AI Article Synopsis

  • The study used resting-state fMRI to examine spontaneous brain activity linked to pathological laughing and crying in stroke patients.
  • It included 12 patients with isolated pontine infarction and pathological emotional expressions, alongside matched controls and patients without these symptoms.
  • Findings revealed changes primarily in brain areas related to the default mode network, sensorimotor network, affective network, and cerebellar lobes, suggesting a loss of control in the volitional system leads to heightened emotional activity in these patients.

Article Abstract

We used resting-state functional magnetic resonance imaging to investigate the global spontaneous neural activity involved in pathological laughing and crying after stroke. Twelve pathological laughing and crying patients with isolated pontine infarction were included, along with 12 age- and gender-matched acute isolated pontine infarction patients without pathological laughing and crying, and 12 age- and gender-matched healthy controls. We examined both the amplitude of low-frequency fluctuation and the regional homogeneity in order to comprehensively evaluate the intrinsic activity in patients with post-stroke pathological laughing and crying. In the post-stroke pathological laughing and crying group, changes in these measures were observed mainly in components of the default mode network (medial prefrontal cortex/anterior cingulate cortex, middle temporal gyrus, inferior temporal gyrus, superior frontal gyrus, middle frontal gyrus and inferior parietal lobule), sensorimotor network (supplementary motor area, precentral gyrus and paracentral lobule), affective network (medial prefrontal cortex/anterior cingulate cortex, parahippocampal gyrus, middle temporal gyrus and inferior temporal gyrus) and cerebellar lobes (cerebellum posterior lobe). We therefore speculate that when disinhibition of the volitional system is lost, increased activation of the emotional system causes pathological laughing and crying.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663617PMC
http://dx.doi.org/10.18632/oncotarget.19307DOI Listing

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