AQP4-IgG and mood disorders: Case series of neuromyelitis optica spectrum disorder
Qing Xu, Yanlin Han, Shuzhan Gao, Siyi Wang, Yanyan Lu, Kuan-Pin Su, Xijia Xu

TL;DR
This paper reports two cases where neuromyelitis optica spectrum disorder and mood disorders co-occur, suggesting a shared neuroinflammatory cause.
Contribution
The study highlights a potential link between AQP4-IgG-mediated neuroinflammation and mood disorders through case reports.
Findings
Two female patients with NMOSD and mood disorders showed frontal lobe demyelination and AQP4-IgG positivity.
Both patients improved with immunosuppressive and psychiatric treatment, indicating a shared inflammatory mechanism.
AQP4-IgG screening may help differentiate organic mood disorders from primary psychiatric conditions.
Abstract
Neuromyelitis optica spectrum disorders (NMOSD) are autoimmune inflammatory demyelinating conditions primarily affecting the optic nerves and spinal cord. While NMOSD pathogenesis is mediated by aquaporin-4 antibody (AQP4-IgG) autoimmunity, increasing evidence suggests significant comorbidity with affective symptoms. The neuropathological mechanisms underlying this comorbidity, however, remain incompletely understood. We reported two cases of female patients with concurrent NMOSD and mood disorders that illustrate a shared neuroinflammatory etiology. Case 1, a 26-year-old female, presented with a decade-long history of mood instability, diagnosed as bipolar disorder (BD) mixed episode, which coincided with her NMOSD diagnosis. Case 2, a 25-year-old female, initially presented with major depressive disorder (MDD) but was subsequently diagnosed with NMOSD following the acute onset of…
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Taxonomy
TopicsMultiple Sclerosis Research Studies · Peripheral Neuropathies and Disorders · Autoimmune Neurological Disorders and Treatments
