Evidence map›Paper›PMID 42410660›Full record

ArticleAnnals of neurology2026

A new Patient-Reported Outcome Scale to assess autoimmune Encephalitis: PROSE.

Juliette Brenner, Yvette S Crijnen, Ilse Kulderij, Sammy H C Olijslagers, Cinthia J Ruhe, Anke A G Tolido, Laura P Kersten, Julia C P Verkoelen, Chelsey N Kret, Brigit Thomassen and 15 more

Abstract read
In one paragraph

Article in Annals of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

25 authors.

Juliette BrennerDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0001-5523-4398
Yvette S CrijnenDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0003-0279-7140
Ilse KulderijDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Sammy H C OlijslagersDepartment of Neurology, Catharina Hospital, Eindhoven, The Netherlands.
Cinthia J RuheDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Anke A G TolidoDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Laura P KerstenDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Julia C P VerkoelenDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Chelsey N KretDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Brigit ThomassenDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Finn I van WijnenDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Juna M de VriesDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Tessa M BienfaitDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Tessa BrandDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Jeroen KerstensDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Robin W van SteenhovenDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.ORCID https://orcid.org/0009-0003-6842-095X
Anna E M BastiaansenDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Marienke A A M de BruijnDepartment of Neurology, Elisabeth TweeSteden Hospital, Tilburg, The Netherlands.
Agnes van SonderenDepartment of Neurology, Haaglanden Medical Centre, The Hague, The Netherlands.
Sharon VeenbergenDepartment of Immunology, Erasmus University Medical Centre Rotterdam, Rotterdam, The Netherlands.
Ava EastonEncephalitis International, Malton, UK.
Peter A E Sillevis SmittDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Esther van den BergDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Melissa MandarakasDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Maarten J TitulaerDepartment of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAutoimmune encephalitis (AIE) has long-lasting effects. Generic clinical assessment-scales insufficiently capture disease-specific sequelae. Patient-reported outcome measures (PROMs) assess outcomes important to patients, ensuring relevance in the clinic and trials. We developed a disease-specific patient-reported outcome scale for encephalitis (PROSE).

methodsExisting PROM-items (n = 235) were evaluated for content-validity and supplemented with focus-group-derived items. Patients with a history of anti-NMDAR, anti-LGI1, or anti-CASPR2 encephalitis completed the preliminary item pool (n = 166). To refine and reduce the item-pool and create the PROSE, we conducted item-, factor-, and Rasch-analyses. Test-retest reliability was assessed over 2 weeks and convergent-validity against established measures.

resultsThe analysis included data from 202 patients with anti-LGI1 (n = 97), anti-NMDAR (n = 85), and anti-CASPR2 (n = 20) encephalitis, median 3.5 years from diagnosis (range = 0.05-14; n = 41 <1 year). Prospective, repeated assessments (n = 52) were available in 22 patients diagnosed <24 months prior. Analyses supported the viability of a 40-item unidimensional interval scale for patient-perceived disease-severity: the PROSE. The person-separation (Cronbach's alpha = 0.92, p < 0.001) and test-retest reliability (intra-class correlation-coefficient = 0.93, p < 0.001, n = 23) were high. PROSE covers cognition, behavior, emotional and physical wellbeing, daily activities, and participation. PROSE scores were normally distributed and informative across subtypes and demographic groups, correlated with time-since-diagnosis (R = -0.32, p = 0.00018) and captured improvement over time prospectively (n = 22). They showed reasonable-to-good agreement with self-reported physical and emotional wellbeing (R = 0.57 and 0.55, p < 0.001) and quality of life (R = 0.57, p < 0.001) on Visual Analogue Scales, to existing PROMs (ρ = 0.42 to ρ = 0.81) and functional scores (mRS ρ = 0.44, p < 0.001, CASE ρ = 0.40, p < 0.001), with strongest correlations to aggregate constructs.

interpretationPROSE is a psychometrically robust, disease-specific patient-reported outcome assessment-tool for encephalitis. ANN NEUROL 2026;100:511-524.

Indexed as

EncephalitisHashimoto DiseasePatient Reported Outcome MeasuresAdolescentAdultAgedAutoantibodiesFemaleHumansIntracellular Signaling Peptides and ProteinsMaleMembrane ProteinsMiddle AgedNerve Tissue ProteinsReproducibility of ResultsYoung AdultAutoantibodiesCNTNAP2 protein, humanIntracellular Signaling Peptides and ProteinsLGI1 protein, humanMembrane ProteinsNerve Tissue Proteins

Identifiers

PMID42410660
PMCPMC13495803

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