Introduction
Pancreatic stone protein (PSP) is a novel biomarker that is reported to be increased in pneumonia and acute conditions, and PSP appears to be superior to procalcitonin (PCT) in discriminating among patients with infection, infection with sepsis, and no infection [
1]. Recently, Van Singer et al., [
2] described the potential advantages of measuring plasma PSP levels in critically ill COVID-19 patients due to the abnormal endothelial activation and inflammatory cytokine cascade that can be observed in COVID-19. Based on these assumptions, the lack of demonstrated clinical biomarkers in coronavirus disease progression requires researchers to further investigate the prognostic role of PSP in critically ill COVID-19 patients [
3,
4]. The measurement of PSP in critical settings has found its application, especially in case of sepsis or in combination with other biomarkers [
5]. Recently Klein et al. described the potential prognostic role of PSP in burns victims, showing the ability to differentiate between septic and non-septic patients during acute burn care [
6]. The serial measurement of this protein over time has shown a prognostic value more than PCT and C-reactive protein (CRP) according to Pugin et al. [
7]. According to Lagadinou et al., the measurement of PSP in hyper-inflammation, such as COVID-19 inflammation, could accurately identify patients requiring prolonged hospitalization [
8].
Methods
Ethical approval was granted by the Ethics Committee of our health system (Azienda Ospedaliero Universitaria di Modena, reference number 784/2021) and the study was carried out in accordance with relevant guidelines and regulations in the Declaration of Helsinki. Informed consent was obtained for all participants when it was possible, in case of impossibility it was waived according to Italian regulations. Patients admitted to a COVID-19 medical intensive care unit who received standard medical care as recommended in COVID-19 sepsis guidelines were screened from March 2021 to June 2021 [
9‐
11] At the same time of blood sample collection, we retrospectively collected information on the mechanical ventilation type; systolic, diastolic and mean arterial pressure measured via a radial or femoral arterial catheter and recorded by the patient’s electronic monitor; urine output per day measured via a urinary catheter; vasopressor and inotropic support dosage; and daily prescribed therapy to describe the patient’s condition at baseline. Physiological variables and medications of interest, the Horowitz index or Sequential Organ Failure Assessment (SOFA) scores were also collected. Finally, patient survival was followed even after discharge from the ICU, and 90 days of mortality data was collected from an electronic register.
Inclusion and exclusion criteria
Inclusion criteria were as follows: age over 18 years, arterial catheter in situ, respiratory failure with mechanical ventilation assistance, urinary catheter in situ, expected ICU length of stay > 24 h, and informed consent signed by patient or next-of-kin when possible, in line with Italian regulations. Exclusion criteria were as follows: patient or next-of-kin refusal or do-not-resuscitate disposals, previous admission to a COVID-19 ICU, and COVID-19-related hemorrhagic or ischemic stroke as the cause of admission to the ICU.
Sample measurement
Patients were positioned lying flat for at least 1 h before the collection of a 4 mL blood sample from the arterial catheter into an ethylene diamine tetra-acetic acid tube (Vacutainer; Becton Dickinson, Franklin Lakes, NJ). PSP levels were measured in whole blood by point-of-care testing using nanofluidic technology (PSP fluorescent immunoassay on the abioSCOPE® IVD device, Abionic SA, Epalinges, Switzerland). PCT and CRP levels were measured upon admission through routine blood tests. Blood samples were drawn at the patient’s time of admission to the ICU, and in the morning (06:00–12:00), PSP, PCT, and CRP levels were measured at the time of admission (T0), 72 h later (T1), five days later (T2) and finally 7 days later (T3).
