Pancreatic stone protein as an early biomarker predicting mortality in a prospective cohort of patients with sepsis requiring ICU management
© Que et al.; licensee BioMed Central Ltd. 2012
Received: 21 January 2012
Accepted: 2 July 2012
Published: 2 July 2012
Biomarkers, such as C-reactive protein [CRP] and procalcitonin [PCT], are insufficiently sensitive or specific to stratify patients with sepsis. We investigate the prognostic value of pancreatic stone protein/regenerating protein (PSP/reg) concentration in patients with severe infections.
PSP/reg, CRP, PCT, tumor necrosis factor-alpha (TNF-α), interleukin 1 beta (IL1-β), IL-6 and IL-8 were prospectively measured in cohort of patients ≥ 18 years of age with severe sepsis or septic shock within 24 hours of admission in a medico-surgical intensive care unit (ICU) of a community and referral university hospital, and the ability to predict in-hospital mortality was determined.
We evaluated 107 patients, 33 with severe sepsis and 74 with septic shock, with in-hospital mortality rates of 6% (2/33) and 25% (17/74), respectively. Plasma concentrations of PSP/reg (343.5 vs. 73.5 ng/ml, P < 0.001), PCT (39.3 vs. 12.0 ng/ml, P < 0.001), IL-8 (682 vs. 184 ng/ml, P < 0.001) and IL-6 (1955 vs. 544 pg/ml, P < 0.01) were significantly higher in patients with septic shock than with severe sepsis. Of note, median PSP/reg was 13.0 ng/ml (IQR: 4.8) in 20 severely burned patients without infection. The area under the ROC curve for PSP/reg (0.65 [95% CI: 0.51 to 0.80]) was higher than for CRP (0.44 [0.29 to 0.60]), PCT 0.46 [0.29 to 0.61]), IL-8 (0.61 [0.43 to 0.77]) or IL-6 (0.59 [0.44 to 0.75]) in predicting in-hospital mortality. In patients with septic shock, PSP/reg was the only biomarker associated with in-hospital mortality (P = 0.049). Risk of mortality increased continuously for each ascending quartile of PSP/reg.
Measurement of PSP/reg concentration within 24 hours of ICU admission may predict in-hospital mortality in patients with septic shock, identifying patients who may benefit most from tailored ICU management.
Despite significant improvements in clinical management, including systematic multimodal approaches , severe forms of infections, such as severe sepsis and septic shock, are the leading causes of mortality in patients admitted to the intensive care unit (ICU) [2–4]. Over the last two decades, several promising therapeutic strategies designed to specifically target pathogen or host-related mediators involved in the septic process have failed to reduce mortality [5–7], and this failure is due, in part, to the heterogeneity of both microbial agents and host inflammatory responses . Since therapeutic strategies should be adapted to each individual patient, the identification of patients who are at high risk of death and who might benefit most from early and aggressive treatment would represent a critical step toward such tailored management . Serum biomarkers may assist clinicians in risk stratification and decision-making processes . An ideal biomarker in patients with sepsis should improve early diagnosis and predict early deterioration toward organ failure and eventually death, thereby identifying patients requiring additional aggressive treatments . Owing to a lack of specificity or sensitivity or both (for example, C-reactive protein (CRP) and procalcitonin (PCT) [10, 12]) or to a narrow time window of expression (for example, interleukin-6 (IL-6) and IL-8 ), currently used biomarkers do not fulfill such requirements. Therefore, further efforts are needed to identify novel sepsis biomarkers.
Pancreatic stone protein/regenerating protein (PSP/reg) is constitutively secreted by pancreatic acinar cells into pancreatic juice along with zymogens and is also secreted by subsets of intestinal and gastric cells . Although its precise physiological roles remain only partly defined, it appears to have protective functions by promoting cellular proliferative responses during beta-cell regenerative processes and epithelial repair . PSP/reg is upregulated during acute and chronic pancreatitis; in animals, its expression may be induced by stress conditions in the absence of any pancreatic inflammation. In a recent clinical study, serum concentrations of PSP/reg were found to be markedly elevated after trauma, and PSP/reg concentrations showed a close correlation with the severity of post-trauma infection . Furthermore, PSP/reg was found to bind to polymorphonuclear cells and seemed to induce or maintain their activation or both; thus, PSP/reg might serve as an acute-phase protein .
