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Expression patterns of serum MicroRNAs related to endothelial dysfunction in patients with subclinical hypothyroidism

BACKGROUND: Increasing evidence has shown that elevated Thyroid stimulating hormone (TSH) levels are positively correlated with atherosclerosis (ATH) in patients with subclinical hypothyroidism (SCH). Some researchers found that the dysfunction of Endothelial Cells (ECs) in SCH plays an important ro...

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Autores principales: Yao, Xuelin, Wang, Ying, Wang, Li, Cao, Mingfeng, Chen, Aifang, Zhang, Xinhuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9485940/
https://www.ncbi.nlm.nih.gov/pubmed/36147570
http://dx.doi.org/10.3389/fendo.2022.981622
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author Yao, Xuelin
Wang, Ying
Wang, Li
Cao, Mingfeng
Chen, Aifang
Zhang, Xinhuan
author_facet Yao, Xuelin
Wang, Ying
Wang, Li
Cao, Mingfeng
Chen, Aifang
Zhang, Xinhuan
author_sort Yao, Xuelin
collection PubMed
description BACKGROUND: Increasing evidence has shown that elevated Thyroid stimulating hormone (TSH) levels are positively correlated with atherosclerosis (ATH) in patients with subclinical hypothyroidism (SCH). Some researchers found that the dysfunction of Endothelial Cells (ECs) in SCH plays an important role in the pathogenesis of ATH in SCH, but the association remains controversial. OBJECTIVES: To determine the expression profiles of serum microRNAs critical to the function of Endothelial cells (ECs) may help reanalyze the possible mechanism underlying ATH in SCH and the association between ATH and SCH. METHODS: We used qRT-PCR to perform microRNA profiling and analysis in normal control subjects (NC), patients with SCH alone (SCH), patients with SCH and ATH (SCH+ATH), and patients with ATH without SCH (ATH). RESULTS: Both miR-221-3p and miR-222-3p showed a decreasing expression trend between the SCH and SCH+ATH groups. In addition, miR-126-3p and miR-150-5p showed a stepwise decrease from the NC to SCH groups and then to the SCH+ATH or ATH group. miR-21-5p was unregulated in the SCH, SCH+ATH, and ATH groups. Furthermore, elevated levels of miR-21-5p in SCH+ATH group were higher than SCH and ATH group. No differences were found in the levels of miR-150, miR-126, miR-221 and miR-222 between the ATH and the SCH+ATH subjects. CONCLUSIONS: miR-21-5p may be involved in the atherosclerosis process in patients with SCH (SCH and SCH+ATH groups). miR-150-5p may be sensitive risk markers for predicting endothelial dysfunction in patients with ATH (ATH and SCH+ATH groups).
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spelling pubmed-94859402022-09-21 Expression patterns of serum MicroRNAs related to endothelial dysfunction in patients with subclinical hypothyroidism Yao, Xuelin Wang, Ying Wang, Li Cao, Mingfeng Chen, Aifang Zhang, Xinhuan Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Increasing evidence has shown that elevated Thyroid stimulating hormone (TSH) levels are positively correlated with atherosclerosis (ATH) in patients with subclinical hypothyroidism (SCH). Some researchers found that the dysfunction of Endothelial Cells (ECs) in SCH plays an important role in the pathogenesis of ATH in SCH, but the association remains controversial. OBJECTIVES: To determine the expression profiles of serum microRNAs critical to the function of Endothelial cells (ECs) may help reanalyze the possible mechanism underlying ATH in SCH and the association between ATH and SCH. METHODS: We used qRT-PCR to perform microRNA profiling and analysis in normal control subjects (NC), patients with SCH alone (SCH), patients with SCH and ATH (SCH+ATH), and patients with ATH without SCH (ATH). RESULTS: Both miR-221-3p and miR-222-3p showed a decreasing expression trend between the SCH and SCH+ATH groups. In addition, miR-126-3p and miR-150-5p showed a stepwise decrease from the NC to SCH groups and then to the SCH+ATH or ATH group. miR-21-5p was unregulated in the SCH, SCH+ATH, and ATH groups. Furthermore, elevated levels of miR-21-5p in SCH+ATH group were higher than SCH and ATH group. No differences were found in the levels of miR-150, miR-126, miR-221 and miR-222 between the ATH and the SCH+ATH subjects. CONCLUSIONS: miR-21-5p may be involved in the atherosclerosis process in patients with SCH (SCH and SCH+ATH groups). miR-150-5p may be sensitive risk markers for predicting endothelial dysfunction in patients with ATH (ATH and SCH+ATH groups). Frontiers Media S.A. 2022-09-06 /pmc/articles/PMC9485940/ /pubmed/36147570 http://dx.doi.org/10.3389/fendo.2022.981622 Text en Copyright © 2022 Yao, Wang, Wang, Cao, Chen and Zhang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Yao, Xuelin
Wang, Ying
Wang, Li
Cao, Mingfeng
Chen, Aifang
Zhang, Xinhuan
Expression patterns of serum MicroRNAs related to endothelial dysfunction in patients with subclinical hypothyroidism
title Expression patterns of serum MicroRNAs related to endothelial dysfunction in patients with subclinical hypothyroidism
title_full Expression patterns of serum MicroRNAs related to endothelial dysfunction in patients with subclinical hypothyroidism
title_fullStr Expression patterns of serum MicroRNAs related to endothelial dysfunction in patients with subclinical hypothyroidism
title_full_unstemmed Expression patterns of serum MicroRNAs related to endothelial dysfunction in patients with subclinical hypothyroidism
title_short Expression patterns of serum MicroRNAs related to endothelial dysfunction in patients with subclinical hypothyroidism
title_sort expression patterns of serum micrornas related to endothelial dysfunction in patients with subclinical hypothyroidism
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9485940/
https://www.ncbi.nlm.nih.gov/pubmed/36147570
http://dx.doi.org/10.3389/fendo.2022.981622
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