Evidence map›Paper›PMID 34658170›Full record

ArticleACR open rheumatology2022

Four Systemic Lupus Erythematosus Subgroups, Defined by Autoantibodies Status, Differ Regarding HLA-DRB1 Genotype Associations and Immunological and Clinical Manifestations.

Lina-Marcela Diaz-Gallo, Vilija Oke, Emeli Lundström, Kerstin Elvin, Yee Ling Wu, Susanna Eketjäll, Agneta Zickert, Johanna T Gustafsson, Andreas Jönsen, Dag Leonard and 8 more

Open access · goldAbstract read
In one paragraph

Article in ACR open rheumatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. [Role of HLA genetic variants in autoimmune diseases].Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2026
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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

18 authors at 6 institutions in 3 countries.

Lina-Marcela Diaz-GalloDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet, Karolinksa University Hospital, Stockholm, Sweden.ORCID https://orcid.org/0000-0002-5688-0102
Vilija OkeDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet, Karolinksa University Hospital, Stockholm, Sweden.ORCID https://orcid.org/0000-0002-1834-2688
Emeli LundströmDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet, Karolinksa University Hospital, Stockholm, Sweden.
Kerstin ElvinDepartment of Clinical Immunology and Transfusion Medicine, Unit of Clinical Immunology, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Yee Ling WuThe Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Susanna EketjällResearch and Early Development, Cardiovascular, Renal and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
Agneta ZickertDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet, Karolinksa University Hospital, Stockholm, Sweden.
Johanna T GustafssonDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet, Karolinksa University Hospital, Stockholm, Sweden.
Andreas JönsenDepartment of Clinical Sciences, Section of Rheumatology, Lund University, Skåne University Hospital, Lund, Sweden.
Dag LeonardDepartment of Medical Sciences, Section of Rheumatology, Uppsala University, Uppsala, Sweden.
Daniel J BirminghamDepartment of Internal Medicine, The Ohio State University, Columbus, Ohio.ORCID https://orcid.org/0000-0002-6803-224X
Gunnel NordmarkDepartment of Medical Sciences, Section of Rheumatology, Uppsala University, Uppsala, Sweden.
Anders A BengtssonDepartment of Clinical Sciences, Section of Rheumatology, Lund University, Skåne University Hospital, Lund, Sweden.
Lars RönnblomDepartment of Medical Sciences, Section of Rheumatology, Uppsala University, Uppsala, Sweden.
Iva GunnarssonDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet, Karolinksa University Hospital, Stockholm, Sweden.
Chack-Yung YuThe Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Leonid PadyukovDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet, Karolinksa University Hospital, Stockholm, Sweden.ORCID https://orcid.org/0000-0003-2950-5670
Elisabet SvenungssonDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet, Karolinksa University Hospital, Stockholm, Sweden.ORCID https://orcid.org/0000-0003-3396-3244
Karolinska University Hospital · SEUppsala University · SELund University · SENationwide Children's Hospital · USAstraZeneca (Sweden) · SEThe Ohio State University · US

Funding

Complement in Human Lupus: Deficiencies, Profiles and ComplicationsR01AR073311 · NIAMS · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI BIRMINGHAM, DANIEL J, YU, CHACK Y · 2018 to 2022
$2.1M
Hjärt-Lungfonden 20170257NIAMS NIH HHS R01 AR073311Reumatikerförbundet R-739631Reumatikerförbundet R-861801Reumatikerförbundet R-930005Reumatikerförbundet R-932138Stiftelsen Konung Gustaf Vs 80-årsfond FAI-2017-0390Stiftelsen Konung Gustaf Vs 80-årsfond FAI-2018-0478Stiftelsen Konung Gustaf Vs 80-årsfond FAI-2018-0518Stiftelsen Konung Gustaf Vs 80-årsfond FAI-2019-0597Stiftelsen Professor Nanna Svartz Fond 2019-00318Stiftelsen Professor Nanna Svartz Fond 2020-00377Stockholms Läns Landsting 20170038Svenska Läkaresällskapet SLS-713911Svenska Läkaresällskapet SLS-936449Ulla och Gustaf af Uggla stiftelse 2018-02670Ulla och Gustaf af Uggla stiftelse 2020-02395Vetenskapsrådet 2014-33867Vetenskapsrådet 2018-02399Vetenskapsrådet 2018-02535
6 · The paper itself

Abstract

objectiveThe heterogeneity of systemic lupus erythematosus (SLE) constitutes clinical and therapeutical challenges. We therefore studied whether unrecognized disease subgroups can be identified by using autoantibody profiling together with HLA-DRB1 alleles and immunological and clinical data.

methodsAn unsupervised cluster analysis was performed based on detection of 13 SLE-associated autoantibodies (double-stranded DNA, nucleosomes, ribosomal P, ribonucleoprotein [RNP] 68, RNPA, Smith [Sm], Sm/RNP, Sjögren's syndrome antigen A [SSA]/Ro52, SSA/Ro60, Sjögren's syndrome antigen B [SSB]/La, cardiolipin [CL]-Immunoglobulin G [IgG], CL-Immunoglobulin M [IgM], and β

resultsOur analysis identified four subgroups among the patients with SLE. Subgroup 1 (29.3%) was dominated by anti-SSA/Ro60/Ro52/SSB autoantibodies and was strongly associated with HLA-DRB1*03 (odds ratio [OR] = 4.73; 95% confidence interval [CI] = 4.52-4.94). Discoid lesions were more common for this disease subgroup (OR = 1.71, 95% CI = 1.18-2.47). Subgroup 2 (28.7%) was dominated by anti-nucleosome/SmRNP/DNA/RNPA autoantibodies and associated with HLA-DRB1*15 (OR = 1.62, 95% CI = 1.41-1.84). Nephritis was most common in this subgroup (OR = 1.61, 95% CI = 1.14-2.26). Subgroup 3 (23.8%) was characterized by anti-ß

conclusionOur findings suggest that four fairly distinct subgroups can be identified on the basis of the autoantibody profile in SLE. These four SLE subgroups differ regarding associations with HLA-DRB1 alleles and immunological and clinical features, suggesting dissimilar disease pathways.

Identifiers

PMID34658170
PMCPMC8754019
OpenAlexW3206909062

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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.