Abstract
Pentraxin 3 (PTX3) is an acute-phase protein that belongs to the pentraxin superfamily. Recently, many clinical studies have demonstrated that plasma PTX3 concentrations rapidly increase in patients with the acute coronary syndrome (ACS). The aim of this study was to evaluate the forensic utility of postmortem plasma PTX3 as a marker of fatal ACS. We compared the plasma PTX3 concentration in cadavers with suspected fatal ACS to that exhibited in control cases (e.g., asphyxia and immediate death due to a fatal injury). The ACS groups included a coronary stenosis group, which exhibited apparent coronary stenosis, but an absence of coronary thrombi, a coronary thrombi group with thrombi found in the coronary artery, and a group of myocardial rupture following an acute myocardial infarction. The plasma PTX3 concentration was significantly higher in the coronary thrombi group than the control group and other ACS groups. The postmortem plasma PTX3 concentration was higher than the clinical reference values, which appeared to be caused by a postmortem release from circulating neutrophils. In conclusion, although the clinical reference value cannot be applied to postmortem samples, the postmortem plasma PTX3 concentration may be a useful marker of death occurring immediately after the onset of fatal ACS.
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Introduction
Most sudden cardiac deaths are caused by acute coronary syndromes (ACS) which include unstable angina pectoris (UAP) and acute myocardial infarction (AMI). Histopathological diagnosis of fatal ACS is challenging to obtain, as the pathological hallmarks of AMI, such as coagulative necrosis, “wavy fibers,” splitting, and contraction band necrosis1,2 are non-specific. Also, biomarkers of myocardium damage, including creatine kinase-MB (CK-MB) isoforms and cardiac troponins, remain unaltered for only a few hours after the onset of AMI. This is because the plasma CK-MB and troponin concentrations only begin to increase between 3–8 h and 4–6 h, respectively, after the onset of an AMI3. A recent report demonstrated that a high-sensitivity cardiac troponin I assay could evaluate the risks of subsequent AMI and cardiac death in patients with suspected ACS4. However, during a postmortem examination, these enzymes present in cardiomyocytes should be used with caution due to the postmortem release into blood5.
In a forensic autopsy, the degree of coronary stenosis is commonly determined to be a possible culprit site of ACS. However, it is generally accepted that fatal ACS is not associated with the progression of the luminal stenosis to a critical degree of narrowing, but rather the rupture of an atherosclerotic plaque6,7. An erosion or rupture of the plaque triggers fatal ACS only when coinciding with thrombus formation at the site of plaque erosion or rupture. However, during a forensic autopsy, it is tough to detect the culprit thrombi remaining in the postmortem coronary artery. During plaque formation, local inflammation occurs, which involves neutrophils, macrophages, and other immune-competent cells8. Several studies have demonstrated that markers of systemic inflammation, including C-reactive protein (CRP)9,10, serum fibrinogen10, leukocyte count11, and cytokines12 are increased in the plasma concentration of patients with atherosclerosis, especially in those with unstable coronary artery diseases. However, the systemic inflammation in which these markers participate is not sensitive enough to quickly respond to a sudden plaque rupture and the subsequent dramatic formation of an occlusive thrombus. For example, Peri et al. reported that the CRP plasma concentration in patients admitted to the coronary care unit (CCU) with AMI symptoms was not elevated at the time of entry to the CCU, finally became raised at 12 h, and peaked at 24 h13.
Recently, pentraxin 3 (PTX3), a component of the same pentraxin superfamily as CRP, has attracted attention as a rapid and sensitive biomarker of ACS, including UAP14,15,16 and AMI13. CRP and serum amyloid P component (SAP), another pentraxin family member, are created primarily in the liver in response to the inflammatory mediator interleukin (IL)-6. In contrast, PTX3 is induced locally at the site of inflammation, but not within the liver. Moreover, PTX3 is secreted following Toll-like receptor activation and proinflammatory cytokine secretion, including tumor necrosis factor-α and IL-1, but not IL-6 (reviewed by17). Therefore, the induction of PTX3 is more rapid than CRP or SAP. In the CCU administration cases described above, the plasma PTX3 concentration in AMI patients was already elevated at the time of entry to the CCU and reached a peak at 7.5 h13. In addition, because the induction of PTX3 is highly sensitive to local inflammation, the plasma PTX3 concentration in patients with vascular atherosclerosis is likely reflective of the inflammatory status of the vasculature (i.e., the presence of plaque formation). In support of this concept, it was reported that the plasma PTX3 concentration increased in patients with high-risk plaque components15 and with UAP, but not in those with effort angina14.
