High-mobility group box 1 is associated with neurological outcome in patients with post-cardiac arrest syndrome after out-of-hospital cardiac arrest
© The Author(s). 2016
Received: 24 March 2016
Accepted: 25 May 2016
Published: 31 May 2016
Alarmins, including high-mobility group box 1 (HMGB-1), can be released from damaged tissues and activated cells as inflammatory mediators. We aimed to evaluate HMGB-1 and mitochondrial DNA dynamics and estimate the prognostic value for neurological outcome in patients with post-cardiac arrest syndrome after out-of-hospital cardiac arrest.
We evaluated the dynamics of HMGB-1, mitochondrial DNA, and other variables in patients with return of spontaneous circulation after out-of-hospital cardiac arrest. Patients were divided into two groups according to the cerebral performance category at 30 days: the favourable outcome group (cerebral performance categories 1 and 2) and unfavourable group (≥3).
Twenty-one patients were included, and 11 demonstrated favourable outcomes. HMGB-1 levels and mitochondrial DNA on day 1 were significantly higher than on days 2, 3, 5, and 7. Plasma levels of HMGB-1 on day 1 correlated with prognostic parameters (estimated interval to return of spontaneous circulation, lactate, and NH3), tissue damage, systemic inflammation, and disease severity. HMGB-1 on day 1 in the unfavourable group was significantly higher than in the favourable group (median [interquartile range] 15.5 [6.65–18.7], 39.4 [17–69.5], P = 0.009). These findings were not observed regarding mitochondrial DNA. Regarding HMGB-1 prediction accuracy for a good neurological outcome, the area under the receiver operating characteristic curve was 0.864 (95 % confidence interval 0.702, 1.000).
HMGB-1 may be involved in acute-phase post-cardiac arrest syndrome pathophysiology, and an increase in plasma levels may be associated with a poor neurological outcome. The study was registered with the University Hospital Medical Information Network Clinical Trials Registry ID: UMIN000006714.
KeywordPost-cardiac arrest syndrome High-mobility group box 1 Mitochondrial DNA Alarmin
In 2008, post-cardiac arrest syndrome (PCAS) was proposed as a new term that incorporates all pathophysiological processes occurring after a return of spontaneous circulation after cardiac arrest . There are four elements to PCAS: (1) hypoxic brain injury, (2) myocardial dysfunction, (3) systemic ischemia/reperfusion response, and (4) persistent precipitating pathology. In particular, systemic ischemia/reperfusion causes systemic inflammatory response syndrome (SIRS), which can lead to organ damage and multiple organ dysfunction in patients with PCAS . Although these pathophysiological changes are caused by non-infectious inflammation, they demonstrate a clinical presentation similar to sepsis . Molecules known as pathogen-associated molecular patterns (PAMPs) have been demonstrated to play a crucial role in the pathophysiology of sepsis . In the pathophysiology of non-infectious inflammatory conditions such as trauma and burns, internal and endogenous molecules are released from damaged tissues and promote immunity, coagulation, and inflammatory responses . These molecules are called “alarmins” . In SIRS associated with PCAS, it has been suggested that alarmins may cause a non-infectious systemic inflammatory response [2, 6].
Recently, the pathophysiological roles of high-mobility group box 1 (HMGB-1) and mitochondrial DNA (mtDNA) were reported as alarmins in critical conditions [4, 7–11]. However, the roles of these molecules in PCAS have not been elucidated clearly. Therefore, the purpose of this study was to evaluate HMGB-1 and mtDNA dynamics, the relationship between HMGB-1, mtDNA, and severity of conditions and estimate the prognostic values of these molecules in patients with post-cardiac arrest syndrome after out-of-hospital cardiac arrest.
We performed a prospective, observational study of patients admitted to an academic tertiary care emergency centre from August 2011 to December 2012. The inclusion criteria were patients who were unresponsive after a return of spontaneous circulation (ROSC) after out-of-hospital cardiac arrest. Cardiac arrest was defined as the absence of spontaneous respiration, a palpable pulse, or responsiveness to stimuli. The exclusion criteria were as follows: trauma, age under 18 years, previous completion of a “Do Not Attempt Resuscitation (DNAR)” form, a Glasgow coma scale (GCS) score >8 at hospital arrival, and the presence of primary brain pathologies. The ethics committee of the institution approved this study (approval reference number: 2011-264), and all study subjects provided written informed consent. The study was registered with the University Hospital Medical Information Network Clinical Trials Registry (UMIN-CTR ID: UMIN000006714).
Procedures after hospital arrival
Clinical management of OHCA and PCAS was performed according to the 2010 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care . If refractory shock from conventional intensive care was not sustained, we initiated therapeutic hypothermia.
