Evidence map›Paper›PMID 39318632›Full record

ArticleFrontiers in immunology2024

Increased serum human epididymis protein 4 is associated with disease activity and systemic involvement in pediatric-onset systemic lupus erythematosus.

Chenxi Liu, Lingyi Yan, Menglan Zhang, Yifei Duan, Jie Luo, Zhijun Liu, Ting Liu, Jiyu Tong, Yongmei Jiang

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. HE4: a potential diagnostic biomarker in autoimmune diseases.Central-European journal of immunology · 2026
    Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Chenxi LiuDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Lingyi YanDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Menglan ZhangDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Yifei DuanDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Jie LuoDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Zhijun LiuDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Ting LiuDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Jiyu TongKey Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Sichuan University, Chengdu, Sichuan, China.
Yongmei JiangDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: We aimed to investigate human epididymis protein 4 (HE4) as a potential biomarker in patients with pediatric-onset systemic lupus erythematosus (pSLE), particularly on the association of serum HE4 levels with disease activity and other laboratory tests. Methods: We included 137 patients with pSLE and 75 age- and sex-matched healthy controls (HCs). Serum HE4 level was measured by a chemiluminescent microparticle on an Abbott ARCHITECT i2000SR Immunoassay Analyzer. Comparisons between groups were performed using the independent Student t-test, Mann-Whitney U test, Chi-square test, or Fisher's exact test, as appropriate. We also determined the relationships between HE4 and clinical parameters and evaluated disease activity using SLE Disease Activity Index (SLEDAI) and renal SLEDAI (rSLEDAI). Results: Serum HE4 levels in patients with pSLE (44.6 pmol/L; IQR, 32.5-73.5) were significantly higher than those in HCs (38.9 pmol/L; IQR, 34-46.1). HE4 levels were significantly higher in moderate to severe disease activities (57.4 pmol/L, IQR 37.7-164.5) than in mild disease activities (38.8 pmol/L, IQR 30.1-48.5) or HCs (38.9 pmol/L, IQR 34.0-46.1), as well as in active renal disease activities (77.2 pmol/L, IQR 47.4-224.1) than in inactive renal disease activities (36.1 pmol/L, IQR 27.8-46.7). The ROC curve analysis showed that HE4 could discriminate pSLE with renal (AUC, 0.717; 95% CI, 0.632-0.801), hematological (AUC, 0.740; 95% CI, 0.648-0.831), and cardiovascular involvement (AUC:0.775, 95% CI 0.669-0.880). Serum HE4 levels significantly correlated with several indicators related to renal morbidity, such as creatinine, blood urea nitrogen, uric acid, cystatin C, urine protein/24 h, etc. Conclusion: Serum HE4 levels in pSLE were elevated and highly associated with disease activity and systemic involvement, indicating HE4 as a potential biomarker for pSLE.

Indexed as

BiomarkersLupus Erythematosus, SystemicWAP Four-Disulfide Core Domain Protein 2AdolescentAge of OnsetCase-Control StudiesChildFemaleHumansMaleROC CurveSeverity of Illness IndexBiomarkersWAP Four-Disulfide Core Domain Protein 2WFDC2 protein, humanbiomarkercorrelationhuman epididymis protein 4lupus nephritispediatric-onset systemic lupus erythematosus

Identifiers

PMID39318632
PMCPMC11419971

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.