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. 2020 Nov 11;15(11):e0241565. doi: 10.1371/journal.pone.0241565

High CSF thrombin concentration and activity is associated with an unfavorable outcome in patients with intracerebral hemorrhage

Harald Krenzlin 1,*, Christina Frenz 1, Jan Schmitt 1, Julia Masomi-Bornwasser 1, Dominik Wesp 1, Darius Kalasauskas 1, Thomas Kerz 1, Johannes Lotz 2, Beat Alessandri 1, Florian Ringel 1, Naureen Keric 1
Editor: Tamil Selvan Anthonymuthu3
PMCID: PMC7657554  PMID: 33175864

Abstract

Background

The cerebral thrombin system is activated in the early stage after intracerebral hemorrhage (ICH). Expression of thrombin leads to concentration dependent secondary neuronal damage and detrimental neurological outcome. In this study we aimed to investigate the impact of thrombin concentration and activity in the cerebrospinal fluid (CSF) of patients with ICH on clinical outcome.

Methods

Patients presenting with space-occupying lobar supratentorial hemorrhage requiring extra-ventricular drainage (EVD) were included in our study. The CSF levels of thrombin, its precursor prothrombin and the Thrombin-Antithrombin complex (TAT) were measured using enzyme linked immune sorbent assays (ELISA). The oxidative stress marker Superoxide dismutase (SOD) was assessed in CSF. Initial clot size and intraventricular hemorrhage (IVH) volume was calculated based on by computerized tomography (CT) upon admission to our hospital. Demographic data, clinical status at admission and neurological outcome were assessed using the modified Rankin Scale (mRS) at 6-weeks and 6-month after ICH.

Results

Twenty-two consecutive patients (9 females, 11 males) with supratentorial hemorrhage were included in this study. CSF concentrations of prothrombin (p < 0.005), thrombin (p = 0.005) and TAT (p = 0.046) were statistical significantly different in patients with ICH compared to non-hemorrhagic CSF samples. CSF concentrations of thrombin 24h after ICH correlated with the mRS index after 6 weeks (r2 = 0.73; < 0.005) and 6 months (r2 = 0.63; < 0.005) after discharge from hospital. Thrombin activity, measured via TAT as surrogate parameter of coagulation, likewise correlated with the mRS at 6 weeks (r2 = 0.54; < 0.01) and 6 months (r2 = 0.66; < 0.04). High thrombin concentrations coincide with higher SOD levels 24h after ICH (p = 0.01).

Conclusion

In this study we found that initial thrombin concentration and activity in CSF of ICH patients did not correlate with ICH and IVH volume but are associated with a poorer functional neurological outcome. These findings support mounting evidence of the role of thrombin as a contributor to secondary injury formation after ICH.

Background

Intracerebral hemorrhage (ICH) accounts for 10–15% of all strokes worldwide [1]. With an annual incidence of 10–30 per 100,000 population, it represents a major public health burden [1]. It is associated with considerable mortality and long-term morbidity [2]. Neuronal damage after ICH is caused by primary tissue disruption and secondary progression due to detrimental processes in the perihematomal zone. Despite ongoing clinical and preclinical research efforts, the underlying pathophysiological mechanisms of secondary deterioration are poorly understood. So far, good prognostic factors and specific treatment targets are missing.

Recently, the importance of the blood coagulation factor IIa (thrombin, FIIa) as key effector after traumatic brain injury and hemorrhagic stroke has become evident [3–5]. Thrombin signaling is mostly mediated through the family of protease-activated receptors (PARs) causing inflammatory responses, cell proliferation/modulation, cell protection and apoptosis [6, 7]. The majority of prothrombin is produced in the liver and, due to its large, spherical shape, it is unable to pass the blood-brain barrier (BBB) [8]. Nevertheless, thrombin and associated factors such as Anti-thrombin III (AT III) have also been detected throughout the central nervous system under physiological conditions [9]. Within the central nervous system (CNS) thrombin exerts both protective and detrimental effects. In pico- to nanomolar ranges (10pM– 10nM), thrombin is protective against a variety of cellular insults, such as glucose deprivation, reactive oxygen species (ROS) or edema formation after ICH [10, 11]. In high concentrations (100 nM–10 μM) thrombin increases edema by TNF-α up-regulation, neuronal damage and death after ischemia in mice [12–14]. These processes lead to extended neuronal injury predominantly mediated via protease-activated receptor-1 signaling [15]. Interestingly, the majority of perihematomal thrombin accumulation has been linked to neuronal expression, rather than systemic influx [16]. The CNS is the only known site of extra-hepatic thrombin production [17]. Neuronal cell loss within the tissue at risk and neurological deficits are associated with higher concentrations of thrombin in mice [16]. This supports the potential role of thrombin as a target of novel therapeutic regimens in the treatment of intracerebral hemorrhage. As human perihematomal tissue samples are not readily available, other specimens need to be analyzed to gain insight into the role of thrombin after ICH. It has previously been shown that thrombin and its inactive precursor prothrombin are detectable in human CSF [5]. However, no published data are available addressing thrombin within CSF after ICH.

