Evidence map›Paper›PMID 37953381›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Serum Metabolic Fingerprints Characterize Systemic Lupus Erythematosus.

Shunxiang Li, Huihua Ding, Ziheng Qi, Jing Yang, Jingyi Huang, Lin Huang, Mengji Zhang, Yuanjia Tang, Nan Shen, Kun Qian and 2 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
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

12 citing papers in PubMed, 21 citations in OpenAlex.

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  12. Serum Metabolic Fingerprints Characterize Systemic Lupus Erythematosus.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
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

12 authors at 2 institutions in 1 country.

Shunxiang LiSchool of Biomedical Engineering, and Med-X Research Institute, Shanghai Jiao Tong University, Shanghai, 200030, P. R. China.
Huihua DingDepartment of Rheumatology, and Shanghai Institute of Rheumatology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200001, P. R. China.
Ziheng QiSchool of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200241, P. R. China.ORCID 0000-0002-5494-2613
Jing YangSchool of Biomedical Engineering, and Med-X Research Institute, Shanghai Jiao Tong University, Shanghai, 200030, P. R. China.
Jingyi HuangSchool of Biomedical Engineering, and Med-X Research Institute, Shanghai Jiao Tong University, Shanghai, 200030, P. R. China.
Lin HuangShanghai Institute of Thoracic Tumors, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, 200030, P. R. China.
Mengji ZhangSchool of Biomedical Engineering, and Med-X Research Institute, Shanghai Jiao Tong University, Shanghai, 200030, P. R. China.
Yuanjia TangDepartment of Rheumatology, and Shanghai Institute of Rheumatology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200001, P. R. China.
Nan ShenDepartment of Rheumatology, and Shanghai Institute of Rheumatology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200001, P. R. China.
Kun QianSchool of Biomedical Engineering, and Med-X Research Institute, Shanghai Jiao Tong University, Shanghai, 200030, P. R. China.
Qiang GuoDepartment of Rheumatology, and Shanghai Institute of Rheumatology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200001, P. R. China.
Jingjing WanSchool of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200241, P. R. China.ORCID 0000-0001-9324-2647
Shanghai Jiao Tong University · CNEast China Normal University · CN

Funding

Innovation Group Project of Shanghai Municipal Health Commission 2019CXJQ03Innovation Research Plan by the Shanghai Municipal Education Commission ZXWF082101Ministry of Science and Technology of the People's Republic of China 2017YFC0909000Ministry of Science and Technology of the People's Republic of China 2017YFE0124400Ministry of Science and Technology of the People's Republic of China 2021YFA0910104Ministry of Science and Technology of the People's Republic of China 2021YFF0703500National Human Genetic Resources Sharing Service Platform 2005DKA21300National Key R&D Program of China 2022YFC2502800National Natural Science Foundation of China 22074044National Natural Science Foundation of China 22122404National Natural Science Foundation of China 81971771National Natural Science Foundation of China 82001709Programme for Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher LearningShanghai Institutions of Higher Learning 2021-01-07-00-02-E00083Shanghai Rising-Star Programme 19QA1404800State Key Laboratory of Oncogenes and Related Genes KF2105
6 · The paper itself

Abstract

Metabolic fingerprints in serum characterize diverse diseases for diagnostics and biomarker discovery. The identification of systemic lupus erythematosus (SLE) by serum metabolic fingerprints (SMFs) will facilitate precision medicine in SLE in an early and designed manner. Here, a discovery cohort of 731 individuals including 357 SLE patients and 374 healthy controls (HCs), and a validation cohort of 184 individuals (SLE/HC, 91/93) are constructed. Each SMF is directly recorded by nano-assisted laser desorption/ionization mass spectrometry (LDI MS) within 1 minute using 1 µL of native serum, which contains 908 mass to charge features. Sparse learning of SMFs achieves the SLE identification with sensitivity/specificity and area-under-the-curve (AUC) up to 86.0%/92.0% and 0.950 for the discovery cohort. For the independent validation cohort, it exhibits no performance loss by affording the sensitivity/specificity and AUC of 89.0%/100.0% and 0.992. Notably, a metabolic biomarker panel is screened out from the SMFs, demonstrating the unique metabolic pattern of SLE patients different from both HCs and rheumatoid arthritis patients. In conclusion, SMFs characterize SLE by revealing its unique metabolic pattern. Different regulation of small molecule metabolites contributes to the precise diagnosis of autoimmune disease and further exploration of the pathogenic mechanisms.

Indexed as

Arthritis, RheumatoidLupus Erythematosus, SystemicBiomarkersHumansSensitivity and SpecificityBiomarkersdiagnosticsmass spectrometrymetabolitessystemic lupus erythematosus

Identifiers

PMID37953381
PMCPMC10787061
OpenAlexW4388616708

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.