Statistical analysis and sample size
We planned a priori analysis of variance (ANOVA), and mixed model test repeated measures correlation coefficients (Rrm) were used for within-patient comparisons, cons is the constant (Y intercept) of the model [
12,
13]. A sample of 10 patients was necessary to have 95% power to detect f = 0.5 (medium size effect) for weekly variation of PSP with alpha = 0.05 (supplementary information, sample size file) [
14]. Results were reported as the mean plus standard deviation (st. dev) and with the 95% confidence interval (CI). The area under the receiver-operator (AUROC) curves was used to test mortality predictions, and the p value (
p) was considered significant if < 0.05. Analysis of variance, the Student T test, and the Wilcoxon rank sum test were also performed depending on type of variable. A probit model was applied for regression with a binary dependent variable. Pearson correlation analysis was performed for continuous variables. Postestimation margins were estimated to plot some results. All analyses were performed with STATA (version 16.0, Stata Corp, College Station, TX, USA) and G Power (Erdfelder, Faul, & Buchner, 1996) software was used to estimate sample size [
15,
16].
Discussion
We investigated the PSP levels in critically ill COVID-19 patients, and we found the PSP level to be a helpful marker in evaluating the severity of illness and in predicting mortality over 90 days. PSP is secreted in the pancreas, small intestine and stomach and has been shown to be upregulated in the presence of infection and organ dysfunction; in fact, PSP plasma levels are significantly increased [
4,
17,
18]. PSP may have an activating effect on leukocytes, triggering polymorphonuclear neutrophil granulocyte activation. This activation facilitates the adherence of selectins and integrins on the neutrophil surface to the vessel walls, i.e., to the endothelial cells; this mechanism plays an essential role in the development of pulmonary oedema and acute respiratory distress syndrome (ARDS) observed in severe COVID-19 infections [
19,
20]. The loss of endothelial integrity is crucial in COVID-19 [
21,
22]. This phenomenon could explain why PSP plasma levels increase over time in critically ill COVID-19 patients. It is important to underline that PSP is not an inflammatory protein but a direct indicator of an inflammatory state. In this study, PSP performed better than PCT and CRP as a biomarker for disease progression, in agreement with Llewelyn et al. [
23]. Plasma biomarkers such as CRP and PCT are insufficiently sensitive or specific in predicting the onset of severe septic shock, ARDS and COVID-19-related acute viral septic shock in these critically ill patients [
17,
24,
25]. Several studies have evaluated the role of CRP in COVID-19. Some of them found that elevated CRP on admission for patients with COVID-19 was associated with increased in-patient mortality and was indicative of disease severity at admission [
26‐
28], while other studies documented no significant differences in the CRP level among mild, severe, and critical patients. The role of CRP remains controversial in the medical literature about its prognostic role: according to Pierrakos et al., quantification of this protein is widely used, but it has limited ability to distinguish sepsis from other inflammatory conditions or to predict the outcome [
29,
30]. PSP has the potential to perform better, and this is the first study documenting the potential role of PSP for risk stratification in COVID-19 patients. Additionally, the availability of this test at the point-of-care may provide further advantages through faster results and timely clinical decisions.
PSP showed an AUROC value higher than 0.7 at each measurement timepoint, as well as a significant result in the mixed model analysis over time and a significant difference in plasma levels between survivors and non-survivors; these differences were not observed for PCT and CRP plasma levels. Multiple studies showed that PCT levels show no significant increase in COVID-19 patients and the presented results for PCT are not surprising [
3,
31]. Therefore, increased PCT levels may be a useful marker to detect the emergence of secondary bacterial infection in critical care patients [
32]. PCT showed a lower sensitivity compared to PSP and these results partially agree with results from Que et al. and Gukasjan et al. PCT probably has better sensitivity in case of septic shock due bacterial infection and severity of sepsis [
17,
33]. Specifically, PCT levels are important markers of disease severity in case of sepsis, as shown be Que et al. [
34] among others.
