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Plasma microRNAs levels are different between pulmonary and extrapulmonary ARDS patients: a clinical observational study

BACKGROUND: Mesenchymal stem cells (MSC) obviously alleviate the damage of the structure and function of pulmonary vascular endothelial cells (VEC). The therapeutic effects of MSC are significantly different between pulmonary ARDS (ARDSp) and extrapulmonary ARDS (ARDSexp). MicroRNAs (miRNAs), as imp...

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Autores principales: Zheng, Yi, Liu, Song-qiao, Sun, Qin, Xie, Jian-feng, Xu, Jing-yuan, Li, Qing, Pan, Chun, Liu, Ling, Huang, Ying-zi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811418/
https://www.ncbi.nlm.nih.gov/pubmed/29442256
http://dx.doi.org/10.1186/s13613-018-0370-1
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author Zheng, Yi
Liu, Song-qiao
Sun, Qin
Xie, Jian-feng
Xu, Jing-yuan
Li, Qing
Pan, Chun
Liu, Ling
Huang, Ying-zi
author_facet Zheng, Yi
Liu, Song-qiao
Sun, Qin
Xie, Jian-feng
Xu, Jing-yuan
Li, Qing
Pan, Chun
Liu, Ling
Huang, Ying-zi
author_sort Zheng, Yi
collection PubMed
description BACKGROUND: Mesenchymal stem cells (MSC) obviously alleviate the damage of the structure and function of pulmonary vascular endothelial cells (VEC). The therapeutic effects of MSC are significantly different between pulmonary ARDS (ARDSp) and extrapulmonary ARDS (ARDSexp). MicroRNAs (miRNAs), as important media of MSC regulating VEC, are not studied between ARDSp and ARDSexp. We aimed to explore the plasma levels difference of miRNAs that regulate VEC function and are associated with MSC (MSC-VEC-miRNAs) between ARDSp and ARDSexp patients. METHODS: MSC-VEC-miRNAs were obtained through reviewing relevant literatures screened in PubMed database. We enrolled 57 ARDS patients within 24 h of admission to the ICU and then collected blood samples, extracted plasma supernatant. Patients’ clinical data were collected. Then, plasma expression of MSC-VEC-miRNAs was measured by real-time fluorescence quantitative PCR. Simultaneously, plasma endothelial injury markers VCAM-1, vWF and inflammatory factors TNF-α, IL-10 were detected by ELISA method. RESULTS: Fourteen miRNAs were picked out after screening. A total of 57 ARDS patients were included in this study, among which 43 cases pertained to ARDSp group and 14 cases pertained to ARDSexp group. Plasma miR-221 and miR-27b levels in ARDSexp group exhibited significantly lower than that in ARDSp group (miR-221, 0.22 [0.12–0.49] vs. 0.57 [0.22–1.57], P = 0.008, miR-27b, 0.34 [0.10–0.46] vs. 0.60 [0.20–1.46], P = 0.025). Plasma vWF concentration in ARDSexp group exhibited significantly lower than that in ARDSp group (0.77 [0.29–1.54] vs. 1.80 [0.95–3.51], P = 0.048). Significant positive correlation was found between miR-221 and vWF in plasma levels (r = 0.688, P = 0.022). Plasma miR-26a and miR-27a levels in non-survival group exhibited significantly lower than that in survival group (miR-26a, 0.17 [0.08–0.20] vs. 0.69 [0.24–2.33] P = 0.018, miR-27a, 0.23 [0.16–0.58] vs. 1.45 [0.38–3.63], P = 0.021) in ARDSp patients. CONCLUSION: Plasma miR-221, miR-27b and vWF levels in ARDSexp group are significantly lower than that in ARDSp group. Plasma miR-26a and miR-27a levels in non-survival group are significantly lower than that in survival group in ARDSp patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13613-018-0370-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-58114182018-02-26 Plasma microRNAs levels are different between pulmonary and extrapulmonary ARDS patients: a clinical observational study Zheng, Yi Liu, Song-qiao Sun, Qin Xie, Jian-feng Xu, Jing-yuan Li, Qing Pan, Chun Liu, Ling Huang, Ying-zi Ann Intensive Care Research BACKGROUND: