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A Free-breathing fMRI Method to Study Human Olfactory Function
Published on: July 30, 2017
Neural Changes in Patients with Post-Traumatic Anosmia: Insights from Resting-State fMRI
Abolhasan Rezaeyan1, Fatemeh Shahi Moridi2, Seyed Kamran Kamrava3
1Cellular and Molecular Gerash Research Center, Gerash University of Medical Sciences, Gerash, Iran.
Journal of Biomedical Physics & Engineering
|June 15, 2026
Summary
Post-traumatic anosmia (PTA) patients exhibit altered brain functional connectivity (FC) in higher-order regions, impacting olfactory performance. Resting-state fMRI (rs-fMRI) reveals these neural-level changes, offering insights into head trauma effects.
Area of Science:
- Neuroscience
- Neuroimaging
- Olfactory Disorders
Background:
- Traumatic brain injury (TBI) frequently causes anosmia (loss of smell).
- Anosmia is a common consequence of severe head trauma.
- Investigating brain changes in anosmia is crucial for understanding TBI sequelae.
Purpose of the Study:
- To examine functional connectivity (FC) changes in patients with post-traumatic anosmia (PTA).
- To compare FC networks in PTA patients versus healthy controls (HCs) using resting-state fMRI (rs-fMRI).
Main Methods:
- Retrospective rs-fMRI study on 44 PTA patients and 43 HCs.
- Olfactory function assessed using the Sniffin' Sticks test.
- Seed-based Analysis (SBA) and Independent Component Analysis (ICA) were performed.
Main Results:
- PTA patients had significantly lower olfactory function (TDI scores) than HCs.
- SBA showed increased FC in anterior cingulate cortex, piriform, insular, and prefrontal areas in PTA patients.
- ICA revealed widespread increased FC in PTA patients, including frontal pole, cerebellum, putamen, and amygdala.
- Global brain network efficiency correlated with olfactory performance in PTA patients.
Conclusions:
- Neural deficits in post-traumatic anosmia extend beyond primary olfactory regions.
- SBA and ICA effectively characterize higher-order brain network alterations in PTA.
- rs-fMRI provides valuable insights into the neural underpinnings of olfactory dysfunction after head trauma.
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