Evidence map›Paper›PMID 26474561›Full record

ArticleBMC genetics2015

The association of CD40 polymorphisms with CD40 serum levels and risk of systemic lupus erythematosus.

Jian-Ming Chen, Jing Guo, Chuan-Dong Wei, Chun-Fang Wang, Hong-Cheng Luo, Ye-Sheng Wei, Yan Lan

Registry-linked trialOpen access · diamondAbstract read
In one paragraph

Article in BMC genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05585944 (" Effect of Single-nucleotide Polymorphism of CD40 Gene rs1883832 C/T on the Risk of Immune Thrombocytopenic Purpura "), which is not on this map. Cited by 24 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 3 pooled it
2.1field-weighted citation impact, top 13% 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.

NCT05585944 naunknown statusnot on this mapstarted 2022, after this paper: background citation

" Effect of Single-nucleotide Polymorphism of CD40 Gene rs1883832 C/T on the Risk of Immune Thrombocytopenic Purpura "

TypeinterventionalSponsorSohag UniversityRan2022 to 2023Enrolled80ConditionsImmune Thrombocytopenic PurpuraArmsGenotyping of rs1883832C/T related single-nucleotide polymorphism
3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 3 syntheses or guidelines pooled it, 41 citations in OpenAlex.

  1. Evaluation ofFrontiers in medicine · 2026
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  4. TheBioMed research international · 2018
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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.

Jian-Ming ChenDepartment of Laboratory Medicine, Affiliated hospital of Youjiang Medical University for Nationalities, Baise, 533000, Guangxi, China. 18777615132@163.com.
Jing GuoDepartment of Dermatology, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, 533000, Guangxi, China. gjnsdy-1987@163.com.
Chuan-Dong WeiDepartment of Laboratory Medicine, Affiliated hospital of Youjiang Medical University for Nationalities, Baise, 533000, Guangxi, China. 1691205864@qq.com.
Chun-Fang WangDepartment of Laboratory Medicine, Affiliated hospital of Youjiang Medical University for Nationalities, Baise, 533000, Guangxi, China. 1918436346@qq.com.
Hong-Cheng LuoDepartment of Laboratory Medicine, Affiliated hospital of Youjiang Medical University for Nationalities, Baise, 533000, Guangxi, China. 2438872699@qq.com.
Ye-Sheng WeiDepartment of Laboratory Medicine, Affiliated hospital of Youjiang Medical University for Nationalities, Baise, 533000, Guangxi, China. wysh22@163.com.
Yan LanDepartment of Dermatology, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, 533000, Guangxi, China. yylanyan@163.com.
Affiliated Hospital of Youjiang Medical University for Nationalities · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCurrent evidence shows that the CD40-CD40 ligand (CD40-CD40L) system plays a crucial role in the development, progression and outcome of systemic lupus erythematosus (SLE). The aim of this study was to investigate whether a CD40 gene single nucleotide polymorphism (SNP) is associated with SLE and CD40 expression in the Chinese population. We included controls (n = 220) and patients with either SLE (n =205) in the study.

methodsThe gene polymorphism was measured using Snapshot SNP genotyping assays and confirmed by sequencing. We analyzed three single nucleotide polymorphisms of CD40 gene rs1883832C/T, rs1569723A/C and rs4810485G/T in 205 patients with SLE and 220 age-and sex-matched controls. Soluble CD40 (sCD40) levels were measured by ELISA.

resultsThere were significant differences in the genotype and allele frequencies of CD40 gene rs1883832C/T polymorphism between the group of patients with SLE and the control group (P < 0.05). sCD40 levels were increased in patients with SLE compared with controls (P < 0.01). Moreover, genotypes carrying the CD40 rs1883832 C/T variant allele were associated with increased CD40 levels compared to the homozygous wild-type genotype in patients with SLE. The rs1883832C/T polymorphism of CD40 and its sCD40 levels were associated with SLE in the Chinese population.

conclusionsOur results suggest that CD40 gene may play a role in the development of SLE in the Chinese population.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseAdultAgedAged, 80 and overCase-Control StudiesCD40 AntigensFemaleGene FrequencyHaplotypesHumansLupus Erythematosus, SystemicMaleMiddle AgedPolymorphism, Single NucleotideRisk FactorsCD40 Antigens

Identifiers

PMID26474561
PMCPMC4608213
OpenAlexW2120970466

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Registered trials

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.