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Updated: Sep 10, 2025

Detection of MicroRNA Expression in the Kidneys of Immunoglobulin A Nephropathic Mice
Published on: July 8, 2020
Attribute-based medicine for IgA nephropathy: risk factor constellations influence kidney prognosis
Hiroshi Kataoka1,2, Shun Manabe1, Takahito Moriyama3
1Department of Nephrology, Tokyo Women's Medical University, Chiba, Japan.
Background And Hypothesis:
Attribute-based medicine emphasizes tailoring care to patient-specific characteristics. Immunoglobulin A nephropathy (IgAN), a heterogeneous glomerular disease, presents varying risks across subgroups. We hypothesized that an attribute-based medicine approach could identify residual risk factors and inform personalized strategies.
Methods:
We analysed data from 996 patients from the Japanese Nationwide Retrospective Cohort Study in IgAN. The primary outcome was kidney replacement therapy initiation or a 1.5-fold increase in serum creatinine. Six pre-specified attributes were assessed: age, sex, body mass index (BMI), chronic kidney disease (CKD) stage, urinary protein excretion (U-Prot) and urine occult blood (U-OB). Cox regression and Kaplan-Meier analyses were performed to evaluate interactions between attributes and risk factors.
Results:
Poor kidney prognosis was associated with lower estimated glomerular filtration rate (eGFR) [per 10 mL/min/1.73 m² increase, hazard ratio (HR) = 0.87], higher U-Prot (log-transformed HR = 4.54) and hyperuricaemia (HR = 1.64), while oral corticosteroids (HR = 0.60) and tonsillectomy (HR = 0.44) were protective factors. Significant interactions included the following: hyperuricaemia with BMI <22 kg/m²; hypertension with female sex; eGFR and age with CKD stage; U-Prot with age, eGFR and corticosteroid use; and U-Prot with U-OB. Prognostic effects of age and eGFR were reversed for CKD stage 3 compared with stages 1-2. U-Prot was the most consistent predictor of poor prognosis, especially in patients with U-OB ≤2+. Corticosteroids improved outcomes in patients with U-Prot ≥1 g/day, while tonsillectomy was effective in those with U-OB ≥3+.
Conclusion:
Attribute-based analysis revealed critical risk modifiers and supported stratified treatment strategies for IgAN. These findings underscore the potential of attribute-based medicine in guiding personalized care for patients with IgAN.
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