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dc.contributor.authorPlaza Florido, Abel Adrián 
dc.contributor.authorPérez Prieto, Inmaculada 
dc.contributor.authorMolina García, Pablo 
dc.contributor.authorOrtega Porcel, Francisco Bartolomé 
dc.contributor.authorAltmae, Signe 
dc.date.accessioned2022-07-29T07:30:53Z
dc.date.available2022-07-29T07:30:53Z
dc.date.issued2022-06-24
dc.identifier.citationPlaza-Florido A... [et al.] (2022) Transcriptional and Epigenetic Response to Sedentary Behavior and Physical Activity in Children and Adolescents: A Systematic Review. Front. Pediatr. 10:917152. doi: [10.3389/fped.2022.917152]es_ES
dc.identifier.urihttp://hdl.handle.net/10481/76419
dc.description.abstractBackground: The links of sedentary behavior and physical activity with health outcomes in children and adolescents is well known. However, the molecular mechanisms involved are poorly understood.We aimed to synthesize the current knowledge of the association of sedentary behavior and physical activity (acute and chronic effects) with gene expression and epigenetic modifications in children and adolescents. Methods: PubMed, Web of Science, and Scopus databases were systematically searched until April 2022. A total of 15 articles were eligible for this review. The risk of bias assessment was performed using the Joanna Briggs Institute Critical Appraisal Tool for Systematic Reviews and/or a modified version of the Downs and Black checklist. Results: Thirteen studies used candidate gene approach, while only 2 studies performed high-throughput analyses. The candidate genes significantly linked to sedentary behavior or physical activity were: FOXP3, HSD11B2, IL-10, TNF-a, ADRB2, VEGF, HSP70, SOX, and GPX. Non-coding Ribonucleic acids (RNAs) regulated by sedentary behavior or physical activity were: miRNA-222, miRNA-146a, miRNA-16, miRNA-126, miR-320a, and long non-coding RNA MALAT1. These molecules are involved in inflammation, immune function, angiogenic process, and cardiovascular disease. Transcriptomics analyses detected thousands of genes that were altered following an acute bout of physical activity and are linked to gene pathways related to immune function, apoptosis, and metabolic diseases. Conclusion: The evidence found to date is rather limited. Multidisciplinary studies are essential to characterize the molecular mechanisms in response to sedentary behavior and physical activity in the pediatric population. Larger cohorts and randomized controlled trials, in combination with multi-omics analyses, may provide the necessary data to bring the field forward.es_ES
dc.description.sponsorshipSpanish Government DEP2013-47540 DEP2016-79512-R DEP2017-91544-EXPes_ES
dc.description.sponsorshipEuropean Commission RYC-2016-21199 ENDORE SAF2017-87526-R 09/UPB/19 45/UPB/20 27/UPB/21 SOMM17/6107/UGRes_ES
dc.description.sponsorshipSpanish Government B-CTS-355 UGR18es_ES
dc.description.sponsorshipUnited States Department of Health & Human Serviceses_ES
dc.description.sponsorshipNational Institutes of Health (NIH) - USA B-CTS-500-UGR18es_ES
dc.description.sponsorshipPERC Systems Biology Fundes_ES
dc.description.sponsorshipHuawei Technologieses_ES
dc.description.sponsorshipEXERNET Research Network on Exercise and Health A-CTS-614-UGR20 FPU 16/02760 FPU19/05561es_ES
dc.description.sponsorshipUO1 TR002004es_ES
dc.description.sponsorshipAlicia Koplowitz Foundationes_ES
dc.description.sponsorshipUniversity of Granadaes_ES
dc.description.sponsorshipJunta de Andalucia, Consejeria de Conocimiento, Investigacion y Universidades and European Regionales_ES
dc.description.sponsorshipDevelopment Fund (ERDF) DEP2005- 00046/ACTI Junta de Andalucia PAIDI P20_00158es_ES
dc.language.isoenges_ES
dc.publisherFrontierses_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectExercise es_ES
dc.subjectMethylationes_ES
dc.subjectOmicses_ES
dc.subjectPhysical fitnesses_ES
dc.subjectRNA-seqes_ES
dc.subjectEpigenomicses_ES
dc.titleTranscriptional and Epigenetic Response to Sedentary Behavior and Physical Activity in Children and Adolescents: A Systematic Reviewes_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.3389/fped.2022.917152
dc.type.hasVersionVoRes_ES


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