Correlation of Oxford Classification Score with Early Response to Treatment in IgA Nephropathy: A Cross-Sectional Study
Abstract
Objective: To evaluate the correlation between the Oxford classification score and early response to treatment in Immunoglobulin A nephropathy (IgAN) in a single-center study in northern Pakistan.
Methods: This cross-sectional study was conducted at the Department of Nephrology, Shifa International Hospital, Islamabad, from July 2024 to January 2025. Patients aged 18 to 65 years with biopsy-proven primary IgAN were included. Baseline demographic, clinical, and laboratory data, including serum creatinine, eGFR, and proteinuria, were recorded. Renal biopsies were assessed using Oxford classification, evaluating mesangial hypercellularity (M), endocapillary hypercellularity (E), segmental glomerulosclerosis (S), tubular atrophy/interstitial fibrosis (T) and crescents (C). Early treatment response was defined as a ≥50% reduction in proteinuria after three months.
Results: Of total 30 patients, the median age was 30.5 (24.5 – 43.5) years. The Oxford classification revealed that 19 (63.3%) patients had M1 and S1 lesions, 16 (53.3%) had E0 lesions, and 12 (40.0%) exhibited T0 lesions. A significant reduction in proteinuria was observed after treatment (p-value < 0.001), with eGFR and serum albumin levels improving significantly (p-value 0.003 and p-value 0.023) respectively. T1-2 lesions demonstrated a strong negative correlation with eGFR (ρ = -0.760, p-value < 0.001), and E1 lesions were moderately correlated with proteinuria (ρ = 0.378, p-value 0.039). Treatment response was observed in 12 (40%) patients, but no significant associations were found with individual Oxford classification scores.
Conclusion: A significant reduction in proteinuria and improvement in eGFR and albumin were observed post-treatment. Histopathological features correlated with renal outcomes, emphasizing their significance in predicting early treatment outcomes.
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Rajasekaran A, Julian BA, Rizk DV. IgA Nephropathy: An interesting autoimmune kidney disease. Am J Med Sci 2021; 361:176-94. doi:10.1016/j.amjms.2020.10.003
Habas E, Ali E, Farfar K, Erayes M, Alfitori J, Habas E, et al. IgA nephropathy pathogenesis and therapy: Review & updates. Medicine (Baltimore) 2022; 101:e31219. doi:10.1097/MD.0000000000031219
Canney M, Barbour SJ, Zheng Y, Coppo R, Zhang H, Liu ZH, et al. International IgA Nephropathy network; International IgA Nephropathy network investigators. Quantifying duration of proteinuria remission and association with clinical outcome in IgA Nephropathy. J Am Soc Nephrol 2021; 32:436-47. doi:10.1681/ASN.2020030349
Xu RC, Guo JY, Cao T, Xu Y, Liao Y, Chn YN, et al. A mixed-method evaluation of the relationship between Oxford classification scores and longitudinal changes in proteinuria in patients with immunoglobulin A nephropathy. Front Endocrinol (Lausanne) 2023; 13:890900. doi:10.3389/fendo.2022.890900
Suzuki H. Biomarkers for IgA nephropathy on the basis multi-hit pathogenesis. Clin Exp Nephrol 2019; 23:26-31. doi:10.1007/s10157-018-1582-2
Wheeler DC, Toto RD, Stefánsson BV, Jongs N, Chertow GM, Greene T, et al. DAPA-CKD Trial Committees and Investigators. A pre-specified analysis of the DAPA-CKD trial demonstrates the effects of dapagliflozin on major adverse kidney events in patients with IgA nephropathy. Kidney Int 2021; 100:215-24. doi:10.1016/j.kint.2021.03.033
EMPA-KIDNEY Collaborative Group. Impact of primary kidney disease on the effects of empagliflozin in patients with chronic kidney disease: secondary analyses of the EMPA-KIDNEY trial. Lancet Diabetes Endocrinol 2024; 12:51-60. doi:10.1016/S2213-8587(23)00322-4
