Paths to hippocampal damage in neuromyelitis optica spectrum disorders

Author:

Zakani Mona1,Nigritinou Magdalini1,Ponleitner Markus2,Takai Yoshiki3,Hofmann Daniel1,Hillebrand Sophie1,Höftberger Romana4,Bauer Jan1,Lasztoczi Balint5,Misu Tatsuro3,Kasprian Gregor6,Rommer Paulus2,Bradl Monika1

Affiliation:

1. Division of Neuroimmunology, Center for Brain Research Medical University of Vienna Vienna Austria

2. Department of Neurology Medical University of Vienna Vienna Austria

3. Department of Neurology Tohoku University Graduate School of Medicine Sendai Japan

4. Department of Neurology, Division of Neuropathology and Neurochemistry Medical University of Vienna Vienna Austria

5. Division of Cognitive Neurobiology, Center for Brain Research Medical University of Vienna Vienna Austria

6. Division of Biomedical Imaging and Image‐guided Therapy Medical University of Vienna Vienna Austria

Abstract

AbstractAimsMany 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.

Funder

Austrian Science Fund

Publisher

Wiley

Subject

Physiology (medical),Neurology (clinical),Neurology,Histology,Pathology and Forensic Medicine

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