We hypothesized that thrombin accumulation occurs in all compartments including the cerebrospinal fluid (CSF) after ICH and, in higher concentrations, might contribute to detrimental neurological outcome. In this study, prothrombin, thrombin and TAT were analyzed in the CSF of ICH patients and correlated with their functional neurological outcome.

Methods

Patient population

From February 2017 to February 2019, 20 consecutive patients (9 female and 11 male) that required extra-ventricular drainage due to space-occupying supratentorial ICH with ventricular hemorrhage were included in our study. Age ranged from 40 to 80 years (66±12 years). All patients had one or more underlying conditions. Arterial hypertension was most common and present in 75% of all patients, chronic heart disease (35%) and malignancies (30%) ranked 2nd and 3rd (S1 Table). All patients received standard intensive care medical treatment according to current clinical guidelines. EVD was established on admission on our neurosurgical intensive care unit. Patients were followed up until six months after discharge or until death occurred. CSF and clinical data were collected and analyzed prospectively. All patients received a thorough clinical examination on admission and before discharge from our hospital. CT was used to analyze hematoma volume and localization as described before [18]. The clinical data and baseline characteristics are summarized in Table 1. Each patient's clinical status was graded according to the modified Rankin scale (mRS) and Glasgow coma scale (GCS) prior to admission. The neurological outcome was measured using the mRS and Glasgow outcome scale extended (GOSE) at 6 weeks and 6 months after ICH occurrence. CSF from patients with normal pressure hydrocephalus was collected and served as controls.

Table 1. Baseline demographics and patients characteristics.

ICH patients Control subject
No of subjects 22 4
Mean age (SD) 65.6 (12.3) 67.0 (5.7)
Sex
Female 8 2
Male 14 2
ICH score 3 (1)
Hematoma localization
frontal 12 n.a.
parietal 8 n.a.
occipital 0 n.a.
Basal ganglia 2 n.a.
Clot volume (cm3) (SD) 26.61 (29.93) n.a.
Intraventricular clot (cm3) (SD) 76.96 (94.88) n.a.
Perihematomal zone (cm3) (SD) 90.54 (44.27) n.a.
CSF concentration (ng/ml)
Prothrombin 20.18 (1.4) 16.68 (1.17)
Thrombin 4.12 (1.3) 0.86 (0.36)
TAT 1.95 (1.7) 0.57 (0.11)
SOD 2.05 (0.95) 1.21 (0.05)
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Sampling procedure

CSF was obtained through extra-ventricular drainage at day 1 and 3 after ICH onset. Concordant blood samples were obtained via an arterial canula. CSF of controls were obtained from either lumbar drainages placed for normal pressure hydrocephalus evaluation or from intraoperative opening of CSF spaces in meningioma and schwannoma patients. Samples were collected in a sterile plastic tube. The tube was centrifuged at 1500 G at 4°C for 5 min. The supernatant was frozen, and aliquots were stored at -80°C until analysis.

Measurement of analytes in CSF and blood samples

The prothrombin (NBP2-60624, Novus Biologicals, Abingdon, UK), thrombin (NBP2-60590, Novus Biologicals, Abingdon, UK) and TAT (NBP2-60605, Novus Biologicals, Abingdon, UK) concentration of each sample was measured with an enzyme-linked immunosorbent assay. SOD and fibrinogen were measured via photometry.

Measurement of hematoma volume

ICH and IVH volumes were calculated by CT, with a slice thickness of 1 mm. On serial slices in one direction, the intraventricular and intracerebral hematomas were segmented separately, while the volume were calculated using the Brainlab software (Brainlab, Munich, Germany) (Tables 1 and 2).

Table 2. Disability and dependence over time (median; IQR).

Admission / prior to ICH 6 weeks 6 month
GCS 10 (3, 14) n.a. n.a.
mRS 1 (0, 1) 5 (3, 5) 5 (3, 6)
GOSE n.a. 3 (2, 3) 1 (1, 3)
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Statistical analysis

Findings were reported as mean or median ± SD. For statistical analysis, we used the non-parametric Mann-Whitney U-test. Relations among FII, FIIa, TAT, SOD and clinical outcome parameters two-way analysis of variance (ANOVA) with Tukey’s multiple comparison post hoc test were performed using GraphPad Prism version 8.4.2 for macOS, GraphPad Software, La Jolla California USA, www.graphpad.com. A value of P < 0.05 was accepted as statistically significant.

