Evidence map›Paper›PMID 42548876›Full record

ArticleFrontiers in neurology

Association between peripheral blood T cell subsets and clinical disability in multiple sclerosis patients.

Penju Liu, Wei Liu, Xiaoting Zhang, Peng Yuan

Abstract read
In one paragraph

Article in Frontiers in neurology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Penju LiuDepartment of Neurology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Wei LiuDepartment of Neurology, The Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou, Gansu Province, China.
Xiaoting ZhangDepartment of Neurology, Hospital of University of Jinan, Jinan, Shandong Province, China.
Peng YuanDepartment of Neurology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Multiple sclerosis (MS) is a chronic immune-mediated disorder involving complex interactions among adaptive and innate immune pathways. The relationship between peripheral blood T cell subsets and clinical disability remains inadequately characterized. This study investigated associations between T cell subsets (CD4+, CD8+, CD4+/CD8 + ratio) and Expanded Disability Status Scale (EDSS) scores in MS patients. Methods: We conducted a cross-sectional study of 48 MS patients who underwent EDSS scoring and flow cytometric analysis of peripheral blood T cell subsets. Clinical and treatment-related characteristics were also collected. Correlations between T cell parameters and EDSS scores were analyzed using Spearman correlation and multivariable linear regression. Exploratory sensitivity analyses were performed to evaluate the potential influence of disease-modifying therapy (DMT) exposure on the association between CD4+/CD8 + ratio and EDSS. Results: Forty-eight MS patients (mean age 35.1 ± 5.8 years, 72.9% female) with mean EDSS score of 3.20 ± 1.50 were included. Mean CD4+/CD8 + ratio was 2.76 ± 1.08 and correlated negatively with EDSS scores ( Conclusion: CD4+/CD8 + ratio was negatively associated with clinical disability in this cross-sectional MS cohort, and stratified analysis showed a progressive decline across disability severity groups. These findings suggest that CD4+/CD8 + ratio may represent an exploratory peripheral immune indicator associated with disability status in MS.

Indexed as

CD4+/CD8+ ratiodisability assessmentmultiple sclerosisneuroimmunologyT cell subsets

Identifiers

PMID42548876
PMCPMC13430141

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.