Combined SuPAR and qSOFA for predicting 28-day mortality in sepsis

doi:10.21203/rs.3.rs-195966/v1

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Combined SuPAR and qSOFA for predicting 28-day mortality in sepsis

https://doi.org/10.21203/rs.3.rs-195966/v1

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Background and Purpose

To determine the prognostic performance of soluble urokinase-type plasminogen activator receptor (suPAR) and quick Sequential Organ Failure Assessment (qSOFA) in predicting the 28-day mortality of sepsis patients admitted to the emergency department (ED).

Methods

A prospective, single-center observational study was conducted between June 2018 and June 2019. In total, 175 patients with sepsis and septic shock admitted to the ED were enrolled based on the Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3). We assessed the qSOFA score on ED admission and measured serum suPAR levels by quantitative enzyme-linked immunosorbent assay. Kaplan–Meier survival curves and areas under the receiver operating characteristic (ROC) curve for 28-day mortality were calculated. We estimated category-free net reclassification improvement (NRI) when suPAR was added to qSOFA.

Results

Increased suPAR levels were significantly associated with 28-day mortality (1337(962–2003) pg/ml in survivors vs. 1742(1238–2514) pg/ml in non-survivors, p = 0.011) and with sepsis severity (1337(986–1979) in sepsis vs. 1742(1215–2649) in septic shock, p = 0.039). Kaplan–Meier curves showed that suPAR ≥ 1382 pg/mL was associated with significantly higher 28-day mortality risk(P = 0.0028). The area under the curve (AUC) for the prediction of 28-day mortality was 0.646 for suPAR, 0.832 for qSOFA, and 0.860 for combined suPAR and qSOFA. Serum suPAR did not significantly increase the AUC of the basic qSOFA, but a model containing suPAR and qSOFA had a continuous NRI of 11% (95% CI :3.5–18.5% ; p = 0.004).

Conclusion

Serum suPAR is associated with sepsis severity and 28-day mortality. Adding suPAR to qSOFA may increase the ROC curve area and improve predictive value of qSOFA for outcome.

Infectious Diseases

Critical Care & Emergency Medicine

Soluble urokinase-type plasminogen activator receptor

quick Sequential Organ Failure Assessment

combined model

sepsis

28-day mortality

Sepsis [1] is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection and is a common cause of morbidity and mortality worldwide. The annual incidence of sepsis has been estimated at approximately 31.5 million cases globally, with 5.3 million deaths per year [2]. The early identification of patients with adverse outcomes and aggressive treatment initiatives has decreased mortality in sepsis [3]. Therefore, the Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3) focused on organ function and emphasized the incorporation of the Sequential Organ Failure Assessment (SOFA) score into the new definition of sepsis [4]. However, SOFA requires multiple laboratory tests and thereby increases the difficulty of detection in emergency department (ED) settings [5]. By contrast, the quick SOFA (qSOFA) provides simple bedside criteria to identify adult patients with suspected infection who are likely to have poor outcomes [1], especially in pre-ED settings. It does not require laboratory tests and can be assessed quickly and repeatedly. But in a recent editorial, qSOFA was described as an early warning system that cannot replace clinical evaluation [6] and has limited utility in early prognostication in high-mortality populations with sepsis. Used at the suggested cut-off ≥ 2, qSOFA showed low sensitivity and high specificity [7].

Existing biomarkers fall short of the ideal accuracy for predicting sepsis mortality [8, 9]. There is an urgent need to identify a simple, accurate, and effective biomarker to predict mortality in sepsis.

SuPAR is the soluble form of the cell membrane-bound urokinase plasminogen activator receptor (uPAR), which is expressed on various cell types, including neutrophils, lymphocytes, monocytes, endothelial cells, and tumor cells.