Ethical approval

Data acquisition and analysis was performed in an anonymous fashion and was approved by the Ethics Committees of the medical association of Rhineland Palatinate and Lower Saxony, Germany (837.374.16). According to the local laws, no informed consent is necessary for such kind of analysis.

Results

Patient outcome and follow-up

Median GCS on admission was 10 ± 5. The mean ICH score on admission was 3 ± 1. Median historical mRS was 1 ± 1. The mRS deteriorated after ICH to 5 ± 1 at week 6 after ICH. The median mRS remained at 5 ± 2 at 6 months after ICH. (Table 2)

CSF FII, FIIa and TAT of controls and ICH patients

24h after ICH mean CSF levels of thrombin were 4.12±1.3 ng/ml compared to 0.86±0.36 ng/ml in healthy controls. Likewise, mean levels of prothrombin within the CSF was 20.18±1.4 ng/ml in patients with ICH and 16.68±1.17 ng/ml in controls. Mean TAT levels were 1.95±1.7 ng/ml or 0.57±0.11 ng/ml respectively. A statistically significant difference was evident between CSF concentrations of prothrombin (p = 0.001), thrombin (p = 0.005) and TAT (p = 0.046) in patients with ICH compared to healthy controls. (Table 1) Plasma levels of FII and FIIa did not correlate with their corresponding CSF levels. (Table 3)

Table 3. CSF prothrombin, thrombin and TAT of patients with ICH and controls.

Prothrombin (FII) Thrombin (FIIa) TAT
Spearman‘s ρ p Spearman‘s ρ p Spearman‘s ρ p
ICH score 0.69 0.005 0.68 0.004 0.04 0.45
mRS 6 weeks 0.3 0.28 0.61 0.004 0.65 0.013
mRS 6 month 0.33 0.22 0.57 0.009 0.65 0.015
Clot size 0.47 0.07 0.23 .35 0.01 0.53
Plasma / CSF 0.007 0.77 0.08 0.3 - -
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CSF fibrinogen and SOD after ICH

CSF levels of fibrinogen were 1.57±0.74 ng/ml 24h- and 1.5±0.89 ng/ml 72h after ICH. SOD levels within the CSF were 2.05±0.9 U/l 24h after ICH and 1.21±0.05 U/l in controls.

While initial levels of CSF fibrinogen and thrombin showed no correlation, both were inversely correlated 72h after onset of ICH (r = -0.68; p = 0.01). Higher levels of CSF thrombin correlate with higher levels of SOD 24h after ICH occurrence (r = 0.64; p = 0.095). (Fig 1)

Fig 1. mRS after ICH is dependent on CSF FIIa and TAT concentrations.

Fig 1

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CSF concentrations of FIIa 24h after ICH correlated with the mRS disability index 6 weeks (r = 0.61; p = 0.004) and 6 months (r = 0.57; p = 0.009) after discharge from hospital. Further, the TAT-complex as surrogate parameter of coagulation correlated with the mRS disability index at 6 weeks (r = 0.65; p = 0.013) and 6 months (r = 0.65; p = 0.015).

Correlation of CSF FII, FIIa and TAT with clinical outcome

CSF concentrations of FIIa 24h after ICH correlated with the initial ICH score (r = 0.68; p = 0.004), as well as the mRS disability index 6 weeks (r = 0.61; p = 0.004) and 6 months (r = 0.57; p = 0.009) after discharge from hospital. Further, the TAT-complex as surrogate parameter of coagulation correlated with the mRS disability index at 6 weeks (r = 0.65; p = 0.013) and 6 months (r = 0.65; p = 0.015). (Table 3, Figs 1 and 2) In contrast, Prothrombin, Thrombin and TAT had no statistically significant correlation neither to the initial ICH volume nor to the IVH volume. Likewise, plasma levels of FII, FIIa and TAT did not correlate with the clinical outcome. (Table 3)

Fig 2. Higher CSF concentrations of thrombin are associated with an unfavourble outcome.

Fig 2

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Higher FIIa CSF concentrations 24h after ICH correlated with an unfavorable outcome after 6 weeks and 6 months.

Correlation of CSF FII, FIIa and TAT with clinical outcome was independent from the type of surgical intervention. In our data, clot evacuation or lysis did not lead to better neurological outcome after 6 weeks or 6 months compared to conservative medical treatment (p = 0.71). High concentrations of FII, FIIa or TAT in CSF did not increase the likelihood of necessary surgical interventions during the acute phase of hospital care.