Additionally, while bacterial sepsis and COVID-19 are two distinct disease entities, each underpinned by its pathophysiology, the two frequently overlap as sepsis is a common late complication of COVID-19 in the ICU population, partly due to direct effects of the primary viral infection on the immune system, but also due to iatrogenic complications of immunomodulatory medications, invasive ventilation as well as other invasive procedure that are commonly performed in this setting. There are several differences between the two, as in the bacterial sepsis the systemic inflammation leads an early and sudden clinical deterioration, while COVID-19 has demonstrated a complex pathogenesis that involves other mechanisms of tissue damage and typically a late clinical deterioration in the disease course [
35]. According to Fidalgo et al. PSP accuracy for the diagnosis of infection and sepsis seems to be at least comparable to the biomarkers currently used in clinical practice. Furthermore, it seems to outperform those biomarkers in the prediction of sepsis, because PSP levels seem to anticipate the clinical diagnosis [
36‐
38]. PSP also seems to have a good prognostic value for mortality at 28 days also in sepsis especially if combined with blood lactate or PCT [
5,
34]. We hypothesize that PSP may have better prognostic performance compared to other biomarkers because it is affected both by the primary viral disease and by sepsis, which is a common complication in the late course of COVID-19. This may be particularly useful for prognostication in the late course of the disease. Other studies that have compared biomarkers for prognosis in COVID-19 have used samples from the time of admission, emergency department presentation or unspecified time and have not found significant differences in performance with PCT or CRP, while ours has used samples collected at multiple times, including in the late phase of disease [
2,
8]. Lastly, the use of this biomarker does not exclude the use of others, as certainly integration of data may provide important and complementary information.
The cytokine storm in COVID-19 suggested that IL-6 might be useful as prognostic biomarker, hence medical research investigated this question [
39‐
41]. Gorham et al. demonstrated the value of repeated measurements of IL-6 in critically severe COVID-19 patients, identifying patients with a high risk of poor prognosis. During the COVID-19 pandemic, IL-6 plasma levels progressively became a routine laboratory exam at our institution. However, due to the high demand and limited capacity during the study period, the serial measurement of plasma IL-6 cytokines was not possible. Consequently, we were not able to compare PSP and IL-6, which has been shown in several studies to be associated with the degree of disease severity [
42‐
45]. In a study by Que et. al that compared PSP and IL-6 in predicting mortality, PSP performed better than IL-6. While IL-6 appears to be an accurate prognostic marker, the measured plasma levels do not seem to perform equally good as treatment response markers [
17]. Unfortunately, due to the availability issues at our institution of IL-6 testing, we could not compare IL-6 and PSP as treatment response biomarkers. Another possible biomarker to predict evolution in COVID-19 patients is D-dimer. In some studies, coagulation measured D-dimer levels were significantly higher in patients who developed ARDS and died than in patients who survived [
46‐
48]. However, the interpretation of D-dimer during disease monitoring is currently unclear, as it may not be directly related to disease severity [
49].
The absence of specific prognostic biomarkers in severe COVID-19 makes the research on the role of PSP through point-of-care technology even more interesting. Observing the post-estimation model (Fig.
3 A), it is possible to infer that a value of PSP, at the time of ICU admission, between 250–300 ng/ml is associated with a probability of death at 90 days above 50% (Fig.
3 panel A). However, while our study has multiple measures for every patient by design, the sample size for PSP levels at admission is not enough to clearly answer this research question. Studies with larger sample size are granted to clearly identify and validate a cut-off of PSP blood levels ad a prognostic biomarker. Recently, medical researchers investigated the role of various endothelial proteins in COVID-19, and some researchers have measured PSP using ELISA methods [
50,
51]. In contrast, point-of-care technology provides a quick result (PSP results are available within 7.5 min with the abioSCOPE platform), which allows physicians to triage patients according to the severity of illness and to start the most appropriate medical treatment as soon as possible, in conformity with the “golden hour”, although a little more expensively than the ELISA method. The advantages of this technology are already widely known, as it is used in coagulation and thromboelastography tests. This study was carried out following the CONSORT guidelines. This research has limitations, mainly in the single-center nature of the study and in the small sample of patients enrolled. As a consequence, our results do not allow for generalization to other settings. We find the prospective observational nature with repeated measures a strength of our study.
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