Donadello et al. [10] suggested that high levels of suPAR correlated with morbidity and outcome, supporting the value of suPAR as a prognostic biomarker in various cohorts of infected patients. A meta-analysis by Huang et al. [11] found that elevated suPAR levels are associated with a high risk of poor outcomes in sepsis. And studies have found that serum suPAR concentrations remained stable for days or weeks in critically ill patients [12, 13].

Although elevated suPAR levels in the initial stage of sepsis are associated with a high risk of death, the value of using suPAR alone to predict prognosis in sepsis is still limited. Hall et al. [14] suggested that it will also be important to compare the performance of suPAR with that of other biomarkers and to evaluate the role of suPAR in combination with existing severity of illness scores.

However, few studies have focused on the combination of suPAR and qSOFA in predicting the mortality of sepsis patients in an emergency setting. The aim of this study was to determine the prognostic accuracy of suPAR combined with qSOFA in predicting the mortality of sepsis patients first admitted to the ED in China.

Study population

This prospective, observational study was conducted during the period of June 2018 through June 2019 among patients hospitalized in the ED of Renji Hospital (South Campus ) affiliated to Shanghai Jiaotong University School of Medicine, a university tertiary hospital with approximately 120,000 ED visitors per year. 190 consecutive non-traumatic patients who fulfilled the Sepsis-3 criteria were enrolled in the study and eventual 175 patients included in the analysis and divided into non-survivors and survivors by 28-day mortality. The treatment and all methods were performed in accordance with the relevant guidelines and regulations of Sepsis 3.0.

Sepsis was defined by the following criteria: infection + SOFA score ≥ 2.

Septic shock should be clinically identified by a requirement for vasopressor to maintain a mean arterial pressure of 65 mmHg or greater and serum lactate level greater than 2 mmol/L (> 18 mg/dL) in the absence of hypovolemia.

The clinical criteria of quick SOFA (qSOFA) were as follows : respiratory rate ≥ 22/min, altered mentation, or systolic blood pressure ≤ 100 mmHg.

The exclusion criteria were age < 18 years or the presence of any of the following: pregnancy, malignant tumor, or end-stage disease. We also excluded patients if they or their relatives declined participation in the study.

Data collection

Data including age, sex, underlying diseases, infection site, clinical data, severity of illness scores (including qSOFA, SOFA and Acute Physiology and Chronic Health Evaluation [APACHE] II scores), and laboratory data of all enrolled patients were recorded.

Measurement of serum suPAR

Peripheral venous blood samples were collected within 24 h of admission prior to intravenous antibiotics in sterile, pro-coagulation tubes and processed within 2 h after venipuncture. After standing for 30 minutes, they were centrifuged at 1914 × g for 10 min to separate the serum from the cellular components. The serum samples were stored at − 80°C for batch analysis[15].

Serum suPAR levels were measured using quantitative enzyme-linked immunosorbent assay (ELISA) kits (DUP00; R&D Systems, Minneapolis, MN, USA) in duplicate as instructed by the manufacturer. The detection sensitivity was 33 pg/mL, and the intra-assay and inter-assay coefficients of variation were < 8%.

Statistical analysis

Continuous variables are expressed as median (interquartile range), and categorical variables are expressed as number (percentage). We used the Fisher’s exact test to compare categorical variables and t-test or Mann–Whitney U test for continuous variables and abnormal distributional variables between two groups. Receiver operating characteristic (ROC) analysis was performed to compare survivors with non-survivors by Sigma Plot 14.0, and cut-off values were calculated according to Youden’s index. Areas under the ROC curve (AUCs), optimal threshold values, sensitivity, and specificity were calculated, the sensitivities and specificities were further used to calculate the positive and negative likelihood ratios.

Curves were compared by using the log-rank test. A two-sided p value < 0.05 was considered statistically significant; confidence intervals (CIs) were set at 95%. To compare the qSOFA models with the suPAR and qSOFA models, the additive information on clinical variables was evaluated by the category-free net reclassification improvement (NRI) [16]. Statistical analyses were performed using the GraphPad Prism version 8.0 software (GraphPad Software, La Jolla, CA, USA) and R statistical software (Foundation for Statistical Computing, Vienna, Austria) version 3.4.0.

