Evidence map›Paper›PMID 28415570›Full record

SynthesisOncotarget2017

Meta-analysis of programmed cell death 1 polymorphisms with systemic lupus erythematosus risk.

Jie Gao, Nan Gai, Li Wang, Kang Liu, Xing-Han Liu, Lin-Ting Wei, Tian Tian, Shan-Li Li, Yi Zheng, Yu-Jiao Deng and 2 more

Open access · diamondAbstract readMeta-AnalysisReview
In one paragraph

Synthesis in Oncotarget, 2017. 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
2.2field-weighted citation impact, top 12% 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, 36 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. The effect of PD-1/PD-L1 signaling axis on the interaction between CD19Advances in rheumatology (London, England) · 2023
    Article
  6. Article
  7. Immunogenetics of Lupus Erythematosus.Advances in experimental medicine and biology · 2022
    Article
  8. Review
  9. Article
  10. Programmed cell death-1Journal of translational autoimmunity · 2021
    Article
  11. Review
  12. Article
  13. 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

12 authors at 1 institution in 1 country.

Jie GaoDepartment of Nephrology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Nan GaiDepartment of Rheumatic Immunology, Xi'an No.5 Hospital, Xi'an, China.
Li WangDepartment of Nephrology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Kang LiuDepartment of Oncology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Xing-Han LiuDepartment of Oncology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Lin-Ting WeiDepartment of Nephrology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Tian TianDepartment of Oncology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Shan-Li LiDepartment of Oncology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Yi ZhengDepartment of Oncology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Yu-Jiao DengDepartment of Oncology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Zhi-Jun DaiDepartment of Oncology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Rong-Guo FuDepartment of Nephrology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Second Affiliated Hospital of Xi'an Jiaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The association of polymorphisms in programmed cell death 1 (PDCD1) gene with systemic lupus erythematosus (SLE) risk is inconsistent across different studies. This meta-analysis is aimed to provide reliable evidence to the association of five common PDCD1 polymorphisms (PD1.1, PD1.2, PD1.3, PD1.5 and PD1.6) with SLE risk. A total of 28 studies with 4,344 SLE cases and 5,474 healthy controls were included in this meta-analysis. PD1.3 polymorphism was significantly associated with SLE in the overall population (A vs. G: OR = 1.35, 95% CI = 1.12-1.63; GA vs.GG: OR = 1.41, 95% CI = 1.12-1.76; AA+GA vs. GG: OR = 1.41, 95% CI = 1.13-1.7). In the stratified analyses based on ethnicity, we found a significant association in Caucasians and in Mexicans. In the subgroup analyses by gender, a significant association was found between PD1.3 polymorphism and SLE risk in males. The results also suggested an association between the PD1.6 polymorphism and decreased SLE risk (A vs. G: OR = 0.84, 95% CI = 0.73-0.96). Our meta-analysis revealed that PD1.3 polymorphism may increase the susceptibility to SLE, particularly in Caucasians, while PD1.6 may be a protective factor to SLE.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseasePolymorphism, Single NucleotideAllelesGenotypeHumansLupus Erythematosus, SystemicOdds RatioProgrammed Cell Death 1 ReceptorPublication BiasRiskProgrammed Cell Death 1 Receptormeta-analysisPDCD1polymorphismriskSLE

Identifiers

PMID28415570
PMCPMC5482706
OpenAlexW2595295182

What OpenQuestion holds

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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 OpenQuestion graph.