Heerspink HJ, Radhakrishnan J, Alpers CE, Barratt J, Bielr S, Diva U, et al. PROTECT Investigators. Sparsentan in patients with IgA nephropathy: a prespecified interim analysis from a randomised, double-blind, active-controlled clinical trial. Lancet 2023; 401:1584-94. doi:10.1016/S0140-6736(23)00569-X
Lv J, Wong MG, Hladunewich MA, Jha V, Hooi LS, Mna-ghan H, et al. TESTING study group. Effect of oral methylprednisolone on decline in kidney function or kidney failure in patients with IgA Nephropathy: The TESTING randomized clinical trial. J Am Med Assoc 2022; 327:1888-98. doi:10.1001/jama.2022.5368
Hou FF, Xie D, Wang J, Xu X, Yang X, Ai J, et al. MAIN trial investigators. Effectiveness of mycophenolate mofetil among patients with progressive IgA Nephropathy: A randomized clinical trial. JAMA Netw Open 2023; 6:e2254054. doi:10.1001/jamanetworkopen.2022.54054
Kidney Disease: Improving Global Outcomes (KDIGO) glomerular diseases work group. KDIGO 2021 clinical practice guideline for the management of glomerular diseases. Kidney Int 2021; 100:S1-276. doi:10.1016/j.kint.2021.05.021
Fellstrom BC, Barratt J, Cook H, Copo R, Feehally J, Fijter JW, et al. NEFIGAN trial investigators. Targeted-release budesonide versus placebo in patients with IgA nephropathy (NEFIGAN): a double-blind, randomised, placebo-controlled phase 2b trial. Lancet 2017; 389:2117-27. doi:10.1016/S0140-6736(17)30550-
Wu H, Xia Z, Gao C, Zhang P, Yang X, Wang R, et al. The correlation analysis between the Oxford classification of Chinese IgA nephropathy children and renal outcome- A retrospective cohort study. BMC Nephrol 2020; 21:247. doi:10.1186/s12882-020-01913-7
Moriyama T, Karasawa K, Miyabe Y, Akiyama K, Ogura S, Takabe T, et al. Validation of the revised Oxford classification for IgA nephropathy considering treatment with corticosteroids/immunosuppressors. Sci Rep 2020; 10:11151. doi:10.1038/s41598-020-68087-y
Coppo R, Troyanov S, Bellur S, Cattran D, Cook HT, Feehally J, et al. VALIGA study of the ERA-EDTA immunonephrology working group. Validation of the Oxford classification of IgA nephropathy in cohorts with different presentations and treatments. Kidney Int 2014; 86:828-36. doi:10.1038/ki.2014.63
Yeter HH, Gonul I, Guz G, Helvaci O, Korucu B, Akcay OF, et al. Combining clinical features and MEST-C score in IgA nephropathy may be a better determinant of kidney survival. Rom J Intern Med 2020; 58:209-18. doi:10.2478/rjim-2020-0025
Haaskjold YL, Bjorneklett R, Bostad L, Bostad LS, Lura NG, Knoop T. Utilizing the MEST score for prognostic staging in IgA nephropathy. BMC Nephrol 2022; 23:26. doi:10.1186/s12882-021-02653-y
Trimarchi H, Barratt J, Cattran DC, Cook HT, Coppo R, Haas M, et al. IgAN classification working group of the international IgA Nephropathy network and the renal pathology society; conference participants. Oxford Classification of IgA nephropathy 2016: an update from the IgA Nephropathy classification working group. Kidney Int 2017; 91:1014-21. doi:10.1016/j.kint.2017.02.003
Yoon CY, Chang TI, Kang EW, Lim BJ, Kie JH, Kee YK, et al. Clinical usefulness of the Oxford classification in determining immunosuppressive treatment in IgA nephropathy. Ann Med 2017; 49:217-29. doi:10.1080/07853890.2016.1252058
Coppo R, D'Arrigo G, Tripepi G, Russo ML, Roberts IS, Bellur S, et al. ERA-EDTA immunonephrology working group. Is there long-term value of pathology scoring in immunoglobulin A nephropathy? A validation study of the Oxford Classification for IgA Nephropathy (VALIGA) update. Nephrol Dial Transplant 2020; 35:1002-09. doi:10.1093/ndt/gfy302
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