The Locus Coeruleus and Memory
Information source: Maastricht University Medical Center
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Alzheimer's Disease
Intervention: 7 Tesla MRI with memory task and non-invasive neurostimulation (Other)
Phase: N/A
Status: Not yet recruiting
Sponsored by: Maastricht University Medical Center Official(s) and/or principal investigator(s): Frans Verhey, Prof, Study Director, Affiliation: Maastricht University Medical Centre
Overall contact: Heidi Jacobs, PhD, Phone: +31433884090, Email: h.jacobs@maastrichtuniversity.nl
Summary
The cause of Alzheimer's disease, the most common form of dementia, remains unknown.
Neuropathological studies suggest that a small area in the brainstem, the locus coeruleus,
might be the site of the onset of the disease. This area is the sole source of noradrenalin
to the brain, a neurotransmitter involved in arousal, but also cognitive functions. Animal
and pharmacological studies have hinted towards an important role of this area in memory
functioning. However, these studies were hampered by the limited spatial resolution, making
it hard to clearly localize the locus coeruleus in the brain. New developments in brain
imaging allow now to visualize the brain with stunning precision. Furthermore, a
non-invasive new stimulation method, transcutaneous vagus nerve stimulation, is believed to
excite the locus coeruleus and thereby influencing neuronal networks and memory functioning.
There are three aims in this project:
1. To investigate how the functional interaction between the locus coeruleus and other
brain areas, in particular the medial temporal lobe areas, during memory processes
(encoding, consolidation and retrieval) change with development of Alzheimer's disease.
2. To investigate associations between noradrenaline, memory performance and brain
functioning. The investigators aim to investigate how acute noradrenalin levels change
during the different memory processes and whether or not this is beneficial for
performance. Furthermore, the investigators will investigate whether this interaction
between noradrenalin, memory performance and brain functioning is different healthy
older individuals (n =35) or patients with prodromal Alzheimer's disease (n =35).
3. To investigate the underlying neural network changes during transcutaneous vagus nerve
stimulation. The investigators will focus on differences in functional connectivity
between the locus coeruleus and the medial temporal lobe areas in healthy older
individuals and prodromal Alzheimer's disease patients. An experimental condition will
be compared with a sham condition in a pseudo-randomized cross-over design.
Clinical Details
Official title: Focus on the Locus Coeruleus Network With 7 T MRI: Link to Memory (Dys)Function
Study design: Observational Model: Case Control
Primary outcome: Blood Oxygen Level Dependent (BOLD) response during a memory taskPerformance on the memory task Noradrenalin levels during the memory task
Secondary outcome: Grey matter volume of the locus coeruleusshape properties of the locus coeruleus Performance on neuropsychological tests
Eligibility
Minimum age: 60 Years.
Maximum age: 85 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
For the patients:
- diagnosis of prodromal Alzheimer's disease based on the latest research criteria
(clinical assessment at the memory clinic : presence of at least a memory impairment,
memory complaints expressed by the patient or informant, no problems in daily life
functioning, no dementia and presence of biomarkers
- Clinical Dementia Rating score of 0. 5 (
- Mini-Mental State Examination (MMSE) ≥ 23 and being mentally competent (in general,
individuals with a MMSE ≥ 18 are considered mentally competent)
- Age: between 60 and 85 years old
- 50% female
- Right-handedness
- Average level of education
- Informed consent before participation in the study
For the healthy older individuals:
- Average neuropsychological test results, in accordance with normative data, corrected
for age, education and gender
- No substantial memory complaints (according to the participant)
- Age: between 60 and 85 years old
- 50% female
- Right-handedness
- Average level of education
- Informed consent before participation in the study
Exclusion Criteria:
- Reduced vision
- Psychoactive medication use
- Abuse of alcohol and drugs
- Cognitive impairment due to alcohol/drug abuse or abuse of other substances
- Past or present psychiatric or neurological disorders (major depression,
schizophrenia, bipolar disorder, psychotic disorder (or treatment for it), epilepsy,
stroke, Parkinson's disease, multiple sclerosis, brain surgery, brain trauma,
electroshock therapy, kidney dialysis, Menière's disease, brain infections)
- Major vascular disorders (e. g. stroke)
- Heart diseases or pacemakers
- Contraindications for scanning (e. g. brain surgery, cardiac pacemaker, metal
implants, claustrophobia, body tattoos)
Locations and Contacts
Heidi Jacobs, PhD, Phone: +31433884090, Email: h.jacobs@maastrichtuniversity.nl Additional Information
Starting date: June 2015
Last updated: March 23, 2015
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