Evidence map›Paper›PMID 32782251›Full record

ArticleScientific reports2020

A novel biomarker of MMP-cleaved prolargin is elevated in patients with psoriatic arthritis.

Dovile Sinkeviciute, Solveig Skovlund Groen, Shu Sun, Tina Manon-Jensen, Anders Aspberg, Patrik Önnerfjord, Anne-Christine Bay-Jensen, Salome Kristensen, Signe Holm Nielsen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
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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

9 authors at 3 institutions in 2 countries.

Dovile SinkeviciuteNordic Bioscience, Biomarkers and Research, Herlev Hovedgade 205-207, Herlev, Denmark. dsi@nordicbio.com.
Solveig Skovlund GroenNordic Bioscience, Biomarkers and Research, Herlev Hovedgade 205-207, Herlev, Denmark.
Shu SunNordic Bioscience, Biomarkers and Research, Herlev Hovedgade 205-207, Herlev, Denmark.
Tina Manon-JensenNordic Bioscience, Biomarkers and Research, Herlev Hovedgade 205-207, Herlev, Denmark.
Anders AspbergDepartment of Clinical Sciences Lund, Lund University, Lund, Sweden.
Patrik ÖnnerfjordDepartment of Clinical Sciences Lund, Lund University, Lund, Sweden.
Anne-Christine Bay-JensenNordic Bioscience, Biomarkers and Research, Herlev Hovedgade 205-207, Herlev, Denmark.
Salome KristensenDepartment of Rheumatology, Aalborg University Hospital, Aalborg, Denmark.
Signe Holm NielsenNordic Bioscience, Biomarkers and Research, Herlev Hovedgade 205-207, Herlev, Denmark.
Nordic Bioscience (Denmark) · DKLund University · SEAalborg University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Psoriatic arthritis (PsA) is a chronic musculoskeletal inflammatory disease found in up to 30% of psoriasis patients. Prolargin-an extracellular matrix (ECM) protein present in cartilage and tendon-has been previously shown elevated in serum of patients with psoriasis. ECM protein fragments can reflect tissue turnover and pathological changes; thus, this study aimed to develop, validate and characterize a novel biomarker PROM targeting a matrix metalloproteinase (MMP)-cleaved prolargin neo-epitope, and to evaluate it as a biomarker for PsA. A competitive ELISA was developed with a monoclonal mouse antibody; dilution- and spiking-recovery, inter- and intra-variation, and accuracy were evaluated. Serum levels were evaluated in 55 healthy individuals and 111 patients diagnosed with PsA by the CASPAR criteria. Results indicated that the PROM assay was specific for the neo-epitope. Inter- and intra- assay variations were 11% and 4%, respectively. PROM was elevated (p = 0.0003) in patients with PsA (median: 0.24, IQR: 0.19-0.31) compared to healthy controls (0.18; 0.14-0.23) at baseline. AUROC for separation of healthy controls from PsA patients was 0.674 (95% CI 0.597-0.744, P < 0.001). In conclusion, MMP-cleaved prolargin can be quantified in serum by the PROM assay and has the potential to separate patients with PsA from healthy controls.

Indexed as

AC133 AntigenAnimalsAntibodies, MonoclonalAntibody FormationArthritis, PsoriaticBiomarkersCase-Control StudiesCohort StudiesEnzyme-Linked Immunosorbent AssayExtracellular Matrix ProteinsFemaleGlycoproteinsHumansMaleMatrix MetalloproteinasesMiceAC133 AntigenAntibodies, MonoclonalBiomarkersExtracellular Matrix ProteinsGlycoproteinsMatrix MetalloproteinasesPRELP protein, humanPROM1 protein, human

Identifiers

PMID32782251
PMCPMC7419545
OpenAlexW3048378744

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Registered trials

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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.