In the present study, we evaluated the forensic utility of the postmortem plasma PTX3 concentration as a biomarker for fatal ACS in cadavers. We compared the plasma PTX3 concentration in forensic autopsy cases of ACS with that in control cases. As inflammation-positive controls, serious infection cases were also investigated.
Results
Plasma PTX3 and CRP concentrations by the cause of death
The plasma PTX3 concentration in the control group was less than 120 ng/mL (43.0 ± 32.0 ng/mL) (Fig. 1a, Table 1). Seven out of nine cases of the coronary stenosis group and 4 out of 5 cases of the myocardial rupture group in the ACS groups exhibited a plasma PTX3 concentration less than 110.0 ng/mL, which is the 97.5th percentile in the control group. Conversely, in the coronary thrombi cases of the ACS group, 5 out of 6 cases exhibited a plasma PTX3 concentration higher than 110.0 ng/mL. In the serious infection group, all cases exhibited a high concentration of PTX3 (462.1 ± 266.6 ng/mL). A multiple-comparison analysis (Steel test following to Kruskal–Wallis test) among these groups determined that the coronary thrombi group and serious infection group were significantly different from the control group (P = 0.0077 and 0.0003, respectively).
Contrary to the plasma PTX3 concentration, the plasma CRP concentration in the ACS groups was significantly higher not in the coronary thrombi group but in the myocardial rupture group (Fig. 1b, Table 1). In the coronary thrombi group, half of the cases had a plasma CRP concentration less than 0.3 ng/mL, which is the upper clinical range limit, whereas in the myocardial rupture group, 4 out of 5 cases were over 0.3 mg/dL. In the serious infection group, all cases exhibited a high concentration of CRP, as well as PTX3 concentration.
Postmortem effects on the plasma PTX3 concentration
The postmortem plasma PTX3 concentration was substantially higher than the clinical reference values reported previously: 43.0 ± 32.0 ng/mL in our control groups versus 1.98 ng/mL for the healthy volunteers14. PTX3 is produced de novo in neutrophil precursors, stored in neutrophil granules, and released in response to inflammatory signals18. Compared with lymphocytes, eosinophils, and monocytes, neutrophils degenerate rapidly following death. Morphological changes (e.g., pyknosis, cytoplasmic and nuclear vacuolation) and disintegration in neutrophils begin as early as 6 h after death19,20,21. These findings led us to investigate the postmortem release of PTX3 from circulating neutrophils. There appeared to be a relationship between the neutrophil counts and plasma PTX3 concentration (Fig. 2a, Table 1). However, this relationship was only present in cases with a plasma PTX3 concentration less than 200 ng/mL. Such high relative PTX3 concentration to neutrophil count ratios were found in only a few cases of the ACS and infection groups (Fig. 2b, Table 1). Accordingly, cases with PTX3/neutrophil count ratios above the 97.5th percentile (2.38) in the control groups (1.13 ± 0.66) were excluded from the correlation analysis. As a result, there was a strong relationship between the plasma PTX3 concentration and neutrophil counts (P < 0.001, r = 0.744) (Fig. 2c). In contrast, the plasma PTX3 concentration did not correlate with the postmortem intervals (P = 0.7221) (Fig. 2d). Following immunostaining of the blood smear samples, the cytoplasm of the neutrophils in fresh blood collected from a healthy volunteer stained positive with an anti-PTX3 antibody (Fig. 3, left panel). The neutrophils in the blood that was incubated at room temperature for 48 h after collection from the same volunteer (Fig. 3, middle panel) and those in the blood derived from a cadaver with a postmortem interval of approximately 16 h (the right panel) exhibited the same morphological changes as previously reported, including pyknosis, cytoplasmic and nuclear vacuolation, nuclear fragmentation, and disintegration19,20,21. Moreover, although the PTX3 concentration in the plasma from the fresh blood was 1.45 ng/mL, the concentration from the blood stored in vitro for 48 h was as high as 8.17 ng/mL (Fig. 3). These results indicate that the plasma PTX3 concentration increases immediately after death via postmortem release from circulating neutrophils. In the ACS groups, the postmortem interval (Fig. 4a), as well as the plasma PTX3 concentration (Fig. 1a), were significantly higher in the coronary thrombi group compared with the control group. However, there was no relationship between the postmortem interval and the plasma PTX3 concentration in the coronary thrombi group (Fig. 4b, Table 1, P = 0.9844).
