Evidence map›Paper›PMID 27441838›Full record

ArticlePloS one2016

Metabolic Profiling of Systemic Lupus Erythematosus and Comparison with Primary Sjögren's Syndrome and Systemic Sclerosis.

Anders A Bengtsson, Johan Trygg, Dirk M Wuttge, Gunnar Sturfelt, Elke Theander, Magdalena Donten, Thomas Moritz, Carl-Johan Sennbro, Frida Torell, Christian Lood and 3 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 2 pooled it
6.8field-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

78 citing papers in PubMed, 2 syntheses or guidelines pooled it, 134 citations in OpenAlex.

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  16. Immunometabolism in systemic lupus erythematosus.Nature reviews. Rheumatology · 2025
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18 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 2 countries.

Anders A BengtssonDepartment of Rheumatology, University Hospital Lund, Lund, Sweden.
Johan TryggComputational Life Science Center (CLiC), Department of Chemistry, Umeå University, Umeå, Sweden.
Dirk M WuttgeDepartment of Rheumatology, University Hospital Lund, Lund, Sweden.
Gunnar SturfeltDepartment of Rheumatology, University Hospital Lund, Lund, Sweden.
Elke TheanderDepartment of Rheumatology, Skåne University Hospital Malmö, Lund University, Lund, Sweden.
Magdalena DontenAcureOmics AB. Tvistevägen 48, Umeå, Sweden.
Thomas MoritzSwedish Metabolomics Centre, Swedish University of Agricultural Sciences, Umeå, Sweden.
Carl-Johan SennbroLeo Pharma A/S, 55 Industriparken, DK-2750 Ballerup, Denmark.
Frida TorellComputational Life Science Center (CLiC), Department of Chemistry, Umeå University, Umeå, Sweden.
Christian LoodDepartment of Rheumatology, University Hospital Lund, Lund, Sweden.
Izabella SurowiecComputational Life Science Center (CLiC), Department of Chemistry, Umeå University, Umeå, Sweden.
Stefan RännarAcureOmics AB. Tvistevägen 48, Umeå, Sweden.
Torbjörn LundstedtAcureOmics AB. Tvistevägen 48, Umeå, Sweden.
Lund University · SEUmeå University · SELeo Pharma (Denmark) · DKSwedish University of Agricultural Sciences · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is a chronic inflammatory autoimmune disease which can affect most organ systems including skin, joints and the kidney. Clinically, SLE is a heterogeneous disease and shares features of several other rheumatic diseases, in particular primary Sjögrens syndrome (pSS) and systemic sclerosis (SSc), why it is difficult to diagnose The pathogenesis of SLE is not completely understood, partly due to the heterogeneity of the disease. This study demonstrates that metabolomics can be used as a tool for improved diagnosis of SLE compared to other similar autoimmune diseases. We observed differences in metabolic profiles with a classification specificity above 67% in the comparison of SLE with pSS, SSc and a matched group of healthy individuals. Selected metabolites were also significantly different between studied diseases. Biochemical pathway analysis was conducted to gain understanding of underlying pathways involved in the SLE pathogenesis. We found an increased oxidative activity in SLE, supported by increased xanthine oxidase activity and an increased turnover in the urea cycle. The most discriminatory metabolite observed was tryptophan, with decreased levels in SLE patients compared to control groups. Changes of tryptophan levels were related to changes in the activity of the aromatic amino acid decarboxylase (AADC) and/or to activation of the kynurenine pathway.

Indexed as

AdultCase-Control StudiesDemographyDiscriminant AnalysisFemaleHumansLeast-Squares AnalysisLupus Erythematosus, SystemicMaleMetabolomicsMiddle AgedPhenotypePrincipal Component AnalysisScleroderma, SystemicSensitivity and SpecificitySjogren's Syndrome

Identifiers

PMID27441838
PMCPMC4956266
OpenAlexW2491155763

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.