# Validation and optimization of classification criteria for childhood-onset systemic lupus erythematosus in a multi-center Chinese cohort

**Authors:** Yudi Zhang, Tian Shen, Sihao Gao, Junxia Yan, Jingcheng Shi, Xuemei Tang, Mo Wang, Jun Yang, Haiguo Yu, Huawei Mao, Lanjun Shuai, Yongzhen Li, Yan Cao, Xiaoyan Li, Ying Wang, Qian Liu, Hongmei Song, Xiaochuan Wu

PMC · DOI: 10.3389/fimmu.2025.1611349 · Frontiers in Immunology · 2025-07-17

## TL;DR

This study tested and improved classification criteria for childhood-onset lupus in a large Chinese cohort to better diagnose the disease.

## Contribution

An optimized classification schema for cSLE was developed by modifying the 2019 EULAR/ACR criteria.

## Key findings

- The 2019 EULAR/ACR criteria had high sensitivity and specificity, with a threshold score of 10.
- Removing alopecia and arthritis criteria and redefining urinary protein improved specificity to 99.3%.
- In ANA-positive patients, the optimized criteria improved specificity without reducing sensitivity.

## Abstract

This study evaluated the diagnostic accuracy of the 2012 SLICC and 2019 EULAR/ACR criteria in Chinese cSLE patients and aimed to develop an optimized classification schema based on the 2019 EULAR/ACR criteria, specifically tailored for cSLE.

Data from cSLE and control cases were extracted from the CAPRID database. Gold-standard diagnosis were established by consensus among 43 rheumatologists (≥80% agreement). From 1,390 consensus cases, a random selection of 1,045 cases (512 cSLE/533 non-cSLE) were allocated to derivation (n=522) and validation (n=523) cohorts. The 2012 SLICC and 2019 EULAR/ACR criteria were evaluated in the total cohort. Multiple optimization schemes were then developed through LASSO regression with expert consultation in the derivation cohort. All potential optimization schemes underwent validation in the validation cohort, from which the optimal scheme was selected and further evaluated in an ANA-positive subgroup.

The 2012 SLICC criteria demonstrated sensitivity of 96.7% and specificity of 96.5%, while the 2019 EULAR/ACR criteria had sensitivity of 95.3% and specificity of 97.8%, with an optimal total score threshold of 10. When both the non-scarring alopecia and arthritis criteria were removed alongside the redefined urinary protein criterion, specificity significantly improved to 99.3% (P < 0.05), while sensitivity remained unaffected at 94.1% (P = 0.210). In the ANA-positive cohort, the optimized integrated scheme significantly improved specificity (97.7% vs. 86.4%, P = 0.012) while maintaining comparable sensitivity (96.2% vs. 97.8%, P = 0.138).

Both criteria performed well in Chinese cSLE patients. Optimizing the 2019 EULAR/ACR criteria by removing alopecia and arthritis criteria and modifying the urinary protein criterion enhanced specificity without compromising sensitivity.

## Linked entities

- **Diseases:** lupus (MONDO:0004670)

## Full-text entities

- **Genes:** BTG3 (BTG anti-proliferation factor 3) [NCBI Gene 10950] {aka ANA, ANA/BTG3, APRO4, TOB5, TOB55, TOFA}, CSF2 (colony stimulating factor 2) [NCBI Gene 1437] {aka CSF, GMCSF}
- **Diseases:** Raynaud's phenomenon (MESH:D011928), joint involvement (MESH:D007592), musculoskeletal involvement (MESH:D009140), autoimmune pancreatitis (MESH:D000081012), alveolar hemorrhage (MESH:D006470), KD (MESH:D009080), alopecia (MESH:D000505), neuropsychiatric (MESH:C000631768), autoimmune hyperthyroidism (MESH:D006111), CRF (MESH:C565541), autoimmune hepatitis (MESH:D019693), memory impairment (MESH:D008569), mesenteric vasculitis (MESH:D014657), rheumatic fever (MESH:D012213), autoimmune disorder (MESH:D001327), headaches (MESH:D006261), juvenile dermatomyositis (MESH:D003882), arthritis (MESH:D001168), effusion (MESH:D000080324), immune dysregulation (OMIM:614878), infectious diseases (MESH:D003141), synovitis (MESH:D013585), necrotizing lymphadenitis (MESH:D008199), Systemic Lupus (MESH:D008180), chronic inflammation (MESH:D007249), ANCA-associated vasculitis (MESH:D056648), alopecia areata (MESH:D000506), neonatal lupus (MESH:C536397), swelling (MESH:D004487), Rheumatic and Immunologic Diseases (MESH:D007154), fever (MESH:D005334), arthralgia (MESH:D018771), neurological symptoms (MESH:D009461), neuropsychiatric manifestations (MESH:D012877), neoplastic diseases (MESH:D004194), interstitial lung disease (MESH:D017563), rheumatic diseases (MESH:D012216), proteinuria (MESH:D011507), renal involvement (MESH:C565423), Takayasu's arteritis (MESH:D013625), JIA (MESH:D001171), involvement (MESH:C564676), tenderness (MESH:D063806), morning stiffness (MESH:D048968), HSP (MESH:D011695)
- **Chemicals:** anti-dsDNA (-), Cr (MESH:D002857)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12310706/full.md

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Source: https://tomesphere.com/paper/PMC12310706