Evidence map›Paper›PMID 35432312›Full record

ArticleFrontiers in immunology2022

Clinical Characteristics and CD4

Yan Yang, Chen Wang, Lei Shi, Shuoran Yang, Yan Liu, Jing Luo, Caihong Wang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.7field-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

13 citing papers in PubMed, 21 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Yan YangDepartment of Rheumatology and Immunology, The Second Hospital of Shanxi Medical University, Taiyuan, China.
Chen WangDepartment of Pathology, The Second Hospital of Shanxi Medical University, Taiyuan, China.
Lei ShiDepartment of Rheumatology and Immunology, The Second Hospital of Shanxi Medical University, Taiyuan, China.
Shuoran YangDepartment of Oral and Maxillofacial Surgery, The Second Hospital of Shanxi Medical University, Taiyuan, China.
Yan LiuDepartment of Rheumatology and Immunology, The Second Hospital of Shanxi Medical University, Taiyuan, China.
Jing LuoDepartment of Rheumatology Laboratory, The Second Hospital of Shanxi Medical University, Taiyuan, China.
Caihong WangDepartment of Rheumatology and Immunology, The Second Hospital of Shanxi Medical University, Taiyuan, China.
Shanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: To characterize the clinical features of IgG4-related disease (IgG4-RD) and analyze the peripheral T lymphocyte subsets and cytokine levels. Methods: A total of 52 patients with newly diagnosed IgG4-RD were enrolled in the retrospective study. Baseline clinical characteristics and examinational findings were systematically reviewed. Results: IgG4-RD patients had a male predominance, with an average age of 57.4 ± 10.3 years (range 27-81). The mean number of involved organs was 2.7 (range 1-8). Submandibular gland (57.7%) and lacrimal gland/orbit (40.4%) were the most commonly involved organs. Serum IgG4 increased in 97.9% of the patients, the median level was 1300 (585.25, 1975) mg/dl. Decreased C3 and C4 accounted for 77.8% and 55.6% of this patient cohort, respectively. Receiver operating characteristic (ROC) test indicated the possibility of lung/pleura involvement when C3 was less than 0.570 g/l (AUC = 0.788, P = 0.014), and kidney involvement when C3 was less than 0.545 g/l (AUC = 0.796, P = 0.014). Compared with healthy controls (HC), the absolute Th1 counts were higher in IgG4-RD patients (157.58 cells/μl Conclusion: Submandibular and lacrimal glands are the most commonly involved organs in IgG4-RD. Serum C3 level could be a predictor of lung/pleura and kidney involvement in the disease process. Elevated Th1 cells are probably related to chronic inflammation and fibrosis. Treg cells are unlikely to play an important role in the pathogenesis of IgG4-RD.

Indexed as

Immunoglobulin G4-Related DiseaseAdultAgedAged, 80 and overFemaleHumansImmunoglobulin GInterleukin-10Interleukin-4MaleMiddle AgedRetrospective StudiesTh1 CellsT-Lymphocyte SubsetsTumor Necrosis Factor-alphaImmunoglobulin GInterleukin-10Interleukin-4Tumor Necrosis Factor-alphaatopyCD4+ T cell subsetscytokineseosinophilsIgG4-related disease

Identifiers

PMID35432312
PMCPMC9010737
OpenAlexW4220945656

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.