Demographic and clinical characteristics of total enrolled patients with sepsis

From June 2018 to June 2019, 190 patients were screened for eligibility. Of these, 15 patients were excluded (1 patient was unable to contact a legal representative, 5 patients declined to participate, and 9 patients’ blood samples were not available in a timely manner on admission). Finally, 175 patients were included in the analysis and divided into non-survivors and survivors (Table 1).

Table 1

Characteristics of the total septic patients at baseline
Characteristic	Total (n = 175)	Non-survivors(n = 41)	Survivors(n = 134)
Age(years) median(IQR)	66(53–77)	69(53–81)	66(53–75)
Sex (male) n(%)	110(62.9)	26(63.4)	84(62.7)
Underlying diseases n(%)
Hypertension	71(40.6)	21(51.2)	50(37.3)
Diabetes mellitus	51(29.1)	8(19.5)	43(32.1)
Coronary heart disease	33(18.9)	17(41.5)	16(11.9)
Cerebral infarction	35(20)	10(24.4)	25(18.7)
Chronic pulmonary disease	15(8.6)	6(14.6)	9(6.7)
Autoimmune disease	34(19.4)	17(41.5)	17(12.7)
Surgical history	36(20.6)	9(22)	27(21.1)
Infection site n(%)
Respiratory tract infection	105(60)	39(95.1)	66(49.3)
Urinary tract infection	36(20.6)	2(4.9)	34(25.4)
Gastrointestinal infection	15(8.6)	2(4.9)	13(9.7)
Hepatobiliary system infection	18(10.3)	1(2.4)	17(12.7)
Skin infection	13(7.4)	4(9.8)	9(6.7)
Intracranial infection	5(2.9)	0	5(3.7)
Bloodstream infection	41(23.4)	5(12.2)	36(26.9)
Unknown origin	10(5.7)	1(2.4)	9(6.7)
Severity related variable n(%) or median(IQR)
Mechanical ventilation	44(25.1)	31(75.6)	13(9.7)
Vasopressor use	53(30.3)	35(85.4)	18(13.4)
CRRT	11(6.3)	5(12.2)	6(4.5)
qSOFA	1(0–2)	3(1.5-3)	1(0–1)
SOFA	4(2–8)	10(7–14)	3(2–6)
APACHE II	14(9–24)	29(21-31.5)	12(8–18)
Septic shock	49(28)	35(85.4)	14(10.4)
Clinical variable median(IQR)
WBC (×10⁹/L)	10.12(6.70–13.40)	12.05(7.19–14.60)	9.56(6.48–13.14)
Hb (g/L)	123(107–137)	119(95–133)	125(108–137)
Plt (×10⁹/L)	161(99–217)	155(64–215)	166(107–217)
CRP (mg/L)	123(39–200)	118(43–190)	125(33–200)
PCT (ng/ml)	1.94(0.46–11.33)	1.75(0.46–7.77)	2.07(0.45–12.21)
Lactate (mmol/L)	2.39(1.60–3.48)	2.80(2.10–4.50)	2.20(1.50–3.12)
Creatinine(umol/L)	91(64–139)	109(60–175)	86(64–126)
suPAR (pg/ml)	1449(1051–2206)	1742(1238–2514)	1337(962–2003)
Outcome variable n(%)
28-day mortality	41(23.4)

The analysis included 134 survivors and 41 non-survivors. The non-survivors group had a more proportion of coronary heart disease (41.5% vs. 11.9%), autoimmune disease (41.5% vs. 12.7%) and respiratory tract infection(95.1% vs. 49.3%).In addition, non-survivors were more likely to be on mechanical ventilation (75.6% vs.9.7%), vasopressor use(85.4% vs.13.4%), and CRRT(12.2% vs. 4.5%) compared with survivors. Furthermore, non-survivors had higher qSOFA, SOFA ,and APACHII score, as well as high lactate levels and suPAR compared with survivors. (3 vs. 1), SOFA score (10 vs. 3), APACHE II score (29 vs. 12), lactate (2.80 vs. 2.20 mmol/L), and higher suPAR(1742 [1238–2514] vs. 1337 [962–2003]pg/mL) compared with survivors. And the total 28-day mortality was 23.4% (41/175).

