Evidence map›Paper›PMID 35273387›Full record

ReviewNature reviews. Rheumatology2022

Effects of targeted therapies on bone in rheumatic and musculoskeletal diseases.

Boglárka Soós, Ágnes Szentpétery, Hennie G Raterman, Willem F Lems, Harjit P Bhattoa, Zoltán Szekanecz

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Rheumatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 pooled it
9.9field-weighted citation impact, top 1% 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

37 citing papers in PubMed, 2 syntheses or guidelines pooled it, 58 citations in OpenAlex.

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  7. Osteoporosis in rheumatoid arthritis: a new perspective on risk factors and clinical prediction models.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2026
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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 2 countries.

Boglárka SoósDepartment of Rheumatology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Ágnes SzentpéteryDepartment of Rheumatology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Hennie G RatermanDepartment of Rheumatology, Northwest Clinics, Alkmaar, Netherlands.ORCID http://orcid.org/0000-0001-9972-2844
Willem F LemsAmsterdam Rheumatology and Immunology Centre, Amsterdam, Netherlands.
Harjit P Bhattoa *Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.ORCID http://orcid.org/0000-0002-4909-0065
Zoltán Szekanecz *Department of Rheumatology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary. szekanecz.zoltan@med.unideb.hu.ORCID http://orcid.org/0000-0002-7794-6844
University of Debrecen · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Generalized bone loss (osteoporosis) and fragility fractures can occur in rheumatic and musculoskeletal diseases including rheumatoid arthritis and spondyloarthritis (SpA; including ankylosing spondylitis and psoriatic arthritis). In addition, rheumatoid arthritis can involve localized, periarticular bone erosion and, in SpA, local (pathological) bone formation can occur. The RANK-RANKL-osteoprotegerin axis and the Wnt-β-catenin signalling pathway (along with its inhibitors sclerostin and Dickkopf 1) have been implicated in inflammatory bone loss and formation, respectively. Targeted therapies including biologic DMARDs and Janus kinase (JAK) inhibitors can stabilize bone turnover and inhibit radiographic joint damage, and potentially also prevent generalized bone loss. Targeted therapies interfere at various points in the mechanisms of local and generalized bone changes in systemic rheumatic diseases, and they effect biomarkers of bone resorption and formation, bone mass and risk of fragility fractures. Studies on the effects of targeted therapies on rates of fragility fracture are scarce. The efficacy of biologic DMARDs for arresting bone formation in axial SpA is debated. Improved understanding of the most relevant therapeutic targets and identification of important targeted therapies could lead to the preservation of bone in inflammatory rheumatic and musculoskeletal diseases.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidBiological ProductsJanus Kinase InhibitorsSpondylarthritisBone and BonesHumansAntirheumatic AgentsBiological ProductsJanus Kinase Inhibitors

Identifiers

PMID35273387
OpenAlexW4221027565

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.