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FABP4 levels in hypothyroidism and its relationship with subclinical atherosclerosis

BACKGROUND/AIM: The aim of this study is to evaluate the relationship between serum fatty acid binding protein 4 (FABP4) levels and carotid intima media thickness (CIMT) in patients with hypothyroidism. MATERIALS AND METHODS: Forty subclinical hypothyroidism patients, 40 overt hypothyroidism patient...

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Autores principales: TAN, Mürşide, KORKMAZ, Hakan, AYDIN, Hüseyin, KUMBUL DOĞUÇ, Duygu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific and Technological Research Council of Turkey 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7018356/
https://www.ncbi.nlm.nih.gov/pubmed/31651119
http://dx.doi.org/10.3906/sag-1904-41
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author TAN, Mürşide
KORKMAZ, Hakan
AYDIN, Hüseyin
KUMBUL DOĞUÇ, Duygu
author_facet TAN, Mürşide
KORKMAZ, Hakan
AYDIN, Hüseyin
KUMBUL DOĞUÇ, Duygu
author_sort TAN, Mürşide
collection PubMed
description BACKGROUND/AIM: The aim of this study is to evaluate the relationship between serum fatty acid binding protein 4 (FABP4) levels and carotid intima media thickness (CIMT) in patients with hypothyroidism. MATERIALS AND METHODS: Forty subclinical hypothyroidism patients, 40 overt hypothyroidism patients, and 40 healthy controls were enrolled in the study. Blood pressure, body mass index, CIMT, fasting blood sugar, creatine, alanine aminotransferase, lipid parameters, insulin, free thyroxine, triiodothyronine, thyroid-stimulating hormone (TSH), thyroid peroxidase antibody (anti-TPO), thyroglobulin antibody (anti-TG), high-sensitivity C-reactive protein (Hs-CRP), and FABP4 levels of all participants were measured. RESULTS: Serum FABP4 levels were significantly higher in patients with subclinical and overt hypothyroidism than healthy controls (HCs) (P = 0.044 and P = 0.014, respectively). There was no significant difference in terms of FABP4 levels between patients with subclinical and overt hypothyroidism (P = 0.641). Serum TSH levels and serum FABP4 levels were positively correlated (r = 0.201, P = 0.039). CIMT was found to be higher in patients with subclinical and overt hypothyroidism than in HCs (P = 0.042 and P < 0.001, respectively). No correlation was found between CIMT and FABP4 levels (r = 0.038, P = 0.702). There was a positive correlation between CIMT and TSH, anti-TPO, anti-TG, triglycerides (TG), and total cholesterol levels. It was found that high TG levels were an independent factor that increased CIMT (r = 0.382, r2 = 0.146). CONCLUSION: In patients with subclinical and overt hypothyroidism, the level of FABP4 increases and this increase is correlated with the increase in TSH level. It is thought that FABP4 does not play a role in atherosclerosis development in patients with hypothyroidism without metabolic disorder.
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spelling pubmed-70183562020-03-23 FABP4 levels in hypothyroidism and its relationship with subclinical atherosclerosis TAN, Mürşide KORKMAZ, Hakan AYDIN, Hüseyin KUMBUL DOĞUÇ, Duygu Turk J Med Sci Article BACKGROUND/AIM: The aim of this study is to evaluate the relationship between serum fatty acid binding protein 4 (FABP4) levels and carotid intima media thickness (CIMT) in patients with hypothyroidism. MATERIALS AND METHODS: Forty subclinical hypothyroidism patients, 40 overt hypothyroidism patients, and 40 healthy controls were enrolled in the study. Blood pressure, body mass index, CIMT, fasting blood sugar, creatine, alanine aminotransferase, lipid parameters, insulin, free thyroxine, triiodothyronine, thyroid-stimulating hormone (TSH), thyroid peroxidase antibody (anti-TPO), thyroglobulin antibody (anti-TG), high-sensitivity C-reactive protein (Hs-CRP), and FABP4 levels of all participants were measured. RESULTS: Serum FABP4 levels were significantly higher in patients with subclinical and overt hypothyroidism than healthy controls (HCs) (P = 0.044 and P = 0.014, respectively). There was no significant difference in terms of FABP4 levels between patients with subclinical and overt hypothyroidism (P = 0.641). Serum TSH levels and serum FABP4 levels were positively correlated (r = 0.201, P = 0.039). CIMT was found to be higher in patients with subclinical and overt hypothyroidism than in HCs (P = 0.042 and P < 0.001, respectively). No correlation was found between CIMT and FABP4 levels (r = 0.038, P = 0.702). There was a positive correlation between CIMT and TSH, anti-TPO, anti-TG, triglycerides (TG), and total cholesterol levels. It was found that high TG levels were an independent factor that increased CIMT (r = 0.382, r2 = 0.146). CONCLUSION: In patients with subclinical and overt hypothyroidism, the level of FABP4 increases and this increase is correlated with the increase in TSH level. It is thought that FABP4 does not play a role in atherosclerosis development in patients with hypothyroidism without metabolic disorder. The Scientific and Technological Research Council of Turkey 2019-10-24 /pmc/articles/PMC7018356/ /pubmed/31651119 http://dx.doi.org/10.3906/sag-1904-41 Text en Copyright © 2019 The Author(s) This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Article
TAN, Mürşide
KORKMAZ, Hakan
AYDIN, Hüseyin
KUMBUL DOĞUÇ, Duygu
FABP4 levels in hypothyroidism and its relationship with subclinical atherosclerosis
title FABP4 levels in hypothyroidism and its relationship with subclinical atherosclerosis
title_full FABP4 levels in hypothyroidism and its relationship with subclinical atherosclerosis
title_fullStr FABP4 levels in hypothyroidism and its relationship with subclinical atherosclerosis
title_full_unstemmed FABP4 levels in hypothyroidism and its relationship with subclinical atherosclerosis
title_short FABP4 levels in hypothyroidism and its relationship with subclinical atherosclerosis
title_sort fabp4 levels in hypothyroidism and its relationship with subclinical atherosclerosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7018356/
https://www.ncbi.nlm.nih.gov/pubmed/31651119
http://dx.doi.org/10.3906/sag-1904-41
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