Evidence map›Paper›PMID 26576067›Full record

ArticleDisease markers2015

Effects of Antitumor Necrosis Factor Therapy on Osteoprotegerin, Neopterin, and sRANKL Concentrations in Patients with Rheumatoid Arthritis.

Katharina Kurz, Manfred Herold, Elisabeth Russe, Werner Klotz, Guenter Weiss, Dietmar Fuchs

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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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

6 authors at 1 institution in 1 country.

Katharina KurzDepartment of Internal Medicine VI, Innsbruck Medical University, 6020 Innsbruck, Austria ; Division of Biological Chemistry, Biocenter, Innsbruck Medical University, 6020 Innsbruck, Austria.
Manfred HeroldDepartment of Internal Medicine VI, Innsbruck Medical University, 6020 Innsbruck, Austria.
Elisabeth RusseDepartment of Internal Medicine VI, Innsbruck Medical University, 6020 Innsbruck, Austria.
Werner KlotzDepartment of Internal Medicine VI, Innsbruck Medical University, 6020 Innsbruck, Austria.
Guenter WeissDepartment of Internal Medicine VI, Innsbruck Medical University, 6020 Innsbruck, Austria.
Dietmar FuchsDepartment of Internal Medicine VI, Innsbruck Medical University, 6020 Innsbruck, Austria ; Division of Biological Chemistry, Biocenter, Innsbruck Medical University, 6020 Innsbruck, Austria.
Innsbruck Medical University · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRheumatoid arthritis is a systemic autoimmune disease characterized by joint erosions, progressive focal bone loss, and chronic inflammation.

methods20 female patients with moderate-to-severe rheumatoid arthritis were treated with anti-TNF-antibody adalimumab in addition to concomitant antirheumatic therapies. Patients were assessed for overall disease activity using the DAS28 score, and neopterin, erythrocyte sedimentation rate (ESR), and C-reactive protein (CRP) concentrations as well as osteoprotegerin (OPG) and soluble receptor activator of NF-κB ligand (sRANKL) concentrations were determined before therapy and at week 12. Neopterin as well as OPG and sRANKL were determined by commercial ELISAs.

resultsBefore anti-TNF therapy patients presented with high disease activity and elevated concentrations of circulating inflammatory markers. OPG concentrations correlated with neopterin (rs = 0.494, p = 0.027), but not with DAS28. OPG concentrations and disease activity scores declined during anti-TNF-treatment (both p < 0.02). Patients who achieved remission (n = 7) or showed a good response according to EULAR criteria (n = 13) presented with initially higher baseline OPG levels, which subsequently decreased significantly during treatment (p = 0.018 for remission, p = 0.011 for good response).

conclusionsAdalimumab therapy was effective in modifying disease activity and reducing proinflammatory and bone remodelling cascades.

Indexed as

AdalimumabAdultAntirheumatic AgentsArthritis, RheumatoidDrug Therapy, CombinationFemaleHumansMiddle AgedNeopterinOsteoprotegerinRANK LigandAdalimumabAntirheumatic AgentsNeopterinOsteoprotegerinRANK Ligand

Identifiers

PMID26576067
PMCPMC4631883
OpenAlexW1763704351

What OpenQuestion holds

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LicenceCC BY
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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.