4.6 Article

An Outcomes-Based Definition of Proteinuria Remission in Focal Segmental Glomerulosclerosis

出版社

AMER SOC NEPHROLOGY
DOI: 10.2215/CJN.04780517

关键词

FSGS; proteinuria; surrogate endpoint; Humans; Glomerulosclerosis; Focal Segmental; glomerular filtration rate; creatinine; Proportional Hazards Models; Propensity Score; Goals; kidney; Renal Insufficiency; Kidney Failure; Chronic; Prognosis; Cohort Studies

资金

  1. National Institutes of Health (NIH)/National Center for Advancing Translational Sciences [U54DK083912]
  2. NIH/National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) [U54DK083912]
  3. NephCure Kidney International
  4. University of Michigan
  5. NIH
  6. NIDDK, NIH
  7. University of Michigan Department of Pediatrics and Communicable Diseases
  8. NIH/NIDDK O'Brien Kidney Center summer research internship (Grace Tsai) [2P30-DK-081943]
  9. University of Michigan Honest Broker Office
  10. NephCure Accelerating Cures Institute
  11. O'Brien Renal Center NIH Grant [P30-DK081943-01]
  12. University of Michigan School of Medicine, Department of Internal Medicine
  13. University of Michigan School of Medicine, Department of Pediatrics and Communicable Diseases

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Background and objectives Proteinuria is used as an indicator of FSGS disease activity, but its use as a clinical trial end point is not universally accepted. The goal of this study was to refine proteinuria definitions associated with long-term kidney survival. Design, setting, participants, & measurements Data on 466 patients with primary FSGS with proteinuria (urine protein-to-creatinine ratio >1 g/g) were analyzed from five independent cohorts. Proteinuria by months 1, 4, and 8 after study baseline was categorized by conventional definitions of complete (<0.3 g/g) and partial remission (<3.5 g/g and 50% reduction in proteinuria). Novel remission definitions were explored using receiver operating curves. Kaplan-Meier methods were used to estimate the associations of proteinuria with progression to ESRD or a 50% loss in kidney function. Propensity score-adjusted Cox proportional hazards models were used to adjust for baseline proteinuria, eGFR, and therapy. Results In the initial derivation cohort, conventional partial remission was not associated with kidney survival. A novel definition of partial remission (40% proteinuria reduction and proteinuria<1.5 g/g) on the basis of receiver operating curve analyses of 89 patients was identified (Sensitivity=0.70; Specificity=0.77). In the validation cohort analyses, complete remission was associated with better prognosis (6 out of 41 patients progressed to kidney failure; 6.6 per 100 patient-years) as was the novel partial remission (13 out of 71 progressed; 8.5 per 100 patient-years), compared with those with no response (51 out of 116 progressed; 20.1 per 100 patient-years). Conventional partial remission at month 8, but not month 4, was also associated with better response (19 out of 85 patients progressed; risk=10.4 per 100 patient-years). Propensity score-adjusted analyses showed the novel partial remission was associated with less progression at months 4 and 8 (month 4: hazard ratio, 0.50; P=0.01; month 8: hazard ratio, 0.30; P=0.002). Conclusions Reaching either a complete or partial remission using a novel or conventional definition was associated with better long-term outcomes in patients with FSGS.

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