TY - JOUR
T1 - MARKERS OF MITOCHONDRIAL ENERGY METABOLISM AND THEIR POTENTIAL RELATIONSHIPS WITH FATIGUE IN HUMAN ADULTS
T2 - A SCOPING REVIEW
AU - Assunção-Luiz, Alan Vinicius
AU - Borges, Paulo Victor
AU - Bacalá, Bruna Tavares
AU - Dos Santos, Jennifer Thalita Targino
AU - Graves, Letitia
AU - Saligan, Leorey
AU - Nascimento, Lucila Castanheira
AU - Flória-Santos, Milena
N1 - Funding Information:
It is a scoping review prepared according to the methodology by the Joanna Briggs Institute (JBI), Reviewer 嬁退 Manual and theoretical recommendations by ?rksey and O ?Ma2l0le0y5 ) ? and based on the Preferred Reporting Items for Systematic reviews and Meta-Analyses extension for Scoping Reviews (PRISMA-ScR) guideline (Page et al. 2021). The research question and search strategy were guided by the PCC (Population, Concept, and Context) tool (Peters et al. 2020). This study considered: P - Human adults; C - Markers of mitochondrial metabolism; C - Fatigue. A combination of descriptors and keywords was used with Boolean operators (Table 缀 to search the literature to answer the research question 圀 帀?re there potential relationships between mitochondrial metabolism markers and fatigue 䴃? ? A comprehensive search was performed in the PubMed, SCOPUS, EMBASE, and Web of Science databases, the screening period was between January 2019 and January 2022, and the search terms were adapted to the specificity of each database. The gray literature was also consulted in the following databases: Brazil - Thesis and Dissertations Portal for the Coordination of Improvement of Higher Education Personnel (CAPES); Brazil - The Digital Library of Theses and Dissertations of the University of São Paulo; Portugal - Scientific Repository of Open Access of Portugal (RCAAP); Europe E-theses Portal (DART); Canada - Theses Canada And World - Cyberthesis; Australia and New Zealand - The National Library of Australia's Trobe (Trove). These databases were included because they somehow represent research performed on different continents. According to the inclusion criteria of the study, the databases of the Asian continent were not investigated due to language limitations. Next, all identified citations were organized and uploaded into Rayyan (Ouzzani et al. 2016), a review software used to aid the initial selection of articles by facilitating title and abstract screening of the selected studies. It also allows removing duplicates and provides practicality for reviewers in selecting the articles of interest.
Publisher Copyright:
© 2022, University Federal de Uberlandia. All rights reserved.
PY - 2022/2/16
Y1 - 2022/2/16
N2 - This scoping review aimed to synthesize the best available evidence of the associations between molecular and genetic markers of mitochondrial metabolism and fatigue in human adults. The research question guiding this review was, “Are there potential relationships between mitochondrial metabolism markers and fatigue?” The literature search used three terms (mitochondria; fatigue; energy metabolism), which yielded 263 manuscripts and 22 theses/dissertations. The studies included in the review had to meet three criteria: (1) Include adult participants (≥18 years of age); (2) Show a relationship between mitochondrial energy metabolism and fatigue; (3) Be published in English, Spanish, or Portuguese. Of the 17 articles included for a full-text review, some had a cross-sectional design (6/17, 35%), and more than half (12/17, 70%) were published between 2015 and 2020. The predominant population studied were patients diagnosed with chronic fatigue syndrome (9/17, 53%). Most studies (15/17, 88%) assessed fatigue with validated instruments. Mitochondrial markers associated with fatigue are a) mitochondrial transport pathways and respiratory chain, b) mutations in mitochondrial DNA, and c) energy disorders in cells of the immune system, such as natural killer cells. Mitochondrial metabolic activities, such as the production and transport of ATP, are significant components that may help understand the etiology of fatigue. Future directions should include longitudinal study designs, characterization of fatigue phenotypes, and the identification of markers involved in production and transport pathways. The clinical relevance in this field can lead to interventions targeting mitochondrial markers to reduce or prevent fatigue.
AB - This scoping review aimed to synthesize the best available evidence of the associations between molecular and genetic markers of mitochondrial metabolism and fatigue in human adults. The research question guiding this review was, “Are there potential relationships between mitochondrial metabolism markers and fatigue?” The literature search used three terms (mitochondria; fatigue; energy metabolism), which yielded 263 manuscripts and 22 theses/dissertations. The studies included in the review had to meet three criteria: (1) Include adult participants (≥18 years of age); (2) Show a relationship between mitochondrial energy metabolism and fatigue; (3) Be published in English, Spanish, or Portuguese. Of the 17 articles included for a full-text review, some had a cross-sectional design (6/17, 35%), and more than half (12/17, 70%) were published between 2015 and 2020. The predominant population studied were patients diagnosed with chronic fatigue syndrome (9/17, 53%). Most studies (15/17, 88%) assessed fatigue with validated instruments. Mitochondrial markers associated with fatigue are a) mitochondrial transport pathways and respiratory chain, b) mutations in mitochondrial DNA, and c) energy disorders in cells of the immune system, such as natural killer cells. Mitochondrial metabolic activities, such as the production and transport of ATP, are significant components that may help understand the etiology of fatigue. Future directions should include longitudinal study designs, characterization of fatigue phenotypes, and the identification of markers involved in production and transport pathways. The clinical relevance in this field can lead to interventions targeting mitochondrial markers to reduce or prevent fatigue.
KW - Energy metabolism
KW - Fatigue
KW - Mitochondria
KW - Oxidative phosphorylation
KW - Review
UR - http://www.scopus.com/inward/record.url?scp=85142501975&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85142501975&partnerID=8YFLogxK
U2 - 10.14393/BJ-v38n0a2022-65195
DO - 10.14393/BJ-v38n0a2022-65195
M3 - Article
AN - SCOPUS:85142501975
SN - 1516-3725
VL - 38
JO - Bioscience Journal
JF - Bioscience Journal
M1 - e38095
ER -