PTX3 also has an inverse relationship with the development of obesity, as the plasma PTX3 concentration has been reported to significantly decrease with an increasing BMI22. In the present study, we found no relationship between the postmortem plasma PTX3 concentration and BMI (P = 0.2303).
Plasma PTX3 concentration is reportedly normalized by cardiovascular drugs, including antihypertensive23,24,25,26,27, antilipemic28, and antithrombotic29 agents. Although the drug screening test detected the antithrombotic drug warfarin in two cases (case Nos. 22 and 39 in Table 1), there seemed to be no influence on the plasma PTX3 concentration.
Discussion
The present study demonstrated that all cases of the coronary thrombi group exhibited a significantly higher plasma PTX3 concentration. Immunohistochemical analysis using an antibody against PTX3 revealed strong positive staining of PTX3 in advanced atherosclerotic plaques of the coronary artery16,30,31. In blood samples collected from sites distal to the plaque lesions, the concentration of PTX3 was significantly higher than that obtained from proximal sites14. This indicates that the increased circulating PTX3 is derived from atherosclerotic plaques. PTX3 is produced by macrophages30,31, endothelial cells30, and smooth muscle cells30 found within atherosclerotic lesions. Furthermore, PTX3 has been detected in neutrophils infiltrating into atherosclerotic plaques and in coronary arterial thrombi removed from a culprit lesion31. Conversely, all but one of the cases in the coronary stenosis group without coronary thrombi had a plasma PTX3 concentration not significantly different from the control group. Consistent with these findings, the plasma PTX3 concentration increases in patients with high-risk plaque components15 and with UAP, but not in those with effort angina14. It seemed that the coronary stenosis case with a high plasma PTX3 concentration failed to detect advanced atherosclerotic plaques.
Plasma PTX3 concentration significantly increased in the coronary thrombi group, whereas in the myocardial rupture group, it returned to levels similar to the control group. Contrary to plasma PTX3 concentration, plasma CRP concentration was less than 0.3 mg/dL, the upper clinical range limit, in 3 out of 5 coronary thrombi cases, whereas CRP concentration was higher than 0.3 mg/dL in 4 out of 5 myocardial rupture cases. The kinetics of plasma PTX3 differs from that of CRP in AMI patients. Specifically, PTX3 peaks at 7.5 h and returns to normal concentration by 48 h after the onset of an AMI, whereas the increase in CRP begins at 18 h and is sustained until hospital discharge (>96 h)13. In a murine model of an AMI involving coronary artery ligation/reperfusion, PTX3 expression was upregulated in the interstitium surrounding the necrotic myocardium at 8 h of reperfusion after ischemia32. In this model, the plasma PTX3 concentration was also found to be elevated at 8 h, peaking at 24 h, and followed by a rapid return to normal concentration levels by 48 h. Myocardial rupture following AMI generally occurs between a few hours and 48 h after an AMI33, and all cases of myocardial rupture in this study exhibited histopathological findings of inflammatory cell infiltration, indicating that death occurred later than 24 h post-AMI34. These results suggest that an increased plasma PTX3 concentration indicates that death occurred immediately after the onset of fatal ACS.
The plasma PTX3 concentration obtained from cadavers was substantially higher than that obtained from patients13,14,15. This is likely due to the postmortem release of PTX3 stored in circulating neutrophils. The morphological changes of neutrophils begin at 6 h following death19,20,21. In this study, the postmortem intervals of the autopsy cases ranged from 5 to 72 h (36.1 ± 15.7 h), which is long enough to cause postmortem changes in neutrophils. There was no relationship between the plasma PTX3 concentration and postmortem intervals, which suggests that the postmortem release of neutrophil-derived PTX3 into the blood occurred simultaneously and immediately after death. Nevertheless, consistent with previous reported clinical data13,14,15, all cases in the coronary thrombi group exhibited a significantly higher plasma PTX3 concentration than the control cases. This finding was observed without being negated by the postmortem release of PTX3 from circulating neutrophils.
