There are several different types of dementia including Alzheimer's Disease (AD) and
Dementia with Lewy Bodies (DLB). Due to the overlapping symptomatology across types of
dementia and the lack of objective biomarkers currently available for dementia,
misdiagnosis rates are high. Additionally, the transition from what is commonly thought
to be an intermediate stage, termed Mild Cognitive Impairment (MCI), to dementia, is not
well defined. Neurovascular and metabolic dysfunction has been strongly linked to
neurodegeneration and dementia, however, a mechanistic understanding of this link has not
been fully developed.
Near-Infrared Spectroscopy (NIRS) is a non-invasive, non-ionising and portable
neuroimaging technique which uses light to quantify changes in concentration of
oxygenated and deoxygenated haemoglobin in the brain. As such, it is a highly attractive
alternative to functional Magnetic Resonance Imaging as it allows access to a larger
variety of individuals, can be used at the bedside or in patients' own homes, and is
significantly less intrusive.
To identify how the brain's haemodynamics and metabolism is altered in dementia, this
study will use NIRS in 25 patients with AD, 25 patients with DLB, 50 patients with MCI
and 100 age-matched healthy controls. This study will be conducted by the School of
Technology and the School of Clinical Medicine at the University of Cambridge.
Firstly, the investigators will perform several cognitive tests in these patient groups
whilst measuring brain activity using a state-of-the-art, dual-wavelength, high-density
NIRS device to map how the brain's haemodynamics are altered in dementia. Secondly, the
investigators will perform further cognitive tests using broadband NIRS to measure how
neurometabolism is altered across the patient groups. The investigators will also relate
the optical data to several facets of cognition that these cognitive tests will measure
including memory, attention, and motor function. Several questionnaires will also be
administered to assess non-cognitive symptoms such as depression and sleep disturbances.
If participants in the patient groups have not had a Magnetic Resonance Imaging (MRI)
scan, or did one over two years ago, they will also undertake an MRI scan to enable the
localisation of brain activity, measured by NIRS, accounting for individual differences
in brain structure and atrophy patterns.
The investigators shall compare all patient groups (AD, DLB, MCI) with healthy controls
to determine how the brain's haemodynamics and metabolism are altered in dementia, as
well as how this relates to both behavioural scores (collected during cognitive testing)
and clinical scores (using either data collected from questionnaires or patient's own
clinical history). Through combining the two NIRS techniques, the investigators shall
also determine the nature of the relationship between the blood oxygenation in the
surrounding vasculature and the intra-neuronal metabolic activity, and how this
relationship may be altered in dementia and across different types of dementia.
Additionally, the investigators shall apply computational methods, such as machine
learning, to identify haemodynamic and/or metabolic signatures for use as biomarkers in
the clinic.