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Perioperative plasma mitochondrial DNA dynamics and correlation with inflammation during infantile cardiopulmonary bypass
OBJECTIVE: Numerous studies in animals and humans have demonstrated that inflammatory mediators such as tumor necrosis factor (TNF)-α, interleukin (IL)-6, and IL-8 play a role in cardiopulmonary bypass (CPB), which might affect surgical outcomes. Plasma mitochondrial DNA (mtDNA), a recently discover...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717290/ https://www.ncbi.nlm.nih.gov/pubmed/29174262 http://dx.doi.org/10.1016/j.ihj.2017.03.009 |
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author | Xu, Fei Liu, Rui-qi Cao, Rong Guo, Lang-tao Zhang, Ning Huang, Ke Cui, Yu Li, Wei-na Li, Lei Huang, Zheng-hua |
author_facet | Xu, Fei Liu, Rui-qi Cao, Rong Guo, Lang-tao Zhang, Ning Huang, Ke Cui, Yu Li, Wei-na Li, Lei Huang, Zheng-hua |
author_sort | Xu, Fei |
collection | PubMed |
description | OBJECTIVE: Numerous studies in animals and humans have demonstrated that inflammatory mediators such as tumor necrosis factor (TNF)-α, interleukin (IL)-6, and IL-8 play a role in cardiopulmonary bypass (CPB), which might affect surgical outcomes. Plasma mitochondrial DNA (mtDNA), a recently discovered pro-inflammatory agent, is released by cells upon insult. This study aimed to detect changes in plasma mtDNA levels at different time points after infantile CPB and explore its potential association with inflammatory mediators. METHODS: In the present study, we analyzed the perioperative plasma mtDNA and inflammatory cytokine levels of 48 infants undergoing ventricular septal defect closure. Blood samples were collected before aortic cross-clamping (T1), at the end of CPB (T2), and 6 h (T3), 12 h (T4), and 24 h (T5) post-CPB. Reverse transcription–polymerase chain reaction and specific enzyme-linked immunosorbent assay were used to quantify the plasma mtDNA and inflammatory cytokines, respectively. Bivariate correlation analysis was used to determine the correlations between plasma mtDNA and inflammatory cytokines. RESULTS: Plasma mtDNA levels increased at T2 and peaked at T3. Significant positive correlations were found between peak plasma mtDNA (at T3) and several inflammatory biomarkers, including IL-6 (at T3) (r = 0.62, P < 0.001), IL-8 (at T2) (r = 0.53, P < 0.001), and TNF-α (at T3) (r = 0.61, P < 0.001). CONCLUSION: Here we report that mtDNA may participate in a systemic inflammatory response to CPB. |
format | Online Article Text |
id | pubmed-5717290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-57172902018-11-01 Perioperative plasma mitochondrial DNA dynamics and correlation with inflammation during infantile cardiopulmonary bypass Xu, Fei Liu, Rui-qi Cao, Rong Guo, Lang-tao Zhang, Ning Huang, Ke Cui, Yu Li, Wei-na Li, Lei Huang, Zheng-hua Indian Heart J Clinico-basic convergence OBJECTIVE: Numerous studies in animals and humans have demonstrated that inflammatory mediators such as tumor necrosis factor (TNF)-α, interleukin (IL)-6, and IL-8 play a role in cardiopulmonary bypass (CPB), which might affect surgical outcomes. Plasma mitochondrial DNA (mtDNA), a recently discovered pro-inflammatory agent, is released by cells upon insult. This study aimed to detect changes in plasma mtDNA levels at different time points after infantile CPB and explore its potential association with inflammatory mediators. METHODS: In the present study, we analyzed the perioperative plasma mtDNA and inflammatory cytokine levels of 48 infants undergoing ventricular septal defect closure. Blood samples were collected before aortic cross-clamping (T1), at the end of CPB (T2), and 6 h (T3), 12 h (T4), and 24 h (T5) post-CPB. Reverse transcription–polymerase chain reaction and specific enzyme-linked immunosorbent assay were used to quantify the plasma mtDNA and inflammatory cytokines, respectively. Bivariate correlation analysis was used to determine the correlations between plasma mtDNA and inflammatory cytokines. RESULTS: Plasma mtDNA levels increased at T2 and peaked at T3. Significant positive correlations were found between peak plasma mtDNA (at T3) and several inflammatory biomarkers, including IL-6 (at T3) (r = 0.62, P < 0.001), IL-8 (at T2) (r = 0.53, P < 0.001), and TNF-α (at T3) (r = 0.61, P < 0.001). CONCLUSION: Here we report that mtDNA may participate in a systemic inflammatory response to CPB. Elsevier 2017 2017-03-28 /pmc/articles/PMC5717290/ /pubmed/29174262 http://dx.doi.org/10.1016/j.ihj.2017.03.009 Text en © 2017 Published by Elsevier B.V. on behalf of Cardiological Society of India. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Clinico-basic convergence Xu, Fei Liu, Rui-qi Cao, Rong Guo, Lang-tao Zhang, Ning Huang, Ke Cui, Yu Li, Wei-na Li, Lei Huang, Zheng-hua Perioperative plasma mitochondrial DNA dynamics and correlation with inflammation during infantile cardiopulmonary bypass |
title | Perioperative plasma mitochondrial DNA dynamics and correlation with inflammation during infantile cardiopulmonary bypass |
title_full | Perioperative plasma mitochondrial DNA dynamics and correlation with inflammation during infantile cardiopulmonary bypass |
title_fullStr | Perioperative plasma mitochondrial DNA dynamics and correlation with inflammation during infantile cardiopulmonary bypass |
title_full_unstemmed | Perioperative plasma mitochondrial DNA dynamics and correlation with inflammation during infantile cardiopulmonary bypass |
title_short | Perioperative plasma mitochondrial DNA dynamics and correlation with inflammation during infantile cardiopulmonary bypass |
title_sort | perioperative plasma mitochondrial dna dynamics and correlation with inflammation during infantile cardiopulmonary bypass |
topic | Clinico-basic convergence |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717290/ https://www.ncbi.nlm.nih.gov/pubmed/29174262 http://dx.doi.org/10.1016/j.ihj.2017.03.009 |
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