recipient organization:** UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH
- **Principal Investigator:** PERRY FRANKLIN RENSHAW
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $488,953
- **Award type:** 5
- **Project period:** 2017-09-15 → 2023-01-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10227185

## Citation

> US National Institutes of Health, RePORTER application 10227185, A Randomized Double-Blind Controlled Trial of Creatine in Female Methamphetamine Users (5R01DA043248-05). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10227185. Licensed CC0.

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