Proteinuria in Immune-Mediated Glomerular Diseases as a Marker of Disease Activity and Therapeutic Response: A Retrospective Study
PDF

Keywords

proteinuria; chronic glomerulonephritis; chronic kidney disease; therapeutic response

Categories

How to Cite

Benkova-Petrova, M., & Bogdanova, S. (2026). Proteinuria in Immune-Mediated Glomerular Diseases as a Marker of Disease Activity and Therapeutic Response: A Retrospective Study. Rheumatology (Bulgaria), 33(4), 28-45. https://doi.org/10.35465/gb6efc68

Abstract

Background: Proteinuria is an established marker of activity, severity, and progression in glomerular diseases. In addition to reflecting damage to the glomerular filtration barrier, it also plays a pathogenetic role in the development of tubulointerstitial inflammation and fibrosis. Objectives: To assess the dynamics of proteinuria in patients with chronic glomerulonephritis and its significance as an indicator of therapeutic response. Methods: A retrospective study of a total of 57 patients with different morphological forms of chronic glomerulonephritis, treated at the Clinic of Nephrology and Dialysis, St. Marina University Hospital – Varna, were followed for a period of 24 months. Twenty-four-hour proteinuria and the protein-to-creatinine ratio (Pr/Cr) in a spot urine sample were analyzed. All patients received optimal nephroprotective therapy, and immunosuppressive treatment was administered when indicated. Results: The mean baseline 24-hour proteinuria was 5.94 g/24 h. By the third month, a statistically significant decrease to 3.65 g/24 h was observed (p≈0.008), followed by a further reduction to 2.7 g/24 h at month 6 and to 1.72 g/24 h at month 12. The observed reduction indicates an early and sustained therapeutic response in the studied patient population. Analysis of the protein-to-creatinine ratio confirmed the same favorable trend and supports its applicability as a reliable marker for monitoring proteinuria in clinical practice. Conclusion: Early and sustained reduction of proteinuria is a reliable indicator of therapeutic efficacy in chronic glomerular diseases and is associated with a more favorable renal prognosis. Proteinuria has substantial value both as a prognostic marker and as a surrogate endpoint in clinical follow-up.

PDF

References

1.Rovin BH, Adler SG, Barratt J et al. Executive summary of the KDIGO 2021 Guideline for the Management of Glomerular Diseases. Kidney Int. 2021 Oct;100(4):753-779. doi: 10.1016/j.kint.2021.05.015. PMID: 34556300.

2. Kidney Disease: Improving Global Outcomes (KDIGO) CKD Work Group. KDIGO 2024 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney Int. 2024;105(4S):S117-S314.

3. Keane WF. Proteinuria: its clinical importance and role in progressive renal disease. Am J Kidney Dis. 2000 Apr;35(4 Suppl 1):S97-105. doi: 10.1016/s0272-6386(00)70237-x. PMID: 10766008.

4. Thompson A, Carroll K, A Inker L et al. Proteinuria Reduction as a Surrogate End Point in Trials of IgA Nephropathy. Clin J Am Soc Nephrol. 2019 Mar 7;14(3):469-481. doi: 10.2215/CJN.08600718. Epub 2019 Jan 11. PMID: 30635299; PMCID: PMC6419287.

5. Remuzzi G, Bertani T. Pathophysiology of progressive nephropathies. N Engl J Med. 1998 Nov 12;339(20):1448-56. doi: 10.1056/NEJM199811123392007. PMID: 9811921.

6. Chen L, Wang Y, Tay YC et al. Proteinuria and tubulointerstitial injury. Kidney Int Suppl. 1997 Oct;61:S60-2. PMID: 9328968.

7. Praga M, Morales E. Renal damage associated with proteinuria. Kidney Int Suppl. 2002 Dec;(82):S42-6. doi: 10.1046/j.1523-1755.62.s82.9.x. PMID: 12410854.

8. Inker LA, Mondal H, Greene T, Masaschi T, Locatelli F, Schena FP, Katafuchi R, Appel GB, Maes BD, Li PK, Praga M, Del Vecchio L, Andrulli S, Manno C, Gutierrez E, Mercer A, Carroll KJ, Schmid CH, Levey ASet al. Early Change in Urine Protein as a Surrogate End Point in Studies of IgA Nephropathy: An Individual-Patient Meta-analysis. Am J Kidney Dis. 2016 Sep;68(3):392-401. doi: 10.1053/j.ajkd.2016.02.042. Epub 2016 Mar 29. PMID: 27032886.

