Evidence map›Paper›PMID 36565348›Full record

Observational studyJournal of neurology2023

Clinical and epidemiological correlates of treatment change in patients with NMOSD: insights from the CIRCLES cohort.

Shervin Gholizadeh, Alex Exuzides, Katelyn E Lewis, Chella Palmer, Michael Waltz, John W Rose, Anna Marie Jolley, Jacinta M Behne, Megan K Behne, Terrence F Blaschke and 5 more

Open access · hybridFull text readObservational Study
In one paragraph

Observational study in Journal of neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

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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

15 authors at 6 institutions in 1 country.

Shervin Gholizadeh *Genentech, Inc, South San Francisco, CA, USA.
Alex Exuzides *Genentech, Inc, South San Francisco, CA, USA.
Katelyn E LewisUniversity of Utah School of Medicine, Salt Lake City, UT, USA.
Chella PalmerUniversity of Utah School of Medicine, Salt Lake City, UT, USA.
Michael WaltzUniversity of Utah School of Medicine, Salt Lake City, UT, USA.
John W RoseUniversity of Utah School of Medicine, Salt Lake City, UT, USA.
Anna Marie JolleyUniversity of Utah School of Medicine, Salt Lake City, UT, USA.
Jacinta M BehneThe Guthy-Jackson Charitable Foundation, Beverly Hills, CA, USA.
Megan K BehneThe Guthy-Jackson Charitable Foundation, Beverly Hills, CA, USA.
Terrence F BlaschkeDepartments of Medicine and of Molecular Pharmacology, Stanford University School of Medicine, Stanford, CA, USA.
Terry J SmithUniversity of Michigan Kellogg Eye Center, Ann Arbor, MI, USA.
Jennifer SinnottUniversity of Utah School of Medicine, Salt Lake City, UT, USA.
Lawrence J CookUniversity of Utah School of Medicine, Salt Lake City, UT, USA.
Michael R YeamanGeffen School of Medicine at UCLA, Los Angeles, CA, USA. MRYeaman@ucla.edu.
Guthy-Jackson Charitable Foundation CIRCLES Study Group
University of Utah · USGuthy-Jackson Charitable Foundation · USStanford University · USUCLA Medical Center · USUniversity of California, Los Angeles · USW.K. Kellogg Foundation · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveNeuromyelitis optica spectrum disorders (NMOSD) represent rare autoimmune diseases of the central nervous system largely targeting optic nerve(s) and spinal cord. The present analysis used real-world data to identify clinical and epidemiological correlates of treatment change in patients with NMOSD.

methodsCIRCLES is a longitudinal, observational study of NMOSD conducted at 15 centers across North America. Patients with ≥ 60 days of follow-up and receiving on-study maintenance treatment were evaluated. The mean annual relapse rate (ARR) was estimated using negative binomial models; the likelihood of treatment change was estimated using Cox proportional hazards models. Relapses were included as time-varying covariates to estimate the relationship to treatment change.

resultsOf 542 patients included, 171 (31.5%) experienced ≥ 1 relapse on the study and 133 patients (24.5%) had ≥ 1 change in the treatment regimen. Two categories of variables significantly correlated with the likelihood of treatment change: (1) relapse: any on-study relapse (hazard ratio [HR] = 2.91; p < 0.001), relapse phenotypes (HR range = 2.15-5.49; p < 0.001), and pre-study ARR > 0.75 (HR 2.28; p < 0.001); 2) disease phenotype: brain syndrome only vs transverse myelitis involvement at onset (HR 2.44; p = 0.008), disease duration < 1 vs > 5 years (HR 1.66; p = 0.028), or autoimmune comorbidity (HR 1.55; p = 0.015). A subset of these factors significantly correlated with shorter time to first rituximab discontinuation.

conclusionsIn CIRCLES, relapse patterns and disease phenotype significantly correlated with changes in the maintenance treatment regimen. Such findings may facilitate the identification of patients with NMOSD who are likely to benefit from treatment change to reduce relapse risk or disease burden and enhance the quality of life.

Indexed as

Neuromyelitis OpticaAquaporin 4AutoantibodiesHumansLongitudinal StudiesNeoplasm Recurrence, LocalQuality of LifeRetrospective StudiesSpinal CordAquaporin 4AutoantibodiesAQP4DemographicsNeuromyelitis optica spectrum disorderRelapseTreatment

Identifiers

PMID36565348
PMCPMC10025181
OpenAlexW4312129189

What Socratic holds

Textfull text, public
LicenceCC BY
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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.