Evidence map›Paper›PMID 23118916›Full record

ArticlePloS one2012

Genome-wide scan identifies variant in TNFSF13 associated with serum IgM in a healthy Chinese male population.

Ming Yang, Yongming Wu, Yanmei Lu, Changyuan Liu, Jielin Sun, Ming Liao, Min Qin, Linjian Mo, Yong Gao, Zheng Lu and 13 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
0.4field-weighted citation impact, top 39% 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 19 citations in OpenAlex.

  1. Pooled it
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  7. Truly selective primary IgM deficiency is probably very rare.Clinical and experimental immunology · 2018
    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

23 authors at 5 institutions in 2 countries.

Ming YangCenter for Genomic and Personalized Medicine, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, People's Republic of China.
Yongming Wu
Yanmei Lu
Changyuan Liu
Jielin Sun
Ming Liao
Min Qin
Linjian Mo
Yong Gao
Zheng Lu
Chunlei Wu
Youjie Zhang
Haiying Zhang
Xue Qin
Yanling Hu
Shijun Zhang
Jianling Li
Min Dong
S Lilly Zheng
Jianfeng Xu
Xiaobo Yang
Aihua Tan
Zengnan Mo
First Affiliated Hospital of GuangXi Medical University · CNGuangxi Medical University · CNWake Forest University · USHuashan Hospital · CNTumor Hospital of Guangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IgM provides a first line of defense during microbial infections. Serum IgM levels are detected routinely in clinical practice. And IgM is a genetically complex trait. We conducted a two-stage genome-wide association study (GWAS) to identify genetic variants affecting serum IgM levels in a Chinese population of 3495, including 1999 unrelated subjects in the first stage and 1496 independent individuals in the second stage. Our data show that a common single nucleotide polymorphism (SNP), rs11552708 located in the TNFSF13 gene was significantly associated with IgM levels (p = 5.00×10(-7) in first stage, p = 1.34×10(-3) in second stage, and p = 4.22×10(-9) when combined). Besides, smoking was identified to be associated with IgM levels in both stages (P<0.05), but there was no significant interaction between smoking and the identified SNP (P>0.05). It is suggested that TNFSF13 may be a susceptibility gene affecting serum IgM levels in Chinese male population.

Indexed as

Polymorphism, Single NucleotideAdultAgedChinaGenome-Wide Association StudyGenotypeHealthHumansImmunoglobulin MMaleMiddle AgedTumor Necrosis Factor Ligand Superfamily Member 13Young AdultImmunoglobulin MTNFSF13 protein, humanTumor Necrosis Factor Ligand Superfamily Member 13

Identifiers

PMID23118916
PMCPMC3485370
OpenAlexW2026823586

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.