4.5 Article

Decreased activity of piriform cortex and orbitofrontal hyperactivation in Usher Syndrome, a human disorder of ciliary dysfunction

期刊

BRAIN IMAGING AND BEHAVIOR
卷 16, 期 3, 页码 1176-1185

出版社

SPRINGER
DOI: 10.1007/s11682-021-00594-6

关键词

Odor discrimination; Olfaction; Piriform; Orbitofrontal cortex; Functional Magnetic Resonance Imaging (fMRI)

资金

  1. Portuguese Funding Agency for Science and Technology (FCT) [E-Rare4/0001/2012, FCT-UID/4950/2020 -COMPETE, POCI-01-0145-FEDER-007440, DSAIPA/DS/0041/2020, PTDC/PSI-GER/1326/2020]
  2. Fundação para a Ciência e a Tecnologia [PTDC/PSI-GER/1326/2020, DSAIPA/DS/0041/2020, E-Rare4/0001/2012] Funding Source: FCT

向作者/读者索取更多资源

USH patients show higher olfactory thresholds and decreased brain activity in response to odorant stimulation in the piriform cortex, but increased activity in the orbitofrontal cortex. This suggests a compensatory mechanism may exist in the orbitofrontal cortex for the under-recruitment of the piriform cortex in USH patients. The study demonstrates that olfactory deficits in USH can be objectively assessed using functional neuroimaging, revealing differential patterns of activity in various regions of the olfactory network.
Usher syndrome (USH) is a condition characterized by ciliary dysfunction leading to retinal degeneration and hearing/vestibular loss. Putative olfactory deficits in humans have been documented at the psychophysical level and remain to be proven at the neurophysiological level. Thus, we aimed to study USH olfactory impairment using functional magnetic resonance imaging. We analyzed differences in whole-brain responses between 27 USH patients and 26 healthy participants during an olfactory detection task with a bimodal odorant (n-butanol). The main research question was whether between-group differences could be identified using a conservative whole-brain approach and in a ROI-based approach in key olfactory brain regions. Results indicated higher olfactory thresholds in USH patients, thereby confirming the hypothesis of reduced olfactory acuity. Importantly, we found decreased BOLD activity for USH patients in response to odorant stimulation in the right piriform cortex, while right orbitofrontal cortex showed increased activity. We also found decreased activity in other higher-level regions in a whole brain approach. We suggest that the hyper activation in the orbitofrontal cortex possibly occurs as a compensatory mechanism after the under-recruitment of the piriform cortex. This study suggests that olfactory deficits in USH can be objectively assessed using functional neuroimaging which reveals differential patterns of activity both in low- and high-level regions of the olfactory network.

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