Background
Mitochondrial DNA (mtDNA), as a potential damage-associated molecular pattern (DAMP), has attracted intense research in recent years since it may contribute to the mechanism by which mitochondria regulate innate immunity [
1]. Cell stress and necrosis caused by injury may result in fragmentation of the mitochondrial genome and disruption of the mitochondrial membrane, ultimately leading to extracellular release of mitochondrial DNA [
2,
3]. Circulating mtDNA is capable of triggering innate immunity through multiple mechanisms, such as activating the Toll-like receptor 9 (TLR-9)/NF-κB pathway or NALP3 inflammasome [
4,
5]. As a consequence, mtDNA may amplify the injury and contribute to the persistent and dysregulated inflammatory response.
Growing evidence has revealed that extracellular mtDNA might act as a biomarker in critically ill patients. Elevated levels of plasma mtDNA are associated with sepsis, trauma or postcardiac arrest [
1,
6‐
9]. Intervention with mtDNA in an animal study induced systemic inflammatory response syndrome (SIRS) and pulmonary edema [
4], and blockade of TLR9 improved the lung histopathological changes, wet/dry ratios and inflammatory factor concentrations [
10]. mtDNA has been shown to increase endothelial cell permeability, either directly or through interactions with endothelial cells and polymorphonuclear leukocytes [
11]. Therefore, circulating mtDNA may account for lung injury during nonpulmonary insults, such as sepsis.
In this study, we explored the relationship between circulating mtDNA and septic lung injury, especially at extrapulmonary infection sites. We hypothesized that plasma mtDNA levels may reflect the level of septic organ dysfunction and prognosis.
Methods
Study design
We performed a prospective study among patients in the Department of Critical Care Medicine of Peking Union Medical College Hospital (PUMCH) from January 2019 to October 2019, which was approved by the PUMCH institutional review board (approval number JS-1985). All methods were performed in accordance with the relevant guidelines and regulations, informed consent was obtained from all enrolled patients through the next of kin of each patient. The inclusion criteria in this study were as follows: (1) age ≥ 18 years, (2) intensive care unit (ICU) stay of more than 24 h, and (3) sepsis diagnosis (see below). Patients who were younger than 18 years old, discharged within 24 h after admitted, or had basic pulmonary disease were excluded.
Sepsis was defined according to consensus international guidelines as life-threatening organ dysfunction caused by a dysregulated host response to infection [
12]. Organ dysfunction was defined as an acute change in total Sequential Organ Failure Assessment (SOFA) score of ≥ 2 points consequent to the infection. Acute lung injury (ALI) was considered to be present if PaO
2/FiO
2 (oxygen index, OI) ≤ 300 mmHg [
13]. The enrolled patients were divided into a control group composed of patients without ALI and an ALI group. The sample size was estimated based on a priori power calculation indicating an 80% power to detect a difference of mtDNA copy number frequency (effect size 0.7) between control and ALI group at the 0.05 significance level using a power and sample size website (
http://powerandsamplesize.com).
Outcome
Vital sign tests, laboratory tests, echocardiography, analysis of plasma mtDNA copies and clinical history evaluation were carried out on the first day after ICU admission. Basic clinical and laboratory characteristics included age, sex, basic cardiological or pulmonary disease, hemodynamic parameters, respiratory parameters, blood chemistry, arterial blood gas analysis, Acute Physiology and Chronic Health Evaluation (APACHE) II score, and SOFA score. Life-sustaining treatment included mechanical ventilation, vasopressor administration, and renal replacement. Follow-up data included ICU stay time and 28-day mortality rate.
Peripheral blood samples were collected within 24 h of ICU admission and centrifuged immediately, and the plasma was withdrawn and stored at − 80 °C until assessment of mtDNA copies. Plasma mtDNA was extracted using a commercially available kit (DP 318, Tiangen Biochemistry, Beijing), quantified using polymerase chain reaction (PCR) for the mitochondrial ND1 gene and measured in triplicate as reported previously. The fold‑change was calculated by the 2
‑ΔΔCq method compared with standards in the kit and showed using log-transformed copy number/µL to ensure normality [
6,
14]. The primers for the mtND1 gene were forward 5′-ATACCCATGGCCAACCTCCT-3′ and reverse 5′-GGGCCTTTGCGTAGTTGTAT-3′.
New onset RV dysfunction was assessed using multimodality parameters as defined by the American Society of Echocardiography (ASE) criteria, i.e., specifically semiquantitative size and function, tricuspid annular plane systolic excursion (TAPSE) < 16 mm by M-mode, tricuspid lateral annulus tissue Doppler systolic velocity < 0.15 cm/s or RV fractional area change < 35% [
15]. Echocardiographic examinations were performed by two experienced intensivists. An ultrasonic machine (M-Turbo Sonosite, Highland Heights, Ohio) equipped with a 15 MHz transducer was used for noninvasive transthoracic echocardiography. Data from 3 consecutive cardiac cycles were analyzed and averaged.