9. Петров А. В търсене на “течната биопсия“: Уринната протеомика като нов подход в диагностиката и прогнозата на хроничното бъбречно заболяване", изд.Стно, Варна, 2025, ISBN 978-619-241-347-7

10. Wang M, Yang J, Fang X et al. Membranous nephropathy: pathogenesis and treatments. MedComm (2020). 2024 Jun 29;5(7):e614. doi: 10.1002/mco2.614. PMID: 38948114; PMCID: PMC11214595.

11. The GISEN Group (Gruppo Italiano di Studi Epidemiologici in Nefrologia). Randomised placebo-controlled trial of effect of ramipril on decline in glomerular filtration rate and risk of terminal renal failure in proteinuric, non-diabetic nephropathy. Lancet. 1997 Jun 28;349(9069):1857-63. PMID: 9217756.

12. Ruggenenti P, Perna A, Gherardi G et al. Renoprotective properties of ACE-inhibition in non-diabetic nephropathies with non-nephrotic proteinuria. Lancet. 1999 Jul 31;354(9176):359-64. doi: 10.1016/S0140-6736(98)10363-X. PMID: 10437863.

13.Heerspink HJL, Stefánsson BV, Correa-Rotter R et al. DAPA-CKD Trial Committees and Investigators. Dapagliflozin in Patients with Chronic Kidney Disease. N Engl J Med. 2020 Oct 8;383(15):1436-1446. doi: 10.1056/NEJMoa2024816. Epub 2020 Sep 24. PMID: 32970396.

14. The EMPA-KIDNEY Collaborative Group. Empagliflozin in patients with chronic kidney disease. N Engl J Med. 2023;388(2):117-127.

15. de Zeeuw D, Coll B, Andress D et al. The endothelin antagonist atrasentan lowers residual albuminuria in patients with type 2 diabetic nephropathy. J Am Soc Nephrol. 2014 May;25(5):1083-93. doi: 10.1681/ASN.2013080830. Epub 2014 Apr 10. PMID: 24722445; PMCID: PMC4005314.

16. Rovin BH, Barratt J, Heerspink HJL et al. DUPRO steering committee and PROTECT Investigators. Efficacy and safety of sparsentan versus irbesartan in patients with IgA nephropathy (PROTECT): 2-year results from a randomised, active-controlled, phase 3 trial. Lancet. 2023 Dec 2;402(10417):2077-2090. doi: 10.1016/S0140-6736(23)02302-4. Epub 2023 Nov 3. PMID: 37931634.

17. Fervenza FC, Appel GB, Barbour SJ et al. MENTOR Investigators. Rituximab or Cyclosporine in the Treatment of Membranous Nephropathy. N Engl J Med. 2019 Jul 4;381(1):36-46. doi: 10.1056/NEJMoa1814427. PMID: 31269364.

18. Hogan MC, Reich HN, Nelson PJ et al. The relatively poor correlation between random and 24-hour urine protein excretion in patients with biopsy-proven glomerular diseases. Kidney Int. 2016 Nov;90(5):1080-1089. doi: 10.1016/j.kint.2016.06.020. Epub 2016 Aug 12. PMID: 27528553; PMCID: PMC5065749.

19. Raza A, Nawaz SH, Rashid R et al. The correlation of spot urinary protein-to-creatinine ratio with 24-h urinary protein excretion in various glomerulopathies. World J Nephrol. 2023 Dec 25;12(5):159-167. doi: 10.5527/wjn.v12.i5.159. PMID: 38230302; PMCID: PMC10789082.

20. Dimitrov S. Shivacheva T, Kadinov V. Our experience with adalimumab in the treatment of patients with inflammatory joint diseases, Revmatologiia (Bulgaria), 2011, Том 19, № 4, стр.53-58

21. Аbushev P, Ganev T, Kirilov P. ROBOT-ASSISTED PARTIAL NEPHRECTOMY FOR T1B RENAL TUMORS: PERIOPERATIVE AND POSTOPERATIVE OUTCOMES, Journal of IMAB, 2025, Issue 31, № Supplement, pp.103-106

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

Copyright (c) 2026 Dr. Miroslava Stancheva Benkova-Petrova, Dr. Simona Bogdanova-Petrova (Author)

Downloads

Download data is not yet available.