Evidence map›Paper›PMID 31162832›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2019

Osteoclast-Derived Autotaxin, a Distinguishing Factor for Inflammatory Bone Loss.

Sacha Flammier, Olivier Peyruchaud, Fanny Bourguillault, François Duboeuf, Jean-Luc Davignon, Derek D Norman, Sylvie Isaac, Hubert Marotte, Gabor Tigyi, Irma Machuca-Gayet and 1 more

Open access · greenAbstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Lipopolysaccharide-Induced Bone Loss in Rodent Models: A Systematic Review and Meta-Analysis.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2023
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Bone mineralisation and glucose metabolism.Current opinion in endocrine and metabolic research · 2023
    Review
  7. Article
  8. Designing Dual Inhibitors of Autotaxin-LPAR GPCR Axis.Molecules (Basel, Switzerland) · 2022
    Review
  9. Autotaxin/Lysophosphatidic Acid Axis: From Bone Biology to Bone Disorders.International journal of molecular sciences · 2022
    Review
  10. Frontiers in immunology · 2022
    Article
  11. Article
  12. 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

11 authors at 4 institutions in 2 countries.

Sacha FlammierINSERM UMR 1033 LYOS and University of Lyon I, Lyon, France.
Olivier PeyruchaudINSERM UMR 1033 LYOS and University of Lyon I, Lyon, France.ORCID 0000-0002-5393-4945
Fanny BourguillaultINSERM UMR 1033 LYOS and University of Lyon I, Lyon, France.
François DuboeufINSERM UMR 1033 LYOS and University of Lyon I, Lyon, France.
Jean-Luc DavignonUniversity of Paul Sabatier Toulouse III, INSERM-CNRS U1043, CPTP, CHU Purpan, and Pierre Paul Riquet Hospital, Toulouse, France.
Derek D NormanUniversity of Tennessee Health Sciences Center, Memphis, Tennessee.
Sylvie IsaacLyon Sud Hospital, Pierre-Bénite, France.
Hubert MarotteSAINBIOSE, INSERM, U1059, LBTO, University of Lyon, and University Hospital of St. Étienne, St. Étienne, France.ORCID 0000-0003-1177-9497
Gabor TigyiUniversity of Tennessee Health Sciences Center, Memphis, Tennessee.
Irma Machuca-GayetINSERM UMR 1033 LYOS and University of Lyon I, Lyon, France.ORCID 0000-0002-3010-9774
Fabienne CouryINSERM UMR 1033 LYOS and University of Lyon I, Lyon, France, and Lyon Sud Hospital, Pierre-Bénite, France.ORCID 0000-0002-9175-8620
Université Claude Bernard Lyon 1 · FRUniversity of Tennessee Health Science Center · USCentre National de la Recherche Scientifique · FRHôpital Lyon Sud · FR

Funding

Ligand Recognition by Phospholipid Growth Factor ReceptorsR01CA092160 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI TIGYI, GABOR J · 2001 to 2022
$5.9M
Agence Nationale de la Recherche ANR-15-CE14-0010-01Fondation ARC pour la Recherche sur le Cancer PJA20151203151Institut National de la Santé et de la Recherche MédicaleLigue Contre le CancerNCI NIH HHS R01 CA092160Pfizer
6 · The paper itself

Abstract

objectiveThe severity of rheumatoid arthritis (RA) correlates directly with bone erosions arising from osteoclast (OC) hyperactivity. Despite the fact that inflammation may be controlled in patients with RA, those in a state of sustained clinical remission or low disease activity may continue to accrue erosions, which supports the need for treatments that would be suitable for long-lasting inhibition of OC activity without altering the physiologic function of OCs in bone remodeling. Autotaxin (ATX) contributes to inflammation, but its role in bone erosion is unknown.

methodsATX was targeted by inhibitory treatment with pharmacologic drugs and also by conditional inactivation of the ATX gene Ennp2 in murine OCs (ΔATX

resultsOCs present at sites of inflammation overexpressed ATX. Pharmacologic inhibition of ATX in hTNF

conclusionOur results identify ATX as a novel OC factor that specifically controls inflammation-induced bone erosions and systemic bone loss. Therefore, ATX inhibition offers a novel therapeutic approach for potentially preventing bone erosion in patients with RA.

Indexed as

AnimalsArthritis, ExperimentalArthritis, RheumatoidBone ResorptionCalcaneusFemaleFemurGene Knockdown TechniquesHumansLysophospholipase DMaleMiceMice, TransgenicOsteoclastsOvariectomyPhosphoric Diester HydrolasesLysophospholipase DPhosphoric Diester HydrolasesTNF protein, humanTumor Necrosis Factor-alpha

Identifiers

PMID31162832
PMCPMC6817375
OpenAlexW2948028899

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.