Discussion

In our study, higher concentrations of thrombin in the CSF of patients suffering from ICH correlated with an unfavorable outcome at 6 weeks and 6 months after discharge from hospital. We further show that prothrombin and thrombin within the CSF does correlate with the ICH score at the time of admission. This is plausible as thrombin has been shown to be neurotoxic both in vitro and in vivo if exceeding a threshold of 100nM [19]. Thrombin is inhibited by antithrombin III, resulting in an inactive proteinase/inhibitor complex (TAT). Interestingly, exceeding concentrations of antithrombin III are also detrimental to neuronal health and might add to adverse thrombin effects [19]. In contrast to thrombin, ATIII mRNA expression has not been detected within normal CNS tissue and is supposed to be largely derived from passage across the blood-brain barrier [20]. It is about 100x higher in plasma, than it is in CSF. In times of BBB disruption, ATIII might enter then CNS and contribute to neuronal damage in the wake of ICH [20]. In our cohort, higher concentrations of thrombin and TAT complex within CSF correlated with a higher mRS at 6 weeks and 6 months after ICH, similar to those of unbound thrombin. These results fall in line with data published from patients with SAH where thrombin activity correlated with the degree of SAH (according to Fisher’s CT classification), the persistence of a subarachnoid clot and the development of vasospasm [14]. In SAH, the Thrombin-Anti-Thrombin complex as surrogate of thrombin activity was found to correlate with the Hunt and Hess grading on admission. Although not statistically significant, larger amounts of TAT persisting over a longer period of time were found to be present in patients with worse neurological outcome [15]. In a preclinical study, nude mice developed hydrocephalus after injection of human hemorrhagic CSF [21]. The authors suggest that various acellular components of CSF inducing secondary brain injury and post-hemorrhagic hydrocephalus. However, in our small patient cohort, the severity and volume of ICH and IVH did not correlate neither with thrombin nor with the occurrence of a post-hemorrhagic hydrocephalus proving the complexity of the underlying pathophysiology.

It is speculated that thrombin induced neurotoxicity is mediated via Par-1, one of 4 members of the protease activated receptors family as activation of Par-1 per se has been linked to neuronal cell death [22]. The increases of oxidative stress and reduction of mitochondrial membrane potential might serve as possible explanation how Par-1 activation subsequently leads to cellular toxicity [23]. Another pathway leading to reactive oxygen species involves activation of microglial NADPH oxidase by thrombin induced upregulation of NADPH oxidation proteins gp91, p47-phox and p67-phox [22]. In our study SOD, higher concentration of thrombin coincided with higher concentrations of SOD at day 1, indirectly indicating the increased occurrence of ROS. Further, higher concentrations of CSF thrombin lead to decreased amounts of fibrinogen 3 days after ICH. As Inhibition of fibrin formation reduces neuroinflammation and improves long-term outcome after intracerebral hemorrhage, this might hint at another mechanism leading to secondary damage induction mediated by thrombin [24].

In contrast to our expectations, thrombin did not correlate with ICH or the IVH volume in our study. It remains a matter of debate, whether thrombin is washed in as a result of blood extravasation and BBB breakdown or mainly produced within the CNS as response to various stressors. Local thrombin expression in the perihematomal zone after ICH might contribute to thrombin levels in CSF [16]. As numerous MRI studies suggests the existence of a perihematomal penumbra with functionally impaired, but potentially reversible neuronal injury, this thin rim of 2 mm to a maximum width of 1 cm surrounding the site of injury, might as well be the area most devastatingly influenced by thrombin [16, 25].

Limitations of the study are due to a rather small and heterogeneous group of patients suffering from severe intracerebral hemorrhage. Limited knowledge of events prior to hospital admission and the number of concomitant illnesses might constitute an additional limitation of our study. Further research combining larger patient cohorts and multivariate analysis could lead to more definitive conclusions on the role of the cerebral thrombin system in the development of secondary brain injury after ICH.

Conclusion

In summary, in the presented data thrombin concentration and activity correlate with the neurological outcome after ICH. Further, generation of ROS seems to be involved in these processes. Our data adds to a mounting body of evidence hinting at the importance of thrombin as a contributor to secondary injury formation after ICH.

Supporting information

S1 Fig. Clot volume is independent from CSF FIIa and TAT concentrations.

CSF concentrations of FIIa (r = 0.13; p = 0.68) and TAT (r = -0.18; p = 0.51) show no correlation with clot volume 24h after ICH. Likewise, no correlation between FIIa (r = 0.36; p = 0.137) and TAT (r = 0.23; p = 0.422) with intraventricular clot volume were found 24h after ICH.

(TIF)

Click here for additional data file. (4.1MB, tif)
S1 Table. Underlying conditions.

(DOCX)

Click here for additional data file. (20.1KB, docx)

Data Availability

All relevant data are within the paper and its Supporting Information files.

Funding Statement

The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The authors received no specific funding for this work.

