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Circulating microRNA-144-5p is associated with depressive disorders

BACKGROUND: Depressive/anxiety disorders are the most common types of mental illnesses in the world. The present study was the first to explore the association between plasma microRNAs (miRNAs) and depression/anxiety in primary care patients. RESULTS: In total, 169 patients (aged 20–64 years) from 1...

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Autores principales: Wang, Xiao, Sundquist, Kristina, Hedelius, Anna, Palmér, Karolina, Memon, Ashfaque A., Sundquist, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4509564/
https://www.ncbi.nlm.nih.gov/pubmed/26199675
http://dx.doi.org/10.1186/s13148-015-0099-8
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author Wang, Xiao
Sundquist, Kristina
Hedelius, Anna
Palmér, Karolina
Memon, Ashfaque A.
Sundquist, Jan
author_facet Wang, Xiao
Sundquist, Kristina
Hedelius, Anna
Palmér, Karolina
Memon, Ashfaque A.
Sundquist, Jan
author_sort Wang, Xiao
collection PubMed
description BACKGROUND: Depressive/anxiety disorders are the most common types of mental illnesses in the world. The present study was the first to explore the association between plasma microRNAs (miRNAs) and depression/anxiety in primary care patients. RESULTS: In total, 169 patients (aged 20–64 years) from 16 primary health centers were enrolled in the present study. The healthy controls were consisted of 52 individuals. We first performed miRNA screening of plasma samples from 11 patients using a Serum/Plasma Focus microRNA Panel comprising 179 miRNA primer sets. Six miRNAs were differentially expressed and were then validated by quantitative real-time (qRT)-PCR in the entire study cohort. The mean plasma miR-144-5p level in the depression/anxiety patients increased significantly compared to baseline (p < 0.0001) after the 8-week follow-up. No significant associations were found between the differentially expressed miRNAs and a change in the Montgomery-Åsberg Depression Rating Scale (MADRS-S) score after the follow-up. In linear regression analysis, the plasma miR-144-5p expression level was inversely related to the depression score (MADRS-S) (β = −0.02, p < 0.01), after adjustment for sex and age, at baseline. In addition, plasma miR-144-5p levels at baseline in the depression/anxiety patients were significantly lower compared with the healthy controls (p < 0.001). CONCLUSIONS: Our findings show that plasma miR-144-5p levels are associated with depressive symptoms. Although confirmatory analyses are required, plasma miRNA-144-5p is a potential peripheral biomarker for pathologic processes related to depression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13148-015-0099-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-45095642015-07-22 Circulating microRNA-144-5p is associated with depressive disorders Wang, Xiao Sundquist, Kristina Hedelius, Anna Palmér, Karolina Memon, Ashfaque A. Sundquist, Jan Clin Epigenetics Research BACKGROUND: Depressive/anxiety disorders are the most common types of mental illnesses in the world. The present study was the first to explore the association between plasma microRNAs (miRNAs) and depression/anxiety in primary care patients. RESULTS: In total, 169 patients (aged 20–64 years) from 16 primary health centers were enrolled in the present study. The healthy controls were consisted of 52 individuals. We first performed miRNA screening of plasma samples from 11 patients using a Serum/Plasma Focus microRNA Panel comprising 179 miRNA primer sets. Six miRNAs were differentially expressed and were then validated by quantitative real-time (qRT)-PCR in the entire study cohort. The mean plasma miR-144-5p level in the depression/anxiety patients increased significantly compared to baseline (p < 0.0001) after the 8-week follow-up. No significant associations were found between the differentially expressed miRNAs and a change in the Montgomery-Åsberg Depression Rating Scale (MADRS-S) score after the follow-up. In linear regression analysis, the plasma miR-144-5p expression level was inversely related to the depression score (MADRS-S) (β = −0.02, p < 0.01), after adjustment for sex and age, at baseline. In addition, plasma miR-144-5p levels at baseline in the depression/anxiety patients were significantly lower compared with the healthy controls (p < 0.001). CONCLUSIONS: Our findings show that plasma miR-144-5p levels are associated with depressive symptoms. Although confirmatory analyses are required, plasma miRNA-144-5p is a potential peripheral biomarker for pathologic processes related to depression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13148-015-0099-8) contains supplementary material, which is available to authorized users. BioMed Central 2015-07-22 /pmc/articles/PMC4509564/ /pubmed/26199675 http://dx.doi.org/10.1186/s13148-015-0099-8 Text en © Wang et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Wang, Xiao
Sundquist, Kristina
Hedelius, Anna
Palmér, Karolina
Memon, Ashfaque A.
Sundquist, Jan
Circulating microRNA-144-5p is associated with depressive disorders
title Circulating microRNA-144-5p is associated with depressive disorders
title_full Circulating microRNA-144-5p is associated with depressive disorders
title_fullStr Circulating microRNA-144-5p is associated with depressive disorders
title_full_unstemmed Circulating microRNA-144-5p is associated with depressive disorders
title_short Circulating microRNA-144-5p is associated with depressive disorders
title_sort circulating microrna-144-5p is associated with depressive disorders
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4509564/
https://www.ncbi.nlm.nih.gov/pubmed/26199675
http://dx.doi.org/10.1186/s13148-015-0099-8
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