All data were collected prospectively. Age, sex, type of bystander-witness status, bystander-initiated cardiopulmonary resuscitation (CPR), origin of cardiac arrest, initially documented electrocardiogram (ECG) rhythms, and the interval from collapse to ROSC were collected. All blood samples from patients were taken at the same time on arrival at the hospital and on the second, third, fifth, and seventh day after ROSC. Blood samples were centrifuged at 3000 rpm for 10 min, and the supernatants were stored in a −80 °C refrigerator until the analyses. HMGB-1 concentrations were measured using an enzyme-linked immunosorbent assay (Shino-Test Corporation, Sagamihara, Kanagawa, Japan). The lower sensitivity limit for HMGB-1 was 1 ng ml−1 and cross-reactivity with HMGB-2 was less than 10 %.
DNA isolation from plasma and mtDNA quantification by real-time quantitative polymerase chain reaction (PCR) were performed as previously described . We centrifuged blood samples at ×1600 rpm for 10 min and then filtered the plasma through a 0.22-μm filter to remove platelets and cellular fragments bound to mtDNA. DNA isolation from filtered plasma samples and quantification of mtDNA by real-time quantitative PCR (qPCR) were performed . Real-time PCR standard curves were created to quantify the mtDNA concentration by using purified mtDNA. The concentration of mtDNA was determined with a spectrophotometer. The purified mtDNA contained <0.1 % nuclear genomic DNA as determined using qPCR. The concentrations of mtDNA were calculated and expressed as micrograms in 1 ml of plasma. The results of biomarker levels were not blinded for outcome assessments.
The severity of illness was evaluated according to the Acute Physiology and Chronic Health Evaluation (APACHE)-II score on the day of enrolment . A diagnosis of disseminated intravascular coagulation (DIC) was made on the basis of the scoring system of the Japanese Association for Acute Medicine (JAAM)  and the International Society on Thrombosis and Haemostasis (ISTH) .
Data analysis and outcomes
The patients’ neurological outcomes were provided by Glasgow-Pittsburgh cerebral performance categories (CPCs)  at 30 days after OHCA. The patients were divided into two groups according to CPC at 30 days after OHCA: the favourable neurological outcome group (CPC = 1 or 2) and the unfavourable group (CPC ≥ 3).
Data are expressed as medians and interquartile ranges or as the number and percentage. All statistical analyses were performed using SPSS 22 for Windows (SPSS, Chicago, IL, USA). Comparisons between the two groups were performed using the Mann-Whitney U test, and categorical variables were compared between the groups using either Pearson’s chi-square or Fisher’s exact test, as appropriate. Correlations between HMGB-1, mtDNA, and other variables were performed using Spearman’s rank correlation test. The Kruskal-Wallis one-way analysis of variance was used for multiple comparisons between groups, and P values were adjusted with a Bonferroni correction for multiple testing. We evaluated the predictive precision of each parameter using the area under the receiver operating characteristic (ROC) curve (AUC). The cutoff values were determined based on the value that maximized the Youden index. Differences with a P value <0.05 were considered to be statistically significant. Furthermore, P < 0.005 (after Bonferroni correction) was used for testing multiple comparisons between groups.
Characteristics of patients with ROSC after OHCA
Characteristics and physiology of patients after out-of-hospital cardiac arrest
All patients (n = 21)
Favourable group (n = 11)
Unfavourable group (n = 10)
Age—years, median (IQR)
Male sex—no. (%)
13 (61.9 %)
8 (72.7 %)
5 (50 %)
Type of bystander-witness status—no. (%)
16 (76.2 %)
8 (72.7 %)
8 (80 %)
Bystander-initiated CPR—no. (%)
14 (66.7 %)
7 (72.7 %)
7 (70 %)
Cardiac origin—no. (%)
17 (81.0 %)
Initially documented rhythms on the scene of cardiac arrest—no.
Estimated interval from collapse to ROSC—min
Therapeutic hypothermia—no. (%)
14 (66.7 %)
9 (81.8 %)
5 (50 %)
Initial lactate—mmol L−1
Initial NH3—μg dl−1
Myoglobin (day 1)—ng ml−1
IL-6 (day 1)—pg ml−1
Max IL-6—pg ml−1
Max JAAM DIC
Max ISTH DIC
Neurological outcomes 30 days after OHCA
Survival (CPCs 1–4)—no. (%)
14 (66.7 %)
CPC 1, good performance
CPC 2, moderate disability
CPC 3, severe disability
CPC 4, vegetative state
CPC 5, death
Plasma levels of HMGB-1 and mtDNA
Relationship between HMGB-1, mtDNA, and clinical variables
Relationship between plasma levels of high-mobility group box 1, mitochondrial DNA, and physiologic parameters in patients after out-of-hospital cardiac arrest with return of spontaneous circulation
HMGB-1 (day 1)
mtDNA (day 1)
Estimated interval from collapse to ROSC
Myoglobin (day 1)
IL-6 (day 1)
Maximal JAAM DIC
Maximal ISTH DIC
Plasma levels of HMGB-1, mtDNA, and neurological outcomes
Our study elucidates the HMGB-1 and mtDNA dynamics in patients with PCAS after OHCA and suggests that plasma levels of HMGB-1 on the day of admission after ROSC might be the prognostic values for neurological outcomes in patients with PCAS after OHCA.
