Evidence map›Paper›PMID 36565347›Full record

ArticleJournal of neurology2023

CSF lymphocytic pleocytosis does not predict a less favourable long-term prognosis in MS.

Lauren Astbury, Seema Kalra, Radu Tanasescu, Cris S Constantinescu

Open access · hybridFull text read
In one paragraph

Article 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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 6 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

4 authors at 2 institutions in 2 countries.

Lauren Astbury *Academic Unit of Mental Health and Clinical Neuroscience, Section of Clinical Neurology, University of Nottingham, Nottingham Centre for MS and Neuroinflammation, Nottingham University Hospitals QMC, Nottingham, NG7 2UH, UK.
Seema Kalra *University Hospitals of North Midlands NHS Trust, Royal Stoke MS Centre of Excellence, Stoke On Trent, UK.
Radu TanasescuAcademic Unit of Mental Health and Clinical Neuroscience, Section of Clinical Neurology, University of Nottingham, Nottingham Centre for MS and Neuroinflammation, Nottingham University Hospitals QMC, Nottingham, NG7 2UH, UK.
Cris S ConstantinescuAcademic Unit of Mental Health and Clinical Neuroscience, Section of Clinical Neurology, University of Nottingham, Nottingham Centre for MS and Neuroinflammation, Nottingham University Hospitals QMC, Nottingham, NG7 2UH, UK. cris.constantinescu@nottingham.ac.uk.ORCID http://orcid.org/0000-0003-2066-7585
Nottingham University Hospitals NHS Trust · GBUniversity of Ulster · GB

Funding

Medical Research Council CARP/T024402/1Medical Research Council MR/T024402/1
6 · The paper itself

Abstract

objectiveThe role of CSF lymphocytic pleocytosis in predicting the clinical outcome of multiple sclerosis is unclear. We explored the impact of CSF pleocytosis at diagnosis on long-term disease progression in a large UK cohort.

methodsWe extracted demographic, clinical and CSF data of people with MS attending the MS clinics between 1996 and 2014 at two MS centres from the English Midlands. We compared EDSS at onset, follow up EDSS and progression indices Multiple Sclerosis Severity Score (MSSS), annualized change in EDSS and transition to secondary progression in the presence/absence of pleocytosis. Two-tailed student t-test, Mann-Whitney U test, Chi-Square or Fisher's exact tests were used for detecting the differences.

resultsA total of 247 patients with MS (178 females; mean age 42.4; 217 with relapsing onset) were followed up for an average of 13.56 years (median 12 years). Almost 18% had lymphocytic CSF ≥ 5 per microliter. CSF pleocytosis was not associated with higher EDSS at the time of LP or at follow up, and other progression indices like MSSS, annualized change in EDSS or transition to secondary progression. DISCUSSION: CSF pleocytosis at MS diagnosis does not predict higher long-term disability and has no long-term prognostic value in routine clinical circumstances. Differences between MS populations and potential differences in disease activity at the time of CSF analysis may account for differences between studies.

Indexed as

Multiple SclerosisMultiple Sclerosis, Chronic ProgressiveAdultDisease ProgressionFemaleHumansLeukocytosisPrognosisCerebrospinal fluidMultiple sclerosisPleocytosisPrognosis

Identifiers

PMID36565347
PMCPMC10025177
OpenAlexW4312129445

What Socratic holds

Textfull text, public
LicenceCC BY
measurements read36
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.