Abstract
Objective
Severe infections are a major cause of morbidity and mortality in patients with systemic lupus erythematosus (SLE). Our primary objective was to use data from a large Spanish cohort to develop a risk score for severe infection in SLE, the SLE Severe Infection Score (SLESIS) and to validate SLESIS in a separate cohort of 699 British patients.
Design and setting
Retrospective longitudinal study in a specialist tertiary care clinic in London, UK.
Participants
Patients fulfilling international classification criteria for SLE (n=209). This included 98 patients who had suffered severe infections (defined as infection leading to hospitalisation and/or death) and 111 randomly selected patients who had never suffered severe infections.
Outcomes
We retrospectively calculated SLESIS at diagnosis for all 209 patients. For the infection cases we also calculated SLESIS just prior to infection and compared it to SLESIS in 98 controls matched for disease duration. We carried out receiver operator characteristic (ROC) analysis to quantify predictive value of SLESIS for severe infection.
Results
Median SLESIS (IQR) at diagnosis was higher in the infection group than in the control group (4.27 (3.18) vs 2.55 (3.79), p=0.0008). Median SLESIS prior to infection was higher than at diagnosis (6.64 vs 4.27, p<0.001). In ROC analysis, predictive value of SLESIS just before the infection (area under the curve (AUC)=0.79) was higher than that of SLESIS at diagnosis (AUC=0.63).
Conclusions
We validated the association of SLESIS with severe infection in an independent cohort. Calculation of SLESIS at each clinic visit may help in management of infection risk in patients with SLE. Prospective studies are needed to confirm these findings.
Keywords: systemic lupus erythematosus, severe infection, risk score
Strengths and limitations of this study.
We developed an algorithm (Systemic Lupus Erythematosus Severe Infection Score (SLESIS)) designed to predict the risk of severe infections in patients with systemic lupus erythematosus (SLE) that could be a useful tool in clinical practice.
SLESIS was developed using data from a Spanish lupus registry (Spanish Society of Rheumatology Lupus Registry (RELESSER)) that includes almost 4000 patients with SLE.
We applied the algorithm in a British cohort of 699 patients with SLE in order to validate it.
The algorithm consists of seven variables that are all obtainable from information obtained in routine clinical practice.
We acknowledge several limitations: the retrospective design of the study, the different ethnicity in the Spanish and British populations and the Katz Index as an item of the score.
Introduction
Systemic lupus erythematosus (SLE) is a systemic autoimmune disease that mainly presents in women aged between 30 years and 50 years. Infection is a major cause of morbidity and mortality in patients with SLE, being responsible for 11%–45% of hospitalisations as well as 20%–55% of deaths, according to different studies.1–6
There are immunological and genetic disorders that predispose to the development of infections in patients with SLE.7 8 Respiratory tract infections are the most common infections in these patients, and bacteraemia the leading cause of mortality. Regarding the aetiology, pathogenic bacteria are most frequently involved in the infection, followed by viruses and fungi.9 10
There are several well-established risk factors for infection such as age at diagnosis, male sex, ethnicity and use of corticosteroids, among others; however, the independent contribution of each factor is not well understood.11–14 On the other hand, severe infections have been associated with decreased survival of patients with SLE, acting as an independent risk factor for mortality at 10 years after diagnosis.2–4 14
This information about the risk factors associated with infection in SLE has not yet been combined into tools to estimate the risk of severe infection in individual patients over time. The development of an algorithm for predicting the risk of severe infection could be very useful to monitor risk factors more closely in a weighted way. It could allow us to implement prophylactic measures such as vaccination in the highest-risk patients and to consider early intervention such as antibiotic therapy in this group of patients with the ultimate goal of reducing morbidity and improving survival.15–17 Similar scores to predict risk of severe infection have been developed and validated in patients with rheumatoid arthritis (RA) with encouraging results.18
In a recent original study from the Spanish Society of Rheumatology Lupus Registry (RELESSER), the authors studied 3658 patients with SLE, of whom 705 (19.3%) had suffered one or more severe infections. A multivariable Cox regression model for repeated events (Andersen-Gill) was used to define the impact of a range of demographic and clinical variables on the risk of developing severe infection, expressed as HR of developing severe infection for patients with each associated factor, compared with those without that factor.17 Seven factors had an HR more than 1.