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Decision Letter 0

Tamil Selvan Anthonymuthu

10 Sep 2020

PONE-D-20-21960

High CSF thrombin concentration and activity is associated with an unfavorable outcome in patients with intracerebral hemorrhage

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It would be better to indicate the exact p value rather than showing the range such as p< 0.01, p<0.05, p<0.09 in Table 3 and in the subsequent text.

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1. Is the manuscript technically sound, and do the data support the conclusions?

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Reviewer #1: Yes

Reviewer #2: Yes

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: I Don't Know

Reviewer #2: Yes

**********

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

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Reviewer #2: Yes

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5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The authors report high CSF thrombin concentration/activity is associated with an unfavorable outcome with intracerebral hemorrhage, and report thrombin concentration/activity in the CSF of patients with ICH on clinical outcomes in patients presenting with space-occupying lobar supratentorial hemorrhage requiring extra-ventricular drainage (EVD). They measured CSF levels of thrombin, prothrombin, thrombin-antithrombin complexes (TATs), and superoxide dismutase (SOD) in CSF. Initial clot size and intraventricular blood volume were calculated by computerized tomography (CT) on admission, and demographic data, clinical status at admission and neurological outcome were assessed using the modified Rankin Scale (mRS) at 6-weeks and 6-months in 22 consecutive patients (9 females, 11 males) with supratentorial hemorrhage. CSF concentrations of prothrombin (p < 0.005), thrombin (p = 0.005) and TAT (p = 0.046) were statistically different in patients with ICH compared to non-hemorrhagic CSF samples. CSF concentrations of thrombin 24h after ICH correlated with the mRS index after 6 weeks (r2 = 0.73; < 0.005) and 6 months (r2 = 0.63; < 0.005) after discharge from hospital. Thrombin activity, measured via TAT as surrogate parameter of coagulation, likewise correlated with the mRS at 6 weeks (r2 = 0.54; < 0.01) and 6 months (r2 = 0.66; < 0.04). High thrombin concentrations coincide with higher SOD levels 24h after ICH (p = 0.01). They conclude that increased thrombin levels and thrombin activity are associated with a poorer neurological outcome after ICH, and have the potential to serve as predictive markers for individual treatment decision making and future novel therapeutic targets.

Overall, the data and presentation are interesting. The authors are to be congratulated for their interesting study.

Comments:

1. From this reviewer’s perspective, it follows that the larger the clot burden and size of the intracranial hemorrhage, the more probability is that levels of thrombin and other thrombin generation thrombin activity biomarkers will be higher. However, as you thoughtfully noted, intraventricular volumes on CT scans did not correlate with your various biomarkers of thrombin activity in particular thrombin levels. I still think it would be helpful to include a scattergram correlating volume with thrombin levels. Also, has this finding been previously reported?

2. You state CSF fibrinogen and thoughtfully have control comparisons. Is there any correlation between plasma and CSF fibrinogen levels?

3. I’m surprised how small your standard deviation values are for your biomarkers. These are standard deviation and not the standard error of the means, correct?

4. You use the term ictus, I think to describe stroke or CNS event. I think another descriptive term would be better.

Additional comments:

Results

1. You state, “Serum levels of FII and FIIa did not correlate with their corresponding CSF levels”. This should be plasma, not serum. You also state this later on as serum levels. Again, coagulation factor levels are obtained from plasma.

2. You state , “Further, the TAT-complex as surrogate parameter of coagulation and fibrinolysis correlated with the mRS disability index at 6 weeks (2 = 0.65; p < 0.01) and 6 months (r = 0.65; p < 0.01)”. How does thrombin – antithrombin complexes provide any surrogate parameter of fibrinolysis? Please specifically explain if not remove the term fibrinolysis.

Discussion

1. Your first paragraph restates information that really should be part of your introduction. My suggestion is in your first paragraph state the novelty and important information from your interesting study, and include your second paragraph is your first paragraph.

2. In your first paragraph, you state, “While small amounts of activated coagulation FII”- be consistent as you described this activated coagulation factor to is thrombin. Is this what you’re referring to? Please be consistent.

3. In your second paragraph, you state, Thrombin is inhibited by antithrombin III, resulting in an inactive proteinase/inhibitor complex (TAT). Interestingly, exceeding concentrations of antithrombin III are also detrimental to neuronal health and might add to adverse thrombin effects.[28]” Antithrombin is primarily a circulating plasma anticoagulant. How does antithrombin get into the CSF? What are the normal levels of antithrombin in the CSF? My understanding is that antithrombin in antithrombin – thrombin complexes are due to active bleeds and breakdown of the blood-brain barrier. Please add this information to your discussion.

