Evidence map›Paper›PMID 38097864›Full record

ArticleClinical rheumatology2024

Sema4D as a biomarker for Predicting rheumatoid arthritis disease activity.

Huiyuan Liu, Yuelin Zhang, Jiaming Cao, Jiahui Li, Haina Liu, Bingbing Dai, Lei Jin, Ruobing Liao, Lingyu Fu

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Article in Clinical rheumatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 50% 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

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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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Huiyuan LiuDepartment of Clinical Epidemiology and Evidence-Based Medicine, the First Affiliated Hospital, China Medical University, Shenyang, China.
Yuelin ZhangDepartment of Clinical Epidemiology and Evidence-Based Medicine, the First Affiliated Hospital, China Medical University, Shenyang, China.
Jiaming CaoDepartment of Clinical Epidemiology and Evidence-Based Medicine, the First Affiliated Hospital, China Medical University, Shenyang, China.
Jiahui LiDepartment of Clinical Epidemiology and Evidence-Based Medicine, the First Affiliated Hospital, China Medical University, Shenyang, China.
Haina LiuDepartment of Rheumatology, the First Affiliated Hospital, China Medical University, Shenyang, China.
Bingbing DaiDepartment of Rheumatology, Dalian Municipal Central Hospital Affiliated of Dalian Medical University, Dalian, China.
Lei JinDepartment of Rheumatology, ShengJing Hospital Affiliated of China Medical University, Shenyang, China.
Ruobing LiaoDepartment of Clinical Epidemiology and Evidence-Based Medicine, the First Affiliated Hospital, China Medical University, Shenyang, China.
Lingyu FuDepartment of Clinical Epidemiology and Evidence-Based Medicine, the First Affiliated Hospital, China Medical University, Shenyang, China. fulingyucmu@sina.com.ORCID http://orcid.org/0000-0003-3400-2509
China Medical University · CNFirst Hospital of China Medical University · CNDalian Medical University · CNSheng Jing Hospital · CN

Funding

Program of the National Natural Science Foundation of China 82173604
6 · The paper itself

Abstract

objectiveThe semaphorins are membrane or secreted proteins first identified in neural development. Semaphorin 4D (Sema4D) is the first family member found to have immune properties. We evaluated the potential of Sema4D as a marker for rheumatoid arthritis (RA) disease activity, singly and in combination with other known biomarkers including rheumatoid factor (RF) and C-reactive protein (CRP).

methodsThree hundred and eleven RA patients were enrolled. The patients were divided into three groups based on their disease activity in 28 joints (DAS28): mild, moderate, and severe. The healthy group included 40 healthy individuals. SerumSema4D was measured by quantitative ELISA and the specificity and sensitivity of biomarkers were evaluated by generating a receiver operating characteristic (ROC) curve to analyze their diagnostic accuracy.

resultsSerum Sema4D levels in the moderate and severe RA groups were elevated significantly above those of the controls (P < 0.01), while levels in the mild RA and control groups did not differ significantly (P > 0.05). The Sema4D cutoff threshold was 15.7 ng/ml when the DAS28 was applied as a reference. Compared to the erythrocyte sedimentation rate (ESR and CRP, Sema4D had the highest specificity (96.8%) and area under the curve (0.80) for diagnosing RA activity. The highest specificity (100%) for the biomarker combinations was obtained when Sema4D was combined with CRP and anti-CCP, the combination of the Sema4D combined with ESR and anti-CCP had the highest sensitivity (99.35%). According to this result, a new model for jointly calculating RA activity of Sema4D,anti-CCP and CRP was constructed. Meanwhile another model is established by using the method of multivariate analysis.Model comparison results showed the the multiple regression algorithm method fitted the patients' disease activity better.

conclusionThe serum Sema 4D level effectively reflects moderate to severe RA activity. Sema4D levels can be used together with conventional RA biomarkers to increase the diagnostic power of RA activity. The multiple regression algorithm method is promising in disease activity calculation.

Indexed as

Antigens, CDArthritis, RheumatoidSemaphorinsAnti-Citrullinated Protein AntibodiesBiomarkersC-Reactive ProteinHumansAnti-Citrullinated Protein AntibodiesAntigens, CDBiomarkersCD100 antigenC-Reactive ProteinSemaphorinsDAS28Diagnostic biomarkerRheumatoid arthritisSemaphorin 4D (Sema4D)

Identifiers

PMID38097864
OpenAlexW4389766620

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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.