In the study reported in the current paper these seven factors were used to generate a score—the Systemic Lupus Erythematosus Severe Infection Score (SLESIS), designed to predict the risk that a patient with lupus will develop a severe infection.
The overarching primary objective of the current study was to validate SLESIS in an independent population of patients with SLE from London, UK.
In the validation cohort, we aimed to answer three questions.
Does SLESIS at the time of diagnosis predict future severe infection?
In patients who suffer a severe infection, does SLESIS change between diagnosis and the time of infection?
Does SLESIS just prior to an infection predict future severe infection?
If (2) and (3) are true, it could support assessing SLESIS at every appointment rather than only at diagnosis.
Patients and methods
Development and definition of SLESIS
SLESIS was developed using variables related to infection from the RELESSER cohort of 3658 patients with SLE who meet ≥4 critera of the American College of Rheumatology (ACR) classification criteria for SLE. The variables, definitions and methodological characteristics of the RELESSER registry have previously been described in detail.19 20
Table 1 shows the seven factors that were found to be associated with increased risk of developing severe infection (defined as infection leading to hospitalisation and/or death) in the RELESSER paper17 together with HR for severe infection associated with each factor. There are four factors that are graded present or absent; age at diagnosis >46 years (HR = 1.12); Latin American ethnicity (HR=2.4); dose of corticosteroid ≥10 mg/day (HR = 1.33); and male sex (HR = 1.49). For each of these factors, the contribution to SLESIS is either 0 (if absent) or 1 × HR (if present).
Table 1.
Variables incorporated into SLESIS
| Variable | β coefficient | HR for severe infection | 95% CI |
| Age at diagnosis (>46 years) | 0.1163 | 1.12 | 1.07 to 1.18 |
| Latin American ethnicity | 0.427 | 2.40 | 2.29 to 2.5 |
| Current dose of corticosteroids ≥10 mg/day | 0.2878 | 1.33 | 1.15 to 1.55 |
| Sex (male) | 0.3692 | 1.49 | 1.22 to 1.81 |
| Previous hospitalisation for SLE | 1.0049 | 2.73 | 2.22 to 3.35 |
| Katz Index21 | 0.062 | 1.06 | 1.03 to 1.1 |
| Each previous severe infection | 0.8739 | 2.40 | 2.29 to 2.50 |
These HR values were derived from the retrospective analysis of 3658 Spanish patients described in ref [17].
SLE, systemic lupus erythematosus; SLESIS, Systemic Lupus Erythematosus Severe Infection Score.
One factor (Katz Index21 of disease severity) is a continuous variable. The contribution of this factor is its absolute value × 1.06 (its HR).
The other factors are previous hospitalisations for SLE (HR = 2.73) and previous severe infection (HR = 2.40). For these factors the contribution to SLESIS is the number of events × HR.
Thus SLESIS for a male Latin American patient, diagnosed at age 22 years, taking 12 mg prednisolone per day with a Katz Index of 2, two previous hospitalisations for SLE and no previous severe infections would be calculated as follows.
(0 × 1.12) + (1 × 2.4) + (1 × 1.33) + (1 × 1.49) + (2 × 1.06) + (2 × 2.73) + (0 × 2.40) = 11.31.
Conversely SLESIS for a female Chinese patient, diagnosed at age 50 years, taking 5 mg prednisolone per day with a Katz Index of 2, no previous hospitalisations for SLE and three previous severe infections would be calculated as follows.
(1 × 1.12) + (0 × 2.4) + (0 × 1.33) + (0 × 1.49) + (2 × 1.06) + (0 × 2.73) + (3 × 2.40) = 10.44.
Validation cohort
Validation was carried out in the lupus clinic at University College London Hospital (UCLH). All patients fulfilled the 1997 revised criteria of ACR for the classification of SLE.22 The clinic has been running continuously since 1979 and has records from 699 patients. Medical records of all the patients were reviewed to identify those who had suffered severe infections. Severe infection was defined as that leading to hospitalisation and/or death. Isolation of the causative agent was not required in every case, with final classification as an infection being made using standard clinical criteria as in the previous RELESSER Study.17 Only infections recorded during the follow-up period (ie, after the diagnosis of lupus) were included as outcomes.
We used a nested case-control design. We identified 98 patients who had suffered at least one severe infection and compared their medical records with those of 111 randomly selected patients with SLE who had never suffered from severe infections. By retrospective analysis of medical records, we obtained comprehensive information about demographic, clinical, serological and treatment factors in these two groups.