Serum suPAR level in sepsis and septic shock groups vs. survivor and non-survivor groups

Comparison of suPAR in patients with sepsis and septic shock, survivors and non-survivors is shown in Fig. 1. Serum suPAR levels were significantly higher in the septic shock and non-survivor groups than in the sepsis and survivor groups (1742(1215–2649) pg/mL and 1742(1238–2514) pg/mL vs.(1337(986–1979)pg/mL and (1337(962–2003) pg/mL, p = 0.0039 and p = 0.011, respectively).

Value of suPAR in predicting 28-day mortality in patients with sepsis

In this study, Kaplan–Meier curves were used to assess the value of suPAR in the prediction of 28-day mortality in patients with sepsis (Fig. 2). The 28-day mortality in high cut-off of suPAR categories (≥ 1382pg/mL) was significantly higher than in low cut-off of suPAR categories (< 1382 pg/mL) (log-rank, p = 0.0028).

Prognostic value of combination suPAR and qSOFA in predicting 28-day mortality in sepsis patients

Table 2 and Fig. 3 shows the ROC analysis for the combination of suPAR and qSOFA and qSOFA alone in predicting the 28-day mortality in sepsis patients. AUCs of various parameters for predicting 28-day mortality in patients with sepsis based on Sepsis-3 are shown in Table 2. The AUC of using a combination of suPAR and qSOFA (0.860) was better than that of using qSOFA (0.832) or suPAR (0.646) alone, and also better than those of using suPAR combined with CRP (0.654) or PCT (0.653), The differences were statistically significant among suPAR + qSOFA compared with suPAR,suPAR + CRP and suPAR + PCT, (P༜0.001༌respectively) but not statistically significant compared with qSOFA (p = 0.082). A model containing suPAR in addition to qSOFA had a continuous NRI of 11% (95% CI :3.5–18.5% ; p = 0.004) (data were not shown). And there was no significant difference between AUC of combined or single model with CHD and without CHD (P = 0.447, data was not shown), on account of that suPAR is independently associated with the presence and severity of heart failure.

Table 2

Results of the ROC analysis of various variables for predicting 28-d mortality of sepsis
Variable	AUC(95%CI)	P value*	Cut-off(≥)	Youden’s index	Sens.	Spec.	LR+	LR-
suPAR (pg/ml)	0.646(0.552–0.741)	༜0.001	1382	0.261	0.732	0.53	0.322	0.777
qSOFA	0.832(0.692–0.923)	0.082	1.5	0.517	0.756	0.761	0.491	0.909
suPAR + qSOFA	0.860(0.795–0.914)		0.335	0.627	0.732	0.895	0.680	0.916
suPAR + CRP	0.654(0.561–0.740)	༜0.001	0.223	0.276	0.634	0.642	0.351	0.852
suPAR + PCT	0.653(0.548–0.745)	༜0.001	0.211	0.323	0.756	0.567	0.348	0.884
*: vs.suPAR + qSOFA

This paper is the first to investigate suPAR levels combined with the qSOFA score in patients with sepsis based on Sepsis-3. We developed a simple risk stratification system for patients with sepsis by taking into consideration qSOFA score and the serum biomarker suPAR .

In the current study, we found that suPAR performed better predictive value for 28-day hospital mortality of patients with sepsis or septic shock than commonly used biomarkers, such as CRP and PCT. Moreover, the predictive abilities were slightly improved when suPAR combined with qSOFA scores.

