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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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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. |
format | Online Article Text |
id | pubmed-6097213 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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