Subject(s)
Adenocarcinoma , Cerebellar Neoplasms , Cerebrospinal Fluid/cytology , Meningeal Carcinomatosis , Meningitis, Bacterial/diagnosis , Stomach Neoplasms , Adenocarcinoma/pathology , Adenocarcinoma/surgery , Brain/diagnostic imaging , Cerebellar Neoplasms/diagnosis , Cerebellar Neoplasms/secondary , Diagnosis, Differential , Fatal Outcome , Gastrectomy/methods , Humans , Magnetic Resonance Imaging/methods , Male , Meningeal Carcinomatosis/diagnosis , Meningeal Carcinomatosis/pathology , Meningeal Carcinomatosis/physiopathology , Middle Aged , Neoplasm Staging , Patient Care/methods , Stomach Neoplasms/pathology , Stomach Neoplasms/surgeryABSTRACT
A 27-year-old man with a diagnosis of new onset refractory status epilepticus (NORSE) was treated with five anti-seizure drugs (ASDs) including clobazam, levetiracetam and topiramate. He received plasma exchange (PE) for presumed autoimmune etiology. Serum ASD levels were serially monitored in two sessions. Levels of clobazam, levetiracetam and topiramate were significant reduced by PE. Serum clobazam level dropped down to at least 85% and 75% of the baseline during and after the procedure respectively; levetiracetam dropped down to 83% and 83%; and topiramate dropped to 86% and 79%. The results may imply a theoretical risk of breakthrough seizure during PE due to low ASD levels.
ABSTRACT
Visual hallucinations carry poor prognosis in Parkinson's disease. Here we tested the hypothesis that the hippocampus and visuospatial memory impairment play a central role in the pathology of PD with visual hallucinations. Multimodal magnetic resonance imaging of the brain was carried out in 12 people with PD and visual hallucinations; 15 PD individuals without hallucinations; and 14 healthy controls. Age, gender, cognitive ability, and education level were matched across the three groups. PD patients were taking dopaminergic medication. Hippocampal volume, shape, mean diffusivity (MD), and functional connectivity within the whole brain were examined. Visuospatial memory was compared between groups, and correlations with hippocampal MD, functional connectivity, and the severity of hallucinations were explored. There were no macrostructural differences across groups, but individuals with hallucinations had higher diffusivity in posterior hippocampus than the other two groups. Visuospatial memory was poorer in both PD groups compared to controls, and was correlated with hallucinations. Finally, hippocampal functional connectivity in the visual cortices was lower in those with hallucinations than other groups, and this correlated with visuospatial memory impairment. In contrast, functional connectivity between the hippocampus and default mode network regions and frontal regions was greater in the PD hallucinators compared to other groups. We suggest that hippocampal pathology, which disrupts visuospatial memory, makes a key contribution to visual hallucinations in PD. These findings may pave the way for future studies of imaging biomarkers to measure treatment response in those with PD who are most at risk of poor outcomes.
Subject(s)
Brain/pathology , Brain/physiopathology , Hallucinations/etiology , Hallucinations/pathology , Hallucinations/physiopathology , Hippocampus/pathology , Hippocampus/physiopathology , Parkinson Disease/complications , Aged , Brain Mapping , Female , Humans , Magnetic Resonance Imaging , Male , Memory/physiology , Middle Aged , Multimodal Imaging , Neural Pathways/pathology , Neural Pathways/physiopathology , Neuropsychological Tests , Spatial Memory/physiologyABSTRACT
BACKGROUND: Visual hallucinations (VH) are one of the most striking nonmotor symptoms in Parkinson's disease (PD), and predict dementia and mortality. Aberrant default mode network (DMN) is associated with other psychoses. Here, we tested the hypothesis that DMN dysfunction contributes to VH in PD. METHODS: Resting state functional data was acquired from individuals with PD with VH (PDVH) and without VH (PDnonVH), matched for levodopa drug equivalent dose, and a healthy control group (HC). Independent component analysis was used to investigate group differences in functional connectivity within the DMN. In addition, we investigated whether the functional changes associated with hallucinations were accompanied by differences in cortical thickness. RESULTS: There were no group differences in cortical thickness but functional coactivation within components of the DMN was significantly lower in both PDVH and PDnonVH groups compared to HC. Functional coactivation within the DMN was found to be greater in PDVH group relative to PDnonVH group. CONCLUSION: Our study demonstrates, for the first time that, within a functionally abnormal DMN in PD, relatively higher "connectivity" is associated with VH. We postulate that aberrant connectivity in a large scale network affects sensory information processing and perception, and contributes to "positive" symptom generation in PD.
