Evidence map›Paper›PMID 38165286›Full record

ReviewCurrent opinion in rheumatology2024

New molecular targets in the treatment of rheumatoid arthritis.

Beth I Wallace, Laura Cooney, David A Fox

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in rheumatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
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

3 authors at 2 institutions in 1 country.

Beth I WallaceDivision of Rheumatology, Department of Internal Medicine, University of Michigan.
Laura CooneyDivision of Rheumatology, Department of Internal Medicine, University of Michigan.
David A FoxDivision of Rheumatology, Department of Internal Medicine, University of Michigan.
University of Michigan–Ann Arbor · USVA Ann Arbor Healthcare System · US

Funding

Using SMART Design to Develop Dynamic Treatment Regimens for Glucocorticoid TaperingIK2CX002430 · VA · VETERANS HEALTH ADMINISTRATION · PI Beth Ilene Wallace · 2022 to 2026
–
CSRD VA IK2 CX002430
6 · The paper itself

Abstract

purpose of reviewThis review will discuss selected emerging molecular targets and associated potential therapeutic agents for rheumatoid arthritis (RA)-directed treatment. RECENT

findingsAgents in active development for RA treatment include those targeted to CD40 and CD40 ligand, programmed death protein 1 (PD-1), and granulocyte-macrophage colony-stimulating factor (GM-CSF). Several other molecules with a strong theoretical role in RA pathogenesis and/or demonstrated efficacy in other autoimmune diseases are also being evaluated as potential drug targets in preclinical or translational studies in RA. These targets include interleukin 1 receptor associated kinases 1 and 4 (IRAK1, IRAK4), tyrosine kinase 2 (Tyk2), bradykinin receptor 1 (B1R), OX40 and OX40 ligand. SUMMARY: Identification of molecular targets for RA treatment remains an active area of investigation, with multiple therapeutic agents in clinical and preclinical development.

Indexed as

Arthritis, RheumatoidHumans

Identifiers

PMID38165286
PMCPMC12165284
OpenAlexW4390498824

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.