4.3 Article

Development of a lupus nephritis suboptimal response prediction tool using renal histopathological and clinical laboratory variables at the time of diagnosis

期刊

LUPUS SCIENCE & MEDICINE
卷 8, 期 1, 页码 -

出版社

BMJ PUBLISHING GROUP
DOI: 10.1136/lupus-2021-000489

关键词

lupus nephritis; outcome assessment; health care; lupus erythematosus; systemic

资金

  1. NIAMS MCRC for Rheumatic Diseases in African Americans [P60 AR062755]
  2. NIAMS Improving Minority Health in Rheumatic Diseases [P30 AR072582]
  3. South Carolina Clinical & Translational Research (SCTR) Institute [UL1 RR029882]
  4. SCTR Institute [UL1 TR001450]
  5. [R01 AR045476]
  6. [R01 AR071947]
  7. [K08 AR002193]
  8. [I01 CX000218]

向作者/读者索取更多资源

This study developed machine learning models using renal pathology results and clinical laboratory data to predict outcomes of lupus nephritis patients at approximately 1 year, providing a valuable tool for clinical decision-making.
Objective Lupus nephritis (LN) is an immune complex-mediated glomerular and tubulointerstitial disease in patients with SLE. Prediction of outcomes at the onset of LN diagnosis can guide decisions regarding intensity of monitoring and therapy for treatment success. Currently, no machine learning model of outcomes exists. Several outcomes modelling works have used univariate or linear modelling but were limited by the disease heterogeneity. We hypothesised that a combination of renal pathology results and routine clinical laboratory data could be used to develop and to cross-validate a clinically meaningful machine learning early decision support tool that predicts LN outcomes at approximately 1 year. Methods To address this hypothesis, patients with LN from a prospective longitudinal registry at the Medical University of South Carolina enrolled between 2003 and 2017 were identified if they had renal biopsies with International Society of Nephrology/Renal Pathology Society pathological classification. Clinical laboratory values at the time of diagnosis and outcome variables at approximately 1 year were recorded. Machine learning models were developed and cross-validated to predict suboptimal response. Results Five machine learning models predicted suboptimal response status in 10 times cross-validation with receiver operating characteristics area under the curve values >0.78. The most predictive variables were interstitial inflammation, interstitial fibrosis, activity score and chronicity score from renal pathology and urine protein-to-creatinine ratio, white blood cell count and haemoglobin from the clinical laboratories. A web-based tool was created for clinicians to enter these baseline clinical laboratory and histopathology variables to produce a probability score of suboptimal response. Conclusion Given the heterogeneity of disease presentation in LN, it is important that risk prediction models incorporate several data elements. This report provides for the first time a clinical proof-of-concept tool that uses the five most predictive models and simplifies understanding of them through a web-based application.

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