2018
DOI: 10.1186/s12883-018-1223-0
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Structural MRI correlates of PASAT performance in multiple sclerosis

Abstract: BackgroundThe Paced Auditory Serial Addition Test (PASAT) is a useful cognitive test in patients with multiple sclerosis (MS), assessing sustained attention and information processing speed. However, the neural underpinnings of performance in the test are controversial. We aimed to study the neural basis of PASAT performance by using structural magnetic resonance imaging (MRI) in a series of 242 patients with MS.MethodsPASAT (3-s) was administered together with a comprehensive neuropsychological battery. Globa… Show more

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Cited by 22 publications
(19 citation statements)
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“…clinical disability and cognitive scores), distinct clinical associations were observed in MOGAD and AQP4+ NMOSD, which might reflect different pathological mechanisms and underlying structural and functional alterations. GM atrophy in hippocampus/parahippocampal gyrus was associated with more clinical disability, implying the potential driving force of underlying GM involvement for the clinical disability and highlighting the role of the hippocampus in prognosis gyrus was associated with cognitive decline in MOGAD, which was consistent with previous findings of cortical and subcortical GM atrophy driving cognitive impairment in neuroimmune and neuroinflammatory diseases, as potential markers for evaluating cognitive impairment in both diseases 34,35. These findings were different from those in AQP4+ NMOSD, where clinical associations were mostly identified with structural and functional characteristics of the visual areas, fornix/stria terminalis and medial lemniscus, some of which are small structures needing further validation.…”
supporting
confidence: 88%
“…clinical disability and cognitive scores), distinct clinical associations were observed in MOGAD and AQP4+ NMOSD, which might reflect different pathological mechanisms and underlying structural and functional alterations. GM atrophy in hippocampus/parahippocampal gyrus was associated with more clinical disability, implying the potential driving force of underlying GM involvement for the clinical disability and highlighting the role of the hippocampus in prognosis gyrus was associated with cognitive decline in MOGAD, which was consistent with previous findings of cortical and subcortical GM atrophy driving cognitive impairment in neuroimmune and neuroinflammatory diseases, as potential markers for evaluating cognitive impairment in both diseases 34,35. These findings were different from those in AQP4+ NMOSD, where clinical associations were mostly identified with structural and functional characteristics of the visual areas, fornix/stria terminalis and medial lemniscus, some of which are small structures needing further validation.…”
supporting
confidence: 88%
“…Episodic memory has been correlated with total grey matter and regional cortical structures (e.g., left precuneus [89]); visuospatial memory has been associated with brain MRI total lesion area, T1 lesion, and FLAIR lesion volume, BPF, third ventricular width, and right superior frontal atrophy, among others [90,91]; verbal episodic memory has been associated with total and regional hippocampal atrophy, total lesion load and BPF [90,91,92,93]; information processing speed has been correlated with thalamus, whole grey matter atrophy, and third ventricle width [94], cerebellum atrophy [95,96], as well as with less white matter integrity, and increases in functional connectivity [79]; executive disfunction has been associated with frontal lobe structural and functional damage [97,98] and with dorsolateral prefrontal, orbitofrontal, anterior cingulate, and insular areas [99], as well as with thalamic structural and functional changes [100]; PASAT-3” scores have been correlated with cortical and subcortical structures such as bilateral precuneus, posterior cingulate, caudate putamen, and cerebellum [101], and acute changes in PASAT score with no physical changes (EDSS) have been associated with presence of acute gadolinium enhancing lesions [102], with similar results observe with transient SDMT changes [103], proposing that patients could also experience “cognitive relapses”.…”
Section: Neural Basis Of Cognitive Impairment In Msmentioning
confidence: 99%
“…Preprocessing and analysis were performed using the toolboxes VBM8 and Lesion Segmentation Tool, implemented in Statistical Parametric Mapping, as have been previously described. 10 Total intracranial volume and white matter lesion load were calculated.…”
Section: Participants and Study Protocolmentioning
confidence: 99%