Evidence map›Paper›PMID 37667491›Full record

ArticleClinical cardiology2023

Circulating Th17/Treg as a promising biomarker for patients with rheumatoid arthritis in indicating comorbidity with atherosclerotic cardiovascular disease.

Hongxuan Fan, Jianqi Zhao, Shaobin Mao, Yongle Wang, Miao Wang, Xiaosu Song, Gaizhen Liu, Caihong Wang, Xin Wang, Bin Liang

Open access · goldAbstract read
In one paragraph

Article in Clinical cardiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 25% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
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  4. Frontiers in pharmacology · 2026
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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

10 authors at 1 institution in 1 country.

Hongxuan FanDepartment of Cardiology, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.ORCID http://orcid.org/0000-0002-1234-544X
Jianqi ZhaoDepartment of Cardiology, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.
Shaobin MaoDepartment of Cardiology, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.ORCID http://orcid.org/0000-0001-6763-4356
Yongle WangDepartment of Neurology, The First Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.
Miao WangDepartment of Cardiology, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.
Xiaosu SongDepartment of Cardiology, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.
Gaizhen LiuDepartment of Cardiology, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.
Caihong WangDepartment of Rheumatology, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.
Xin WangDepartment of Rheumatology, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.
Bin LiangDepartment of Cardiology, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.
Shanxi Medical University · CN

Funding

"Four a batch of" talent of Shanxi Province 2021RC08Fund Program for the Scientific Activities of Selected Returned Overseas Professionals in Shanxi Province 20190041Fund Program for the Scientific Activities of Selected Returned Overseas Professionals in Shanxi Province 20220043National Natural Science Foundation of China 81970391
6 · The paper itself

Abstract

backgroundImmune and inflammatory responses have a pivotal role in the pathogenesis of rheumatoid arthritis (RA) and atherosclerotic cardiovascular disease (ASCVD). This study aims to explore the change of peripheral lymphocytes, especially the absolute and relative changes in peripheral T cells in RA patients with and without ASCVD. HYPOTHESIS: The changes in the lymphocyte subsets were assessed to provide a novel insight in diagnosing and preventing ASCVD in patients with RA.

methodsA propensity score matching system (1:1) was conducted to perform a matched case-control study with 169 pairs RA-ASCVD and RA participants. Univariate and multivariate analyses were performed to determine the association between peripheral lymphocytes and RA-ASCVD.

resultMultivariate logistic regression analysis demonstrated that Th17 cell absolute, Th17 cell Ratio, Th17/Treg were associated with a significantly higher risk of ASCVD after model adjustment. Then we focused on Th17/Treg, multivariate logistic analyses in tri-sectional Th17/Treg groups showed that the odds of ASCVD is gradually increasing with Th17/Treg rank's rising after model adjustment. Finally, the restricted cubic spline of Th17/Treg and odds ratio of RA-ASCVD was conducted. Interestingly, we found a critical point of Th17/Treg (critical point = 0.2399). Th17/Treg shows a protective role in the odds of ASCVD when Th17/Treg < 0.2399. With smaller Th17/Treg, the protective efficiency is more obvious when Th17/Treg < 0.2399.

conclusionsOur study suggested that increasing absolute and percentage of Th17 cells in the peripheral blood of patients with RA was associated with the development of ASCVD. And Th17/Treg may be a promising biomarker for patients with RA in indicating comorbidity with ASCVD.

Indexed as

Arthritis, RheumatoidCardiovascular DiseasesBiomarkersCase-Control StudiesComorbidityHumansTh17 CellsT-Lymphocytes, RegulatoryBiomarkersbiomarkerscardiovascularlymphocytesrheumatoid arthritisT cellsTh17/Treg

Identifiers

PMID37667491
PMCPMC10716320
OpenAlexW4386439137

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.