Published online Dec 25, 2025. doi: 10.5527/wjn.v14.i4.112082
Revised: August 8, 2025
Accepted: November 4, 2025
Published online: December 25, 2025
Processing time: 159 Days and 14.1 Hours
Immunoglobulin A nephropathy is a leading cause of primary glomerulonephritis globally. Predicting disease progression using clinical markers alone is often in
To determine the correlation between MEST-C scores and clinical parameters, as well as their utility in predicting long-term kidney outcomes.
A retrospective analysis was conducted on biopsy-confirmed immunoglobulin A nephropathy cases diagnosed from 1998 to 2019 at the Sindh Institute of Urology and Transplantation, with a minimum follow-up of 12 months.
Among 118 patients (mean age: 29.03 ± 10.58 years), median proteinuria was 2.13 g/day, and mean estimated glomerular filtration rate (eGFR) was 67.82 ± 44.60 mL/minute/1.73 m2. Upon admission, 26.4% required kidney replacement the
The E1, T1/2, and C1/C2 components of the MEST-C score showed strong correlations with baseline clinical markers. Delayed diagnosis has led to poor long-term kidney outcomes.
Core Tip: This study highlights the prognostic significance of the Oxford MEST-C score classification in immunoglobulin A nephropathy patients in Pakistan. Among 118 biopsy-confirmed cases, higher MEST-C scores - particularly E1, T1/2, and C1/C2 lesions - correlated with worse clinical parameters like proteinuria and estimated glomerular filtration rate, and predicted poor kidney survival. Remission rates declined, and end-stage kidney disease rates increased over time, with only 33.3% kidney survival at 10 years. These findings emphasize the value of integrating histopathological scoring with clinical data for early risk stratification. Delayed diagnosis contributed to adverse outcomes, underscoring the need for timely recognition and intervention in immunoglobulin A nephropathy management.