Statistical analysis
The normality of the data was evaluated using the Kolmogorov–Smirnov test. Normally distributed data were expressed as the mean and standard deviation and were compared using Student’s t-test. Nonnormally distributed data are presented as the median, and interquartile intervals were analyzed with the Mann–Whitney U test. Categorical variables were recorded as proportions. Univariate logistic regression was performed to identify mtDNA and other parameters with predictive value for 28-day mortality and ALI risk. The Cox proportional hazard survival model was applied to identify the independent contribution of prognostic factors to the prediction of the 28-day outcome. The results are expressed as the Wald index, odds ratio (OR), hazard ratio (HR) and 95% CIs. Discrimination of values was calculated using receiver operating characteristic (ROC) curve analysis using the Hanley-McNeil test. Survival curves up to day 28 were estimated using the Kaplan–Meier method, and the log-rank (Mantel–Cox) test was used to estimate differences among the predefined groups. All comparisons were two-tailed, and a p value less than 0.05 was required to exclude the null hypothesis. Statistical analyses were performed using the SPSS 13.0 software package (SPSS, Chicago, IL).
Discussion
To explore the relationship between circulating mtDNA and septic lung injury, we investigated the level of plasma mtDNA within 24 h after admission in different septic patient groups. We revealed that higher plasma mtDNA levels were associated with ALI incidence and mortality in septic patients. The association was stronger in patients with abdominal infection than in those with pulmonary infection.
Mounting evidence has revealed that extracellular mtDNA might be useful as a biomarker in critically ill patients and is associated with disease severity and mortality [
16‐
18]. Circulating mtDNA may contribute to the mechanism linking distant injury to subsequent lung injury. An increasing number of studies have found elevated mtDNA levels in hip fracture patients with lung injury [
19,
20], an acute respiratory distress syndrome (ARDS) population from a mixed ICU unit [
6] and a cohort of trauma patients [
21]. In our study, we further explored whether higher plasma mtDNA levels were associated with ALI incidence and mortality in septic patients. Plasma mtDNA levels were significantly increased in the group of septic patients with ALI compared with those in the control group patients [5.01 (3.38–6.64) vs 4.13 (3.20–5.07) log copies/µL, p 0.0172]. The sensitivity of other inflammatory biomarkers, such as procalcitonin, CRP IL-6, IL-8, IL-10 and TNFα, was inferior to mtDNA among septic.
Consistent with a previous study, we revealed that the mtDNA level (HR, 3.2052; 95% CI 1.1608–8.8500; p 0.0253) was independently associated with mortality, and the area under the ROC curve was 0.856 (95% CI 0.748–0.930). Patients with high mtDNA levels had worse outcomes, and post hoc tests showed significant differences in 28-day survival rates (log-rank [Mantel-Cox], 6.842; p 0.0089). Patients with high mtDNA levels experienced longer ICU stay times [21.5 (11.3–42.8) vs 6.0 (4.0–12.0) days, p < 0.0001], more severe organ dysfunction [SOFA score, 10.9 (7.6–14.2) vs 6.8 (3.8–9.7), p < 0.0001] and worse respiratory and hemodynamic conditions.
MtDNA level (odds ratio 2.7506; 95% CI 1.1647–6.4959; p 0.0210) was also independently associated with ALI risk. The interaction between mtDNA and innate immunity helps us to understand the mechanism of SIRS caused by injury, such as trauma or sepsis. Due to the bacterial ancestry of mitochondria, mtDNA contains unmethylated CpG repeats and formylated peptides that could be recognized by pattern-recognition receptors [
22,
23]. mtDNA released into the cytosol or circulation could activate the TLR-9-mediated NF-κB pathway [
5,
8] or interact with inflammasomes, leading to caspase-1 activation or secretion of proinflammatory cytokines such as IL-1β and IL-18 [
3,
24]. Based on the molecular biology of mtDNA as a potent DAMP, circulating mtDNA may contribute to the mechanism linking distant injury to subsequent lung injury. Therefore, we hypothesized that the association between circulating mtDNA and septic ALI would be strongest in patients with extrapulmonary sepsis sources. The basic clinical characteristics of all patients showed that bloodstream and abdominal infection seemed to be more common than pulmonary infection in patients with ALI. As we expected, a higher amount of mtDNA [5.14 (4.39–5.87) vs 4.79 (2.52–5.54) log copies/µL, p 0.0492] was seen in patients with abdominal infection than in those with pulmonary infection. The OI of abdominal infection patients was even worse than that of pulmonary infection patients [215 (178–243) vs 256 (230–271) mmHg, p 0.0369]. Consistent with our hypothesis, higher levels of inflammatory biomarkers such as PCT and IL-6 and higher HR and NE doses all indicated a more severe inflammatory response in abdominal infection.
There are still several limitations in our study. This is a single center study, which may limit generalizability. A larger sample size or multicenter study and subgroup analysis, especially among patients with specific infectious sources, may help. Second, an increasing number of studies have suggested that mtDNA copy numbers may vary among different disease courses [
21,
25]. Our study collected only blood samples within 24 h after admission, and a dynamic view of mtDNA copy number may be significant and worthy of further study.
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