Evidence map›Paper›PMID 42080421›Full record

ArticleAnnals of clinical and translational neurology2026

MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children.

Chaitanya Aduru, Akansha Chandrasekar, Kyla Blasingame, Jonathan Rosen, Jesse M Levine, Karla Salazar, Madhuri Chilakapati, Rod Foroozan, Victoria Hardwick, Jonathan M Yarimi and 4 more

Abstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

14 authors.

Chaitanya AduruDepartment of Pediatrics, Section of Neurology and Developmental Neuroscience, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.ORCID https://orcid.org/0009-0005-7048-7912
Akansha ChandrasekarDepartment of Pediatrics, Section of Neurology and Developmental Neuroscience, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.
Kyla BlasingameDepartment of Pediatrics, Section of Neurology and Developmental Neuroscience, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.
Jonathan RosenDepartment of Pediatrics, Section of Neurology and Developmental Neuroscience, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.
Jesse M LevineDepartment of Pediatrics, Section of Neurology and Developmental Neuroscience, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.ORCID https://orcid.org/0009-0002-6919-0036
Karla SalazarDepartment of Pediatrics, Section of Neurology and Developmental Neuroscience, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.
Madhuri ChilakapatiDepartment of Ophthalmology, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.
Rod ForoozanDepartment of Ophthalmology, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.
Victoria HardwickDepartment of Pediatrics, Section of Neurology and Developmental Neuroscience, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.
Jonathan M YarimiDepartment of Pediatrics, Section of Neurology and Developmental Neuroscience, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.ORCID https://orcid.org/0000-0003-0246-9964
Nikita ShuklaDepartment of Pediatrics, Section of Neurology and Developmental Neuroscience, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.ORCID https://orcid.org/0000-0002-7322-676X
Timothy E LotzeDepartment of Pediatrics, Section of Neurology and Developmental Neuroscience, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.ORCID https://orcid.org/0009-0003-2898-1963
Kristen S FisherDepartment of Pediatrics, Section of Neurology and Developmental Neuroscience, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.ORCID https://orcid.org/0000-0002-1598-8571
Alexander J SandweissDepartment of Pediatrics, Section of Neurology and Developmental Neuroscience, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.ORCID https://orcid.org/0000-0002-8213-2941

Funding

Through support from the Research Vision at Texas Children's Hospital
6 · The paper itself

Abstract

objectivesThe study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first-time pediatric ON in the post-MOG-IgG era.

methodsThis was a single-center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first-time ON between 2018-2024, with follow-up data collected through 2025. Inclusion criteria required monocular or binocular subacute vision loss with supportive paraclinical signs. Subjects were excluded if they had a prior history of demyelinating disease or extra-orbital demyelinating lesions on initial brain/spine MRI. Primary outcomes were the proportion of MOG-IgG seropositivity, retinal nerve fiber layer thickness, and visual acuity at onset and most recent follow-up.

resultsOf 73 children with ON, 38 met criteria for isolated first-time ON. Etiologies included MOGAD (n = 27, 71.1%) and idiopathic/monophasic (n = 9, 23.7%), while none of the 38 subjects were later diagnosed with multiple sclerosis. MOGAD-ON was associated with less severe vision loss at presentation (p < 0.01) compared to idiopathic cases. At most recent follow-up, both groups achieved excellent functional recovery, yet both demonstrated significant retinal nerve fiber layer thinning from ON presentation. Linear regression revealed worse presenting LogMAR significantly correlated to thinner follow-up RNFL (F(1,18) = 8.467, R

interpretationIn isolated pediatric ON, no patients were diagnosed with MS, and MOGAD is the predominant etiology. The linear correlation between initial LogMAR and subsequent RNFL atrophy suggests a permanent reduction in neurological reserve dependent on the degree of functional severity at ON onset.

Indexed as

demyelinationmultiple sclerosisneuroinflammatoryoptic nervepediatric neurology

Identifiers

PMID42080421
PMCPMC13394016

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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.