Although mtDNA has been recognized as one of the alarmins and showed similar serial changes to those of HMGB-1 in patients with PCAS after OHCA, plasma levels of mtDNA on the day of admission did not correlate with parameters associated with prognosis, tissue damage, or disease severity, and the values were not different between the favourable and unfavourable outcome groups. In previous study, we demonstrated that changes in plasma HMGB-1 and mtDNA levels in patients with severe trauma and sepsis . Although plasma levels of HMGB-1 and mtDNA on the day of admission were higher than those of the other days, which decrease gradually during the initial 7 days, in patients with severe trauma, plasma HMGB-1 and mtDNA were sustained in elevated levels in patients with sepsis. Present study showed that the dynamics of plasma HMGB-1 and mtDNA levels were similar to those in patients with trauma. However, relationship between the plasma levels of HMGB-1, mtDNA, and disease severities and outcomes in patients with PCAS were different from those of severe trauma. Therefore, it is suggested that the role of HMGB-1 and mtDNA in the pathogenesis of PCAS after OHCA, including brain injuries, might be different from those in severe trauma.
HMGB-1 is known as a late mediator in sepsis . Moreover, it has been reported that HMGB-1 levels increased in the early phase of trauma and correlated with the severity of injury [9, 17]. Active leakage (secretion) and passive leakage are known as mechanisms that increase plasma levels of HMGB-1 [7, 8, 18], and these mechanisms may contribute differently to the pathophysiologies of sepsis and trauma. Active secretion occurs when HMGB-1 is actively released extracellularly from the stimulation of tumour necrosis factor-α, interferon-γ, and other inflammatory mediators in sepsis [19–25]. Passive leakage is caused by the necrosis of injured cells due to trauma, infections, and tissue ischemia [8, 26–28]. On the contrary, the mechanism of mtDNA release has been suggested to be passive discharge into the extracellular space from injured mitochondria in the necrotic cell . Therefore, the pathophysiological role and clinical significance may differ between HMGB-1 and mtDNA in various critical conditions.
PCAS is a complex pathologic condition and includes ischemic tissue damage and SIRS, leading to multiple organ dysfunction [2, 6]. Although HMGB-1 can be released as a consequence of ischemic injury, it may also play a role as an early trigger of inflammation and may be involved as a late modulator of inflammation. HMGB-1 induces the release of proinflammatory cytokines, and then promotes further inflammation in the brain [29, 30]. Therefore, an increase in plasma levels of HMGB-1 may be involved in the pathogenesis of a poor neurological outcome and post-resuscitation inflammatory status. In recent study, an association between HMGB-1 in cerebrospinal fluid and neurological outcomes in patients with PCAS after OHCA was reported . In contrast, serum HMGB-1 levels did not correlated to neurological outcomes. However, the study may consist of small sample size with only seven patients of the favourable neurological outcome, which may be insufficient to evaluate the prognostic value adequately. As demonstrated in this study, plasma levels of HMGB-1 on the day of admission might have the prognostic value in patients with PCAS after OHCA. To clarify the pathophysiological role of HMGB-1 in patients with PCAS, further large-scale study is required.
This study has some limitations. The main limitations are the observational study design, small sample size, and the distribution of aetiologies in cardiac arrest and neurological severity levels. In addition, although there are some confounding factors with respect to the levels of HMGB-1 and mtDNA, and clinical impacts of these mediators exist, their influences have not been adjusted because of the limited number of patients. Further evaluations in a larger number of patients are therefore needed to determine whether HMGB-1 can be a reliable biomarker predicting neurological outcome and to clarify its pathophysiological significance.
HMGB-1 may be involved in the pathophysiology of systemic inflammation and neurological sequences in patients with PCAS after OHCA and an increase in plasma levels may be associated with a poor neurological outcome. To verify the role of HMGB-1, further evaluations in a larger number of patients are necessary.
Availability of supporting data
The datasets supporting the conclusions of this article are included within the article and its additional file.
APACHE-II, Acute Physiology and Chronic Health Evaluation II; DIC, disseminated intravascular coagulation; DNAR, Do Not Attempt Resuscitation; GCS, Glasgow coma scale; HMGB-1, high-mobility growth box 1; mtDNA, mitochondrial DNA; OHCA, out-of-hospital cardiac arrest; PAMP, pathogen-associated molecular pattern; PCAS, post-cardiac arrest syndrome; ROSC, return of spontaneous circulation; SIRS, systemic inflammatory response syndrome
This work was supported by the JSPS KAKENHI Grant Number 25462810 and the General Insurance Association of Japan.
The authors were supported by JSPS KAKENHI for data collections and analysis.
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.
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