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Association of Thyroid Function with Blood Pressure and Cardiovascular Disease: A Mendelian Randomization

Thyroid function has a widespread effect on the cardiometabolic system. However, the causal association between either subclinical hyper- or hypothyroidism and the thyroid hormones with blood pressure (BP) and cardiovascular diseases (CVD) is not clear. We aim to investigate this in a two-sample Men...

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Autores principales: Giontella, Alice, Lotta, Luca A., Overton, John D., Baras, Aris, Sartorio, Andrea, Minuz, Pietro, Gill, Dipender, Melander, Olle, Fava, Cristiano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704995/
https://www.ncbi.nlm.nih.gov/pubmed/34945778
http://dx.doi.org/10.3390/jpm11121306
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author Giontella, Alice
Lotta, Luca A.
Overton, John D.
Baras, Aris
Sartorio, Andrea
Minuz, Pietro
Gill, Dipender
Melander, Olle
Fava, Cristiano
author_facet Giontella, Alice
Lotta, Luca A.
Overton, John D.
Baras, Aris
Sartorio, Andrea
Minuz, Pietro
Gill, Dipender
Melander, Olle
Fava, Cristiano
author_sort Giontella, Alice
collection PubMed
description Thyroid function has a widespread effect on the cardiometabolic system. However, the causal association between either subclinical hyper- or hypothyroidism and the thyroid hormones with blood pressure (BP) and cardiovascular diseases (CVD) is not clear. We aim to investigate this in a two-sample Mendelian randomization (MR) study. Single nucleotide polymorphisms (SNPs) associated with thyroid-stimulating hormone (TSH), free tetraiodothyronine (FT4), hyper- and hypothyroidism, and anti-thyroid peroxidase antibodies (TPOAb), from genome-wide association studies (GWAS), were selected as MR instrumental variables. SNPs–outcome (BP, CVD) associations were evaluated in a large-scale cohort, the Malmö Diet and Cancer Study (n = 29,298). Causal estimates were computed by inverse-variance weighted (IVW), weighted median, and MR-Egger approaches. Genetically increased levels of TSH were associated with decreased systolic BP and with a lower risk of atrial fibrillation. Hyperthyroidism and TPOAb were associated with a lower risk of atrial fibrillation. Our data support a causal association between genetically decreased levels of TSH and both atrial fibrillation and systolic BP. The lack of significance after Bonferroni correction and the sensitivity analyses suggesting pleiotropy, should prompt us to be cautious in their interpretation. Nevertheless, these findings offer mechanistic insight into the etiology of CVD. Further work into the genes involved in thyroid functions and their relation to cardiovascular outcomes may highlight pathways for targeted intervention.
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spelling pubmed-87049952021-12-25 Association of Thyroid Function with Blood Pressure and Cardiovascular Disease: A Mendelian Randomization Giontella, Alice Lotta, Luca A. Overton, John D. Baras, Aris Sartorio, Andrea Minuz, Pietro Gill, Dipender Melander, Olle Fava, Cristiano J Pers Med Article Thyroid function has a widespread effect on the cardiometabolic system. However, the causal association between either subclinical hyper- or hypothyroidism and the thyroid hormones with blood pressure (BP) and cardiovascular diseases (CVD) is not clear. We aim to investigate this in a two-sample Mendelian randomization (MR) study. Single nucleotide polymorphisms (SNPs) associated with thyroid-stimulating hormone (TSH), free tetraiodothyronine (FT4), hyper- and hypothyroidism, and anti-thyroid peroxidase antibodies (TPOAb), from genome-wide association studies (GWAS), were selected as MR instrumental variables. SNPs–outcome (BP, CVD) associations were evaluated in a large-scale cohort, the Malmö Diet and Cancer Study (n = 29,298). Causal estimates were computed by inverse-variance weighted (IVW), weighted median, and MR-Egger approaches. Genetically increased levels of TSH were associated with decreased systolic BP and with a lower risk of atrial fibrillation. Hyperthyroidism and TPOAb were associated with a lower risk of atrial fibrillation. Our data support a causal association between genetically decreased levels of TSH and both atrial fibrillation and systolic BP. The lack of significance after Bonferroni correction and the sensitivity analyses suggesting pleiotropy, should prompt us to be cautious in their interpretation. Nevertheless, these findings offer mechanistic insight into the etiology of CVD. Further work into the genes involved in thyroid functions and their relation to cardiovascular outcomes may highlight pathways for targeted intervention. MDPI 2021-12-06 /pmc/articles/PMC8704995/ /pubmed/34945778 http://dx.doi.org/10.3390/jpm11121306 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Giontella, Alice
Lotta, Luca A.
Overton, John D.
Baras, Aris
Sartorio, Andrea
Minuz, Pietro
Gill, Dipender
Melander, Olle
Fava, Cristiano
Association of Thyroid Function with Blood Pressure and Cardiovascular Disease: A Mendelian Randomization
title Association of Thyroid Function with Blood Pressure and Cardiovascular Disease: A Mendelian Randomization
title_full Association of Thyroid Function with Blood Pressure and Cardiovascular Disease: A Mendelian Randomization
title_fullStr Association of Thyroid Function with Blood Pressure and Cardiovascular Disease: A Mendelian Randomization
title_full_unstemmed Association of Thyroid Function with Blood Pressure and Cardiovascular Disease: A Mendelian Randomization
title_short Association of Thyroid Function with Blood Pressure and Cardiovascular Disease: A Mendelian Randomization
title_sort association of thyroid function with blood pressure and cardiovascular disease: a mendelian randomization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704995/
https://www.ncbi.nlm.nih.gov/pubmed/34945778
http://dx.doi.org/10.3390/jpm11121306
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