Evidence map›Paper›PMID 33134397›Full record

ArticleJournal of immunology research2020

Cytokine Profiling in Chinese SLE Patients: Correlations with Renal Dysfunction.

Chen Yan, Le Yu, Xiu-Ling Zhang, Jing-Jing Shang, Jie Ren, Jie Fan, Xue-Qin Feng, Rong-Wei Zhang, Zhong-Bin Xia, Xin-Wang Duan

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. TFF3 as a Diagnostic Biomarker in Kidney Transplant Patients.International journal of molecular sciences · 2023
    Article
  4. AlteredDiagnostics (Basel, Switzerland) · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. 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

10 authors at 1 institution in 1 country.

Chen YanDepartment of Rheumatology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, China.ORCID https://orcid.org/0000-0003-3808-1259
Le YuDepartment of Rheumatology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Xiu-Ling ZhangDepartment of Rheumatology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Jing-Jing ShangDepartment of Rheumatology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Jie RenDepartment of Rheumatology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Jie FanDepartment of Rheumatology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Xue-Qin FengDepartment of Rheumatology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Rong-Wei ZhangDepartment of Rheumatology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Zhong-Bin XiaDepartment of Rheumatology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Xin-Wang DuanDepartment of Rheumatology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, China.ORCID https://orcid.org/0000-0002-0432-3638
Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSystemic lupus erythematosus (SLE) is a chronic, systemic autoimmune disease that commonly causes kidney damage. Therefore, we measured plasma levels of cytokines that may be related to renal dysfunction in SLE patients.

methodsTo explore the differences between SLE patients with renal dysfunction and healthy volunteers, the levels of cytokines in plasma were screened using a human cytokine antibody array. Then, we chose fourteen of the elevated cytokines for verification with an expanded sample size by a human magnetic Luminex assay. Plasma samples were isolated from SLE patients (

resultsCytokine antibody array data showed elevated plasma cytokines in SLE patients with renal dysfunction compared with healthy volunteers. By using the human magnetic Luminex assay, we found that plasma levels of CHI3L1, GDF-15, IGFBP-2, MIF, ST2, TFF3, and uPAR were significantly higher in SLE patients than in healthy volunteers. Plasma levels of CXCL4 were significantly lower in the active group than in the inactive group, and plasma levels of CHI3L1, IGFBP-2, MIF, and MPO were significantly higher in the active group than in the inactive group. We also analyzed the correlation between plasma cytokine levels and the SLEDAI-2K, and our results showed that the plasma levels of the fourteen selected cytokines were weakly correlated or not correlated with the SLEDAI-2K. We further analyzed the correlation between cytokines and renal dysfunction. Plasma levels of GDF-15 and TFF3 were highly positively correlated with serum creatinine levels and 24-hour urine protein levels.

conclusionOur data suggest that plasma levels of GDF-15 and TFF3 are potential renal dysfunction markers in SLE patients, but plasma levels of these cytokines are not correlated with the SLEDAI-2K. Further study is warranted to determine how these cytokines regulate inflammatory responses and renal dysfunction in SLE.

Indexed as

AdultBiomarkersChinaCytokinesFemaleGene Expression ProfilingGene Expression RegulationGrowth Differentiation Factor 15HumansKidney DiseasesLupus Erythematosus, SystemicMalePlatelet Factor 4Severity of Illness IndexTrefoil Factor-3BiomarkersCytokinesGrowth Differentiation Factor 15Platelet Factor 4TFF3 protein, humanTrefoil Factor-3

Identifiers

PMID33134397
PMCPMC7568803
OpenAlexW3092298866

What Socratic 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 Socratic graph.