The overall goal of this project is to define and characterize congenital anosmia-related neural plasticity in the human brain and its behavioral consequences. We hypothesize that individuals suffering from congenital anosmia demonstrate wide-spread…
ID
Source
Brief title
Condition
- Congenital and hereditary disorders NEC
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Main parameters within this study are:
- Morphological (anatomical) differences in brain areas between healthy and
anosmic individuals.
- Differences in functional connectivity during resting-state between healthy
and anosmic individuals.
- Differences in functional connectivity during uni- versus multi-sensory
stimulation within healthy and anosmic individuals.
- Differences in functional connectivity during uni- and multi-sensory
stimulation between healthy and anosmic individuals.
Secondary outcome
A secondary study parameter are differences between groups in behavioral
outcomes of the multisensory integration task. This will be calculated by means
of Hierarchical Drift Diffusion Model (HDDM), to combine speed versus accuracy
in responses.
Background summary
In contrast to the three sensory modalities of vision, audition, and touch, few
studies have explored what impact sensory loss in the chemical senses
(olfaction and gustation) might have on our cortical organization and
behavioral performance. The few studies that have explored cerebral changes
mediated by a loss of olfactory functions demonstrate remarkable little changes
in either morphology or functional remapping.
To date, studies exploring anosmia-related morphological changes have utilized
classical voxel-based GLM analyses where large localized changes is needed to
reach statistically established levels. This project is based on the assumption
that changes within such wide-spread network that encompass only heterogeneous
processing areas should demonstrate subtle but wide-spread alteration rather
than uniquely impacting one specific area. Thus, by using novel multivoxel- and
network-based analyzing techniques, we can define and characterize
anosmia-related neural plasticity in the human brain from a network perspective
rather from than of a single-voxel.
Finally, previous studies exploring blind and deaf individuals have
demonstrated enhancement of sensory functions in remaining sensory modalities
but none have assessed whether sensory loss alters individuals ability to
integrate and utilize information gain from multiple sensory sources, so-called
sensory integration gain.
Study objective
The overall goal of this project is to define and characterize congenital
anosmia-related neural plasticity in the human brain and its behavioral
consequences. We hypothesize that individuals suffering from congenital anosmia
demonstrate wide-spread morphological changes and that these changes render
them be better at multisensory integration tasks.
We will investigate the following two major issues in the proposed experiments:
1) Are there differences in the basic morphology and functionality of the human
brain between humans who were born with and humans who were born without the
sense of smell?
2) Are there differences in neural processing of other senses (vision and
hearing) between humans who were born with and humans who were born without the
sense of smell?
Study design
This is an observational case-control study. Duration of the protocol will be
one session of 2 hours. On the study day participants will perform a
behavioural task (Sniffin' Sticks smell test) as well as engage in an fMRI
session that consists of four subparts:
* Whole brain anatomical image
* Functional resting-state scan
* Multisensory integration task consisting of identifying objects within
degraded stimuli
* Object identification task of clear visual and auditory objects.
Study burden and risks
The study is non-therapeutic to the participants. No immediate benefits for the
participants are expected from participation in this study. The risk associated
with participation is negligible. The participant*s burden is as follows,
regarding time: the experimental session will take approximately 2hrs: one hour
of behavioral (olfactory) testing, and one hour inside the scanner. MRI is an
eminently safe technique; there are no risks that have been associated with the
acquisition of MRI data per se.
Chance findings of pathology: The MRI-scans in this study are not made with the
intention to diagnose pathologies, however, chance findings of pathology may
occur. Participants will be informed of this possibility and need to be willing
to receive information about incidental findings of pathology, as this is one
of the inclusion criteria. In case of a possible chance finding, a radiologist
will inspect the scans. If any pathology is found or suspected by the
radiologist, the subject will be referred to his/her general physician or a
medical specialist. The participant and her/his general physician will be
informed of the finding.
Stippeneng 4
Wageningen 6708 WE
NL
Stippeneng 4
Wageningen 6708 WE
NL
Listed location countries
Age
Inclusion criteria
For patients, in order to be eligible to participate in this study, a subject must meet all of the following criteria:
- Have congenital anosmia
- Labelled as anosmic according to our standardized clinical olfactory test
- Age between 18-65 years
- Have a normal eyesight or an eye deviation that can be corrected with glasses or contact lenses.
- Willing to comply with the study procedures
- Willing to be informed about incidental findings of pathology
- Having given written informed consent;For age- and sex- matched healthy controls, in order to be eligible to participate in this study, a subject must meet all of the following criteria:
- Self-reported healthy
- No know smell disorder
- Labelled as having a normal sense of smell according to our standardized clinical test
- Age between 18-65 years
- Have a normal eyesight or an eye deviation that can be corrected with glasses or contact lenses.
- Willing to comply with the study procedures
- Willing to be informed about incidental findings of pathology
- Having given written informed consent
- Matched on sex to patient
- Matched on age (within 3 years) to patient
Exclusion criteria
A potential subject who meets any of the following criteria will be excluded from participation in this study:
- Being deaf (or having any other hearing problems) or blind
- Being an employee of the division of Human Nutrition, Wageningen University
- Performing an internship or thesis at the chair group Sensory Science and Eating Behaviour of the division of Human Nutrition, Wageningen University
- Having a contra-indication to MRI scanning (including, but not limited to):
* Pacemakers and defibrillators
* Intraorbital or intraocular metallic fragments
* Ferromagnetic implants
* Presence of non-removable piercings
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL60948.081.17 |