Evidence map›Paper›PMID 29323343›Full record

ReviewNature reviews. Rheumatology2018

Targeting lymphatic function as a novel therapeutic intervention for rheumatoid arthritis.

Echoe M Bouta, Richard D Bell, Homaira Rahimi, Lianping Xing, Ronald W Wood, Clifton O Bingham, Christopher T Ritchlin, Edward M Schwarz

Abstract readReview
In one paragraph

Review in Nature reviews. Rheumatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 1 pooled it
6.3field-weighted citation impact, top 2% 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

78 citing papers in PubMed, 1 synthesis or guideline pooled it, 143 citations in OpenAlex.

  1. Pooled it
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  8. The Function ofbioRxiv : the preprint server for biology · 2026
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18 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 1 country.

Echoe M BoutaCenter for Musculoskeletal Research, University of Rochester School of Medicine and Dentistry.
Richard D BellCenter for Musculoskeletal Research, University of Rochester School of Medicine and Dentistry.
Homaira RahimiCenter for Musculoskeletal Research, University of Rochester School of Medicine and Dentistry.
Lianping XingCenter for Musculoskeletal Research, University of Rochester School of Medicine and Dentistry.
Ronald W WoodDepartment of Obstetrics and Gynecology, University of Rochester School of Medicine and Dentistry.
Clifton O BinghamDivisions of Rheumatology and Allergy and Clinical Immunology, Johns Hopkins University, 600 North Wolfe Street Baltimore, Maryland 21205, USA.
Christopher T RitchlinCenter for Musculoskeletal Research, University of Rochester School of Medicine and Dentistry.
Edward M SchwarzCenter for Musculoskeletal Research, University of Rochester School of Medicine and Dentistry.
University of Rochester · USJohns Hopkins University · US

Funding

The University of Rochester's Clinical and Translational Science InstituteUL1TR000042 · NCATS · UNIVERSITY OF ROCHESTER · PI BENNETT, NANCY M, KIEBURTZ, KARL D. · 2012 to 2015
$14.4M
Rochester Resource-Based Center for Bone, Muscle and Orthopaedic Research (ROCSTARR) (Overall Application)P30AR069655 · NIAMS · UNIVERSITY OF ROCHESTER · PI Edward M. Schwarz · 2016 to 2026
$7.8M
Elucidating the Mechanisms of Arthritic Flare and Developing TreatmentsR01AR056702 · NIAMS · UNIVERSITY OF ROCHESTER · PI SCHWARZ, EDWARD M. · 2009 to 2025
$4.9M
Training in Orthopaedic Researchhttps://apps.era.nih.gov/grantfolder/viewInternalGF.era?applId=8841318&folderId=90T32AR053459 · NIAMS · UNIVERSITY OF ROCHESTER · PI ZUSCIK, MICHAEL J · 2006 to 2017
$3.4M
The University of Rochester Core Center for Musculoskeletal Biology and MedicineP30AR061307 · NIAMS · UNIVERSITY OF ROCHESTER · PI SCHWARZ, EDWARD M. · 2011 to 2015
$3.0M
DC-STAMP: Regulator of Osteoclastogenesis and Response Marker in PsAR01AR069000 · NIAMS · UNIVERSITY OF ROCHESTER · PI RITCHLIN, CHRISTOPHER TREVOR · 2016 to 2020
$1.7M
Study of osteoblast regulation in TNF-mediated bone lossR01AR063650 · NIAMS · UNIVERSITY OF ROCHESTER · PI XING, LIANPING · 2013 to 2016
$1.4M
sGC beta1: A Potential Critical Regulator of the Lymphatic Pulse and Novel Target in Arthritic FlareK08AR067885 · NIAMS · UNIVERSITY OF ROCHESTER · PI RAHIMI, HOMAIRA · 2016 to 2020
$844k
Protein modification in bone cell regulationR21AR069789 · NIAMS · UNIVERSITY OF ROCHESTER · PI BOECKMAN, ROBERT K, XING, LIANPING · 2016 to 2017
$372k
NCATS NIH HHS UL1 TR000042NIAMS NIH HHS K08 AR067885NIAMS NIH HHS P30 AR061307NIAMS NIH HHS P30 AR069655NIAMS NIH HHS R01 AR056702NIAMS NIH HHS R01 AR063650NIAMS NIH HHS R01 AR069000NIAMS NIH HHS R21 AR069789NIAMS NIH HHS T32 AR053459
6 · The paper itself

Abstract

Although clinical outcomes for patients with rheumatoid arthritis (RA) have greatly improved with the use of biologic and conventional DMARDs, approximately 40% of patients do not achieve primary clinical outcomes in randomized trials, and only a small proportion achieve lasting remission. Over the past decade, studies in murine models point to the critical role of the lymphatic system in the pathogenesis and therapy of inflammatory-erosive arthritis, presumably by the removal of catabolic factors, cytokines and inflammatory cells from the inflamed synovium. Murine studies demonstrate that lymphatic drainage increases at the onset of inflammatory-erosive arthritis but, as inflammation progresses to a more chronic phase, lymphatic clearance declines and both structural and cellular changes are observed in the draining lymph node. Specifically, chronic damage to the lymphatic vessel from persistent inflammation results in loss of lymphatic vessel contraction followed by lymph node collapse, reduced lymphatic drainage, and ultimately severe synovitis and joint erosion. Notably, clinical pilot studies in patients with RA report lymph node changes following treatment, and thus draining lymphatic vessels and nodes could represent a potential biomarker of arthritis activity and response to therapy. Most importantly, targeting lymphatics represents an innovative strategy for therapeutic intervention for RA.

Indexed as

AnimalsArthritis, RheumatoidClinical Trials as TopicDisease Models, AnimalGenetic TherapyGenetic VectorsHumansLymphatic SystemMiceVascular Endothelial Growth Factor CVascular Endothelial Growth Factor C

Identifiers

PMID29323343
PMCPMC6475908
OpenAlexW2782987256

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.