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Author Spotlight: New Insights into PBMC Mitochondrial Responses Using Fluorespirometry
Published on: May 24, 2024
Association between peripheral blood cells mitochondrial DNA content and severity of coronary heart disease
Li-Peng Liu1, Kang Cheng2, Ming-An Ning3
1Department of Cardiovascular Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.
Insights
Lower leukocyte mitochondrial DNA (mtDNA) content is associated with coronary heart disease (CHD) and its severity. This finding suggests mtDNA may play a role in atherosclerosis development and could be a predictive marker for coronary atherosclerosis.
Area of Science:
- Cardiovascular Disease Research
- Molecular Biology
- Biomarker Discovery
Background:
- Leukocyte mitochondrial DNA (mtDNA) content indicates oxidant-induced cell damage, relevant to cardiovascular diseases.
- The relationship between mtDNA content and coronary heart disease (CHD), a condition linked to oxidative stress, remains unclear.
Purpose of the Study:
- To investigate the association between leukocyte mitochondrial DNA (mtDNA) content and the presence and severity of coronary heart disease (CHD).
Main Methods:
- Quantitative real-time PCR measured relative mtDNA content in peripheral blood cells (PBCs) of 400 individuals (290 with CHD, 110 controls).
- Gensini score assessed coronary stenotic lesion severity.
- Unconditional multivariate logistic regression analyzed the association between CHD risk and mtDNA content.
Main Results:
- CHD patients exhibited lower mtDNA content compared to controls (0.78 vs. 0.83, p < 0.001).
- mtDNA levels significantly decreased with increasing Gensini scores (p < 0.001).
- Higher quartiles of mtDNA content showed significantly increased odds ratios for CHD presence.
Conclusions:
- Leukocyte mtDNA content may be linked to atherogenesis.
- Peripheral blood mtDNA levels show potential as a predictive marker for coronary atherosclerosis severity.
Background And Aims:
Leukocyte mitochondrial DNA (mtDNA) content reflects the oxidant-induced cell damage, which has been observed in a wide range of cardiovascular diseases. However, whether it correlates with coronary heart disease (CHD), which closely relates to oxidative stress, has never been elucidated before. The aim of this study was to explore association between mtDNA content and the presence and severity of CHD.
Methods:
The study population consisted of 400 individuals (290 with CHD and 110 controls). A quantitative real-time PCR was performed to measure the relative content of mtDNA in peripheral blood cells (PBCs). Gensini score was used to evaluate the severity of coronary stenotic lesions. An unconditional multivariate logistic regression was developed to estimate the association between CHD risk and mtDNA content by using odds ratio (OR). This study is registered with ClinicalTrials.gov, number NCT02500823.
Results:
CHD patients, compared to controls, had lower mtDNA content (median, 0.78 vs. 0.83, p < 0.001), and mtDNA levels significantly decreased following an increasing Gensini score (p < 0.001). By using the first (highest mtDNA content) quartile of mtDNA content of controls as reference, the adjusted ORs (95% CIs) for individuals in the second, third and highest quartile of mtDNA content were 1.78 (95% CI, 1.15-3.51), 2.21 (95% CI, 1.65-3.74) and 4.83 (95% CI, 2.67-8.64), respectively (p for trend <0.001).
Conclusions:
These preliminary results suggest that expression of mtDNA may be associated with atherogenesis. The level of peripheral blood mtDNA in predicting the severity of coronary atherosclerosis may have a relatively certain value.
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