Evidence map›Paper›PMID 39762123›Full record

Trial reportRMD open2025

Association between resolution of MRI-detected inflammation and improved clinical outcomes in axial spondyloarthritis under long-term anti-TNF therapy.

Murat Torgutalp, Judith Rademacher, Fabian Proft, Kay-Geert Hermann, Christian Althoff, H Haibel, Mikhail Protopopov, Joachim Sieper, Valeria Rios Rodriguez, Denis Poddubnyy

Registry-linked trialAbstract readClinical Trial
In one paragraph

Trial report in RMD open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00844142 (Randomized Controlled 12 Months Trial With Etanercept), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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.

NCT00844142 phase2unknown statusnot on this map

Randomized Controlled 12 Months Trial With Etanercept (Enbrel ®) vs. Sulfasalazine in Early Axial Spondyloarthritis With Focus on Improvement of Acute Inflammatory Lesions as Detected by MRI. Amendment 4: 1-Year Extension of Study

TypeinterventionalSponsorCharite University, Berlin, GermanyRan2005 to 2013Enrolled80ConditionsModerate to Severe Active Axial SpondyloarthritisArmsEtanercept 25mg, Sulfasalazine
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Murat TorgutalpCorporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Gastroenterology, Infectious Diseases and Rheumatology (including Nutrition Medicine), Charite Universitatsmedizin Berlin, Berlin, Germany.ORCID 0000-0003-4600-9484
Judith RademacherCorporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Gastroenterology, Infectious Diseases and Rheumatology (including Nutrition Medicine), Charite Universitatsmedizin Berlin, Berlin, Germany.ORCID 0000-0001-7442-2570
Fabian ProftCorporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Gastroenterology, Infectious Diseases and Rheumatology (including Nutrition Medicine), Charite Universitatsmedizin Berlin, Berlin, Germany.ORCID 0000-0003-4306-033X
Kay-Geert HermannCorporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Radiology (including Pediatric Radiology), Charité Universitätsmedizin Berlin, Berlin, Germany.
Christian AlthoffHELIOS Klinikum Emil von Behring GmbH, Berlin, Germany.
H HaibelCorporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Gastroenterology, Infectious Diseases and Rheumatology (including Nutrition Medicine), Charite Universitatsmedizin Berlin, Berlin, Germany.
Mikhail ProtopopovCorporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Gastroenterology, Infectious Diseases and Rheumatology (including Nutrition Medicine), Charite Universitatsmedizin Berlin, Berlin, Germany.ORCID 0000-0003-4840-5069
Joachim SieperCorporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Gastroenterology, Infectious Diseases and Rheumatology (including Nutrition Medicine), Charite Universitatsmedizin Berlin, Berlin, Germany.ORCID 0000-0003-0285-9890
Valeria Rios Rodriguez *Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Gastroenterology, Infectious Diseases and Rheumatology (including Nutrition Medicine), Charite Universitatsmedizin Berlin, Berlin, Germany valeria.rios-rodriguez@charite.de.ORCID 0000-0001-5612-043X
Denis Poddubnyy *Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Gastroenterology, Infectious Diseases and Rheumatology (including Nutrition Medicine), Charite Universitatsmedizin Berlin, Berlin, Germany.ORCID 0000-0002-4537-6015

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesIn this post-hoc analysis of ESTHER trial, we aimed to investigate the longitudinal relationship between inflammation on MRI and the achievement of inactive disease/low disease activity in patients with axial spondyloarthritis (axSpA) treated with long-term tumor necrosis factor (TNF) inhibitor etanercept.

methodsOf the 76 patients with active axSpA in the ESTHER trial, we included all patients treated with etanercept for at least 6 months for main analysis. All clinical and MRI data from 4.5 years of follow-up were used in the analysis. MRIs of the spine and sacroiliac (SI) joints were performed at baseline, week 24, week 48 and yearly thereafter and were evaluated for active inflammatory lesions according to the Berlin MRI score.

resultsLongitudinal analysis showed that higher SI joint osteitis score was associated with higher Axial Spondyloarthritis Disease Activity Score (ASDAS) at the same time point (β=0.08, 95% CI (0.05; 0.11)) and at the next time point 6 months later (β=0.05, 95% CI (0.02; 0.07)). Furthermore, resolution of osteitis in the SI joint (Berlin MRI osteitis score of ≤1) was associated with lower ASDAS at the next time point (β=-0.26, 95% CI (-0.42; -0.09)), higher odds of achieving ASDAS low disease activity (OR=5.61, 95% CI (1.06; 29.67)) and inactive disease status (OR=2.23, 95% CI (1.01; 4.94)) at the next time point.

conclusionsThe presence of inflammation on SI joints-MRI is associated with higher disease activity in axSpA. Resolution of inflammation on MRI is associated with better clinical outcomes in the long-term follow-up. Thus, achieving complete resolution of inflammation is favourable for meeting the treatment goals in axSpA. TRIAL REGISTRATION NUMBER: NCT00844142.

Indexed as

Axial SpondyloarthritisEtanerceptMagnetic Resonance ImagingSacroiliac JointAdultAntirheumatic AgentsClinical Trials, Phase II as TopicFemaleHumansInflammationLongitudinal StudiesMaleMiddle AgedOsteitisRandomized Controlled Trials as TopicSeverity of Illness IndexAntirheumatic AgentsEtanerceptTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsAxial SpondyloarthritisEtanerceptMagnetic Resonance ImagingSpondylitis AnkylosingTumor Necrosis Factor Inhibitors

Identifiers

PMID39762123
PMCPMC11749430

What OpenQuestion holds

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Registered trials

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.