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Clinical Significance of Crescent Formation in IgA Nephropathy - a Multicenter Validation Study
Sehoon Park1,2, Chung Hee Baek3, Su-Kil Park3
1Division of Nephrology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Insights
The C score in IgA nephropathy (IgAN) is a significant predictor of kidney disease progression. Higher C scores (C1 and C2) are associated with an increased risk of adverse renal outcomes, including end-stage renal disease.
Area of Science:
- Nephrology
- Pathology
- Clinical Medicine
Background:
- Immunoglobulin A nephropathy (IgAN) is a common glomerular disease.
- The Oxford classification aids in IgAN prognosis, with the C score (crescents) recently added.
- Validation of the C score's clinical significance is needed.
Purpose of the Study:
- To validate the clinical significance of the C score in the Oxford classification for IgAN.
- To assess the association between crescent presence and IgAN prognosis.
Main Methods:
- Multicenter retrospective cohort study of 3,380 biopsy-confirmed IgAN patients in Korea.
- Clinicopathologic parameters, including crescent degree, were analyzed using Cox regression.
- Composite renal outcome: progression to end-stage renal disease (ESRD) or halving of estimated glomerular filtration rate (eGFR).
Main Results:
- Crescent scores C1 (19.6%) and C2 (1.8%) were identified.
- Both C1 (aHR 1.33) and C2 (aHR 2.24) scores were linked to increased composite outcome risk.
- C2 predicted ESRD and eGFR decline; C1 predicted eGFR decline. Crescent proportion correlated linearly with adverse outcomes.
Conclusions:
- The C score is a valid prognostic parameter for IgAN.
- IgAN patients with crescents require increased clinical attention.
- The C score aids in predicting IgAN progression.
Background/Aims:
Additional validation study was warranted to confirm the clinical significance of C score, which was recently added to the Oxford classification for immunoglobulin A nephropathy (IgAN).
Methods:
We performed a multicenter retrospective cohort study in four hospitals in Korea. Patients who had biopsied glomeruli less than eight or inadequate follow-up information were excluded. Clinicopathologic parameters, including the degree of cellular or fibrocellular crescents, were collected and included in multivariable models for Cox regression analysis. The main outcome was a composite renal outcome, defined as a merge of progression to end-stage renal disease (ESRD) and halving of estimated glomerular filtration rate (eGFR) from baseline.
Results:
Among included 3,380 biopsy-confirmed IgAN patients, there were 664 (19.6%) patients with C1 and 60 (1.8%) patients with C2 scores in the study population. Although C0 and C1 patients shared similar baseline characteristics, C2 patients frequently had more clinicopathologic risk factors for poor prognosis of IgAN. Both C1 [adjusted HR 1.33 (1.11-1.58), P=0.002] and C2 [adjusted HR 2.24 (1.46-3.43), P< 0.001] scores were associated with an increased risk of the composite outcome. C2 was a strong predictive parameter associated with both progression to ESRD and halving of eGFR, whereas C1 was mainly associated with the increased risk of halving of eGFR. Notably, the proportion of crescent showed a linear association with the risk of adverse renal outcome.
Conclusion:
The C score in the Oxford classification is a valid predictive parameter for IgAN prognosis. Additional clinical attention is necessary for IgAN patients with identified cellular or fibrocellular crescents.
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