Circulating early biomarkers of atherogenesis in participants of the Longitudinal Study of Adult Health (ELSA-Brasil) without diabetes or cardiovascular disease

Detalhes bibliográficos
Autor(a) principal: Pititto, Bianca de Almeida
Data de Publicação: 2016
Outros Autores: Ribeiro Filho, Fernando de Souza Flexa, Barreto, Sandhi Maria, Duncan, Bruce Bartholow, Schmidt, Maria Inês, Lotufo, Paulo Andrade, Benseñor, Isabela Judith Martins, Ferreira, Sandra Roberta Gouvêa
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/152701
Resumo: Objective: Our aim was to describe the distribution of selected biomarkers according to age and sex, adjusted for HOMA-IR and adiposity, in a subset of middle-aged individuals of Brazilian Longitudinal Study of Adult Health-ELSA without diabetes mellitus or CVD. Subjects and methods: This crosssectional study was conducted in 998 participants of the ELSA-Brasil without diabetes and/or cardiovascular disease. In addition to the traditional risk factors, several biomarkers concentrations were compared according to sex, age groups (35-44; 45-54 yrs) and HOMA-IR tertiles. Linear regression was used to examine independent associations of sex and age with selected novel biomarkers, adjusted for body adiposity and HOMA-IR. Results: Fifty-five percent were women. Men had higher mean values of body mass index, waist circumference, blood pressure, plasma glucose, HOMA-IR, worse lipid profile and higher E-selectin and lower leptin concentrations than women; while women had higher levels of HDL-cholesterol and leptin than men. Mean values of waist circumference, systolic BP, plasma glucose and apolipoprotein B (Apo B) increased with age in both sexes. Leptin and E-selectin concentrations increased across HOMA-IR tertiles. Independent associations of Apo B with age were found only in male sex, while of leptin with body mass index and HOMA-IR, and of E-selectin with HOMA-IR in both sexes. Conclusions: In conclusion, our data indicate age, sex, adiposity and, consequently, insulin resistance, influence circulating levels of Apo B, leptin and E-selectin, suggesting that those aspects should be taken into consideration when assessing these parameters for research or clinical purposes in individuals at relatively low cardiometabolic risk.
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spelling Pititto, Bianca de AlmeidaRibeiro Filho, Fernando de Souza FlexaBarreto, Sandhi MariaDuncan, Bruce BartholowSchmidt, Maria InêsLotufo, Paulo AndradeBenseñor, Isabela Judith MartinsFerreira, Sandra Roberta Gouvêa2017-02-17T02:33:13Z20162359-4292http://hdl.handle.net/10183/152701001013230Objective: Our aim was to describe the distribution of selected biomarkers according to age and sex, adjusted for HOMA-IR and adiposity, in a subset of middle-aged individuals of Brazilian Longitudinal Study of Adult Health-ELSA without diabetes mellitus or CVD. Subjects and methods: This crosssectional study was conducted in 998 participants of the ELSA-Brasil without diabetes and/or cardiovascular disease. In addition to the traditional risk factors, several biomarkers concentrations were compared according to sex, age groups (35-44; 45-54 yrs) and HOMA-IR tertiles. Linear regression was used to examine independent associations of sex and age with selected novel biomarkers, adjusted for body adiposity and HOMA-IR. Results: Fifty-five percent were women. Men had higher mean values of body mass index, waist circumference, blood pressure, plasma glucose, HOMA-IR, worse lipid profile and higher E-selectin and lower leptin concentrations than women; while women had higher levels of HDL-cholesterol and leptin than men. Mean values of waist circumference, systolic BP, plasma glucose and apolipoprotein B (Apo B) increased with age in both sexes. Leptin and E-selectin concentrations increased across HOMA-IR tertiles. Independent associations of Apo B with age were found only in male sex, while of leptin with body mass index and HOMA-IR, and of E-selectin with HOMA-IR in both sexes. Conclusions: In conclusion, our data indicate age, sex, adiposity and, consequently, insulin resistance, influence circulating levels of Apo B, leptin and E-selectin, suggesting that those aspects should be taken into consideration when assessing these parameters for research or clinical purposes in individuals at relatively low cardiometabolic risk.application/pdfengArchives of endocrinology and metabolism. São Paulo. Vol. 60, n. 6 (Nov./Dec. 2016), p. 573-581.BiomarcadoresAteroscleroseAdiposidadeResistência à insulinaBiomarkersAtherogenesisAdiposityInsulin resistanceCirculating early biomarkers of atherogenesis in participants of the Longitudinal Study of Adult Health (ELSA-Brasil) without diabetes or cardiovascular diseaseinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL001013230.pdf001013230.pdfTexto completo (inglês)application/pdf195817http://www.lume.ufrgs.br/bitstream/10183/152701/1/001013230.pdf5c02213cf793ebd68869a168818b1f9fMD51TEXT001013230.pdf.txt001013230.pdf.txtExtracted Texttext/plain38684http://www.lume.ufrgs.br/bitstream/10183/152701/2/001013230.pdf.txt99de0c3a0c953b6e60a5fce6a15a2adfMD5210183/1527012023-05-21 03:27:33.462384oai:www.lume.ufrgs.br:10183/152701Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-05-21T06:27:33Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Circulating early biomarkers of atherogenesis in participants of the Longitudinal Study of Adult Health (ELSA-Brasil) without diabetes or cardiovascular disease
