Evidence map›Paper›PMID 27893410›Full record

ArticleAging2016

Characterization of variations in IL23A and IL23R genes: possible roles in multiple sclerosis and other neuroinflammatory demyelinating diseases.

Fei-Feng Li, Xi-Dong Zhu, Peng Yan, Mei-Hua Jin, Hui Yue, Qiong Zhang, Jin Fu, Shu-Lin Liu

Open access · greenAbstract read
In one paragraph

Article in Aging, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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  7. Article
  8. The Association Study ofFrontiers in neuroscience · 2020
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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

8 authors at 3 institutions in 2 countries.

Fei-Feng LiSystemomics Center, College of Pharmacy, and Genomics Research Center (one of the State-Province Key Laboratory of Biopharmaceutical Engineering, China), Harbin Medical University, Harbin, China.
Xi-Dong ZhuDepartment of Neurology, the Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Peng YanDepartment of Colorectal Surgery of the Second Affiliated Hospital, Harbin Medical University, Harbin, China.
Mei-Hua JinDepartment of Neurology, the Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Hui YueDepartment of Neurology, the Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Qiong ZhangDepartment of Antibiotics, Heilongjiang province food and drug inspection testing Institute, Harbin, China.
Jin FuDepartment of Neurology, the Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Shu-Lin LiuSystemomics Center, College of Pharmacy, and Genomics Research Center (one of the State-Province Key Laboratory of Biopharmaceutical Engineering, China), Harbin Medical University, Harbin, China.
Second Affiliated Hospital of Harbin Medical University · CNHarbin Medical University · CNHeilongjiang Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis is among the most serious inflammatory demyelinating diseases (IDD). Interleukin-23A (IL23A) regulates and coordinates the activities of immune cells by interacting with its receptor IL23R and plays key roles in the pathogenesis of immune inflammatory diseases. IDD, deemed to be a kind of autoimmune diseases, may involve IL23A in the pathogenesis. The aim of this work was to validate the hypothesized involvement of IL-23A and its receptor in IDD. We sequenced the

Indexed as

AdolescentAdultAgedAsian PeopleChinaDemyelinating DiseasesFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseHumansInterleukin-23 Subunit p19MaleMiddle AgedMultiple SclerosisPolymorphism, Single NucleotideIL23A protein, humanIL23R protein, humanInterleukin-23 Subunit p19Receptors, Interleukingene expression levelIDDinterleukin-23Amultiple sclerosisSNP

Identifiers

PMID27893410
PMCPMC5191866
OpenAlexW2556345717

What OpenQuestion holds

Textmetadata
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.