We therefore hypothesized that PSP/reg concentration may represent a potential biomarker of sepsis-related inflammation. To address this hypothesis, we prospectively measured plasma concentrations of PSP/reg within 24 hours of ICU admission in 107 patients with clinically diagnosed forms of severe infections. (Some of the results of these studies have been reported in the form of an abstract .)
Materials and methods
This study was performed between February 2008 and June 2010 in a 32-bed adult medico-surgical ICU of a community and referral university hospital. Patients who were at least 18 years old were evaluated within 24 hours of ICU admission for severe sepsis or septic shock. Owing to organizational constraints, inclusion was prospective but could not be strictly consecutive. The study was approved by the Institutional Review Board (Commission cantonale [VD] d'éthique de la recherche sur l'être humain, Lausanne, Switzerland). Written informed consent was obtained from patients or relatives. Infections, sepsis, severe sepsis, and septic shock were defined according to commonly used criteria  (Additional file 1). Patients were followed until death or discharge from the hospital. In-hospital mortality was the primary endpoint.
In addition to recording clinical variables collected from the computerized information system (Metavision; IMDsoft, Tel Aviv, Israel), we recorded the age, sex, admission category, origin (home, emergency room, or ward), and McCabe score of each patient . Severity of illness was evaluated on the first day in the ICU by using the Simplified Acute Physiology Score (SAPS) II  and III  and the Acute Physiology and Chronic Health Evaluation II (APACHE II) score . Organ dysfunction was evaluated by the Sequential Organ Failure Assessment (SOFA) score . Severe comorbidities were described by using definitions of the APACHE II score and SAPS II and III.
Measurement of plasma biomarker concentrations
At the time of enrollment, heparinized plasma was obtained from each patient for measurements of biomarkers. (Detailed measurement protocols are presented in Additional file 1.) PSP/reg was quantified by using an isoform-specific enzyme-linked immunosorbent assay as described previously . Briefly, plasma samples were incubated with plates precoated with guinea pig anti-PSP/reg antibody. Rabbit anti-PSP/reg was added and subsequently detected by phosphatase-conjugated anti-rabbit immunglobulin G. This assay had a detection limit of less than 0.1 ng/mL and an inter-plate variance of less than 10% .
Continuous variables are reported as mean and standard deviation (SD) or medians and interquartile ranges (IQRs) as indicated. Categorical variables are reported as frequencies and percentages. Because the distributions of the biomarkers were skewed, continuous variables between severity of infection or between survivors and non-survivors were compared by using non-parametric two-sided Wilcoxon-Mann-Whitney rank sum tests. APACHE II, SAPS II and III, and SOFA scores are expressed as mean and SD.
Receiver operating characteristic (ROC) curves using concentrations of acute-phase proteins (CRP, PCT, and PSP/reg), pro-inflammatory cytokines (IL-6, IL-8, and IL-10), and acute severity scores (APACHE II and SAPS II and III) as independent variables and mortality as a dependent variable were computed first for the entire population and then specifically for patients with septic shock only. From these curves, we computed areas under the curve (AUCs) and 95% confidence intervals (CIs) to assess the discrimination ability of each marker for predictive purposes. Multiple logistic regression analysis and age-adjusted predicted hospital mortality (expressed as age-adjusted beta regression coefficients) were used to assess the relationship (for example, linearity and distribution) between biomarker concentrations and in-hospital mortality. Finally, we estimated the odds ratios (ORs) for mortality and trends across biomarker quartiles. All P values were two-sided, and statistical significance was set at a P value of less than 0.05. We used Stata (version 11.2; StataCorp LP, College Station, TX, USA) for data processing and analyses.
