Background: Infection is the most common complication of Idiopathic Nephrotic Syndrome (INS) and the main cause of INS recurrence, severe infection and even leading to mortality. The purpose of this study was to investigate the risk factors of severe infection in INS children and the clinical parameters influencing prognosis.
Methods: Totally 147 children with INS and concomitant infections were enrolled and classified into the severe infection group (SIG) and Non-severe infection group (Non-SIG). The clinical characteristics and auxiliary examination results were compared between the two groups, and the early-warning parameters for severe infection and risk factors for poor prognosis were evaluated.
Results: There were 49 patients in the SIG, 98 patients in the Non-SIG. In the SIG, the most common severe infections disease included severe pneumonia (63.6%), severe sepsis (30.6%), septic shock (4.1%). In SIG, Gram-positive bacteria (GPB) were more common, as was respiratory syncytial virus (RSV), and the three most common strains were Pseudomonas aeruginosa, Staphylococcus aureus (SA) and Staphylococcus epidermidis. There were more steroid-resistant nephrotic syndrome and combination of steroids and immunosuppressants in SIG, compared with the Non-SIG (P = 0.000). Patients in the SIG has lower complement 3 (C3, ≤ 0.55 g/L,) and absolute lymphocyte count (ALC, ≤ 1.5 × 109/L) (P = 0.004). Logistic regression analysis revealed that the independent risk factors for severe infections were the combined use of immunosuppressants [95% confidence interval (CI):1.569–463.541, P = 0.023], steroid resistance (95% CI: 4.845–2,071.880, P = 0.003), C-reactive protein (CRP) ≥8 mg/L (95% CI: 43.581–959, 935.668, P = 0.001), and infections caused by GPB (95% CI: 27.126–2,118, 452.938, P = 0.002), influenza (95% CI: 2.494–1, 932.221, P = 0.012) and RSV (95% CI: 5.011–24 963.819, P = 0.007). The patients in the SIG were classified into the survival group (N = 39) and the mortality group (N = 5). Logistic regression analysis showed that white blood cell count (WBC) >15 × 109/L (95% CI: 1.046–2.844, P = 0.033) was an independent risk factor of poor prognosis for these patients.
Conclusions: Resistance to steroids, combined with steroids and IS agents, and GPB infections (especially SA) are high-risk factors for severe infection in children with INS. We should monitor CRP ≥ 8 mg/L, C3 ≤ 0.55 g/L and ALC ≤ 1.5 × 109/L to avoid developing severe infection. Accompanied by an increase in ANC, WBC significantly increased, suggesting a fatal infection.
Idiopathic nephrotic syndrome (INS) is one of the most common kidney diseases in children. It is characterized by heavy proteinuria, pitting edema, hypoalbuminemia, and hyperlipidemia. INS occurs in 1.15–16.9 per 100,000 children, and its incidence varies by ethnicity and region (1). Infection is the most common complication of INS; it hampers the treatment of the underlying kidney disease, leads to INS relapse, increases rates of unplanned hospitalizations, and even leads to increased mortality. Several recent reports have evaluated the clinical characteristics and risk factors in children with INS and infections (2, 3). However, few studies have assessed the risk factors for serious infections associated with INS and the risk factors for poor prognosis of infections. The purpose of this study was to investigate the risk factors of severe infections in children with INS and the clinical parameters leading to poor prognosis.
This study enrolled children aged 0–18 years with INS and concomitant infections who were hospitalized in the Children's Hospital of Chongqing Medical University and the Affiliated Hospital of Guizhou Medical University, from January 2013 to October 2019. Written informed consent was obtained from parents or legal guardians, and this study complied with the ethical principles of the Helsinki Declaration of the World Medical Association. All the patients met the following criteria: (1) An onset age from birth to 18 years. (2) The definition of nephrotic syndrome (NS) included: ➀ nephrotic- range proteinuria: urine protein/creatinine ratio (UPCR) ≥ 200.0 (mg/mmol) in spot morning urine or 24 h urine quantification ≥50 mg/kg/day ➁ hypoproteinaemia: serum albumin 0.05) (Table 3). Among the children, the shortest and longest disease durations were 0.03 and 106.13 months, respectively, and the median was 0.67 months. There were 49 children in the SIG and 98 in the Non-SIG. The SIG primarily developed severe pneumonia (n = 31, 63.3%), severe sepsis (n = 15, 30.6%), septic shock (n = 2, 4.1%), and severe chickenpox (n = 1, 2.0%); whereas, the Non-SIG primarily developed pneumonia (n = 81, 82.7%), urinary tract infection (UTI) (n = 12, 12.2%), and upper respiratory tract infection (URTI) (n = 5, 5.1%).
