Evidence map›Paper›PMID 18338203›Full record

ArticleClinical rheumatology2008

Reduction of urinary levels of pyridinoline and deoxypyridinoline and serum levels of soluble receptor activator of NF-kappaB ligand by etanercept in patients with rheumatoid arthritis.

Kageyama Yasunori, Takahashi Masaaki, Nagafusa Tetsuyuki, Kobayashi Hayato, Nagano Akira

Abstract read
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In one paragraph

Article in Clinical rheumatology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Observational
  5. Observational
  6. Article
  7. Article
  8. Osteoblast Role in Rheumatic Diseases.International journal of molecular sciences · 2017
    Review
  9. Characterization of Smad3 knockout mouse derived skin cells.In vitro cellular & developmental biology. Animal · 2017
    Article
  10. Biologic therapies and bone loss in rheumatoid arthritis.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2017
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Effects of anti-tumor necrosis factor α agents on bone.Current opinion in rheumatology · 2012
    Review
  16. Review
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

5 authors at 3 institutions in 1 country.

Kageyama YasunoriDepartment of Orthopaedic Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan. Tsukatonpipi@nifty.com
Takahashi Masaaki
Nagafusa Tetsuyuki
Kobayashi Hayato
Nagano Akira
Hamamatsu University · JPHamamatsu University School of Medicine · JPFujieda Municipal General Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The effects of soluble TNF-alpha receptor, etanercept, on bone metabolism were investigated in patients with rheumatoid arthritis (RA). Thirty RA patients were administered etanercept once or twice a week for more than 6 months. We evaluated clinical and laboratory parameters and measured urinary excretion levels of pyridinoline (PYD), deoxypyridinoline (DPD), cross-linked N-telopeptides of type I collagen (NTX), and serum levels of bone alkaline phosphatase (BAP), osteoprotegerin (OPG), and soluble receptor activator of NFkappaB ligand (sRANKL) at the baseline and at 3 and 6 months after initial treatment with etanercept. Etanercept treatment resulted in an improvement of symptoms due to RA and in a reduction of urinary excretion levels of PYD and DPD as well as serum sRANKL levels, with a significant difference at 6 months, and an increase of serum BAP levels at 3 and 6 months after the initial treatment with etanercept. Urinary NTX and serum OPG levels did not show a significant change at 3 and 6 months after the initial treatment, but serum OPG levels did show a reverse correlation with serum CRP levels, suggesting that the regulation of inflammation in RA may result in an induction of OPG production. Etanercept may have the ability to reduce the levels of bone resorption markers and to increase the levels of a bone formation marker while reducing sRANKL formation in RA patients.

Indexed as

Alkaline PhosphataseAmino AcidsArthritis, RheumatoidBiomarkersBone and BonesCollagen Type IEtanerceptFemaleHumansImmunoglobulin GMaleMiddle AgedOsteoprotegerinPeptidesRANK LigandReceptors, Tumor Necrosis FactorAlkaline PhosphataseAmino AcidsBiomarkersCollagen Type Icollagen type I trimeric cross-linked peptidedeoxypyridinolineEtanerceptImmunoglobulin GOsteoprotegerinPeptidespyridinolineRANK LigandReceptors, Tumor Necrosis FactorTNFSF11 protein, human

Identifiers

PMID18338203
OpenAlexW2065758044

What OpenQuestion holds

Textmetadata
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.