Abstract

Systemic lupus erythematosus (SLE) patients are vulnerable to infections. We aim to explore the approach to differentiate active infection from disease activity in pediatric SLE patients. Fifty pediatric SLE patients presenting with 185 clinical visits were collected. The associations between both clinical and laboratory parameters and the outcome groups were analyzed using generalized estimating equations (GEEs). These 185 visits were divided into 4 outcome groups: infected-active (n = 102), infected-inactive (n = 11), noninfected-active (n = 59), and noninfected-inactive (n = 13) visits. Multivariate GEE (generalized estimating equation) analysis showed that SDI, SLEDAI-2K, neutrophil‐to‐lymphocyte ratio (NLR), hemoglobin, platelet, RDW-to-platelet ratio (RPR), and C3 are predictive of flare (combined calculated AUC of 0.8964 and with sensitivity of 82.2% and specificity of 90.9%). Multivariate GEE analysis showed that SDI, fever temperature, CRP, procalcitonin (PCT), lymphocyte percentage, NLR, hemoglobin, and renal score in SLEDAI-2k are predictive of infection (combined calculated AUC of 0.7886 and with sensitivity of 63.5% and specificity of 89.2%). We can simultaneously predict 4 different outcome with accuracy of 70.13% for infected-active group, 10% for infected-inactive group, 59.57% for noninfected-active group, and 84.62% for noninfected-inactive group, respectively. Combination of parameters from four different domains simultaneously, including inflammation (CRP, ESR, PCT), hematology (Lymphocyte percentage, NLR, PLR), complement (C3, C4), and clinical status (SLEDAI, SDI) is objective and effective to differentiate flares from infections in pediatric SLE patients.

Highlights

  • Systemic lupus erythematosus (SLE) patients are vulnerable to infections

  • Using generalized estimating equations (GEEs), we found that acute infection was associated with SLICC/ACR Damage Index (SDI) score, fever temperature (°C), CRP level, PCT level, neutrophil‐to‐lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and renal score of Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) 2 K but that lymphocyte percentage, Hb level (g/dL), and urine nitrate were negative predictors of infectious events (Supplementary Table S1b)

  • Multivariate GEE analysis showed that SDI score, fever temperature (°C), CRP level, PCT level, lymphocyte percentage, NLR, Hb level (g/dL), and SLEDAI 2 K renal score were independent parameters for predicting acute infection in SLE patients (Table 5)

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Summary

Introduction

Systemic lupus erythematosus (SLE) patients are vulnerable to infections. We aim to explore the approach to differentiate active infection from disease activity in pediatric SLE patients. Combination of parameters from four different domains simultaneously, including inflammation (CRP, ESR, PCT), hematology (Lymphocyte percentage, NLR, PLR), complement (C3, C4), and clinical status (SLEDAI, SDI) is objective and effective to differentiate flares from infections in pediatric SLE patients. Abbreviations AR Autoregressive CRP C-reactive protein ESR Erythrocyte sedimentation rate GEE Generalized estimating equation NLR Neutrophil-to-lymphocyte ratio PCT Procalcitonin PLR Platelet-to-lymphocyte ratio RPR RDW-to-platelet ratio SLE Systemic lupus erythematosus SLEDAI Systemic Lupus Erythematosus Disease Activity Index SDI Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage www.nature.com/scientificreports/. Clinicians have to make treatment decisions based on clinical judgment and laboratory parameters to distinguish between active disease and infection Most such studies to date have been performed in adult populations, whereas data regarding pediatric SLE are lacking. New scores, which include combinations of different biomarkers, may represent better solutions for d­ ifferentiation

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