Evidence map›Paper›PMID 29148078›Full record

ArticleClinical and experimental immunology2018

Soluble TAM receptor tyrosine kinases in rheumatoid arthritis: correlation with disease activity and bone destruction.

L Xu, F Hu, H Zhu, X Liu, L Shi, Y Li, H Zhong, Y Su

Open access · greenAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

21 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Observational
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. The Role of TAM Receptors in Bone.International journal of molecular sciences · 2023
    Review
  10. Article
  11. Observational
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Protective Role of the MER Tyrosine KinaseFrontiers in immunology · 2018
    Article
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 1 institution in 1 country.

L XuDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.ORCID 0000-0002-2095-0906
F HuDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
H ZhuDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
X LiuDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
L ShiDepartment of Rheumatology and Immunology, Peking University International Hospital, Beijing, China.
Y LiDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
H ZhongDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Y SuDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Peking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The TAM receptor tyrosine kinases (TAM RTK) are a subfamily of receptor tyrosine kinases, the role of which in autoimmune diseases such as systemic lupus erythematosus has been well explored, while their functions in rheumatoid arthritis (RA) remain largely unknown. In this study, we investigated the role of soluble TAM receptor tyrosine kinases (sAxl/sMer/sTyro3) in patients with RA. A total of 306 RA patients, 100 osteoarthritis (OA) patients and 120 healthy controls (HCs) were enrolled into this study. The serum concentrations of sAxl/sMer/sTyro3 were measured by enzyme-linked immunosorbent assay (ELISA), then the associations between sAxl/sMer/sTyro3 levels and clinical features of RA patients were analysed. We also investigated whether sTyro3 could promote osteoclast differentiation in vitro in RA patients. The results showed that compared with healthy controls (HCs), sTyro3 levels in the serum of RA patients were elevated remarkably and sMer levels were decreased significantly, whereas there was no difference between HCs and RA patients on sAxl levels. The sTyro3 levels were correlated weakly but positively with white blood cells (WBC), immunoglobulin (Ig)M, rheumatoid factor (RF), swollen joint counts, tender joint counts, total sharp scores and joint erosion scores. Conversely, there were no significant correlations between sMer levels and the above indices. Moreover, RA patients with high disease activity also showed higher sTyro3 levels. In-vitro osteoclast differentiation assay showed further that tartrate-resistant acid phosphatase (TRAP)

Indexed as

AdultAgedArthritis, RheumatoidAxl Receptor Tyrosine KinaseBone and BonesCase-Control StudiesCell Differentiationc-Mer Tyrosine KinaseEnzyme-Linked Immunosorbent AssayFemaleHumansMaleMiddle AgedOsteoarthritisOsteoclastsProto-Oncogene ProteinsAXL protein, humanAxl Receptor Tyrosine Kinasec-Mer Tyrosine KinaseMERTK protein, humanProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesTYRO3 protein, humanbone destructiondisease activityrheumatoid arthritisTAM receptor tyrosine kinases

Identifiers

PMID29148078
PMCPMC5842405
OpenAlexW2769289468

What OpenQuestion holds

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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.