Evidence map›Paper›PMID 39435961›Full record

ArticleAnnals of clinical and translational neurology2024

Matched oligoclonal bands: Diagnostic utility and clinical characteristics.

Yoji Hoshina, Justin R Abbatemarco, Stefanie J Rodenbeck, Jason T Poon, Suzanne C Liu, M Mateo Paz Soldan, John E Greenlee, John W Rose, Lisa K Peterson, Lisa Johnson and 3 more

Abstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2024. 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. Exploring the Type 4 Cerebrospinal Fluid Oligoclonal Band Pattern: Clinical and Paraclinical Features with Diagnostic Implications.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Article
  2. Article
  3. Review
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

13 authors.

Yoji Hoshina *Department of Neurology, University of Utah, Salt Lake City, Utah, USA.ORCID 0000-0003-0228-664X
Justin R Abbatemarco *Department of Neurology, University of Utah, Salt Lake City, Utah, USA.
Stefanie J RodenbeckDepartment of Neurology, University of Utah, Salt Lake City, Utah, USA.
Jason T PoonDepartment of Neurology, University of Utah, Salt Lake City, Utah, USA.
Suzanne C LiuPediatric Neurology Division, Department of Pediatrics, University of Utah, Salt Lake City, Utah, USA.
M Mateo Paz SoldanDepartment of Neurology, University of Utah, Salt Lake City, Utah, USA.
John E GreenleeDepartment of Neurology, University of Utah, Salt Lake City, Utah, USA.ORCID 0000-0001-7788-6178
John W RoseDepartment of Neurology, University of Utah, Salt Lake City, Utah, USA.
Lisa K PetersonARUP Institute for Clinical and Experimental Pathology, Salt Lake City, Utah, USA.
Lisa JohnsonARUP Institute for Clinical and Experimental Pathology, Salt Lake City, Utah, USA.
Alen DelicDepartment of Neurology, University of Utah, Salt Lake City, Utah, USA.
Tammy L SmithDepartment of Neurology, University of Utah, Salt Lake City, Utah, USA.
Stacey L ClardyDepartment of Neurology, University of Utah, Salt Lake City, Utah, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo describe patient clinical characteristics associated with matched oligoclonal bands (OCB).

methodsA retrospective review at the University of Utah examined patients with matched OCB from 2015 to 2020. Clinical data, diagnosis, and outcomes were collected. Patients were classified with either multiple sclerosis (MS), other inflammatory neurologic disorder (other-IND), or noninflammatory neurologic disorder (NIND).

resultsOf 539 identified patients, 436 (53.4% female) were matched-only, while 103 (43.7% female) were matched + unique. Patients with matched-only bands were older (57.4 ± 16 vs. 52 ± 14.2, p < 0.001) and more likely to have a history of autoimmune disease (40.1% vs. 28.2%, p = 0.024) and/or cancer (28.7% vs. 16.5%, p = 0.012). Patients with matched + unique bands were more likely to have CSF pleocytosis (52.4% vs. 25.9%, p < 0.001), high IgG index (52.2% vs. 7.6%, p < 0.001), and an abnormal MRI (86.9% vs. 63.1%, p < 0.001). More than two-thirds of matched-only patients had NIND, while 33% and 41.7% of matched + unique patients had MS and other-IND, respectively. Patients exhibiting matched-only bands and a high IgG index demonstrated a significantly higher incidence of other-IND compared to those with matched-only bands and a normal IgG index (55.6% vs. 30.4%, p = 0.013). While Kaplan-Meier survival curves demonstrated higher mortality in the matched-only cohort compared to the matched + unique cohort (p = 0.02), multivariable Cox regression analysis showed this difference was not statistically significant when adjusting for various factors. A history of cancer was the significant predictor of increased mortality risk (Hazard ratio = 3.147, 95% CI [2.196, 4.51]).

interpretationPatients with matched only versus matched + unique OCB have distinct clinical profiles.

Indexed as

Multiple SclerosisOligoclonal BandsAdultAgedFemaleHumansMaleMiddle AgedRetrospective StudiesOligoclonal Bands

Identifiers

PMID39435961
PMCPMC11572730

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