Evidence map›Paper›PMID 30157968›Full record

ArticleArthritis research & therapy2018

Interferon-λ3/4 genetic variants and interferon-λ3 serum levels are biomarkers of lupus nephritis and disease activity in Taiwanese.

Ji-Yih Chen, Chin-Man Wang, Tai-Di Chen, Yeong-Jian Jan Wu, Jing-Chi Lin, Ling Ying Lu, Jianming Wu

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 43 citations in OpenAlex.

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  16. Regulation of B Cell Responses in SLE by Three Classes of Interferons.International journal of molecular sciences · 2021
    Review
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  19. 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

7 authors at 4 institutions in 2 countries.

Ji-Yih ChenDepartment of Medicine, Division of Allergy, Immunology and Rheumatology, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, No. 5, Fu-Shin St. Kwei-Shan, Tao-Yuan, Taiwan. jychen31@adm.cgmh.org.tw.
Chin-Man WangDepartment of Rehabilitation, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, No. 5, Fu-Shin St. Kwei-Shan, Tao-Yuan, Taiwan.
Tai-Di ChenDepartment of Anatomic Pathology, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Tao-Yuan, Taiwan.
Yeong-Jian Jan WuDepartment of Medicine, Division of Allergy, Immunology and Rheumatology, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, No. 5, Fu-Shin St. Kwei-Shan, Tao-Yuan, Taiwan.
Jing-Chi LinDepartment of Medicine, Division of Allergy, Immunology and Rheumatology, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, No. 5, Fu-Shin St. Kwei-Shan, Tao-Yuan, Taiwan.
Ling Ying LuDepartment of Medicine, Division of Allergy Immunology and Rheumatology, Kaohsiung Veterans General Hospital, No. 386, Dazhong 1st Rd, Zuoying District, Kaohsiung City, 81362, Taiwan. lylu@vghks.gov.tw.
Jianming WuDepartment of Veterinary and Biomedical Sciences, Department of Medicine, University of Minnesota, 235B Animal Science/Vet. Med. Bldg, 1988 Fitch Avenue, St. Paul, MN, 55108, USA. jmwu@umn.edu.
Chang Gung Memorial Hospital · TWChang Gung University · TWKaohsiung Veterans General Hospital · TWUniversity of Minnesota · US

Funding

High affinity IgG Fc receptor FcγRIA variants as novel genetic markers for sarcoidosisR21AI125729 · NIAID · UNIVERSITY OF MINNESOTA · PI WU, JIANMING · 2016 to 2017
$419k
NIAID NIH HHS R21 AI125729
6 · The paper itself

Abstract

backgroundType III interferons (IFNs) or IFN-λs are the newly discovered cytokines that primarily target the cells of epithelial and myeloid lineages, which are major components of kidneys. The current study aimed to investigate whether IFN-λs are involved in the pathogenesis of systemic lupus erythematosus (SLE) and lupus nephritis.

methodsTaqMan allele discrimination assays were used to determine IFNL3/4 SNP genotypes of 1620 healthy controls and 1013 SLE patients (two independent cohorts consisting of 831 and 182 subjects, respectively) from Taiwan. The distributions of IFNL3/4 SNP genotypes and allele frequencies were compared between SLE patients and healthy controls and among SLE patients stratified by clinical phenotypes. ELISA was used to determine the serum IFN-λ3 concentrations of SLE patients.

resultsAll major IFN3/4 SNP alleles were significantly associated with the risk for lupus nephritis (rs8099917T, P

conclusionsIFN-λ3/4 genetic variants play a unique role in the development of lupus nephritis and SLE.

Indexed as

Polymorphism, Single NucleotideAdultAsian PeopleBiomarkersFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHaplotypesHumansInterferon LambdaInterferonsInterleukinsLupus Erythematosus, SystemicLupus NephritisMaleBiomarkersIFNL4 protein, humanInterferon Lambdainterferon-lambda, humanInterferonsInterleukinsInterferon λLupus nephritisSystemic lupus erythematosus

Identifiers

PMID30157968
PMCPMC6116434
OpenAlexW2889414963

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.