Through statistical analysis of clinical data, we found that there were many differences between SIG and Non-SIG. The percentage of relapsed cases and SRNS in SIG were higher than those Non- SIG (63.3 vs. 30.6%, 51.0 vs. 10.2%, respectively). The number of steroids (≥0.5 mg/kg) users and immunosuppressant users in SIG was significantly higher than that in the Non-SIG (46.9 vs. 16.3%, 36.7 vs. 4.1%). There were 18 cases using immunosuppressive agents, including 12 cases using tacrolimus, of which 2 cases were combined with mycophenolate mofetil and 1 case was combined with cyclophosphamide. The remaining 4 cases used mycophenolate mofetil alone and 2 cases used cyclophosphamide alone. Steroids and immunosuppressants for SIG were used longer than for Non -SIG. In the auxiliary examination, we also found that there were significant differences between the two groups. The ANC, PCT, PT, and APTT in the SIG were significantly higher than those in the Non-SIG, while ALC, Tch, LDL, and C3 were significantly lower than those in the Non-SIG. Other indicators were also significantly different, such as WBC, CRP, uric acid, urea nitrogen, and other indicators SIG are higher than Non-SIG. The SIG group's Fib, serum potassium, sodium, etc. were lower than the Non-SIG group (Table 3).
Based on the data from blood, sputum, and urine cultures obtained from 147 children with INS and infections during hospitalization, 30 of them were detected and 46 strains were isolated. The three most common types in the SIG were Pseudomonas aeruginosa (three strains), Staphylococcus aureus (SA) (three strains), and Staphylococcus epidermidis (three strains). On the contrary, the three most common types in the Non-SIG were Haemophilus influenzae (three strains), Streptococcus pneumonia (SP) (three strains), and Enterococcus faecium (three strains). The detection rate of Gram-positive bacteria (GPB) was higher in the SIG than in the Non-SIG (Table 4). The pathogen profiles indicated that the SIG was more likely to be infected with GPB, respiratory syncytial virus (RSV) and influenza viruses (FLu), and fungi than the Non-SIG (P < 0.05). In total, 10 drug-resistant strains were detected in the two groups. The incidence of Methicillin-resistant strains was significantly higher in the SIG (n = 4) than in the Non-SIG (n = 0) (P = 0.000).
To identify the risk factors of severe infections in children with INS, the aforementioned clinical parameters that were statistically different between the two groups were entered into the binary logistic regression analysis model. The results obtained using the “forward Wald” method were shown in Table 5. Binary logistic regression analysis showed that the combined use of immunosuppressants (OR: 26.969, 95% CI: 1.569–463.541), CRP ≥8 mg/L (OR: 6,468.029, 95% CI: 43.581–959,935.668), steroid resistance (OR: 100.191, 95% CI: 4.845–2,071.880), infection with gram-positive cocci (OR: 7,580.545, 95% CI: 27.126–2,118,452.938), infection with influenza virus (OR: 69.426, 95% CI: 2.494–1,932.221), and infection with respiratory syncytial virus (OR: 353.681, 95% CI: 5.011–24,963.819) were independent risk factors for severe infections in children with INS. ALC (increase > 1.5 × 10/L) (OR: 0.356, 95% CI: 0.188–0.675) and complement C3 (increase > 0.55 g/L) (OR: 0.000, 95% CI: 0.000–0.276) were protective factors.
Through the ROC curve model analysis, it was found that when children with nephropathy were co-infected, the risk of infection progression often needed to consider the combined effect of multiple influencing factors at the same time. The sensitivity and specificity reflected by the area under the ROC curve (AUC) showed that when infection occurred in children with INS, when one or more factors including steroid resistance, IS treatment and increased CRP were combined, a more severe infection was very likely to occur (Figures 2A,B).
In the SIG, 39 patients survived, five died, and five gave up treatment. Five patients who gave up treatment were excluded because of incomplete data and unclear prognosis. The causes of death included multiple organ failure syndromes (2 cases), brain herniation (1 case), and circulatory failure (2 cases). The patients were classified into the survival group (N = 39) and the mortality group (N = 5). The statistically significant parameters between two groups by univariate analysis entered into the binary logistic regression analysis model. There was no significant difference in baseline characteristics, treatment, and disease condition between the two groups. However, in the auxiliary examination, WBC, Serum chlorine, and ANC in the mortality group were significantly higher than those in the survival group, and ALT, AST, serum calcium, IgG, IgA, and C3 were significantly lower than those in the survival group (Table 6). Binary logistic regression analysis showed that WBC (increased > 15 × 10/L) (OR: 1.725, 95% CI: 1.046–2.844) is an independent risk factor for the poor prognosis of INS children with severe infections, often accompanied by an increase in the ANC(>10 × 10/L), whereas serum calcium level (increase > 1.30 mmol/L) (OR: 0.000, 95% CI: 0.000–0.698) was a protective factor. The area under the ROC curve shows that serum calcium and WBC are highly specific and sensitive in predicting the risk of poor prognosis (Figures 2C,D).
