Obesity Increases Gene Expression of Markers Associated With Immunosenescence in Obese Middle-Aged Individuals

Detalhes bibliográficos
Autor(a) principal: Brunelli, Diego T.
Data de Publicação: 2021
Outros Autores: Boldrini, Vinicius O., Bonfante, Ivan L. P., Duft, Renata G., Mateus, Keryma, Costa, Leonardo Santos, Chacon-Mikahil, Mara P. T., Teixeira, Ana M., Farias, Alessandro S., Cavaglieri, Cláudia R.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/103252
https://doi.org/10.3389/fimmu.2021.806400
Resumo: Recently, it has been argued that obesity leads to a chronic pro-inflammatory state that can accelerate immunosenescence, predisposing to the early acquisition of an immune risk profile and health problems related to immunity in adulthood. In this sense, the present study aimed to verify, in circulating leukocytes, the gene expression of markers related to early immunosenescence associated with obesity and its possible relationships with the physical fitness in obese adults with type 2 diabetes or without associated comorbidities. The sample consisted of middle-aged obese individuals (body mass index (BMI) between 30-35 kg/m²) with type 2 diabetes mellitus (OBD; n = 17) or without associated comorbidity (OB; n = 18), and a control group of eutrophic healthy individuals (BMI: 20 - 25 kg/m²) of same ages (E; n = 18). All groups (OBD, OB and E) performed the functional analyses [muscle strength (1RM) and cardiorespiratory fitness (VO2max)], anthropometry, body composition (Air Displacement Plethysmograph), blood collections for biochemical (anti-CMV) and molecular (gene expression of leptin, IL-2, IL-4, IL-6, IL-10, TNF-α, PD-1, P16ink4a, CCR7, CD28 and CD27) analyses of markers related to immunosenescence. Increased gene expression of leptin, IL-2, IL-4, IL-10, TNF-α, PD-1, P16ink4a, CCR7 and CD27 was found for the OBD and OB groups compared to the E group. Moreover, VO2max for the OBD and OB groups was significantly lower compared to E. In conclusion, obesity, regardless of associated disease, induces increased gene expression of markers associated with inflammation and immunosenescence in circulating leukocytes in obese middle-aged individuals compared to a eutrophic group of the same age. Additionally, increased adipose tissue and markers of chronic inflammation and immunosenescence were associated to impairments in the cardiorespiratory capacity of obese middle-aged individuals.
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spelling Obesity Increases Gene Expression of Markers Associated With Immunosenescence in Obese Middle-Aged Individualstype 2 diabetes mellitusinflammationagingphysical fitnessadipose tissueRecently, it has been argued that obesity leads to a chronic pro-inflammatory state that can accelerate immunosenescence, predisposing to the early acquisition of an immune risk profile and health problems related to immunity in adulthood. In this sense, the present study aimed to verify, in circulating leukocytes, the gene expression of markers related to early immunosenescence associated with obesity and its possible relationships with the physical fitness in obese adults with type 2 diabetes or without associated comorbidities. The sample consisted of middle-aged obese individuals (body mass index (BMI) between 30-35 kg/m²) with type 2 diabetes mellitus (OBD; n = 17) or without associated comorbidity (OB; n = 18), and a control group of eutrophic healthy individuals (BMI: 20 - 25 kg/m²) of same ages (E; n = 18). All groups (OBD, OB and E) performed the functional analyses [muscle strength (1RM) and cardiorespiratory fitness (VO2max)], anthropometry, body composition (Air Displacement Plethysmograph), blood collections for biochemical (anti-CMV) and molecular (gene expression of leptin, IL-2, IL-4, IL-6, IL-10, TNF-α, PD-1, P16ink4a, CCR7, CD28 and CD27) analyses of markers related to immunosenescence. Increased gene expression of leptin, IL-2, IL-4, IL-10, TNF-α, PD-1, P16ink4a, CCR7 and CD27 was found for the OBD and OB groups compared to the E group. Moreover, VO2max for the OBD and OB groups was significantly lower compared to E. In conclusion, obesity, regardless of associated disease, induces increased gene expression of markers associated with inflammation and immunosenescence in circulating leukocytes in obese middle-aged individuals compared to a eutrophic group of the same age. Additionally, increased adipose tissue and markers of chronic inflammation and immunosenescence were associated to impairments in the cardiorespiratory capacity of obese middle-aged individuals.2021info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/103252http://hdl.handle.net/10316/103252https://doi.org/10.3389/fimmu.2021.806400eng1664-3224350695891664-3224Brunelli, Diego T.Boldrini, Vinicius O.Bonfante, Ivan L. P.Duft, Renata G.Mateus, KerymaCosta, Leonardo SantosChacon-Mikahil, Mara P. T.Teixeira, Ana M.Farias, Alessandro S.Cavaglieri, Cláudia R.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-10-26T20:32:49Zoai:estudogeral.uc.pt:10316/103252Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:20:07.179075Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Obesity Increases Gene Expression of Markers Associated With Immunosenescence in Obese Middle-Aged Individuals
title Obesity Increases Gene Expression of Markers Associated With Immunosenescence in Obese Middle-Aged Individuals
spellingShingle Obesity Increases Gene Expression of Markers Associated With Immunosenescence in Obese Middle-Aged Individuals
Brunelli, Diego T.
