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Increased leptin/adiponectin ratio relates to low-normal thyroid function in metabolic syndrome
BACKGROUND: Low-normal thyroid function within the euthyroid range may contribute to increased atherosclerosis susceptibility. The leptin/adiponectin (L/A) ratio is associated with cardiovascular disease and reflects adipose tissue dysfunction. Relationships of the L/A ratio with low-normal thyroid...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225648/ https://www.ncbi.nlm.nih.gov/pubmed/28077136 http://dx.doi.org/10.1186/s12944-016-0403-4 |
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author | van Tienhoven-Wind, Lynnda J. N. Dullaart, Robin P. F. |
author_facet | van Tienhoven-Wind, Lynnda J. N. Dullaart, Robin P. F. |
author_sort | van Tienhoven-Wind, Lynnda J. N. |
collection | PubMed |
description | BACKGROUND: Low-normal thyroid function within the euthyroid range may contribute to increased atherosclerosis susceptibility. The leptin/adiponectin (L/A) ratio is associated with cardiovascular disease and reflects adipose tissue dysfunction. Relationships of the L/A ratio with low-normal thyroid function are unknown. METHODS: Relationships of thyroid stimulating hormone (TSH) and free thyroxine (free T(4)) with leptin, adiponectin and the L/A ratio in euthyroid subjects were documented in 67 fasting subjects with metabolic syndrome (Mets) and 86 euthyroid subjects without MetS (TSH and free T(4) levels within the institutional reference range). RESULTS: Neither plasma leptin nor adiponectin was significantly correlated with TSH or free T(4) in subjects with and without MetS. In the whole group, high sensitivity C-reactive protein (hs-CRP) was positively correlated with the L/A ratio (r = 0.485, P < 0.001). Notably, the L/A ratio was positively correlated with TSH in subjects with MetS (r = 0.252, P = 0.040) but not in subjects without MetS (r = −0.068, P = 0.54; interaction term, P = 0.027). In MetS subjects, the L/A ratio remained positively related with TSH after adjustment for age, sex, diabetes status, hs-CRP and the use of antihypertensive and glucose lowering medication (β = 0.283, P = 0.018), as well as after adjustment for individual MetS components (β = 0.294, P = 0.020). CONCLUSIONS: In the context of MetS, a higher TSH within the euthyroid range confers an increased L/A ratio, a proposed marker of atherosclerosis susceptibility and adipocyte dysfunction. |
format | Online Article Text |
id | pubmed-5225648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-52256482017-01-17 Increased leptin/adiponectin ratio relates to low-normal thyroid function in metabolic syndrome van Tienhoven-Wind, Lynnda J. N. Dullaart, Robin P. F. Lipids Health Dis Research BACKGROUND: Low-normal thyroid function within the euthyroid range may contribute to increased atherosclerosis susceptibility. The leptin/adiponectin (L/A) ratio is associated with cardiovascular disease and reflects adipose tissue dysfunction. Relationships of the L/A ratio with low-normal thyroid function are unknown. METHODS: Relationships of thyroid stimulating hormone (TSH) and free thyroxine (free T(4)) with leptin, adiponectin and the L/A ratio in euthyroid subjects were documented in 67 fasting subjects with metabolic syndrome (Mets) and 86 euthyroid subjects without MetS (TSH and free T(4) levels within the institutional reference range). RESULTS: Neither plasma leptin nor adiponectin was significantly correlated with TSH or free T(4) in subjects with and without MetS. In the whole group, high sensitivity C-reactive protein (hs-CRP) was positively correlated with the L/A ratio (r = 0.485, P < 0.001). Notably, the L/A ratio was positively correlated with TSH in subjects with MetS (r = 0.252, P = 0.040) but not in subjects without MetS (r = −0.068, P = 0.54; interaction term, P = 0.027). In MetS subjects, the L/A ratio remained positively related with TSH after adjustment for age, sex, diabetes status, hs-CRP and the use of antihypertensive and glucose lowering medication (β = 0.283, P = 0.018), as well as after adjustment for individual MetS components (β = 0.294, P = 0.020). CONCLUSIONS: In the context of MetS, a higher TSH within the euthyroid range confers an increased L/A ratio, a proposed marker of atherosclerosis susceptibility and adipocyte dysfunction. BioMed Central 2017-01-11 /pmc/articles/PMC5225648/ /pubmed/28077136 http://dx.doi.org/10.1186/s12944-016-0403-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research van Tienhoven-Wind, Lynnda J. N. Dullaart, Robin P. F. Increased leptin/adiponectin ratio relates to low-normal thyroid function in metabolic syndrome |
title | Increased leptin/adiponectin ratio relates to low-normal thyroid function in metabolic syndrome |
title_full | Increased leptin/adiponectin ratio relates to low-normal thyroid function in metabolic syndrome |
title_fullStr | Increased leptin/adiponectin ratio relates to low-normal thyroid function in metabolic syndrome |
title_full_unstemmed | Increased leptin/adiponectin ratio relates to low-normal thyroid function in metabolic syndrome |
title_short | Increased leptin/adiponectin ratio relates to low-normal thyroid function in metabolic syndrome |
title_sort | increased leptin/adiponectin ratio relates to low-normal thyroid function in metabolic syndrome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225648/ https://www.ncbi.nlm.nih.gov/pubmed/28077136 http://dx.doi.org/10.1186/s12944-016-0403-4 |
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