Development of clinical and laboratory biomarkers in an international cohort of 428 children with lupus nephritis
- PMID: 38802607
- DOI: 10.1007/s00467-024-06405-6
Development of clinical and laboratory biomarkers in an international cohort of 428 children with lupus nephritis
Abstract
Background: Lupus nephritis (LN) is a very severe manifestation of lupus. There is no consensus on which treatment goals should be achieved to protect kidney function in children with LN.
Methods: We retrospectively analyzed trends of commonly used laboratory biomarkers of 428 patients (≤ 18 years old) with biopsy-proven LN class ≥ III. We compared data of patients who developed stable kidney remission from 6 to 24 months with those who did not.
Results: Twenty-five percent of patients maintained kidney stable remission while 75% did not. More patients with stable kidney remission showed normal hemoglobin and erythrocyte sedimentation rate from 6 to 24 months compared to the group without stable kidney remission. eGFR ≥ 90 ml/min/1.73m2 at onset predicted the development of stable kidney remission (93.8%) compared to 64.7% in those without stable remission (P < 0.00001). At diagnosis, 5.9% and 20.2% of the patients showed no proteinuria in the group with and without stable kidney remission, respectively (P = 0.0001). dsDNA antibodies decreased from onset of treatment mainly during the first 3 months in all groups, but more than 50% of all patients in both groups never normalized after 6 months. Complement C3 and C4 increased mainly in the first 3 months in all patients without any significant difference.
Conclusions: Normal eGFR and the absence of proteinuria at onset were predictors of stable kidney remission. Significantly more children showed normal levels of Hb and erythrocyte sedimentation rate (ESR) from 6 to 24 months in the group with stable kidney remission.
Keywords: Biomarkers; Lupus nephritis; Pediatric; Proteinuria; Remission; eGFR.
© 2024. The Author(s), under exclusive licence to International Pediatric Nephrology Association.
Similar articles
-
Clinico-pathological associations of serum VCAM-1 and ICAM-1 levels in patients with lupus nephritis.Lupus. 2021 Jun;30(7):1039-1050. doi: 10.1177/09612033211004727. Epub 2021 Mar 26. Lupus. 2021. PMID: 33765901
-
Comparison of urinary parameters, biomarkers, and outcome of childhood systemic lupus erythematosus early onset-lupus nephritis.Adv Rheumatol. 2020 Feb 1;60(1):10. doi: 10.1186/s42358-020-0114-4. Adv Rheumatol. 2020. PMID: 32005292
-
Clinical and immunological biomarkers can identify proliferative changes and predict renal flares in lupus nephritis.Arthritis Res Ther. 2025 Mar 31;27(1):72. doi: 10.1186/s13075-025-03536-5. Arthritis Res Ther. 2025. PMID: 40165257 Free PMC article.
-
Lupus nephritis: redefining the treatment goals.Kidney Int. 2025 Feb;107(2):198-211. doi: 10.1016/j.kint.2024.10.018. Epub 2024 Nov 8. Kidney Int. 2025. PMID: 39521057 Review.
-
Something new about prognostic factors for lupus nephritis? A systematic review.Lupus. 2021 Dec;30(14):2256-2267. doi: 10.1177/09612033211061475. Epub 2021 Dec 15. Lupus. 2021. PMID: 34907831
References
-
- Hagelberg S, Lee Y, Bargman J, Mah G, Schneider R, Laskin C et al (2002) Longterm follow up of childhood lupus nephritis. J Rheumatol 29:2635–2642 - PubMed
-
- Chan EY, Yap DY, Wong WT, Wong WH, Wong SW, Lin KY, Hui FY, Yee-Ming J, Lam SS, Wong JK, Lai FF, Ho TW, Tong PC, Lai WM, Chan TM, Ma AL (2022) Long-term outcomes of children and adolescents with biopsy-proven childhood-onset lupus nephritis. Kidney Int Rep 8:141–150. https://doi.org/10.1016/j.ekir.2022.10.014 - DOI - PubMed - PMC
-
- Suhlrie A, Hennies I, Gellermann J, Büscher A, Hoyer P, Waldegger S et al (2020) Twelve-month outcome in juvenile proliferative lupus nephritis: results of the German registry study. Pediatr Nephrol 35:1235–1246. https://doi.org/10.1007/s00467-020-04501-x - DOI - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous