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Role of Adiponectin in Coronary Heart Disease Risk: A Mendelian Randomization Study

RATIONALE: Hypoadiponectinemia correlates with several coronary heart disease (CHD) risk factors. However, it is unknown whether adiponectin is causally implicated in CHD pathogenesis. OBJECTIVE: We aimed to investigate the causal effect of adiponectin on CHD risk. METHODS AND RESULTS: We undertook...

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Autores principales: Borges, Maria Carolina, Lawlor, Debbie A., de Oliveira, Cesar, White, Jon, Horta, Bernardo Lessa, Barros, Aluísio J.D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959825/
https://www.ncbi.nlm.nih.gov/pubmed/27252388
http://dx.doi.org/10.1161/CIRCRESAHA.116.308716
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author Borges, Maria Carolina
Lawlor, Debbie A.
de Oliveira, Cesar
White, Jon
Horta, Bernardo Lessa
Barros, Aluísio J.D.
author_facet Borges, Maria Carolina
Lawlor, Debbie A.
de Oliveira, Cesar
White, Jon
Horta, Bernardo Lessa
Barros, Aluísio J.D.
author_sort Borges, Maria Carolina
collection PubMed
description RATIONALE: Hypoadiponectinemia correlates with several coronary heart disease (CHD) risk factors. However, it is unknown whether adiponectin is causally implicated in CHD pathogenesis. OBJECTIVE: We aimed to investigate the causal effect of adiponectin on CHD risk. METHODS AND RESULTS: We undertook a Mendelian randomization study using data from genome-wide association studies consortia. We used the ADIPOGen consortium to identify genetic variants that could be used as instrumental variables for the effect of adiponectin. Data on the association of these genetic variants with CHD risk were obtained from CARDIoGRAM (22 233 CHD cases and 64 762 controls of European ancestry) and from CARDIoGRAMplusC4D Metabochip (63 746 cases and 130 681 controls; ≈ 91% of European ancestry) consortia. Data on the association of genetic variants with adiponectin levels and with CHD were combined to estimate the influence of blood adiponectin on CHD risk. In the conservative approach (restricted to using variants within the adiponectin gene as instrumental variables), each 1 U increase in log blood adiponectin concentration was associated with an odds ratio for CHD of 0.83 (95% confidence interval, 0.68–1.01) in CARDIoGRAM and 0.97 (95% confidence interval, 0.84–1.12) in CARDIoGRAMplusC4D Metabochip. Findings from the liberal approach (including variants in any locus across the genome) indicated a protective effect of adiponectin that was attenuated to the null after adjustment for known CHD predictors. CONCLUSIONS: Overall, our findings do not support a causal role of adiponectin levels in CHD pathogenesis.
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spelling pubmed-49598252016-08-14 Role of Adiponectin in Coronary Heart Disease Risk: A Mendelian Randomization Study Borges, Maria Carolina Lawlor, Debbie A. de Oliveira, Cesar White, Jon Horta, Bernardo Lessa Barros, Aluísio J.D. Circ Res Clinical Track RATIONALE: Hypoadiponectinemia correlates with several coronary heart disease (CHD) risk factors. However, it is unknown whether adiponectin is causally implicated in CHD pathogenesis. OBJECTIVE: We aimed to investigate the causal effect of adiponectin on CHD risk. METHODS AND RESULTS: We undertook a Mendelian randomization study using data from genome-wide association studies consortia. We used the ADIPOGen consortium to identify genetic variants that could be used as instrumental variables for the effect of adiponectin. Data on the association of these genetic variants with CHD risk were obtained from CARDIoGRAM (22 233 CHD cases and 64 762 controls of European ancestry) and from CARDIoGRAMplusC4D Metabochip (63 746 cases and 130 681 controls; ≈ 91% of European ancestry) consortia. Data on the association of genetic variants with adiponectin levels and with CHD were combined to estimate the influence of blood adiponectin on CHD risk. In the conservative approach (restricted to using variants within the adiponectin gene as instrumental variables), each 1 U increase in log blood adiponectin concentration was associated with an odds ratio for CHD of 0.83 (95% confidence interval, 0.68–1.01) in CARDIoGRAM and 0.97 (95% confidence interval, 0.84–1.12) in CARDIoGRAMplusC4D Metabochip. Findings from the liberal approach (including variants in any locus across the genome) indicated a protective effect of adiponectin that was attenuated to the null after adjustment for known CHD predictors. CONCLUSIONS: Overall, our findings do not support a causal role of adiponectin levels in CHD pathogenesis. Lippincott Williams & Wilkins 2016-07-22 2016-07-21 /pmc/articles/PMC4959825/ /pubmed/27252388 http://dx.doi.org/10.1161/CIRCRESAHA.116.308716 Text en © 2016 The Authors. Circulation Research is published on behalf of the American Heart Association, Inc., by Wolters Kluwer. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial-NoDervis (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited, the use is noncommercial, and no modifications or adaptations are made.
spellingShingle Clinical Track
Borges, Maria Carolina
Lawlor, Debbie A.
de Oliveira, Cesar
White, Jon
Horta, Bernardo Lessa
Barros, Aluísio J.D.
Role of Adiponectin in Coronary Heart Disease Risk: A Mendelian Randomization Study
title Role of Adiponectin in Coronary Heart Disease Risk: A Mendelian Randomization Study
title_full Role of Adiponectin in Coronary Heart Disease Risk: A Mendelian Randomization Study
title_fullStr Role of Adiponectin in Coronary Heart Disease Risk: A Mendelian Randomization Study
title_full_unstemmed Role of Adiponectin in Coronary Heart Disease Risk: A Mendelian Randomization Study
title_short Role of Adiponectin in Coronary Heart Disease Risk: A Mendelian Randomization Study
title_sort role of adiponectin in coronary heart disease risk: a mendelian randomization study
topic Clinical Track
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959825/
https://www.ncbi.nlm.nih.gov/pubmed/27252388
http://dx.doi.org/10.1161/CIRCRESAHA.116.308716
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