Mesenchymal stem cells (MSC) obviously alleviate the damage of the structure and function of pulmonary vascular endothelial cells (VEC). The therapeutic effects of MSC are significantly different between pulmonary ARDS (ARDSp) and extrapulmonary ARDS (ARDSexp). MicroRNAs (miRNAs), as important media of MSC regulating VEC, are not studied between ARDSp and ARDSexp. We aimed to explore the plasma levels difference of miRNAs that regulate VEC function and are associated with MSC (MSC-VEC-miRNAs) between ARDSp and ARDSexp patients. METHODS: MSC-VEC-miRNAs were obtained through reviewing relevant literatures screened in PubMed database. We enrolled 57 ARDS patients within 24 h of admission to the ICU and then collected blood samples, extracted plasma supernatant. Patients’ clinical data were collected. Then, plasma expression of MSC-VEC-miRNAs was measured by real-time fluorescence quantitative PCR. Simultaneously, plasma endothelial injury markers VCAM-1, vWF and inflammatory factors TNF-α, IL-10 were detected by ELISA method. RESULTS: Fourteen miRNAs were picked out after screening. A total of 57 ARDS patients were included in this study, among which 43 cases pertained to ARDSp group and 14 cases pertained to ARDSexp group. Plasma miR-221 and miR-27b levels in ARDSexp group exhibited significantly lower than that in ARDSp group (miR-221, 0.22 [0.12–0.49] vs. 0.57 [0.22–1.57], P = 0.008, miR-27b, 0.34 [0.10–0.46] vs. 0.60 [0.20–1.46], P = 0.025). Plasma vWF concentration in ARDSexp group exhibited significantly lower than that in ARDSp group (0.77 [0.29–1.54] vs. 1.80 [0.95–3.51], P = 0.048). Significant positive correlation was found between miR-221 and vWF in plasma levels (r = 0.688, P = 0.022). Plasma miR-26a and miR-27a levels in non-survival group exhibited significantly lower than that in survival group (miR-26a, 0.17 [0.08–0.20] vs. 0.69 [0.24–2.33] P = 0.018, miR-27a, 0.23 [0.16–0.58] vs. 1.45 [0.38–3.63], P = 0.021) in ARDSp patients. CONCLUSION: Plasma miR-221, miR-27b and vWF levels in ARDSexp group are significantly lower than that in ARDSp group. Plasma miR-26a and miR-27a levels in non-survival group are significantly lower than that in survival group in ARDSp patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13613-018-0370-1) contains supplementary material, which is available to authorized users. Springer International Publishing 2018-02-13 /pmc/articles/PMC5811418/ /pubmed/29442256 http://dx.doi.org/10.1186/s13613-018-0370-1 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.
spellingShingle Research
Zheng, Yi
Liu, Song-qiao
Sun, Qin
Xie, Jian-feng
Xu, Jing-yuan
Li, Qing
Pan, Chun
Liu, Ling
Huang, Ying-zi
Plasma microRNAs levels are different between pulmonary and extrapulmonary ARDS patients: a clinical observational study
title Plasma microRNAs levels are different between pulmonary and extrapulmonary ARDS patients: a clinical observational study
title_full Plasma microRNAs levels are different between pulmonary and extrapulmonary ARDS patients: a clinical observational study
title_fullStr Plasma microRNAs levels are different between pulmonary and extrapulmonary ARDS patients: a clinical observational study
title_full_unstemmed Plasma microRNAs levels are different between pulmonary and extrapulmonary ARDS patients: a clinical observational study
title_short Plasma microRNAs levels are different between pulmonary and extrapulmonary ARDS patients: a clinical observational study
title_sort plasma micrornas levels are different between pulmonary and extrapulmonary ards patients: a clinical observational study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811418/
https://www.ncbi.nlm.nih.gov/pubmed/29442256
http://dx.doi.org/10.1186/s13613-018-0370-1
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