Sepsis is a physiopathological process rather than a specific syndrome[17], and it is too complex and cannot be simply described by a single measure. For this reason, neither clinical nor biological markers have been demonstrated to be perfect prognostic tools. Severity scores such as the Acute Physiology and Chronic Health Evaluation (APACHE) II score and Sequential Organ Failure Assessment (SOFA) score are the gold standard for severity assessment of critically ill patients [18]. However, the assessment of scoring systems to guide decision making in sepsis is sophisticated and is not readily available in pre-ED.

Recently, some authors reported that qSOFA could be a useful tool in hospital ED settings outside the intensive care unit. In this case, qSOFA could predict death of sepsis patients, but it could be overcome by rapid and accurate laboratory diagnostic tests [19]. qSOFA score with a cut-off value of ≥ 2 showed a low sensitivity and high specificity. Our study found that the AUC of qSOFA alone was 0.832 for 28-day mortality. Furthermore, the present study showed that qSOFA alone has a low post-test probability that increased significantly when associated with PCT [7]. In the analysis by Giamarellos-Bourboulis et al [20], qSOFA score had inadequate sensitivity for early risk assessment.

Classical biomarkers have not been shown to be better than generic scores in predicting outcome in septic patients [21]. Many studies focus on the prognostic value of suPAR which has been proposed as a biomarker for the risk of death. Early increase in suPAR has also been reported to be strongly associated with risk of in-hospital-, 30-day-, and 90-day mortality in sepsis patients and correlated with sepsis severity [22–24]. In our study, we found that serum suPAR levels were significantly higher in the septic shock and non-survivor groups than in the sepsis and survivor groups. Our results are consistent with those of previous studies. The AUC for suPAR in predicting in-hospital mortality ranges from 0.67 to 0.84 [17, 23, 25, 26]. Several studies have showed the superiority of suPAR over conventional biomarkers such as CRP and PCT [13, 25, 27–29]. Consistent with previous reports, the AUC for suPAR of out study to predict mortality was 0.646 which was also better than CRP and PCT(0.483 vs 0.470).

Kaplan–Meier curves showed that suPAR ≥ 1382 pg/mL was associated with significantly higher 28-day mortality risk; this threshold value is identical to that reported in prior studies [17, 30].

Based on the above analysis, we indicate that suPAR may provide a promising prognostic biomarker in sepsis.

There were several studies of suPAR combined with other indicators or qSOFA combined with other indicators in prediction of mortality of infected patients. Kofoed et al. [31] demonstrated that suPAR levels had a better prognostic value than PCT and CRP, equal to that of the admission SOFA score and almost as good as that of the Simplified Acute Physiology Score( SAPS ) II score and that the combination of suPAR and age had a better prognostic value than the SAPS II score alone. Julián-Jiménez et al found that qSOFA scores achieved better results for 30-day mortality than systemic inflammatory response syndrome, and that qSOFA plus mid regional pro-adrenomedullin [MR-proADM] could increase the predictive power in elderly patients visit ED due to infections than qSOFA alone[32].

There has been no report on the prognostic value of combining suPAR and qSOFA. We propose to improve prognostication of 28-day mortality of sepsis by using the qSOFA score combined with suPAR, a serum biomarker that is easily performed on-site and provides information within 1 h [33]. Our results show that the AUC of the combination of suPAR and qSOFA was better than that of qSOFA or suPAR alone and combined model(suPAR + CRP and suPAR + PCT).

There is a fact that suPAR is a non-specific inflammatory marker and a strong and independent predictor of mortality in patients with CHF[34], Data presented in Tabel 1 showed that non-survivors compared with survivors included more patients with coronary heart disease (41.5% vs. 11.9%). So we assessed the ROC of the combined model and single model that was no significant difference between two groups stratified by CHD and without CHD (P = 0.447,data was not shown).