title Circulating early biomarkers of atherogenesis in participants of the Longitudinal Study of Adult Health (ELSA-Brasil) without diabetes or cardiovascular disease
spellingShingle Circulating early biomarkers of atherogenesis in participants of the Longitudinal Study of Adult Health (ELSA-Brasil) without diabetes or cardiovascular disease
Pititto, Bianca de Almeida
Biomarcadores
Aterosclerose
Adiposidade
Resistência à insulina
Biomarkers
Atherogenesis
Adiposity
Insulin resistance
title_short Circulating early biomarkers of atherogenesis in participants of the Longitudinal Study of Adult Health (ELSA-Brasil) without diabetes or cardiovascular disease
title_full Circulating early biomarkers of atherogenesis in participants of the Longitudinal Study of Adult Health (ELSA-Brasil) without diabetes or cardiovascular disease
title_fullStr Circulating early biomarkers of atherogenesis in participants of the Longitudinal Study of Adult Health (ELSA-Brasil) without diabetes or cardiovascular disease
title_full_unstemmed Circulating early biomarkers of atherogenesis in participants of the Longitudinal Study of Adult Health (ELSA-Brasil) without diabetes or cardiovascular disease
title_sort Circulating early biomarkers of atherogenesis in participants of the Longitudinal Study of Adult Health (ELSA-Brasil) without diabetes or cardiovascular disease
author Pititto, Bianca de Almeida
author_facet Pititto, Bianca de Almeida
Ribeiro Filho, Fernando de Souza Flexa
Barreto, Sandhi Maria
Duncan, Bruce Bartholow
Schmidt, Maria Inês
Lotufo, Paulo Andrade
Benseñor, Isabela Judith Martins
Ferreira, Sandra Roberta Gouvêa
author_role author
author2 Ribeiro Filho, Fernando de Souza Flexa
Barreto, Sandhi Maria
Duncan, Bruce Bartholow
Schmidt, Maria Inês
Lotufo, Paulo Andrade
Benseñor, Isabela Judith Martins
Ferreira, Sandra Roberta Gouvêa
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Pititto, Bianca de Almeida
Ribeiro Filho, Fernando de Souza Flexa
Barreto, Sandhi Maria
Duncan, Bruce Bartholow
Schmidt, Maria Inês
Lotufo, Paulo Andrade
Benseñor, Isabela Judith Martins
Ferreira, Sandra Roberta Gouvêa
dc.subject.por.fl_str_mv Biomarcadores
Aterosclerose
Adiposidade
Resistência à insulina
topic Biomarcadores
Aterosclerose
Adiposidade
Resistência à insulina
Biomarkers
Atherogenesis
Adiposity
Insulin resistance
dc.subject.eng.fl_str_mv Biomarkers
Atherogenesis
Adiposity
Insulin resistance
description Objective: Our aim was to describe the distribution of selected biomarkers according to age and sex, adjusted for HOMA-IR and adiposity, in a subset of middle-aged individuals of Brazilian Longitudinal Study of Adult Health-ELSA without diabetes mellitus or CVD. Subjects and methods: This crosssectional study was conducted in 998 participants of the ELSA-Brasil without diabetes and/or cardiovascular disease. In addition to the traditional risk factors, several biomarkers concentrations were compared according to sex, age groups (35-44; 45-54 yrs) and HOMA-IR tertiles. Linear regression was used to examine independent associations of sex and age with selected novel biomarkers, adjusted for body adiposity and HOMA-IR. Results: Fifty-five percent were women. Men had higher mean values of body mass index, waist circumference, blood pressure, plasma glucose, HOMA-IR, worse lipid profile and higher E-selectin and lower leptin concentrations than women; while women had higher levels of HDL-cholesterol and leptin than men. Mean values of waist circumference, systolic BP, plasma glucose and apolipoprotein B (Apo B) increased with age in both sexes. Leptin and E-selectin concentrations increased across HOMA-IR tertiles. Independent associations of Apo B with age were found only in male sex, while of leptin with body mass index and HOMA-IR, and of E-selectin with HOMA-IR in both sexes. Conclusions: In conclusion, our data indicate age, sex, adiposity and, consequently, insulin resistance, influence circulating levels of Apo B, leptin and E-selectin, suggesting that those aspects should be taken into consideration when assessing these parameters for research or clinical purposes in individuals at relatively low cardiometabolic risk.
publishDate 2016
dc.date.issued.fl_str_mv 2016
dc.date.accessioned.fl_str_mv 2017-02-17T02:33:13Z
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Archives of endocrinology and metabolism. São Paulo. Vol. 60, n. 6 (Nov./Dec. 2016), p. 573-581.
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