Evidence map›Paper›PMID 26411424›Full record

ReviewClinical reviews in allergy & immunology2016

Bone as a Target Organ in Rheumatic Disease: Impact on Osteoclasts and Osteoblasts.

Rebecca Baum, Ellen M Gravallese

Abstract readReview
In one paragraph

Review in Clinical reviews in allergy & immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
7.2field-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

56 citing papers in PubMed, 100 citations in OpenAlex.

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  9. Fu-zi decoction attenuate rheumatoid arthritisFrontiers in pharmacology · 2024
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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

2 authors at 1 institution in 1 country.

Rebecca BaumDepartment of Medicine and Division of Rheumatology, University of Massachusetts Medical School, Lazare Research Building Suite 223, 364 Plantation Street, Worcester, MA, 01605, USA.
Ellen M GravalleseDepartment of Medicine and Division of Rheumatology, University of Massachusetts Medical School, Lazare Research Building Suite 223, 364 Plantation Street, Worcester, MA, 01605, USA. ellen.gravallese@umassmed.edu.
University of Massachusetts Chan Medical School · US

Funding

Medical Scientist Training at UMMS Administrative SupplementT32GM107000 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KIEFE, CATARINA I. · 2013 to 2022
$4.9M
Innate Immunity Training ProgramT32AI095213 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SILVERMAN, NEAL · 2011 to 2025
$2.5M
Inhibition of osteoblast function in bone erosion in rheumatoid arthritisR01AR055952 · NIAMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI GRAVALLESE, ELLEN M · 2009 to 2013
$1.7M
NIAID NIH HHS T32 AI095213NIAMS NIH HHS R01 AR055952NIGMS NIH HHS T32 GM107000
6 · The paper itself

Abstract

Dysregulated bone remodeling occurs when there is an imbalance between bone resorption and bone formation. In rheumatic diseases, including rheumatoid arthritis (RA) and seronegative spondyloarthritis, systemic and local factors disrupt the process of physiologic bone remodeling. Depending upon the local microenvironment, cell types, and local mechanical forces, inflammation results in very different effects on bone, promoting bone loss in the joints and in periarticular and systemic bone in RA and driving bone formation at enthesial and periosteal sites in diseases such as ankylosing spondylitis (AS), included within the classification of axial spondyloarthritis. There has been a great deal of interest in the role of osteoclasts in these processes and much has been learned over the past decade about osteoclast differentiation and function. It is now appreciated that osteoblast-mediated bone formation is also inhibited in the RA joint, limiting the repair of erosions. In contrast, osteoblasts function to produce new bone in AS. The Wnt and BMP signaling pathways have emerged as critical in the regulation of osteoblast function and the outcome for bone in rheumatic diseases, and these pathways have been implicated in both bone loss in RA and bone formation in AS. These pathways provide potential novel approaches for therapeutic intervention in diseases in which inflammation impacts bone.

Indexed as

AnimalsArthritis, RheumatoidAutoantibodiesBone and BonesBone Morphogenetic ProteinsBone RemodelingBone ResorptionCell DifferentiationHumansMicroRNAsOsteoblastsOsteoclastsOsteogenesisRheumatic DiseasesSignal TransductionWnt Signaling PathwayAutoantibodiesBone Morphogenetic ProteinsMicroRNAsAnkylosing spondylitisBone erosionsBone formationBone remodelingDKK1EnthesesIL-23InflammationmicroRNAsOsteoblastOsteoclastRheumatoid arthritisSclerostinWnt

Identifiers

PMID26411424
PMCPMC4809775
OpenAlexW1908326960

What OpenQuestion 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 OpenQuestion graph.