Evidence map›Paper›PMID 35522124›Full record

ArticleJournal of clinical laboratory analysis2022

Th1, Th2, and Th17 cells are dysregulated, but only Th17 cells relate to C-reactive protein, D-dimer, and mortality risk in Stanford type A aortic dissection patients.

Mowei Song, Li Deng, Hongtao Shen, Guofu Zhang, Hang Shi, Erjun Zhu, Qingping Xia, Hongguang Han

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2022. 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
2.6field-weighted citation impact, top 9% 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, 18 citations in OpenAlex.

  1. Article
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  6. CD36-mediated ferroptosis destabilizes CD4Cell death & disease · 2024
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  8. Correlation of the serum cell division cycle 42 with CD4Frontiers in cardiovascular medicine · 2024
    Article
  9. Editorial: Novel biomarkers in acute aortic dissection.Frontiers in cardiovascular medicine · 2024
    Article
  10. Review
  11. Review
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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

8 authors at 3 institutions in 1 country.

Mowei SongDepartment of Cardiology, The First Affiliated Hospital, Harbin Medical University, Harbin, China.
Li DengDepartment of Extracorporeal Life Support, The People's Hospital of Gaozhou, Gaozhou, China.
Hongtao ShenDepartment of Orthopedic Surgery, The First Affiliated Hospital, Harbin Medical University, Harbin, China.
Guofu ZhangDepartment of Cardiovascular Surgery, The First Affiliated Hospital, Harbin Medical University, Harbin, China.
Hang ShiDepartment of Cardiovascular Surgery, The First Affiliated Hospital, Harbin Medical University, Harbin, China.
Erjun ZhuDepartment of Cardiovascular Surgery, The First Affiliated Hospital, Harbin Medical University, Harbin, China.
Qingping XiaDepartment of Science and Education, The People's Hospital of Gaozhou, Gaozhou, China.
Hongguang HanDepartment of Cardiovascular Surgery, General Hospital of Northern Theater Command, Shenyang, China.ORCID https://orcid.org/0000-0003-1187-2421
Harbin Medical University · CNGaozhou People's Hospital · CNGeneral Hospital of Shenyang Military Region · CN

Funding

National Natural Science Foundation of China 81900369Natural Science Foundation of Heilongjiang Science and Technology Department H2015055Research on Monitoring System of Vital Signs Based on Air Transport and Wear for Critical Patients in Battlefield 20QNPY090Research on Synergistic Innovation of Vital Signs Signal Collection and Transmission and Intelligent Processing in Emergency Medical Evacuation 20-205-4-016
6 · The paper itself

Abstract

backgroundT helper (Th) cells are closely involved in vascular inflammation, endothelial dysfunction, and atherogenesis, which are the hallmarks of aortic dissection (AD). This study aimed to evaluate the clinical value of Th1, Th2, and Th17 cell measurements in Stanford type A AD patients.

methodsStanford type A AD patients (N=80) and non-AD patients with chest pain (N = 40) were recruited. Then, Th1, Th2, and Th17 cells in peripheral blood CD4

resultsTh1 and Th17 cells were higher, while Th2 cells were lower in Stanford type A AD patients compared with non-AD patients (all p < 0.001). Meanwhile, Th1 cells (area under curve (AUC): 0.734, 95% confidence interval (CI): 0.640-0.828), Th2 cells (AUC: 0.841, 95% CI: 0.756-0.925), and Th17 cells (AUC: 0.898, 95% CI: 0.839-0.957) could distinguish Stanford type A patients from non-AD patients. Moreover, Th1 cells (p = 0.037) and Th17 cells (p = 0.001) were positively related to CRP, and Th17 cells (p = 0.039) were also positively associated with D-dimer in Stanford type A AD patients. Furthermore, Th17 cells were elevated in deaths compared with survivors (p = 0.001), also, it could estimate 30-day mortality risk in Stanford type A AD patients with an AUC of 0.741 (95% CI: 0.614-0.867), which was similar to the value of CRP (AUC: 0.771, 95% CI: 0.660-0.882), but lower than the value of D-dimer (AUC: 0.818, 95% CI: 0.722-0.913).

conclusionTh1, Th2, and Th17 cells are dysregulated, but only the Th17 cells relate to CRP, D-dimer, and 30-day mortality risk in Stanford type A AD patients.

Indexed as

Aortic DissectionTh17 CellsC-Reactive ProteinCytokinesFibrin Fibrinogen Degradation ProductsHumansTh1 CellsTh2 CellsC-Reactive ProteinCytokinesFibrin Fibrinogen Degradation Productsfibrin fragment DC-reactive proteinD-dimer; 30-day mortality riskstanford type A aortic dissectionT helper cells

Identifiers

PMID35522124
PMCPMC9169215
OpenAlexW4228997453

What OpenQuestion holds

Textmetadata
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.