Evidence map›Paper›PMID 40172495›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2025

Recurrence Risk in Pediatric Noninfectious Uveitis During Adalimumab Tapering: An International Multicenter Retrospective Study.

Achille Marino, Maria Vittoria Cicinelli, Elisabetta Miserocchi, Stefania Costi, Francesco Baldo, Maurizio Virgilio Gattinara, Pierluigi Scandale, Scott D Smith, Debra A Goldstein, Dina Baddar and 22 more

Abstract readMulticenter Study
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Observational
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

32 authors.

Achille MarinoASST Gaetano Pini-CTO, Milan, Italy.
Maria Vittoria CicinelliVita-Salute San Raffaele University and IRCCS San Raffaele Scientific Institute, Milan, Italy.
Elisabetta MiserocchiVita-Salute San Raffaele University and IRCCS San Raffaele Scientific Institute, Milan, Italy.
Stefania CostiASST Gaetano Pini-CTO, Milan, Italy.
Francesco BaldoASST Gaetano Pini-CTO, Milan, Italy.
Maurizio Virgilio GattinaraASST Gaetano Pini-CTO, Milan, Italy.
Pierluigi ScandaleVita-Salute San Raffaele University and IRCCS San Raffaele Scientific Institute, Milan, Italy.
Scott D SmithCleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates, and Cleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, Ohio.
Debra A GoldsteinNorthwestern University, Chicago, Illinois.
Dina BaddarWatany Eye Hospital, Cairo, Egypt, and Research Institute of Ophthalmology, Giza, Egypt.
Terese K A GergesWatany Eye Hospital, Cairo, Egypt.
Timothy M JanetosNorthwestern University, Chicago, Illinois.
Matilde Ruiz-CruzAsociación Para Evitar la Ceguera en México, I. A. P, Mexico City, Mexico.
Kazuichi MaruyamaOsaka University, Osaka, Japan.
Massimiliano SerafinoIRCCS Giannina Gaslini Institute, Genoa, Italy.
Paola CamicioneIRCCS Giannina Gaslini Institute, Genoa, Italy.
Vishali GuptaPost Graduate Institute of Medical Education and Research, Chandigarh, India.
Radgonde AmerHadassah Medical Center, Jerusalem, Israel.
Emilio M DoddsConsultores Oftalmológicos, Buenos Aires, Argentina.
Sebastian InchauspeConsultores Oftalmológicos, Buenos Aires, Argentina.
Marion R MunkNorthwestern University, Chicago, Illinois, and Inselspital, University Hospital Bern and Augenarzt-Praxisgemeinschaft Gutblick AG, Bern, Switzerland.
Ester CarreñoHospital Universitario Fundación Jiménez Díaz, Madrid, Spain.
Soon-Phaik CheeSingapore National Eye Centre, National University of Singapore, Singapore Eye Research Institute, and Duke-NUS Medical School, Singapore.
Aniruddha AgarwalCleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates, and Cleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, Ohio.
Ariel SchlaenHospital Universitario Austral and Hospital De Clinicas "José de San Martín," Universidad de Buenos Aires, Buenos Aires, Argentina.
Ramiro A GómezHospital De Clinicas "José de San Martín," Universidad de Buenos Aires, Buenos Aires, Argentina.
Cristobal A CoutoHospital De Clinicas "José de San Martín," Universidad de Buenos Aires, Buenos Aires, Argentina.
Moncef KhairallahFattouma Bourguiba University Hospital, University of Monastir, Tunisia.
Piergiorgio NeriCleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates, and Cleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, Ohio.
Cecilia B ChighizolaASST Gaetano Pini-CTO and University of Milan, Milan, Italy.ORCID https://orcid.org/0000-0002-3787-9632
Roberto F CaporaliASST Gaetano Pini-CTO and University of Milan, Milan, Italy.
Francesco PichiCleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates, and Cleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, Ohio.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aims to assess the risk of noninfectious uveitis (NIU) relapse in pediatric patients undergoing adalimumab (ADA) tapering, evaluating potential predictors of such risk.

methodsWe conducted a multicenter retrospective cohort study involving pediatric patients with NIU who underwent ADA tapering due to inactive uveitis. Cox proportional hazards regression was used to analyze risk factors for NIU recurrence.

resultsThe study cohort comprised 114 patients (65 girls; 57%). Most commonly, patients presented with juvenile idiopathic arthritis-associated uveitis (JIA-U) (52 of 114; 46%) or idiopathic uveitis (46 of 114; 40%). At ADA tapering, 46% of patients (53 of 114) experienced NIU recurrence after an overall median time of 30 weeks (interquartile range [IQR] 15-58 weeks) from the start of ADA tapering. Patients without recurrences were observed for a median of 70 weeks (IQR 48-98 weeks). Multivariate Cox regression analysis showed that a slower ADA tapering schedule was associated with a lower recurrence rate during the waning (hazard ratio [HR] 0.40, 95% confidence interval [CI] 0.21-0.74; P < 0.01). Subgroup analysis of patients with JIA-U indicated that beginning ADA tapering after at least two years of disease inactivity significantly reduced recurrence risk (HR 0.65, 95% CI 0.43-0.95; P = 0.05). Among 59 patients (52%) who discontinued ADA, recurrence rates were similar between fast- and slow-tapering groups (21% vs 33%; P = 0.6), but median time to recurrence was shorter with fast tapering (10 weeks vs 37 weeks; P = 0.05).

conclusionThis study highlights the significant clinical impact of ADA tapering on uveitis recurrence risk, recommending a gradual, slow-tapering approach with close monitoring.

Indexed as

AdalimumabAntirheumatic AgentsUveitisAdolescentArthritis, JuvenileChildChild, PreschoolFemaleHumansMaleProportional Hazards ModelsRecurrenceRetrospective StudiesRisk FactorsAdalimumabAntirheumatic Agents

Identifiers

PMID40172495
PMCPMC12401805

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.