In conclusion, the postmortem plasma PTX3 concentration is a useful marker to indicate when death occurred immediately after the onset of fatal ACS. However, the postmortem plasma PTX3 concentration was higher than the clinical reference, which appeared to be caused by a postmortem release from circulating neutrophils. This study first demonstrated that the clinical reference value of plasma PTX3 cannot be applied to postmortem samples. Further postmortem plasma PTX3 data should be collected to aid in the creation of a specific reference value for cadavers.
Methods
Autopsy materials
Medico-legal autopsy cases in our department, including ACS, serious infection, asphyxia and immediate death due to fatal injury were investigated. The ACS groups (n = 20 total) were composed of coronary stenosis, coronary thrombi, and myocardial rupture groups. The coronary stenosis group (n = 9) exhibited apparent coronary stenosis, but an absence of coronary thrombi. In the coronary thrombi group (n = 6), thrombi were found in the coronary artery. The myocardial rupture group (n = 5) presented with myocardial rupture following an AMI. No large injuries were evident on these bodies. The serious infection group (n = 10) consisted of one meningitis and two sepsis cases. The control groups (n = 12 total) consisted of six asphyxia cases, including drowning, flail chest, and aspiration and six immediate death cases due to a fatal injury, including cerebral contusion, traumatic myocardial rupture, traumatic aortic rupture, and spinal cord injury. The summary of these groups is presented in Table 1. The cause of death and postmortem interval were determined on the basis of the autopsy findings and the circumstantial evidence in the autopsy documents. A drug screening test was performed on the database with a forensic toxicology library (MassLynx 4.1 TOF Toxicology Database 1, Waters, Milford, MA, USA) using an LC–TOF-MS system (ACQUITY UPLC-Xevo® G2-S QTof, Waters). Plasma samples were prepared from whole heart blood immediately after the autopsy and stored at −20 °C. After routine examinations, the remnants were used for the PTX3 assay. All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. The use of autopsy materials without informed consent was approved by the Ethical Review Board of Kyoto Prefectural University (reference number ERB-C-442).
Assay
The plasma PTX3 concentration was determined using an ELISA assay kit for human PTX3 (Human Pentraxin3/TSG-14 ELISA System; Perseus Proteomics, Tokyo, Japan)14. White blood cell-large cell count (W-LCC) values were determined by an automated hematology analyzer (pocH®-100i, Sysmex, Kobe, Japan) and were considered as the neutrophil counts. The plasma CRP concentration was determined using latex agglutination turbidimetry in LSI Medience Corporation (Tokyo, Japan). Body mass index (BMI) was calculated using the height and weight data measured at autopsy.
Immunostaining
For PTX3 immunostaining of hemocytes, whole blood from a healthy volunteer or a cadaver was smeared onto a glass slide, dried by cold air for 30 min, and fixed with buffered formalin/acetone (4:6) for 30 s. The blood smear samples were then incubated for 3 h at room temperature with an anti-PTX3 antibody (Perseus Proteomics) diluted at 1:200 and then with biotin-conjugated anti-mouse IgG followed by streptavidin-conjugated alkaline phosphatase each for 30 min (SAB-AP kit, Nichirei Biosciences, Tokyo, Japan). New Fuchsin was used as the chromogenic substrate.
Statistical analysis
Quantitative data are presented as means ± SD. A Pearson’s product-moment correlation coefficient was used to test the correlation between two variables. All statistical analyses were performed using EZR (ver. 1.11) (Saitama Medical Center, Jichi Medical University)35. P < 0.05 was considered to be statistically significant.
Data Availability
All data generated or analysed during this study are included in this published article (and its Supplementary Information files).
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Acknowledgements
This study was funded by JSPS KAKENHI (Grant Numbers JP16K09214 and JP17K09271).
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M.T. and K.S.: study conception and design, analysis and interpretation of data. M.T.: acquisition of data. K.S.: drafting of the manuscript. H.T., M.N., N.I. and H.I.: discussion and critical revision of the manuscript.
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Tojo, M., Shintani-Ishida, K., Tsuboi, H. et al. Postmortem plasma pentraxin 3 is a useful marker of fatal acute coronary syndrome. Sci Rep 9, 8090 (2019). https://doi.org/10.1038/s41598-019-44472-0
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DOI: https://doi.org/10.1038/s41598-019-44472-0
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