Patient characteristics, by sepsis severity (n = 107)
( n = 107)
( n = 33)
( n = 74)
Age in years, mean ± SD
59 ± 17.5
55 ± 20
61 ± 16
Community (home/emergency room)
Nosocomial (hospital transfer)
Referral from other hospital
Chronic obstructive pulmonary disease
End-stage renal disease
Score, mean ± SD
30 ± 8
27 ± 86
31 ± 8
71 ± 17
65 ± 16
74 ± 17
76 ± 18
67 ± 21
80 ± 15
SOFA (day 1)
11 ± 3
11 ± 3
11 ± 3
Ultimately fatal (< 5 years)
Rapid fatal (< 6 months)
CNS and ENT
Gram-positive (number of positive blood cultures)
Staphylococcus aureus (8)
Streptococcus pyogenes (2)
Streptococcus pneumoniae (8)
Escherichia coli (14)
Other Enterobacteriacae (5)
Pseudomonas aeruginosa (5)
Candida albicans (1)
Plasma levels of CRP, PCT, PSP/reg, and inflammatory cytokines in patients with severe sepsis and septic shock
Plasma concentrations of biomarkers and severity scores, by sepsis severity
Biomarker or severity scoring system
All (n= 107)
Severe sepsis (n= 33)
Septic shock (n= 74)
PSP/reg was further measured in the plasma of burned patients who were previously admitted to our ICU and in whom trace element supplementation resulted in improved clinical outcome, including fewer pulmonary infections and better wound healing . In these 20 patients with severe non-infectious inflammation (mean age of 43 ± 16 years, mean total surface body area burned of 45% ± 22%, and median SAPS II of 32 and IQR of 14), the median PSP/reg within the first 24 hours of admission was 13.0 ng/mL (IQR of 4.8). Figure S3 of Additional file 4 displays the individual values of PSP/reg in these patients compared with those with severe sepsis and septic shock.
Association between plasma levels of CRP, PCT, PSP/reg, and inflammatory cytokines and in-hospital mortality
Plasma concentrations of biomarkers and severity scores, by survival status
Biomarker or severity scoring system
All (n= 107)
Death ( n = 22)
Survival ( n = 85)
Biomarkers and severity scores as predictors of in-hospital mortality
The age-adjusted beta regression coefficients - that is, the change in probability of in-hospital mortality per standard unit (one SD) change in biomarker concentration - were 0.16 (SD of 0.07) per 100 ng/mL increase of PSP/reg (P = 0.03), 0.17 (SD of 0.10) per 50 ng/mL increase of IL-6 (P = 0.08), and -0.00076 (SD of 0.0587) per 10 ng/mL increase of PCT (P = 0.99). When restricted to patients with septic shock, the age-adjusted beta regression coefficients were 0.16 (SD of 0.08) per 100 ng/mL increase of PSP/reg (P = 0.048), 0.15 (SD of 0.10) per 50 ng/mL increase of IL-6 (P = 0.15), and -0.0167 (SD of 0.062) per 10 ng/mL increase of PCT (P = 0.79).
Moreover, in contrast to IL-6 and PCT, the age-adjusted ORs (95% CIs) of mortality among patients with septic shock increased continuously across PSP/reg quartiles: PSP/reg OR 1.0 [reference group], 1.5 (0.19 to 10.0), 5.1 (0.8 to 32.0), and 6.4 (0.96 to 42.0), respectively (test for trend P = 0.02). For IL-6 quartiles, the age-adjusted ORs (95% CIs) for mortality among patients with septic shock were 1.0 [reference group], 2.0 (0.36 to 10.0), 1.3 (0.23 to 7.5), and 2.4 (0.45 to 12.0), respectively (test for trend P = 0.41), whereas, for PCT, the corresponding values were 1.0 [reference group], 0.4 (0.7 to 2.0), 0.7 (0.16 to 3.1), and 0.4 (0.08 to 1.9), respectively (test for trend P = 0.35).
Our results suggest that PSP/reg, a novel acute-phase protein, measured within 24 hours of ICU admission, may predict the risk of mortality in patients with severe sepsis and septic shock. PSP/reg was identified in patients with pancreatitis and further associated with islet regeneration [13, 23]. The findings that its expression was not restricted to the pancreas [24, 25] and that it can be induced by stress in animals  opened the way to investigate its role as a potential acute-phase protein. A recent study in 83 trauma patients reported that PSP/reg concentrations were 15-fold higher from baseline (5 to 15 ng/mL) in patients developing septic complications .
Our results suggest that PSP/reg, measured within 24 hours of ICU admission, may be used as a biomarker to identify septic patients at highest risk of death. PSP/reg performed better than CRP and PCT, which are widely used to diagnose infection but which, owing to their poor accuracy in this indication, should not be used to predict disease outcome [10, 12, 27, 28]. A similar observation was recently reported in a cohort of 101 patients with ventilator-associated pneumonia . In this cohort, PSP/reg measured after 7 days of mechanical ventilation predicted subsequent organ failure development and, eventually, outcome. A major advantage of PSP/reg over the currently available predictors of disease evolution, such as cytokines, may be its presence in the plasma of all septic patients at the time of ICU admission. This sharply contrasts with the pro-inflammatory cytokines tumor necrosis factor-alpha, IL-1, and IL-6, which showed very good predictive values in dedicated trials [30, 31] but whose use in daily life was finally hampered by their short window of expression in plasma, making them difficult to interpret at the bedside in a population of patients in whom the time between the onset of sepsis and the blood test cannot be standardized .