type 2 diabetes mellitus
inflammation
aging
physical fitness
adipose tissue
title_short Obesity Increases Gene Expression of Markers Associated With Immunosenescence in Obese Middle-Aged Individuals
title_full Obesity Increases Gene Expression of Markers Associated With Immunosenescence in Obese Middle-Aged Individuals
title_fullStr Obesity Increases Gene Expression of Markers Associated With Immunosenescence in Obese Middle-Aged Individuals
title_full_unstemmed Obesity Increases Gene Expression of Markers Associated With Immunosenescence in Obese Middle-Aged Individuals
title_sort Obesity Increases Gene Expression of Markers Associated With Immunosenescence in Obese Middle-Aged Individuals
author Brunelli, Diego T.
author_facet Brunelli, Diego T.
Boldrini, Vinicius O.
Bonfante, Ivan L. P.
Duft, Renata G.
Mateus, Keryma
Costa, Leonardo Santos
Chacon-Mikahil, Mara P. T.
Teixeira, Ana M.
Farias, Alessandro S.
Cavaglieri, Cláudia R.
author_role author
author2 Boldrini, Vinicius O.
Bonfante, Ivan L. P.
Duft, Renata G.
Mateus, Keryma
Costa, Leonardo Santos
Chacon-Mikahil, Mara P. T.
Teixeira, Ana M.
Farias, Alessandro S.
Cavaglieri, Cláudia R.
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Brunelli, Diego T.
Boldrini, Vinicius O.
Bonfante, Ivan L. P.
Duft, Renata G.
Mateus, Keryma
Costa, Leonardo Santos
Chacon-Mikahil, Mara P. T.
Teixeira, Ana M.
Farias, Alessandro S.
Cavaglieri, Cláudia R.
dc.subject.por.fl_str_mv type 2 diabetes mellitus
inflammation
aging
physical fitness
adipose tissue
topic type 2 diabetes mellitus
inflammation
aging
physical fitness
adipose tissue
description Recently, it has been argued that obesity leads to a chronic pro-inflammatory state that can accelerate immunosenescence, predisposing to the early acquisition of an immune risk profile and health problems related to immunity in adulthood. In this sense, the present study aimed to verify, in circulating leukocytes, the gene expression of markers related to early immunosenescence associated with obesity and its possible relationships with the physical fitness in obese adults with type 2 diabetes or without associated comorbidities. The sample consisted of middle-aged obese individuals (body mass index (BMI) between 30-35 kg/m²) with type 2 diabetes mellitus (OBD; n = 17) or without associated comorbidity (OB; n = 18), and a control group of eutrophic healthy individuals (BMI: 20 - 25 kg/m²) of same ages (E; n = 18). All groups (OBD, OB and E) performed the functional analyses [muscle strength (1RM) and cardiorespiratory fitness (VO2max)], anthropometry, body composition (Air Displacement Plethysmograph), blood collections for biochemical (anti-CMV) and molecular (gene expression of leptin, IL-2, IL-4, IL-6, IL-10, TNF-α, PD-1, P16ink4a, CCR7, CD28 and CD27) analyses of markers related to immunosenescence. Increased gene expression of leptin, IL-2, IL-4, IL-10, TNF-α, PD-1, P16ink4a, CCR7 and CD27 was found for the OBD and OB groups compared to the E group. Moreover, VO2max for the OBD and OB groups was significantly lower compared to E. In conclusion, obesity, regardless of associated disease, induces increased gene expression of markers associated with inflammation and immunosenescence in circulating leukocytes in obese middle-aged individuals compared to a eutrophic group of the same age. Additionally, increased adipose tissue and markers of chronic inflammation and immunosenescence were associated to impairments in the cardiorespiratory capacity of obese middle-aged individuals.
publishDate 2021
dc.date.none.fl_str_mv 2021
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/103252
http://hdl.handle.net/10316/103252
https://doi.org/10.3389/fimmu.2021.806400
url http://hdl.handle.net/10316/103252
https://doi.org/10.3389/fimmu.2021.806400
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1664-3224
35069589
1664-3224
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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