4. You state, “In our cohort, higher concentrations of thrombin and TAT complex within CSF correlated with a higher mRS at 6 weeks and 6 months after ICH, similar to those of unbound thrombin. These results fall in line with data published from patients with SAH where thrombin activity correlated with the degree of SAH (according to Fisher’s CT classification), the persistence of a subarachnoid clot, and the development of vasospasm.[29]” as previously stated, at least providing a box plot correlation of the intracranial hemorrhage with thrombin generation in your study would be useful.

Reviewer #2: The introduction could be shortened by 50%.

Probably should report variables as median with interquartile range (rather than standard deviation). It's a bit more informative.

How were controls selected? Were they matched for any demographics or comorbidities with patients? If not, how might this limit your results? How was CSF obtained from controls? How might different sampling methods affect your results?

I could not find mention of whether any patients had intraventricular hematoma, and if so, how much?

Need consistency in the number of decimal places used to report out p-values in tables.

Please report mean/median time to CSF sample collection from ICH ictus, if you have it, or list this as a limitation.

Given the very small sample size, the conclusion of both the abstract and the manuscript are over-stated. It is possible that CSF thrombin may be associated with outcome, but it's also quite possible that a larger, better powered, more random sample would prove your current findings wrong. Or that a larger study would find that only certain patients (perhaps with certain hematomas) demonstrate the associations that you found. Alot left to learn and your data are very preliminary.

What do you think of your findings in the context of the translational science work using preclinical SAH models - Wan, S., Wei, J., Hua, Y. et al. Cerebrospinal Fluid from Aneurysmal Subarachnoid Hemorrhage Patients Leads to Hydrocephalus in Nude Mice. Neurocrit Care (2020). https://doi.org/10.1007/s12028-020-01031-0?

Overall, nicely done.

**********

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PLoS One. 2020 Nov 11;15(11):e0241565. doi: 10.1371/journal.pone.0241565.r002

Author response to Decision Letter 0

12 Oct 2020

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Response: Table 1 has now been included with the main file. Supplementary Table 1 remained as individual file and has been uploaded as supporting information" file.

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Response: The authors received no specific funding for this work. The statement has been included within the cover letter.

• Please ensure that you refer to Figure 2 in your text as, if accepted, production will need this reference to link the reader to the figure.

Response: Fig 1 and Fig 2 are now cited under results “Correlation of CSF FII, FIIa and TAT with clinical outcome”.

• Please include captions for your Supporting Information files at the end of your manuscript, and update any in-text citations to match accordingly. Please see our Supporting Information guidelines for more information: http://journals.plos.org/plosone/s/supporting-information.

3. Additional Editor Comments (if provided):

• It would be better to indicate the exact p value rather than showing the range such as p< 0.01, p<0.05, p<0.09 in Table 3 and in the subsequent text.

Response: All p values have been changed to exact values within the manuscript, tables and figures.

Reviewer 1:

Reviewer #1: The authors report high CSF thrombin concentration/activity is associated with an unfavorable outcome with intracerebral hemorrhage, and report thrombin concentration/activity in the CSF of patients with ICH on clinical outcomes in patients presenting with space-occupying lobar supratentorial hemorrhage requiring extra-ventricular drainage (EVD). They measured CSF levels of thrombin, prothrombin, thrombin-antithrombin complexes (TATs), and superoxide dismutase (SOD) in CSF. Initial clot size and intraventricular blood volume were calculated by computerized tomography (CT) on admission, and demographic data, clinical status at admission and neurological outcome were assessed using the modified Rankin Scale (mRS) at 6-weeks and 6-months in 22 consecutive patients (9 females, 11 males) with supratentorial hemorrhage. CSF concentrations of prothrombin (p < 0.005), thrombin (p = 0.005) and TAT (p = 0.046) were statistically different in patients with ICH compared to non-hemorrhagic CSF samples. CSF concentrations of thrombin 24h after ICH correlated with the mRS index after 6 weeks (r2 = 0.73; < 0.005) and 6 months (r2 = 0.63; < 0.005) after discharge from hospital. Thrombin activity, measured via TAT as surrogate parameter of coagulation, likewise correlated with the mRS at 6 weeks (r2 = 0.54; < 0.01) and 6 months (r2 = 0.66; < 0.04). High thrombin concentrations coincide with higher SOD levels 24h after ICH (p = 0.01). They conclude that increased thrombin levels and thrombin activity are associated with a poorer neurological outcome after ICH, and have the potential to serve as predictive markers for individual treatment decision making and future novel therapeutic targets.

Overall, the data and presentation are interesting. The authors are to be congratulated for their interesting study.

Comments:

1. From this reviewer’s perspective, it follows that the larger the clot burden and size of the intracranial hemorrhage, the more probability is that levels of thrombin and other thrombin generation thrombin activity biomarkers will be higher. However, as you thoughtfully noted, intraventricular volumes on CT scans did not correlate with your various biomarkers of thrombin activity in particular thrombin levels. I still think it would be helpful to include a scattergram correlating volume with thrombin levels. Also, has this finding been previously reported?

