Evidence map›Paper›PMID 36811295›Full record

ArticleNeuropathology and applied neurobiology2023

Paths to hippocampal damage in neuromyelitis optica spectrum disorders.

Mona Zakani, Magdalini Nigritinou, Markus Ponleitner, Yoshiki Takai, Daniel Hofmann, Sophie Hillebrand, Romana Höftberger, Jan Bauer, Balint Lasztoczi, Tatsuro Misu and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Neuropathology and applied neurobiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. 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

13 authors at 2 institutions in 2 countries.

Mona ZakaniDivision of Neuroimmunology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Magdalini NigritinouDivision of Neuroimmunology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Markus PonleitnerDepartment of Neurology, Medical University of Vienna, Vienna, Austria.
Yoshiki TakaiDepartment of Neurology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Daniel HofmannDivision of Neuroimmunology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Sophie HillebrandDivision of Neuroimmunology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Romana HöftbergerDepartment of Neurology, Division of Neuropathology and Neurochemistry, Medical University of Vienna, Vienna, Austria.
Jan BauerDivision of Neuroimmunology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Balint LasztocziDivision of Cognitive Neurobiology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Tatsuro MisuDepartment of Neurology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Gregor KasprianDivision of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria.
Paulus RommerDepartment of Neurology, Medical University of Vienna, Vienna, Austria.
Monika BradlDivision of Neuroimmunology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Medical University of Vienna · ATTohoku University · JP

Funding

Austrian Science Fund FWF DOC 33
6 · The paper itself

Abstract

aimsMany patients with neuromyelitis optica spectrum disorders (NMOSD) suffer from cognitive impairment affecting memory, processing speed and attention and suffer from depressive symptoms. Because some of these manifestations could trace back to the hippocampus, several magnetic resonance imaging (MRI) studies have been performed in the past, with a number of groups describing volume loss of the hippocampus in NMOSD patients, whereas others did not observe such changes. Here, we addressed these discrepancies.

methodsWe performed pathological and MRI studies on the hippocampi of NMOSD patients, combined with detailed immunohistochemical analysis of hippocampi from experimental models of NMOSD.

resultsWe identified different pathological scenarios for hippocampal damage in NMOSD and its experimental models. In the first case, the hippocampus was compromised by the initiation of astrocyte injury in this brain region and subsequent local effects of microglial activation and neuronal damage. In the second case, loss of hippocampal volume was seen by MRI in patients with large tissue-destructive lesions in the optic nerves or the spinal cord, and the pathological work-up of tissue derived from a patient with such lesions revealed subsequent retrograde neuronal degeneration affecting different axonal tracts and neuronal networks. It remains to be seen whether remote lesions and associated retrograde neuronal degeneration on their own are sufficient to cause extensive volume loss of the hippocampus, or whether they act in concert with small astrocyte-destructive, microglia-activating lesions in the hippocampus that escape detection by MRI, either due to their small size or due to the chosen time window for examination.

conclusionsDifferent pathological scenarios can culminate in hippocampal volume loss in NMOSD patients.

Indexed as

Neuromyelitis OpticaAquaporin 4AutoantibodiesBrainHippocampusHumansMagnetic Resonance ImagingSpinal CordAquaporin 4Autoantibodiesaquaporin 4hippocampusmicroglial activationneuromyelitis opticaretrograde degeneration

Identifiers

PMID36811295
PMCPMC10947283
OpenAlexW4321498524

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.