We calculated SLESIS for each of the 209 patients at the time of diagnosis. For each of the 98 patients with infection we also calculated SLESIS for the clinical assessment carried out at the last consultation prior to the infection. For comparison, we calculated SLESIS in 98 controls matched for disease duration, as follows. For each infection case we selected one control case from the 111 who had never suffered severe infections. For the control we calculated SLESIS at the time point after diagnosis corresponding to the duration after diagnosis when the matched case suffered severe infection.
Statistical analysis
Demographic and clinical characteristics were compared between patients who developed severe infection and patients who did not, using a Pearson χ2 for categorical variables or a Student’s t-test for normally distributed continuous variables (data expressed as mean±SD). For non-normally distributed variables, either a Mann-Whitney U test or a logarithmic transformation was performed, and data are expressed as median and IQR. Multivariable logistic regression analysis was performed to establish which factors were independently associated with severe infection.
We compared SLESIS scores between case and control groups using the Mann-Whitney U test. Receiver operator characteristics (ROC) analysis was used to define the area under the curve (AUC) for SLESIS at diagnosis and SLESIS just prior to infection. We also identified several possible cut-off scores for SLESIS with different combinations of specificity and sensitivity for severe infection.
The STATA for Windows statistical software package (V.13.1) was used for all statistical analysis. Significance was defined as p<0.05.
Patients and/or public involvement
Patients and/or public were not involved in this study.
Results
Table 2 shows a comparison of 98 patients (14% of the total cohort of 699 patients) who developed severe infection and a control group of 111 patients who never suffered from severe infection. These two groups did not differ in age, sex or ethnicity.
Table 2.
Descriptive data: patients with systemic lupus erythematosus (SLE) with infection versus without infection
| Study (infection) group (n=98) | Control (non-infection) group (n=111) | P values | |
| Gender, n (%) | 90 (92) | 103 (93) | |
| Female (male) | 8 (8) | 8 (7) | ns |
| Median age at diagnosis of SLE (IQR), years | 30.5 (27) | 31 (18) | ns |
| Median age at time of infection (IQR), years | 43 (25) | Not applicable | |
| Ethnicity, n (%) | |||
| Caucasian | 48 (49) | 72 (65) | ns |
| Hispanics | 3 (3) | 2 (2) | |
| Afro-Caribbean | 28 (29) | 20 (18) | |
| Asian | 7 (7) | 6 (5) | |
| Other | 12 (12) | 12 (11) | |
| Median length of follow-up (IQR), years | 9.5 (14) | 14 (9) | ns |
| Previous infection before SLE diagnosis,n (%) | 16 (16) | 3 (2) | 0.001 |
| Previous hospitalisations due to SLE n (%) | 55 (56) | 36 (32) | 0.001 |
| SLE main features (cumulative) n, (%) | |||
| Skin disease | 76 (78) | 67 (60) | 0.012 |
| Joint disease | 72 (74) | 101 (91) | 0.001 |
| Renal disease | 42 (43) | 24 (22) | 0.004 |
| Neuropsychiatric disease | 13 (13) | 12 (11) | ns |
| Serositis | 19 (19) | 33 (30) | ns |
| Previous drug treatment n (%) | |||
| Corticosteroids | 89 (91) | 43 (39) | <0.001 |
| Corticosteroids (≥10 mg per day at any time) | 54 (55) | 25 (23) | 0.009 |
| No hydroxychloroquine | 32 (33) | 25 (23) | ns |
| Azathioprine | 47 (48) | 35 (32) | 0.015 |
| Mycophenolate | 36 (35) | 28 (25) | ns |
| Cyclophosphamide | 28 (29) | 13 (13) | 0.004 |
| Rituximab | 26 (27) | 25 (23) | ns |
| Laboratory data, n(%) at any time | |||
| Neutropenia | 33 (34) | 19 (17) | 0.006 |
| Lymphopenia | 76 (78) | 73(66) | ns |
| Anti-dsDNA + | 67 (68) | 66 (60) | ns |
| Low C3 | 57 (58) | 50 (45) | ns |
| Outcomes | |||
| Deaths | 26 (27) | 2 (2) | |
| Patients with >1 infection | 18 (18) | 0 | 0.03 |
Patients who developed severe infections after diagnosis of SLE were more likely to have suffered previous severe infections before diagnosis of SLE (Pearson χ2=11.69, p=0.001) or to have been hospitalised for SLE (Pearson χ2=11.89, p=0.001) compared with those patients who never had severe infections. In terms of SLE manifestations, skin and renal disease were more common in the infection group (Pearson χ2=6.25, p=0.012; Pearson χ2=9.5, p=0.004) whereas joint involvement was more frequent in the non-infection group (Pearson χ2=11.21, p=0.001).
