Katherine R. Tuttle , Lindsey M. Kornowske , Cami R. Jones , Kenn B. Daratha , Radica Z. Alicic , Christina L. Reynolds , Joshua J. Neumiller , Mark E. Bensink , Wu Gong , Keith C. Norris , Susanne B. Nicholas , CURE-CKD Consortium
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引用次数: 0
Abstract
Rationale & Objective
Although IgA nephropathy (IgAN) therapies are advancing quickly, therapeutic interventions are hampered by a lack of kidney disease identification and risk assessment. The study aim was to use population-level data from health systems to identify IgAN and assess risks.
Study Design
A longitudinal and real-world cohort study.
Setting & Participants
Electronic health record data for patients ≥18 years old with IgAN at Providence and University of California Los Angeles health systems during 2016-2022.
Predictors
Health insurance and care utilization along with age, gender, race, ethnicity, estimated glomerular filtration rate (eGFR), urine albumin/creatinine ratio (UACR) or urine protein/creatinine ratio (UPCR), diabetes, hypertension, and medications.
Outcomes
Time to first major adverse kidney event (MAKE): ≥40% eGFR decline; eGFR <15 mL/min/1.73 m2; administrative codes for kidney failure, dialysis, or transplant; and death.
Analytical Approach
Kaplan-Meier survival curves and Cox proportional hazards models.
Results
Patients with IgAN (n = 2,571) were 50% (n = 1,277) women and 58 ± 18 (mean ± SD) years old. At baseline, eGFR was 78 ± 27 mL/min/1.73 m2 (chronic kidney disease epidemiologic 2021 equation); median UACR and UPCR were 166 (interquartile range 25-795) mg/g and 0.7 (0.2-1.8) g/g, respectively, among those with baseline measurements (n = 669). MAKE occurred in 22% of the cohort by 3 years. In Cox proportional hazards models, MAKE was predicted by noncommercial (Medicare or Medicaid) health insurance, hospitalization, more frequent outpatient encounters, lower eGFR, and a higher UACR or UPCR.
Limitations
Missingness, miscoding, and retrospective data.
Conclusions
Substantial loss of kidney function, kidney failure, and death were common events over a short period of time in patients with IgAN. Within health system populations, noncommercial health insurance and greater care utilization augmented risk prediction and could help to identify those who may benefit from closer monitoring and implementation of therapeutic interventions.
Plain Language Summary
IgA nephropathy therapies have advanced quickly. However, therapeutic interventions are hampered by lack of disease identification and risk assessment. We identified patients with IgA nephropathy at 2 United States health systems and assessed predictors of risk for major adverse kidney events (major adverse kidney event [MAKE]—substantial loss of kidney function, kidney failure, or death). More than one in 5 patients experienced MAKE by 3 years. In addition to demographic and clinical predictors, MAKE was predicted by noncommercial health insurance, hospitalization, and more frequent outpatient encounters. A population health approach within health systems could improve outcomes by identification of IgA nephropathy and assessment of health insurance status and care utilization to help risk stratify patients for closer monitoring and implementation of therapeutic interventions.