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The inverted pattern of circulating miR-221-3p and miR-222-3p associated with isolated low HDL-C phenotype

BACKGROUND: We investigated the baseline characterization of cardiovascular disease (CVD)-derived circulating miR-221-3p/222-3p in isolated low HDL-C phenotype (ILHP) to enhance our understanding on their molecular pathological pattern prior to disease onset. METHODS: We screened 174 asymptomatic su...

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Autores principales: Zhou, Yuntao, Liu, Mengdi, Li, Jinrong, Wu, Bing, Tian, Wei, Shi, Lu, Zhang, Jing, Sun, Zening
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097213/
https://www.ncbi.nlm.nih.gov/pubmed/30115076
http://dx.doi.org/10.1186/s12944-018-0842-1
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author Zhou, Yuntao
Liu, Mengdi
Li, Jinrong
Wu, Bing
Tian, Wei
Shi, Lu
Zhang, Jing
Sun, Zening
author_facet Zhou, Yuntao
Liu, Mengdi
Li, Jinrong
Wu, Bing
Tian, Wei
Shi, Lu
Zhang, Jing
Sun, Zening
author_sort Zhou, Yuntao
collection PubMed
description BACKGROUND: We investigated the baseline characterization of cardiovascular disease (CVD)-derived circulating miR-221-3p/222-3p in isolated low HDL-C phenotype (ILHP) to enhance our understanding on their molecular pathological pattern prior to disease onset. METHODS: We screened 174 asymptomatic subjects with isolated low HDL-C phenotype (n = 88) and normal lipid phenotype (n = 86), and detected circulating levels of CVD-derived circulating miR-221-3p/222-3p using TaqMan miRNA Real-time PCR detection system. RESULTS: We found the inverted pattern of decreased circulating miR-221-3p (0.415 [0.249, 1.004] vs 0.658 [0.347, 1.534], p = 0.002) versus increased miR-222-3p levels (0.379 [0.101, 0.701] vs 0.156 [0.043, 0.407], p < 0.001) in ILHP. The baseline levels of circulating miR-221-3p and miR-222-3p are correlated with serum HDL-C levels (miR-221-3p: r = 0.306, p < 0.001; miR-222-3p: r = − 0.201, p = 0.008). Gender-based analysis showed female-specific elevation of circulating miR-221-3p in asymptomatic individual. Multiple logistic regression analysis showed that circulating miR-222-3p is robustly independent factor (adjusted OR = 8.42, 95%CI: 2.53–27.98, p < 0.001) and significantly improved the performance of the predictive clinical model distinguished ILHP from normal lipid phenotype (AUC: 0.816, 95%CI (0.754, 0.879) vs AUC: 0.771, 95%CI (0.702, 0.840); Z = 2.169, p = 0.030). Moreover, the increased original Ct ratio of miR-221-3p to miR-222-3p in male ILHP (1.003 [0.927, 1.063] vs 0.927 [0.858, 0.967], p < 0.001) significantly enhanced the ability to classify male ILHP compared with the male predictive clinical model (AUC: 0.851, 95%CI (0.770, 0.933) vs AUC: 0.759, 95%CI (0.659, 0.859); Z = 2.474, p < 0.05). CONCLUSIONS: The inverted pattern of circulating miR-221-3p and miR-222-3p are potentially clinically actionable signature for molecular pathology in isolated low HDL-C phenotype. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12944-018-0842-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-60972132018-08-20 The inverted pattern of circulating miR-221-3p and miR-222-3p associated with isolated low HDL-C phenotype Zhou, Yuntao Liu, Mengdi Li, Jinrong Wu, Bing Tian, Wei Shi, Lu Zhang, Jing Sun, Zening Lipids Health Dis Research BACKGROUND: We investigated the baseline characterization of cardiovascular disease (CVD)-derived circulating miR-221-3p/222-3p in isolated low HDL-C phenotype (ILHP) to enhance our understanding on their molecular pathological pattern prior to disease onset. METHODS: We screened 174 asymptomatic subjects with isolated low HDL-C phenotype (n = 88) and normal lipid phenotype (n = 86), and detected circulating levels of CVD-derived circulating miR-221-3p/222-3p using TaqMan miRNA Real-time PCR detection system. RESULTS: We found the inverted pattern of decreased circulating miR-221-3p (0.415 [0.249, 1.004] vs 0.658 [0.347, 1.534], p = 0.002) versus increased miR-222-3p levels (0.379 [0.101, 0.701] vs 0.156 [0.043, 0.407], p < 0.001) in ILHP. The baseline levels of circulating miR-221-3p and miR-222-3p are correlated with serum HDL-C levels (miR-221-3p: r = 0.306, p < 0.001; miR-222-3p: r = − 0.201, p = 0.008). Gender-based analysis showed female-specific elevation of circulating miR-221-3p in asymptomatic individual. Multiple logistic regression analysis showed that circulating miR-222-3p is robustly independent factor (adjusted OR = 8.42, 95%CI: 2.53–27.98, p < 0.001) and significantly improved the performance of the predictive clinical model distinguished ILHP from normal lipid phenotype (AUC: 0.816, 95%CI (0.754, 0.879) vs AUC: 0.771, 95%CI (0.702, 0.840); Z = 2.169, p = 0.030). Moreover, the increased original Ct ratio of miR-221-3p to miR-222-3p in male ILHP (1.003 [0.927, 1.063] vs 0.927 [0.858, 0.967], p < 0.001) significantly enhanced the ability to classify male ILHP compared with the male predictive clinical model (AUC: 0.851, 95%CI (0.770, 0.933) vs AUC: 0.759, 95%CI (0.659, 0.859); Z = 2.474, p < 0.05). CONCLUSIONS: The inverted pattern of circulating miR-221-3p and miR-222-3p are potentially clinically actionable signature for molecular pathology in isolated low HDL-C phenotype. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12944-018-0842-1) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-16 /pmc/articles/PMC6097213/ /pubmed/30115076 http://dx.doi.org/10.1186/s12944-018-0842-1 Text en © The Author(s). 2018 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
Zhou, Yuntao
Liu, Mengdi
Li, Jinrong
Wu, Bing
Tian, Wei
Shi, Lu
Zhang, Jing
Sun, Zening
The inverted pattern of circulating miR-221-3p and miR-222-3p associated with isolated low HDL-C phenotype
title The inverted pattern of circulating miR-221-3p and miR-222-3p associated with isolated low HDL-C phenotype
title_full The inverted pattern of circulating miR-221-3p and miR-222-3p associated with isolated low HDL-C phenotype
title_fullStr The inverted pattern of circulating miR-221-3p and miR-222-3p associated with isolated low HDL-C phenotype
title_full_unstemmed The inverted pattern of circulating miR-221-3p and miR-222-3p associated with isolated low HDL-C phenotype
title_short The inverted pattern of circulating miR-221-3p and miR-222-3p associated with isolated low HDL-C phenotype
title_sort inverted pattern of circulating mir-221-3p and mir-222-3p associated with isolated low hdl-c phenotype
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097213/
https://www.ncbi.nlm.nih.gov/pubmed/30115076
http://dx.doi.org/10.1186/s12944-018-0842-1
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