The strength of our study is that it is representative of the usual population of patients admitted to a mixed ICU. Inclusion criteria were simple, making the setting correspond to what any clinician could encounter in his or her daily practice, increasing the chances of PSP/reg measurement implementation at the bedside to predict patient outcome. The small number of patients may explain the absence of a correlation of APACHE II or SAPS II with mortality in a cohort of patients with severe infections . In this context, the strong association of PSP/reg with mortality might be viewed as indirect evidence of its better specificity for sepsis. The fact that stratification of patients with sepsis could occur within 24 hours of admission would eventually exclude from stratification most patients without a clear diagnosis of sepsis (this strategy resulted in a low number of non-documented infections in our study) as well as those dying rapidly despite resuscitation and for whom very early evaluation of prognosis (< 18 hours) would probably not result in a different initial management .
This single-center study also has several limitations. First, since 18 (10%) patients died before consent could be obtained, selection bias cannot be excluded. This may also have contributed to the lower mortality rate of our patients with septic shock compared with rates reported earlier [2–4]. Second, owing to organizational constraints, patient recruitment was restricted to periods when co-investigators worked as attending physicians. Third, since the purpose of the study was to explore the accuracy of PSP/reg compared with that of other commonly used or studied predictors (such as pro-inflammatory cytokines) in a homogenous population of patients with a definite diagnosis of sepsis at the time of ICU admission and not between populations of septic and non-septic patients, patients without sepsis were not included. This may have resulted in an apparently modest absolute predicting power (ROC of 0.65). Finally, owing to the relatively small number of patients, these results require further validation in a larger and preferentially multicentric cohort of patients with sepsis.
Though preliminary, our data still suggest that PSP/reg determination could be useful in the stratification of patients with septic shock. After initial resuscitation, PSP/reg blood levels that are measured within 24 hours of ICU admission may help to detect patients at high risk of death and to reduce the number of those susceptible to receive new and costly adjunctive treatments, such as specific immunotherapy , anti-cytokines , or extra-corporeal lipopolysaccharide removal .
We conclude that a single measurement of PSP/reg concentration within 24 hours of ICU admission stratifies patients with sepsis according to severity of infection and risk of death. If our findings are confirmed by further studies, this promising biomarker may help physicians to tailor treatments to individual patients according to risk of death.
Commonly used biomarkers, such as C-reactive protein and procalcitonin, are insufficiently sensitive or specific to stratify patients with sepsis.
Pancreatic stone protein/regenerating protein (PSP/reg) is an accurate biomarker to stratify septic patients admitted to intensive care units (ICUs).
PSP/reg blood measurement within 24 hours of ICU admission predicts risk of death more accurately than procalcitonin and pro-inflammatory cytokines.
PSP/reg may help to identify, among all patients admitted for sepsis, those most susceptible to benefit from aggressive management.
- APACHE II:
Acute Physiology and Chronic Health Evaluation II
area under the curve
intensive care unit
pancreatic stone protein/regenerating protein
receiver operating characteristic
Simplified Acute Physiology Score
Sequential Organ Failure Assessment.
We thank Laurence Leone for outstanding technical assistance and the members of the Lausanne Sepsis Group - Anne Angelilo-Scherrer, Jacques Bille, Philippe Jolliet, Philippe Moreillon, Guy Prod'hom, Thierry Roger, and Pierre-Yves Bochud - for their constructive support. This study was funded by an unrestricted grant from the 'Loterie Romande' and the 'Fondation pour la Recherche en Soins Intensifs'. Y-AQ is supported by Swiss National Science Foundation (SNF)/Swiss Medical Association (FMH) grant PASMP3-123226 and a grant from the SICPA Foundation. LL is supported by the SNF (grants 32000-118174/1 and 310030-135394/1). IG is supported by an SNF grant (SNF 33CM30-124087/1). TC is supported by grants from the SNF (310030-118266), the Leenaards Foundation, and the Santos-Suarez Foundation for Medical Research.
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