Infection is one of the main complications of childhood idiopathic nephrotic syndrome, which can lead to frequent relapses of INS, treatment failures, and even death (14). Children with INS are more likely to have a poor prognosis after infection due to the primary disease and therapeutic drugs. At present, most studies on children's INS focus on the analysis of risk factors for infection, and there is a lack of large-scale reports on the risk factors and outcome factors for severe infection. Referring to the definition of severe infection in adult INS and the indicators of severe infection in children (7, 8), we defined the manifestations of severe infection in children with INS and analyzed the relevant risk factors.
In this study, it was observed that pneumonia and urinary tract infection were dominant in Non-severely infective INS children, while severe pneumonia, sepsis was dominant in severely infective INS children. In Taiwan (15), pneumonia is the main type of infection in children with INS, which is consistent with the Non-SIG in our study, while in India, Saudi Arabia, and other regions (2, 16, 17), the upper respiratory tract infection is the main type, but these studies did not grade the infection. Although in Israel (18), the infections were mainly pneumonia and bacteremia/sepsis, but they defined the infection as a serious bacterial infection, which has limitations. From our research, it is found that both severe and Non-severe infections are mainly respiratory infections. Therefore, our treatment should be more active when pneumonia is complicated. We found that the pathogen spectrum of the two groups is significantly different, and GPB are an independent risk factor for severe infections. In SIG, the respiratory pathogens are mainly SA, while Non-SIG is mainly composed of SP and Haemophilus influenzae, and it is more common for SIG strains to have drug resistance. Therefore, when patients are infected with methicillin-resistant SA or other methicillin-resistant GPB, they are more likely to cause serious infections. So, children with INS must vaccinate pneumococcal vaccine. Previous studies have confirmed that the use of high cumulative doses of steroids and IS agents (8, 17, 19–23) all increase the risk of INS infection. Besides, we found that children with SRNS or relapse are more susceptible to severe infection, and the risk of severe infection is higher when treated with steroids combined with immunosuppressive agents such as tacrolimus or mycophenolate mofetil. From the auxiliary inspection point of view, SIG has higher CRP and PCT, but their Tch and LDL are lower. The Tch and LDL of the two groups were higher than the normal range, but studies have shown that inflammation can cause a decrease in Tch (24), so the LDL of SIG is lower than that of Non-SIG. When the Tch and LDL of infected children with INS decrease, we need to be vigilant. SIG's PT and APTT are also higher, suggesting that when there is a problem with the coagulation function of Non-SIG, we need to be alert to the progress of the infection, and even cause diffuse intravascular coagulation. C3 (15 × 10/L).
Several limitations of this study should be mentioned. First, although we have found some risk factors of severe infection in children with INS, as a retrospective study, it might lead to the bias in data collection and uniform availability of information from the medical records. Second, the age span of children in this study was large, and the results could not well-reflect the clinical characteristics of children with INS complicated with severe infection in each age period. We tried to divide the children into infant, childhood and adolescence group based on tanner staging. However, due to the relatively small sample size, it was hard to perform statistical analysis. In the future, we will expand the sample size and design a prospective study based on the results of this study, so as to avoid poor prognosis of children with INS caused by severe infection, and to find more risk factors of severe infection in children with INS in different age period.
In summary, our double-center retrospective study showed that resistance to steroids, combined use of steroids and IS agents, and GPB infections (especially SA) are high risk factors for severe infection. We should monitor CRP ≥ 8 mg/L, C3 ≤ 0.55 g/L and ALC ≤ 1.5 × 10/L to avoid developing severe infection. The WBC of severely infected patients increases significantly, especially when ANC increases, which can lead to fatal infections.
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
The studies involving human participants were reviewed and approved by Ethics Committee of the Children's Hospital of Chongqing Medical University (reference number 2020-12, 2020-03-24). Written informed consent to participate in this study was provided by the participants' legal guardian/next of kin.
MW and XZ designed this study. HZ and SQ wrote the draft. CZ, LS, and TZ has participated in data collection and case follow-up. JL designed the statistical analysis of the study. All authors contributed to the article and approved the submitted version.
This study was funded by the central government directs special funds for local science and technology development, Social Development Project of Guizhou Provincial Department of Science and Technology (2020-4Y124).
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
First, we would like to thank Western Pediatric Development Union of China for setting up a platform for academic exchange. Besides, we would thank all of the medical staff at the department of nephrology, Children's Hospital of Chongqing Medical University, and the department of pediatrics, the Affiliated Hospital of Guizhou Medical University for their support in this research. At last, we would like to thank Haiping Yang, Gaofu Zhang, Qin Yang, Daoqi Wu for their help in data collection.