Patients in the infection group were more likely to have been treated with high doses of corticosteroids or an immunosuppressant (IS). Whereas 55% of the infection group had ever been treated with corticosteroids at a dose >10 mg per day, this only happened in 22% of the non-infected group (Pearson χ2=10.54, p=0.009). Significantly increased risk of infection was found for azathioprine (Pearson χ2=5.89 p=0.015) and cyclophosphamide (Pearson χ2=8.26, p=0.004) but not for mycophenolate or rituximab. Hydroxychloroquine (HCQ) had been taken by 77% of the non-infection group compared with 67% of the infection group with no significant difference between groups.
Regarding laboratory data, only neutropenia, which was twice as common in the infection group (34% vs 17%), was significantly different between both groups (Pearson χ2=7.63, p=0.006).
After multivariable analysis adjusted for age, only previous infection (β coefficient: 2.20, 95% CI 0.77 to 3.62; p=0.003), previous hospitalisations for SLE (β coefficient: 1.12, 95% CI 0.19 to 2.07; p=0.021) and treatment with corticosteroids ≥10 mg/day, (β coefficient: 3.39, 95% CI 2.33 to 4.44; p<0.001) remained statistically significant.
Type of infection
The most common type of severe infection was respiratory tract infection (n=29; 29.6% of all infections), followed by urinary tract infection (n=22, 22.4%) and gastrointestinal infection (n=22, 22.4%). Less frequent were soft tissue infection (n=11, 11.2%) and nervous system infections (n=4, 4.1%). Twelve (12.4%) of the patients developed documented bacteraemia on blood culture and 15 (15.3%) had multiple organ involvement.
Mortality
About a quarter (26.5%) of the patients died during their admission for severe infection, though this does not imply that death was always due to infection as many patients had comorbidities or active lupus as well. Having recorded this high proportion of deaths, we analysed the differences between the group of 26 patients who died during their admission for infection and the 72 patients who survived. These results are summarised in table 3.
Table 3.
Comparison of patients who died during admission for severe infection and those who survived
| Deceased patients n=26 (26.5%) | Alive patients n=72 (73.5%) | P values | |
| Mean age at diagnosis (SD) | 33.8 (14.1) | 31.2 (15.1) | ns |
| Mean age at infection (SD) | 42.88 (16.7) | 40.88 (16.7) | ns |
| Follow-up between diagnosis and first infection (years) | 9.11 (7.04) | 10.8 (10.3) | ns |
| Ethnicity n, (%) | |||
| Caucasian | 16 (61.5) | 31 (43.1) | ns |
| Hispanics | NA | 3 (4.2) | |
| Afro-Caribbean | 8 (30.8) | 20 (27.8) | |
| Asian | 2 (7.7) | 4 (5.6) | |
| Others | NA | 12 (16.7) | |
| Gender (female), n (%) | 25 (96) | 65 (90) | ns |
| Previous hospitalisations, n (%) | 2 (8) | 53 (74) | <0.001 |
| Previous severe infection before diagnosis of SLE, n (%) | 9 (35) | 7 (10) | 0.003 |
| Skin disease, n (%) | 18 (69) | 58 (81) | ns |
| Renal disease, n (%) | 10 (39) | 32 (44) | ns |
| Joint disease, n (%) | 22 (85) | 50 (69) | ns |
| Neuropsychiatric disease, n (%) | 4 (15) | 9 (13) | ns |
| Serositis, n (%) | 7 (27) | 12 (17) | ns |
| Corticosteroids per day at any time), n (%) | 20 (77) | 69 (96) | 0.02 |
| Corticosteroids ≥10 mg/day at any time, n (%) | 17 (65) | 37 (51) | ns |
| Hydroxychloroquine, n (%) | 20 (77) | 46 (64) | ns |
| Rituximab, n (%) | 1 (4) | 25 (35) | 0.002 |
| Cyclophosphamide, n (%) | 11 (42) | 17 (24) | ns |
| Azathioprine, n (%) | 14 (54) | 33 (46) | ns |
| Mycophenolate, n (%) | 10 (39) | 26 (36) | ns |
| Splenectomy, n (%) | 0 | 3 (4) | ns |
| Bacteraemia, n (%) | 4 (15) | 9 (13) | ns |
| Multiple organ involvement, n (%) | 12 (46) | 5 (7) | <0.001 |
| Low complement, n (%) | 11 (42) | 46 (64) | ns |
| Neutropenia, n (%) | 5 (19) | 28 (39) | ns |
| Lymphopenia, n (%) | 20 (77) | 56 (78) | ns |
| a-dsDNA, n (%) | 20 (77) | 47 (65) | ns |
a-dsDNA, Anti-double stranded DNAantibodies; SLE, systemic lupus erythematosus.
