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Prediction of outcomes in crescentic IgA nephropathy in a multicenter cohort study
Jicheng Lv1, Yihe Yang, Hong Zhang
1Renal Division, Peking University First Hospital, Institute of Nephrology, Peking University, Key Laboratory of Renal Disease, Ministry of Health of China, Beijing, China;
Insights
Crescentic IgA nephropathy (IgAN) has a poor prognosis. Initial serum creatinine levels, not crescent percentage, independently predict kidney failure in IgAN patients, aiding in risk assessment.
Area of Science:
- Nephrology
- Glomerular Diseases
- Renal Pathology
Background:
- Crescentic IgA nephropathy (IgAN) is a common cause of rapidly progressive glomerulonephritis.
- Few studies have characterized the risk factors and prognosis of crescentic IgAN.
Purpose of the Study:
- To identify risk factors for end-stage renal disease (ESRD) in crescentic IgAN.
- To develop a prediction model for kidney failure in patients with crescentic IgAN.
Main Methods:
- Retrospective analysis of two cohorts (discovery and validation) of patients with crescentic IgAN (≥14 years old, followed ≥12 months).
- Multivariate Cox and logistic regression analyses to identify independent risk factors for ESRD.
- Evaluation of serum creatinine (SCr) and percentage of crescents as predictors of kidney survival.
Main Results:
- Initial SCr level was the sole independent predictor of ESRD (HR 1.32, P=0.002).
- The percentage of crescents did not independently associate with ESRD.
- High SCr levels (>6.8 mg/dl) were associated with poor kidney survival and reduced likelihood of dialysis recovery.
Conclusions:
- Crescentic IgAN carries a poor prognosis.
- Initial serum creatinine concentration is a valuable predictor of kidney failure in crescentic IgAN.
- The findings may inform clinical management and risk stratification for patients with crescentic IgAN.
Abstract:
Crescentic IgA nephropathy (IgAN), defined as >50% crescentic glomeruli on kidney biopsy, is one of the most common causes of rapidly progressive GN. However, few studies have characterized this condition. To identify risk factors and develop a prediction model, we assessed data from patients ≥ 14 years old with crescentic IgAN who were followed ≥ 12 months. The discovery cohort comprised 52 patients from one kidney center, and the validation cohort comprised 61 patients from multiple centers. At biopsy, the mean serum creatinine (SCr) level ± SD was 4.3 ± 3.4 mg/dl, and the mean percentage of crescents was 66.4%± 15.8%. The kidney survival rates at years 1, 3, and 5 after biopsy were 57.4%± 4.7%, 45.8%± 5.1%, and 30.4%± 6.6%, respectively. Multivariate Cox regression revealed initial SCr as the only independent risk factor for ESRD (hazard ratio [HR], 1.32; 95% confidence interval [CI], 1.10 to 1.57; P=0.002). Notably, the percentage of crescents did not associate independently with ESRD. Logistic regression showed that the risk of ESRD at 1 year after biopsy increased rapidly at SCr>2.7 mg/dl and reached 90% at SCr>6.8 mg/dl (specificity=98.5%, sensitivity=64.6% for combined cohorts). In both cohorts, patients with SCr>6.8 mg/dl were less likely to recover from dialysis. Analyses in additional cohorts revealed a similar association between initial SCr and ESRD in patients with antiglomerular basement membrane disease but not ANCA-associated systemic vasculitis. In conclusion, crescentic IgAN has a poor prognosis, and initial SCr concentration may predict kidney failure in patients with this disease.
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