Response: It is enticing to presume, that larger clot volumes might result in higher CSF thrombin levels. However, given the short half-life of thrombin of about 56.4 ± 4.7 seconds (Ruehl et al. 2012 Thromb haemost.) washed in thrombin might be long gone at the point of analysis. The connection of thrombin and clot volume is now depicted in supplement figure 1. In 2011 Wu et al (European Journal of Neurology) reported a positive correlation of TAT measured in intracerebral hematoma (obtained during surgical removal) and a detrimental outcome. To our knowledge, no correlation between CSF thrombin or TAT levels and clot volume has been reported yet.

2. You state CSF fibrinogen and thoughtfully have control comparisons. Is there any correlation between plasma and CSF fibrinogen levels?

Response: Similar to the absence of a correlation between thrombin and clot volume, we found also no correlation between thrombin levels in CSF and plasma.

3. I’m surprised how small your standard deviation values are for your biomarkers. These are standard deviation and not the standard error of the means, correct?

Response: Figure 2 shows the correlation of thrombin with good and unfavorable outcome at 6 weeks and 6 months after ICH. The box itself represents the interquartile range, while the whiskers indicate the minimum and maximum values.

4. You use the term ictus, I think to describe stroke or CNS event. I think another descriptive term would be better.

Response: The term ictus has been changed to ICH or onset of ICH respectively.

Additional comments:

Results

5. You state, “Serum levels of FII and FIIa did not correlate with their corresponding CSF levels”. This should be plasma, not serum. You also state this later on as serum levels. Again, coagulation factor levels are obtained from plasma.

Response: The word serum has been replaced by plasma throughout the manuscript.

6. You state , “Further, the TAT-complex as surrogate parameter of coagulation and fibrinolysis correlated with the mRS disability index at 6 weeks (2 = 0.65; p < 0.01) and 6 months (r = 0.65; p < 0.01)”. How does thrombin – antithrombin complexes provide any surrogate parameter of fibrinolysis? Please specifically explain if not remove the term fibrinolysis.

Response: It is true that TAT does actually not allow any conclusion about fibrinolysis. The word fibrinolysis has therefore been removed.

Discussion

7. Your first paragraph restates information that really should be part of your introduction. My suggestion is in your first paragraph state the novelty and important information from your interesting study, and include your second paragraph is your first paragraph.

Response: This is an insightful remark which we gladly adhered to. We have now incorporated the recapitulating information into our introduction with the former second paragraph now being the first of the discussion. Additionally, the introduction was revised and shortened adhering to remarks made by reviewer 2.

8. In your first paragraph, you state, “While small amounts of activated coagulation FII”- be consistent as you described this activated coagulation factor to is thrombin. Is this what you’re referring to? Please be consistent.

Response: The sentence has been deleted due to the restructuring of our introduction. We rechecked the remainder of our manuscript for consistency when referring to FIIa.

9. In your second paragraph, you state, Thrombin is inhibited by antithrombin III, resulting in an inactive proteinase/inhibitor complex (TAT). Interestingly, exceeding concentrations of antithrombin III are also detrimental to neuronal health and might add to adverse thrombin effects.[28]” Antithrombin is primarily a circulating plasma anticoagulant. How does antithrombin get into the CSF? What are the normal levels of antithrombin in the CSF? My understanding is that antithrombin in antithrombin – thrombin complexes are due to active bleeds and breakdown of the blood-brain barrier. Please add this information to your discussion.

Response: This is an insightful remark and important line of thought. Evidence suggests that ATIII plasma levels are 100x higher than in CSF. It is hypothesized that ATIII in CSF is largely derived from passage across the blood-brain barrier. (Zetterberg et al. “CSF Antithrombin III and Disruption of the Blood-Brain Barrier” Journal of Clinical Oncology 2009) This observation falls in line with the mentioned line of thought and has been added to our discussion.

10. You state, “In our cohort, higher concentrations of thrombin and TAT complex within CSF correlated with a higher mRS at 6 weeks and 6 months after ICH, similar to those of unbound thrombin. These results fall in line with data published from patients with SAH where thrombin activity correlated with the degree of SAH (according to Fisher’s CT classification), the persistence of a subarachnoid clot, and the development of vasospasm.[29]” as previously stated, at least providing a box plot correlation of the intracranial hemorrhage with thrombin generation in your study would be useful.

Response: In order to clarify the interrelation of CSF thrombin and TAT with clot volume, a supplementary figure has been added depicting both together with either intraventricular clot volume or total clot volume.

Reviewer #2:

1. The introduction could be shortened by 50%.

2. Probably should report variables as median with interquartile range (rather than standard deviation). It's a bit more informative.

