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DC Field | Value | Language |
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dc.contributor.author | Davies-Tuck M.L. | en |
dc.contributor.author | Ellery S.J. | en |
dc.contributor.author | de Guingand D.L. | en |
dc.contributor.author | Palmer, Kirsten R. | en |
dc.contributor.author | Snow R.J. | en |
dc.date.accessioned | 2021-05-14T09:44:14Z | en |
dc.date.available | 2021-05-14T09:44:14Z | en |
dc.date.copyright | 2020 | en |
dc.date.created | 20200727 | en |
dc.date.issued | 2020-07-27 | en |
dc.identifier.citation | Nutrients. 12 (6) (pp 1-26), 2020. Article Number: 1780. Date of Publication: 2020. | en |
dc.identifier.issn | 2072-6643 (electronic) | en |
dc.identifier.uri | https://repository.monashhealth.org/monashhealthjspui/handle/1/28888 | en |
dc.description.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. | en |
dc.language | en | en |
dc.language | English | en |
dc.publisher | MDPI AG (Postfach, Basel CH-4005, Switzerland. E-mail: rasetti@mdpi.com) | en |
dc.relation.ispartof | Nutrients | en |
dc.subject.mesh | muscle mass | - |
dc.subject.mesh | muscle strength | - |
dc.subject.mesh | Roux-en-Y gastric bypass | - |
dc.subject.mesh | urea nitrogen blood level | - |
dc.subject.mesh | biological marker | - |
dc.subject.mesh | creatine | - |
dc.subject.mesh | creatine kinase | - |
dc.subject.mesh | programmed 1 receptor | - |
dc.subject.mesh | adverse outcome | - |
dc.subject.mesh | body composition | - |
dc.subject.mesh | body mass | - |
dc.subject.mesh | body weight | - |
dc.subject.mesh | body weight gain | - |
dc.subject.mesh | creatinine clearance | - |
dc.subject.mesh | diet supplementation | - |
dc.subject.mesh | dietary supplement | - |
dc.subject.mesh | estimated glomerular filtration rate | - |
dc.subject.mesh | glycemic index | - |
dc.subject.mesh | heart rate | - |
dc.subject.mesh | liquid chromatography-mass spectrometry | - |
dc.subject.mesh | liver function | - |
dc.title | Risk of adverse outcomes in females taking oral creatine monohydrate: A systematic review and meta-analysis. | en |
dc.type | Review | en |
dc.identifier.affiliation | Obstetrics and Gynaecology (Monash Women's) | - |
dc.type.studyortrial | Systematic review and/or meta-analysis | - |
dc.identifier.doi | http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.3390/nu12061780 | - |
dc.publisher.place | Switzerland | en |
dc.identifier.pubmedid | 32549301 [http://www.ncbi.nlm.nih.gov/pubmed/?term=32549301] | en |
dc.identifier.source | 2004558069 | en |
dc.identifier.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 | en |
dc.description.address | D.L. de Guingand, The Ritchie Centre, Hudson Institute of Medical Research, Melbourne 3168, Australia. E-mail: Deborah.deguingand@hudson.org.au | en |
dc.description.publicationstatus | Embase | en |
dc.rights.statement | Copyright 2020 Elsevier B.V., All rights reserved. | en |
dc.subect.keywords | Adverse outcomes Creatine monohydrate Female Human Safety Supplementation | en |
dc.identifier.authoremail | de Guingand D.L.; Deborah.deguingand@hudson.org.au Davies-Tuck M.L.; miranda.tuck@hudson.org.au Ellery S.J.; stacey.ellery@hudson.org.au Palmer K.R.; kirsten.palmer@monash.edu Snow R.J.; rod.snow@deakin.edu.au | en |
dc.description.grant | Organization: (MU) *Monash University* Organization No: 501100001779 Country: Australia No: CRD42018105999 Organization: (NHMRC) *National Health and Medical Research Council* Organization No: 501100000925 Country: Australia | en |
item.fulltext | No Fulltext | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.openairetype | Review | - |
crisitem.author.dept | Obstetrics and Gynaecology (Monash Women's) | - |
Appears in Collections: | Articles |
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