There were some limitations of ROC curves in evaluating biomarkers [35]. Thus, the net reclassification improvement (NRI) was applied to estimate the strength of associations in this study .The NRI captures the relative improvement in classification associated with the additional predictive variable, while explicitly balancing trade off between changes in sensitivity and specificity. NRI is the sum of 2 percentages with different denominators and hence, is reported as a proportion (possible range, − 2.0 to 2.0)[36].Although serum suPAR did not significantly increase the AUC of the basic qSOFA, a model containing suPAR in addition to qSOFA had a continuous NRI of 11% (95% CI: 3.5–18.5%, p = 0.004). In other words, the addition of suPAR to the clinical predictive model (qSOFA) could improve its discrimination and predictive value for outcomes than qSOFA alone.

Our study has substantial limitations. First, serum suPAR levels were only detected at the time of admission; dynamic and follow-up changes (in response to treatment) were not investigated. Second, several comorbidities (e.g., diabetes mellitus[37], CHD[34]) may also influence the suPAR values, however this reflected a real world setting and we did a subgroup analysis according to the presence or absence of CHD. Finally, we did not examine the suPAR levels of healthy controls for comparison owing to limitations of funding and ethical considerations. Hence, the effects of changes in suPAR expression during the pathogenesis of sepsis should be investigated in future studies with a larger sample size. Further research is required to evaluate the predictive efficacy of suPAR in combination with other indicators.

We demonstrated that serum suPAR levels were associated with sepsis severity and 28-day mortality in patients with sepsis. The addition of suPAR to the clinical model (qSOFA) may increased the ROC curve area and improve predictive value of qSOFA for outcome.

suPAR, soluble urokinase-type plasminogen activator receptor; qSOFA, quick Sequential Organ Failure Assessment; SOFA, Sequential Organ Failure Assessment; ED, emergency department; NRI, net reclassification improvement; BNP, B-type natriuretic peptide; CRP, C-reactive protein; PCT, procalcitonin; WBC, Whole blood leukocyte count; OR, odds ratio; CI, confidence interval; IQR, Interquartile range; Sepsis-3, Third International Consensus Definitions for Sepsis and Septic Shock; APACHE, Acute Physiology and Chronic Health Evaluation; SAPS, Simplified Acute Physiology Score ; MR-proADM, Mid regional pro-adrenomedullin; CHD, coronary heart disease; CHF, congestive heart failure

Ethics approval and consent to participate：The study was approved by the Ethics Committee of Renji Hospital Affiliated to Shanghai Jiaotong University School of Medicine (ethics NO.:2016-109k) and the 1964 Helsinki declaration and its later amendments or comparable ethical standards, and all patients and legally authorized representative of deceased/non-survivor patients provided written informed consent for the study.

Consent for publication：Not applicable.

Availability of data and materials：The datasets used and/or analysed during the current study available from the corresponding author on reasonable request.

Competing interests: All of the authors have no competing interests.
Funding: Not applicable.
Authors' contributions: LW and CT contributed equally to the writing of this manuscript. SH and YC participated in data interpretation and statistical analysis. CX revised the whole manuscript. All authors read and approved the final manuscript.

Acknowledgements: The authors thank professor Shuang Ye and Dr. Chenyu Fan for their excellent assistance with study coordination and laboratory analyses.

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No competing interests reported.

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Combined SuPAR and qSOFA for predicting 28-day mortality in sepsis

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Abstract

Background and Purpose

Methods

Results

Conclusion

Figures

Background

Methods

Study population

Data collection

Measurement of serum suPAR

Statistical analysis

Results

Demographic and clinical characteristics of total enrolled patients with sepsis

Serum suPAR level in sepsis and septic shock groups vs. survivor and non-survivor groups

Value of suPAR in predicting 28-day mortality in patients with sepsis

Prognostic value of combination suPAR and qSOFA in predicting 28-day mortality in sepsis patients

Discussion

Limitations

Conclusions

Abbreviations

Declarations

References

Additional Declarations

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