Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/28888
Title: Risk of adverse outcomes in females taking oral creatine monohydrate: A systematic review and meta-analysis.
Authors: Davies-Tuck M.L.;Ellery S.J.;de Guingand D.L.;Palmer, Kirsten R. ;Snow R.J.
Monash Health Department(s): Obstetrics and Gynaecology (Monash Women's)
Institution: (de Guingand, Davies-Tuck, Ellery) The Ritchie Centre, Hudson Institute of Medical Research, Melbourne 3168, Australia (Palmer, Ellery) Department of Obstetrics and Gynaecology, Monash University, Melbourne 3168, Australia (Palmer) Monash Health, Monash Medical Centre, Melbourne 3168, Australia (Snow) Institute of Physical Activity and Nutrition, Deakin University, Melbourne 3125, Australia
Issue Date: 27-Jul-2020
Copyright year: 2020
Publisher: MDPI AG (Postfach, Basel CH-4005, Switzerland. E-mail: rasetti@mdpi.com)
Place of publication: Switzerland
Publication information: Nutrients. 12 (6) (pp 1-26), 2020. Article Number: 1780. Date of Publication: 2020.
Journal: Nutrients
Abstract: Creatine Monohydrate (CrM) is a dietary supplement routinely used as an ergogenic aid for sport and training, and as a potential therapeutic aid to augment different disease processes. Despite its increased use in recent years, studies reporting potential adverse outcomes of CrM have been mostly derived from male or mixed sex populations. A systematic search was conducted, which included female participants on CrM, where adverse outcomes were reported, with meta-analysis performed where appropriate. Six hundred and fifty-six studies were identified where creatine supplementation was the primary intervention; fifty-eight were female only studies (9%). Twenty-nine studies monitored for adverse outcomes, with 951 participants. There were no deaths or serious adverse outcomes reported. There were no significant differences in total adverse events, (risk ratio (RR) 1.24 (95% CI 0.51, 2.98)), gastrointestinal events, (RR 1.09 (95% CI 0.53, 2.24)), or weight gain, (mean difference (MD) 1.24 kg pre-intervention, (95% CI -0.34, 2.82)) to 1.37 kg post-intervention (95% CI -0.50, 3.23)), in CrM supplemented females, when stratified by dosing regimen and subject to meta-analysis. No statistically significant difference was reported in measures of renal or hepatic function. In conclusion, mortality and serious adverse events are not associated with CrM supplementation in females. Nor does the use of creatine supplementation increase the risk of total adverse outcomes, weight gain or renal and hepatic complications in females. However, all future studies of creatine supplementation in females should consider surveillance and comprehensive reporting of adverse outcomes to better inform participants and health professionals involved in future trials.Copyright © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.3390/nu12061780
PubMed URL: 32549301 [http://www.ncbi.nlm.nih.gov/pubmed/?term=32549301]
ISSN: 2072-6643 (electronic)
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/28888
Type: Review
Subjects: muscle mass
muscle strength
Roux-en-Y gastric bypass
urea nitrogen blood level
biological marker
creatine
creatine kinase
programmed 1 receptor
adverse outcome
body composition
body mass
body weight
body weight gain
creatinine clearance
diet supplementation
dietary supplement
estimated glomerular filtration rate
glycemic index
heart rate
liquid chromatography-mass spectrometry
liver function
Type of Clinical Study or Trial: Systematic review and/or meta-analysis
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