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Glucocorticoids associate with cardiometabolic risk factors in black South Africans

Circulating glucocorticoids are associated with metabolic syndrome and related cardiometabolic risk factors in non-Africans. This study investigated these associations in Africans, whose metabolic phenotype reportedly differs from Europeans. Adiposity, blood pressure, glycaemia, insulin resistance,...

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Autores principales: Dlamini, Siphiwe N, Lombard, Zané, Micklesfield, Lisa K, Crowther, Nigel, Norris, Shane A, Snyman, Tracy, Crawford, Andrew A, Walker, Brian R, Goedecke, Julia H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8346194/
https://www.ncbi.nlm.nih.gov/pubmed/34261039
http://dx.doi.org/10.1530/EC-21-0195
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author Dlamini, Siphiwe N
Lombard, Zané
Micklesfield, Lisa K
Crowther, Nigel
Norris, Shane A
Snyman, Tracy
Crawford, Andrew A
Walker, Brian R
Goedecke, Julia H
author_facet Dlamini, Siphiwe N
Lombard, Zané
Micklesfield, Lisa K
Crowther, Nigel
Norris, Shane A
Snyman, Tracy
Crawford, Andrew A
Walker, Brian R
Goedecke, Julia H
author_sort Dlamini, Siphiwe N
collection PubMed
description Circulating glucocorticoids are associated with metabolic syndrome and related cardiometabolic risk factors in non-Africans. This study investigated these associations in Africans, whose metabolic phenotype reportedly differs from Europeans. Adiposity, blood pressure, glycaemia, insulin resistance, and lipid profile, were measured in 316 African men and 788 African women living in Soweto, Johannesburg. The 2009 harmonized criteria were used to define metabolic syndrome. Serum glucocorticoids were measured using liquid chromatography-mass spectrometry. Cortisol was associated with greater odds presenting with metabolic syndrome (odds ratio (95% CI) =1.50 (1.04, 2.17) and higher systolic (beta coefficient, β (95% CI) =0.04 (0.01, 0.08)) and diastolic (0.05 (0.02, 0.09)) blood pressure, but higher HDL (0.10 (0.02, 0.19)) and lower LDL (−0.14 (−0.24, −0.03)) cholesterol concentrations, in the combined sample of men and women. In contrast, corticosterone was only associated with higher insulin sensitivity (Matsuda index; 0.22 (0.03, 0.41)), but this was not independent of BMI. Sex-specific associations were observed, such that both cortisol and corticosterone were associated with higher fasting glucose (standardized β (95% CI): 0.24 (0.12, 0.36) for cortisol and 0.12 (0.01, 0.23) for corticosterone) and HbA1c (0.13 (0.01, 0.25) for cortisol and 0.12 (0.01, 0.24) for corticosterone) in men only, but lower HbA1c (0.10 (−0.20, −0.01) for cortisol and −0.09 (−0.18, −0.03) for corticosterone) in women only. Our study reports for the first time that associations between circulating glucocorticoid concentrations and key cardiometabolic risk factors exhibit both glucocorticoid- and sex-specificity in Africans.
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spelling pubmed-83461942021-08-10 Glucocorticoids associate with cardiometabolic risk factors in black South Africans Dlamini, Siphiwe N Lombard, Zané Micklesfield, Lisa K Crowther, Nigel Norris, Shane A Snyman, Tracy Crawford, Andrew A Walker, Brian R Goedecke, Julia H Endocr Connect Research Circulating glucocorticoids are associated with metabolic syndrome and related cardiometabolic risk factors in non-Africans. This study investigated these associations in Africans, whose metabolic phenotype reportedly differs from Europeans. Adiposity, blood pressure, glycaemia, insulin resistance, and lipid profile, were measured in 316 African men and 788 African women living in Soweto, Johannesburg. The 2009 harmonized criteria were used to define metabolic syndrome. Serum glucocorticoids were measured using liquid chromatography-mass spectrometry. Cortisol was associated with greater odds presenting with metabolic syndrome (odds ratio (95% CI) =1.50 (1.04, 2.17) and higher systolic (beta coefficient, β (95% CI) =0.04 (0.01, 0.08)) and diastolic (0.05 (0.02, 0.09)) blood pressure, but higher HDL (0.10 (0.02, 0.19)) and lower LDL (−0.14 (−0.24, −0.03)) cholesterol concentrations, in the combined sample of men and women. In contrast, corticosterone was only associated with higher insulin sensitivity (Matsuda index; 0.22 (0.03, 0.41)), but this was not independent of BMI. Sex-specific associations were observed, such that both cortisol and corticosterone were associated with higher fasting glucose (standardized β (95% CI): 0.24 (0.12, 0.36) for cortisol and 0.12 (0.01, 0.23) for corticosterone) and HbA1c (0.13 (0.01, 0.25) for cortisol and 0.12 (0.01, 0.24) for corticosterone) in men only, but lower HbA1c (0.10 (−0.20, −0.01) for cortisol and −0.09 (−0.18, −0.03) for corticosterone) in women only. Our study reports for the first time that associations between circulating glucocorticoid concentrations and key cardiometabolic risk factors exhibit both glucocorticoid- and sex-specificity in Africans. Bioscientifica Ltd 2021-07-14 /pmc/articles/PMC8346194/ /pubmed/34261039 http://dx.doi.org/10.1530/EC-21-0195 Text en © The authors https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License. (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Research
Dlamini, Siphiwe N
Lombard, Zané
Micklesfield, Lisa K
Crowther, Nigel
Norris, Shane A
Snyman, Tracy
Crawford, Andrew A
Walker, Brian R
Goedecke, Julia H
Glucocorticoids associate with cardiometabolic risk factors in black South Africans
title Glucocorticoids associate with cardiometabolic risk factors in black South Africans
title_full Glucocorticoids associate with cardiometabolic risk factors in black South Africans
title_fullStr Glucocorticoids associate with cardiometabolic risk factors in black South Africans
title_full_unstemmed Glucocorticoids associate with cardiometabolic risk factors in black South Africans
title_short Glucocorticoids associate with cardiometabolic risk factors in black South Africans
title_sort glucocorticoids associate with cardiometabolic risk factors in black south africans
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8346194/
https://www.ncbi.nlm.nih.gov/pubmed/34261039
http://dx.doi.org/10.1530/EC-21-0195
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