Patients who did not die had more previous hospitalisations due to SLE, compared with those who died (Pearson χ2=33.71, p=<0.001). In contrast, those who died were more likely to have suffered from severe infections prior to the diagnosis of SLE (Pearson χ2=8.66, p=0.003).
There were no statistically significant differences among the clinical manifestations of SLE between these two groups.
Regarding treatment, there were statistically significant differences for steroids at any time (Pearson χ2=8.19, p=0.004) and rituximab (Pearson χ2=9.34, p=0.002). However, for both these variables, patients who survived were more likely to have taken these drugs than those who died. Importantly, we only considered use of drugs in the period between diagnosis and first infection so survival from first infection would not affect the proportion of patients recorded as taking any drug.
Multiple organ involvement by infection was more common in deceased patients than in patients who survived (Pearson χ2=20.5, p=<0.001). Patients who died were more likely to have had positive anti-dsDNA compared with those who survived.
After multivariable analysis adjusted for age, previous hospitalisations due to SLE, previous infection and the presence of multiple organ involvement remained statistically significant as factors differentiating patients who died from those who survived (β coefficient: −6.15, 95% CI −9.57 to −2.73; p<0.001; β coefficient: 3.55, 95% CI 0.47 to 6.63; p=0.024 and β coefficient 3.51 95% CI 0.9 to 6.12; p=0.008).
Analysis of SLESIS values over time
Median (IQR) SLESIS at diagnosis of SLE in patients with infection was 4.27 (3.18) which was significantly higher than in the control (no infection) group (median 2.55, IQR 3.79 (z = −3.34; p=0.0008). Median (IQR) SLESIS just before the infection in the infection group was 6.64 (4.18) which was statistically higher than the median SLESIS at diagnosis in those patients (z=−5.73, p=<0.001) and also higher than median SLESIS in the duration-matched control group at a comparable time point in their disease course (median 3.32, IQR 3.16, z=−6.99; p=<0.001). There were no statistically significant differences between the first and second SLESIS values (ie, diagnosis and comparable time point to infection) for the matched controls.
Figure 1 shows the ROC analysis for SLESIS at diagnosis. The AUC was 0.6332 (SD 0.04; 95% CI 0.56 to 0.70). We defined three possible cut-offs to distinguish patients with and without severe infection. We selected the cut-offs which had classified correctly the maximum percentage of the sample taking into account sensitivity and specificity. A cut-off for SLESIS at diagnosis ≥3.18 identified patients who would develop severe infection with sensitivity 77% and specificity 51%. For SLESIS ≥3.46, sensitivity was 66% and specificity 55%. For SLESIS ≥4.24, sensitivity was 64% and specificity 60%.
Figure 1.
Receiver operator characteristics (ROC) curve analysis—Systemic Lupus Erythematosus Severe Infection Score (SLESIS) at diagnosis.
Figure 2 shows the ROC curve for SLESIS just prior to the infection. The AUC was 0.79 (SD 0.03 95% CI 0.73 to 0.85), which was better than for SLESIS at diagnosis. We selected three cut-offs: ≥3.67 identified patients who would develop severe infection with sensitivity of 90% and specificity of 43%. Similar results were obtained using ≥3.79 as a cut-off (sensitivity of 88%, specificity of 50%). For SLESIS ≥4.24, sensitivity was 86% and specificity 60%.
Figure 2.
Receiver operator characteristics (ROC) curve analysis Systemic Lupus Erythematosus Severe Infection Score (SLESIS) before infection.
