The causes of neurodegenerative dementias such as Frontotemporal Dementia, Lewy Body Disease and Alzheimer's disease are still largely unknown. While the contribution of some genetic mutations and polymorphisms is associated with autosomal dominant patterns of inheritance of these dementias, in many cases, the specific causative mutation in these families is not yet identified. Further, in many patients, polygenic risk is thought to give rise to pathophysiologic changes, but which specific genes affect risk are largely yet unknown. By examining genotypes in patients that present to our Cognitive Neurology and Alzheimer's Research Clinic with suspected or confirmed neurodegenerative dementia, or have a history of a familial dementia, we aim to help identify and characterize genetic mutations or polymorphisms that give rise to neurodegenerative diseases.
Study Type
OBSERVATIONAL
Enrollment
1,000
Blood draw.
Parkwood Institute
London, Ontario, Canada
RECRUITINGBlood draw for genetic status or polymorphism result.
The blood draw is taken at the time of the clinic visit. Up to 30ml will be collected by standard venipuncture.
Time frame: A one-time visit, taking the participant approximately 20 minutes total for all study procedures.
Demographic information.
Demographic information will be collected at the time of the clinic visit.
Time frame: A one-time visit, taking the participant approximately 20 minutes total for all study procedures.
Medical history/Clinical diagnoses.
Will be obtained via chart review when available. This information is collected already as part of the patient's standard care.
Time frame: Typically within 1 month of the clinic visit, taking approximately 5 minutes.
Pathological diagnoses.
Will be obtained via chart review when available. This information is collected already as part of the patient's standard care.
Time frame: Typically within 1 month of the clinic visit, taking approximately 5 minutes.
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