Evidence map›Paper›PMID 33792986›Full record

ArticleJournal of clinical laboratory analysis2021

A novel CD209 polymorphism is associated with rheumatoid arthritis patients in Taiwan.

Hua-Chen Chan, Shu-Chen Wang, Chia-Hui Lin, Yuan-Zhao Lin, Ruei-Nian Li, Jeng-Hsien Yen

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Differences in IDO1Frontiers in immunology · 2024
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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

6 authors at 2 institutions in 1 country.

Hua-Chen ChanCenter for Lipid Biosciences, Kaohsiung Medical University Hospital, Kaohsiung City, Taiwan.ORCID https://orcid.org/0000-0001-7016-8392
Shu-Chen WangDepartment of Laboratory Medicine, Kaohsiung Medical University Hospital, Kaohsiung City, Taiwan.ORCID https://orcid.org/0000-0002-9287-6901
Chia-Hui LinDivision of Rheumatology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung City, Taiwan.ORCID https://orcid.org/0000-0002-2819-237X
Yuan-Zhao LinDivision of Rheumatology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung City, Taiwan.ORCID https://orcid.org/0000-0001-5358-0203
Ruei-Nian LiDepartment of Biomedical Science and Environmental Biology, College of Life Science, Kaohsiung Medical University, Kaohsiung City, Taiwan.ORCID https://orcid.org/0000-0003-2569-1314
Jeng-Hsien YenDivision of Rheumatology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung City, Taiwan.ORCID https://orcid.org/0000-0002-1291-1739
Kaohsiung Medical University · TWNational Sun Yat-sen University · TW

Funding

Kaohsiung Medical University DK106010Kaohsiung Medical University SH000151Kaohsiung Medical University TP105D07Kaohsiung Medical University TP105D14Kaohsiung Medical University Chung-Ho Memorial HospitalTaiwan Ministry of Science and Technology MOST 106-2628-B-037-001-MY3Taiwan Ministry of Science and Technology MOST 109-2314-B-037-124
6 · The paper itself

Abstract

Single nucleotide polymorphisms (SNPs) in the promoter region of CD209 (cluster of differentiation 209) may influence expression levels, and higher expression of CD209 on immune cells correlate with severity of cartilage destruction in patients with rheumatoid arthritis (RA). Due to the lack of a comprehensive study, this study aimed to investigate the CD209 promoter variants and haplotypes in a Taiwanese population and the association with RA development. Deoxyribonucleic acid (DNA) of peripheral blood mononuclear cells from 126 RA patients and 124 healthy controls was purified, and the CD209 gene promoter was amplified by polymerase chain reaction and analyzed by Sanger sequencing. Results showed that a novel variant -96C>A polymorphism in CD209 promoter was identified in the Taiwanese population, and the frequency was significantly higher in RA patients than in controls (11.51% vs. 2.42%, P < .0001). The odds ratio (OR) for the development of RA was 5.88 (95% CI 2.35-14.74, P < .0001). Other known variants were also evaluated; for instance, -1180 T/T (rs7359874) was increased in RA patients, and the OR for the development of RA was 3.26, 95% CI 0.85-12.52, P = .07). Besides, the haplotype frequencies were calculated; -1180A-939C-871 T-336 T-139 T-96A and -1180 T-939 T-871C-336 T-139C-96A were increased in RA patients (P = .004 and 0.05, respectively). In summary, CD209-96A variant could be an important factor for the development of RA in the Taiwanese population.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseAllelesArthritis, RheumatoidBase SequenceCase-Control StudiesCell Adhesion MoleculesDC-Specific ICAM-3 Grabbing NonintegrinFemaleGene FrequencyHaplotypesHumansLectins, C-TypeLinkage DisequilibriumMaleMiddle AgedCell Adhesion MoleculesDC-Specific ICAM-3 Grabbing NonintegrinLectins, C-TypeReceptors, Cell SurfaceautoimmunityCD209 polymorphismrheumatoid arthritis

Identifiers

PMID33792986
PMCPMC8128313
OpenAlexW3151026787

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.