Discussion
In patients with SLE it has been reported that the prevalence of life-threatening infections appears to be highest within the first 5 years after disease onset.23 However, severe infection represents a threat throughout the course of the disease, especially when these patients become older and develop more comorbidities related to age. Given the potential mortality in patients with SLE due to such infections, it is pertinent to pursue new options that allow us to predict which groups of patients will have higher risk of developing major infections. Our aim was to develop a risk score (SLESIS) to aid in this purpose. This study fulfils the important task of testing the properties of this SLESIS score in a cohort independent of the RELESSER19 20 population in which it was developed. Our London cohort differs from the Spanish cohort in terms of ethnicity but SLESIS still exhibits a valid and statistically significant association with severe infection.
During the last few years, there have been several publications aiming to develop algorithms that could measure the risk of developing severe infections in patients with other autoimmune diseases. Crowson et al 24 developed a score in order to detect severe infection promptly in a cohort of 410 patients with RA. The score was designed and validated to predict the 1-year risk of severe infection whereas SLESIS was elaborated to predict the risk of severe infection ever. Zink et al 18 built a score based on the Rheumatoid Arthritis Observation of Biologic Therapy cohort in order to predict serious infection in patients on biologic treatment, with promising results. However, the authors suggested that their risk score was valid only in Caucasian populations in Western Europe. Beca et al 25 designed a risk calculator algorithm to differentiate flares from infections in patients with SLE with fever. The study encompassed 130 patients with SLE who presented with fever over a period of 13 years. ROC curve analysis in both papers showed that both scores were able to predict infection with an AUC between 0.8 and 0.9. Nonetheless, both studies validated the algorithms in similar cohorts in terms of ethnicity distribution compared with the original cohorts. In contrast, we selected a validation cohort of patients in a different country, with a different range of ethnicities. In the Spanish cohort, 93% of patients were Caucasian and fewer than 1% African/Caribbean. In London, 68% were Caucasian and 28% African/Caribbean, an ethnic group recognised as suffering more severe SLE.
Patients with previous severe infection were predisposed to developing major infection and were also more likely to die during admission for severe infection. Impaired immune system functions in a subgroup of patients with SLE may contribute to increase the infection risk in those patients. There are immunological and genetic disorders that predispose to the development of infections in patients with SLE. Furthermore, other clinical and treatment factors might play a crucial role in the predisposition of patients with SLE to develop infection. For instance, the infection group were more likely than the controls to have had previous hospitalisations for SLE. These findings are comparable to other previous reports.2 26–28 In contrast, in the study of Ruiz-Irastorza et al, lung disease was the only clinical manifestation that was considered a predictor of major infection after the multivariate analysis.29
In carrying out this project, we noted the fact that a quarter of the patients recorded as suffering severe infections died during their admission for infection. To investigate this mortality further, we carried out univariable and multivariable analyses of factors that could potentially influence whether or not these patients died. Surprisingly, though previous hospitalisation due to SLE was a factor independently associated with increased risk of severe infection it was also associated with increased chance of surviving that severe infection, even after multivariable analysis. There is no obvious explanation for this apparent paradox. Perhaps the threshold for starting antibiotics was lower in such patients. We considered the possibility that deaths from severe infection had all occurred many years ago, during a period when more patients were treated with high-dose IS such as cyclophosphamide. However, this is not the case as 12 patients died between 2000 and 2012 while the other 14 died before the year 2000.
SLESIS was significantly higher just before the severe infection in comparison to the value at the diagnosis of SLE. This reinforces the idea that repeated measurement of SLESIS may be a helpful clinical assessment tool. As lupus activity and treatment change over time, it is predictable that SLESIS would change over time, but it was important to investigate whether this makes SLESIS at diagnosis a poorer predictor of infection. Development of chronic damage over time, as well as cumulative use of corticosteroids and immunosuppressive drugs, could contribute to these changes in SLESIS related to increased infection risk. Some variables of SLESIS will never change over time, such as age at diagnosis, ethnicity and gender, whereas others, such as number of previous severe infections, Katz Index and current dose of corticosteroids, could change and may thus contribute to changes in SLESIS. One strategy could be to recalculate SLESIS annually and after every severe infection and hospitalisation. In this way, a prospective study could be carried out to calculate SLESIS multiple times during follow-up in order to assess its variation over time and see if its peak (vs lower values during follow-up) is really associated with a higher probability of severe infection.