Response: The SD in Table 2 has been changed to Median + IQR.

3. How were controls selected? Were they matched for any demographics or comorbidities with patients? If not, how might this limit your results? How was CSF obtained from controls? How might different sampling methods affect your results?

Response: Patients requiring lumbar drainage for normal pressure hydrocephalus evaluation and patients with meningiomas or schwannomas, who need intraoperative opening of CSF spaces were used as controls. This aspect was added to our Methods section. The intention was to compare CSF from patients with ICH to those without. We do not expect that thrombin or ATIII concentration would differ throughout the CSF. Nevertheless, to our knowledge, no comparison of these factors according to site of CSF acquisition has been reported so far. The controls were similar in age and sex distribution. As comorbidities were widely spread among patients with ICH (Supp. Table 1), arterial hypertension was the sole common denominator.

4. I could not find mention of whether any patients had intraventricular hematoma, and if so, how much?

Response: All patients had at least minimal aspects of intraventricular hemorrhage. The mean (SD) intraventricular blood volume is shown in table 1. An explanatory graph of intraventricular clot and thrombin/TAT correlation has been added as supp. Fig.1

5. Need consistency in the number of decimal places used to report out p-values in tables.

Response: Number and p-value formatting has been revised throughout the manuscript.

6. Please report mean/median time to CSF sample collection from ICH ictus, if you have it, or list this as a limitation.

Response: This is an import observation. As our data concerning the events prior to hospital admission are limited, this circumstance has been added as limitation of our study.

7. Given the very small sample size, the conclusion of both the abstract and the manuscript are over-stated. It is possible that CSF thrombin may be associated with outcome, but it's also quite possible that a larger, better powered, more random sample would prove your current findings wrong. Or that a larger study would find that only certain patients (perhaps with certain hematomas) demonstrate the associations that you found. Alot left to learn and your data are very preliminary.

Response: We agree that conclusion from this small and heterogenous cohort have to be drawn with caution and therefor somewhat dampened the conclusions in our manuscript.

8. What do you think of your findings in the context of the translational science work using preclinical SAH models - Wan, S., Wei, J., Hua, Y. et al. Cerebrospinal Fluid from Aneurysmal Subarachnoid Hemorrhage Patients Leads to Hydrocephalus in Nude Mice. Neurocrit Care (2020). https://doi.org/10.1007/s12028-020-01031-0?

Response: This is an interesting study suggesting that various a-cellular components of CSF might influence secondary injury formation via macrophage activation and consecutive cell damage after SAH. These results might be transferable to intraventricular hemorrhages altering CSF composition and thus effecting secondary injury.

Overall, nicely done.

Attachment

Submitted filename: Revision_Thrombin CSF_PLOS_Reviewer response.docx

Click here for additional data file. (25KB, docx)

Decision Letter 1

Tamil Selvan Anthonymuthu

19 Oct 2020

High CSF thrombin concentration and activity is associated with an unfavorable outcome in patients with intracerebral hemorrhage

PONE-D-20-21960R1

Dear Dr. Krenzlin,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

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Kind regards,

Tamil Selvan Anthonymuthu, Ph. D

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: All comments have been addressed

Reviewer #2: (No Response)

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: (No Response)

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: I Don't Know

Reviewer #2: (No Response)

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: (No Response)

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: (No Response)

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The authors have done an excellent job of revising their manuscript, answering the comments, and providing important responses. I have no further comments.

Reviewer #2: Well done. All of my concerns have been addressed.

For some reason, PLOS ONE requires a character count for these statements, which I have now met.

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: No

Acceptance letter

Tamil Selvan Anthonymuthu

3 Nov 2020

PONE-D-20-21960R1

High CSF thrombin concentration and activity is associated with an unfavorable outcome in patients with intracerebral hemorrhage

Dear Dr. Krenzlin:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Tamil Selvan Anthonymuthu

Academic Editor

PLOS ONE

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Fig. Clot volume is independent from CSF FIIa and TAT concentrations.

    CSF concentrations of FIIa (r = 0.13; p = 0.68) and TAT (r = -0.18; p = 0.51) show no correlation with clot volume 24h after ICH. Likewise, no correlation between FIIa (r = 0.36; p = 0.137) and TAT (r = 0.23; p = 0.422) with intraventricular clot volume were found 24h after ICH.

    (TIF)

    Click here for additional data file. (4.1MB, tif)
    S1 Table. Underlying conditions.

    (DOCX)

    Click here for additional data file. (20.1KB, docx)
    Attachment

    Submitted filename: Revision_Thrombin CSF_PLOS_Reviewer response.docx

    Click here for additional data file. (25KB, docx)

    Data Availability Statement

    All relevant data are within the paper and its Supporting Information files.

    Articles from PLoS ONE are provided here courtesy of PLOS

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