In line with other reports,30 31 we found that ever-use of corticosteroids ≥10 mg/day was associated with increased infection risk. In fact, more than 50% of patients of our cohort who suffered from severe infections had been treated with ≥10 mg/day of corticosteroids. Other immunosuppressive treatments have been associated with high risk of infections although results have been controversial among the different cohorts.31 In our study, cyclophosphamide and azathioprine were associated with increased risk of severe infection in the univariate analysis but that significance was lost after the multivariable analysis.
There was a trend with HCQ which seemed to be the opposite to corticosteroids or IS, since fewer patients in the study group than the control group had ever been treated with HCQ. This finding is in agreement with previous reports29 32 although in our study, it did not reach statistical significance. Ruiz-Irastorza et al 29 found that patients taking antimalarials were 16 times less likely to suffer a major infection. Similarly, Sisó et al 32, found a lower frequency of infections among those previously treated with antimalarials in a retrospective study. Bultink et al, in a study designed to analyse the effect of the deficiency of functional mannose-binding lectin, also found that treatment with HCQ was associated with fewer severe infections although the authors attributed this association to the presumed lesser severity of patients with lupus who take HCQ.33
Overall, the AUCs in our study were not as high as for previous scores developed for RA.18 24 However, this is the first score that has been developed to predict severe infections in SLE and may represent the first step in developing tools to do this accurately. We acknowledge several limitations in our study. First is the retrospective design of the study. Second, the ethnicity item in SLESIS distinguishes only Latin-American ethnicity as a separate group, which was not helpful in the London population. A modified SLESIS including HR for other ethnic groups would be more widely applicable globally but could not have been derived from the RELESSER cohort (too ethnically homogeneous) or the UCLH cohort (too small). Thirdly, the Katz Index used by RELESSER is a simple and helpful measure of disease severity (not just activity) but is not widely used in clinical practice. However, in the original RELESSER Study,17 from which SLESIS was derived, Systemic Lupus International Collaborating Clinics (SLICC)/ACR/Damage Index, Katz Index and SELENA-SLEDAI (Safety of Estrogen in Lupus National Assessmentstudy-Systemic Lupus Erythematosus Disease Activity Index) activity score were all measured and the Katz Index was the only one statistically associated with severe infection. Notwithstanding these limitations, we have shown that SLESIS at diagnosis was significantly higher in the group of patients who later suffered severe infections than in the control group of patients with SLE who did not suffer severe infection.
How might SLESIS be used in clinical practice? It is important to bear in mind that both sensitivity and specificity for severe infection were modest for SLESIS at diagnosis. For SLESIS just before the infection, sensitivity was high (90%) but specificity was low (54%). The low specificity means that SLESIS could not be used to decide on use of management measures with a high risk of adverse effects. We would suggest that patients with high SLESIS (>3.5) at any point could be followed up with a higher index of suspicion for infection and lower threshold for using antibiotics. Although this may be an obvious extrapolation of the data, it is not possible to conclude that the early use of antibiotics in patients with high SLESIS will impact on the outcomes, and therefore, this strategy cannot be suggested based solely on the results of our work. SLESIS at diagnosis, together with other factors, might also help in deciding which patients might benefit from vaccination against bacterial infections (eg, pneumococcus) and considering a benefit-risk balance of corticosteroids (≥10 mg/day) and other IS.
In summary, despite the limitations, our study has demonstrated strong arguments to perform future prospective studies to assess if SLESIS, or an improved form of SLESIS, could be clinically useful in the early diagnosis and prevention of severe infections in patients with SLE.
Supplementary Material
Acknowledgments
The authors thank the researchers of the RELESSER group and Research Unit of Spanish Society of Rheumatology, who carried out the original study from which SLESIS was derived (Ref 17). BTS, CW, DI and AR work in a department supported by the National Institute for Health Research University College London Hospitals Biomedical Research Centre.
Footnotes
Contributors: AR and BTS designed the study. IR-F, JMP-R and VdC developed the SLESIS score and advised on design of the study. BTS, AR, CW and DI collected the data. BTS and VdC carried out the statistical analysis. BTS, JMP-R, IR-F, VdC, DI and AR all took part in interpreting the results and writing the final manuscript.
Funding: This work was supported by the National Institute for Health Research University College London Hospitals Biomedical Research Centre and the Spanish Foundation of Rheumatology (FER).
Competing interests: None declared.
Provenance and peer review: Not commissioned; externally peer reviewed.
Data sharing statement: No additional data are available.
Patient consent for publication: Not required.
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