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- Study Description
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- Instructions for requestors
- Data Use Certification (DUC) Agreement
- Talking Glossary of Genetic Terms
GenADA is a multi-site collaborative study, involving GlaxoSmithKline Inc and nine medical centres in Canada, to develop a dataset containing 1000 Alzheimer's disease patients and 1000 ethnically-matched controls in order to associate DNA sequence (allelic) variations in candidate genes with Alzheimer's disease phenotypes. The study consists of both retrospective and prospective components, that is, patients with an existing diagnosis of Alzheimer's disease as well as newly diagnosed patients were enrolled in the study. Thus, clinical data was retrospectively or prospectively obtained on Day 1 of entry into GenADA. Where possible, biological relatives with Alzheimer's (up to third degree relationship such as cousins) and unaffected siblings of AD cases were also recruited. Note that recruitment numbers for biological relatives were lower than expected and genotypic data has not been submitted to dbGap for these subjects.
The purpose of this study is:
- To identify DNA sequence variations (genotype) in candidate genes that are associated with the clinical symptoms and behavioural features of Alzheimer's disease (phenotype), which differ between study participants with and without the disease.
- To identify other genotype-phenotype associations in cognitively impaired study participants such as age of onset, family history, rate of cognitive decline, patterns of behavioural/psychiatric non-cognitive symptoms factors, response to treatment co-morbid conditions, and risks/exposure.
The final subject recruitment for this study included 875 Alzheimer's disease patients, 850 ethnically-matched controls, and 37 family members.
GenADA LONG is a longitudinal assessment to the original GenADA study. Eligible subjects were recruited from five of the nine memory clinics that participated in the GenADA study. Mild to moderate AD participants, a matched subset of controls, and biological related siblings (both affected and unaffected) or other blood relatives affected with AD, were initially examined a minimum of 12 months from recruitment into the original GenADA study, then at two further intervals of 12 and 18 months after time of entry into GenADA LONG. This enables an evaluation of the disease progression in AD patients and a determination of whether controls show evidence of cognitive decline. The overall goal of this extension study is to identify genetic differences and environmental influences that modulate the age of onset of the disease, the course of the disease, and/or biomarkers for neurodegenerative processes.
Three of the five memory clinics that participated in the GenADA LONG study recruited eligible patients into GenADA Imaging.
A concurrent neuroimaging sub-study was conducted at three of the five memory clinics participating in GenADA LONG. Eligible AD cases with mild to moderate AD, who were recruited into the original GenADA study and participated in the GenADA LONG extension study, were enrolled. Additionally, controls that showed signs of cognitive decline, as part of the assessment in GenADA LONG, were imaged at baseline, 12 and 18 month scanning intervals. The objective of this study is to find genes that: affect changes in AD brain volume measure by magnetic resonance in order to investigate how well change in brain volume predicts other key clinical measures in AD, such as neurodegenerative scales; that correlate changes in brain volume for other genotype-phenotype associations in cognitively impaired study participants; and that correlate with other clinically applicable magnetic resonance measures of pathology that can be conducted at the same time as structural volume measures, and are complementary to the volume measures.
The ultimate aim of this research is to obtain a better understanding and definition of Alzheimer's Disease in order to develop new improved medicines.
- Study Design:
- Study Type:
- dbGaP estimated ancestry using GRAF-pop
- Subject Sample Telemetry Report (SSTR)
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- Publicly Available Data (Public ftp)
- Study Inclusion/Exclusion Criteria
All study participants voluntarily provided an informed and signed consent by self and/or legal representative.
AD Patient Inclusion Criteria
An Alzheimer patient was eligible for inclusion in this study only if all of the following criteria applied:
- Met ADRDA/NINCDS criteria for diagnosis of probable Alzheimer's disease
- Positive diagnosis of Dementia of the Alzheimer's Type (DAT) on the DSM-IV check list, with a diagnostic code based on age of onset (to be determined by first symptoms noted by friends and family) and predominant clinical features: early onset (age 65 or less) uncomplicated (290.10), with delirium as mode of presentation (290.11), with delusions as mode of presentation (290.12), with depressed mood as mode of presentation (290.13), versus late onset (after age 65) uncomplicated (290.0), with delirium as mode of presentation (290.3), with delusions as mode of presentation (290.20), with depressed mood as mode of presentation (290.21)
- Global Deterioration Scale of Reisberg et al., score of 3 to 7
- Have clinical data available confirming Alzheimer diagnosis
Patient Exclusion Criteria
An Alzheimer's patient was not eligible for inclusion in this study if any of the following criteria applied:
- Was currently in a Major Depressive Episode, psychosis, acute manic or depressive episode of Bipolar Disorder
A control was ethnically matched, and when feasible gender- and age- matched (or older) to the cases and eligible for inclusion in this study only if all of the following criteria applied:
Control Inclusion Criteria
- No history of memory problems
- MMSE higher than the appropriate cut-off dementia score taking into account age and education level
- DRS -2 AEMSS (Age and Education adjusted MOANS scale score) of 9 or higher (after adjustment for age and education)
- Clock test (11:10) with a score > or = 14.
- No impairment of the 7 instrumental ADL questions from the Duke Older American Resources and Services Procedures caused by cognitive decline (allow for 'never did' or 'physical disability'): use the telephone, get to places, go shopping, prepare meals, do housework, take own medicine, handle money)
Control Exclusion Criteria
A control was not eligible for inclusion in this study if any of the following criteria applied:
- Was currently in a Major Depressive Episode, psychosis or acute manic or depressive episode of Bipolar Disorder
- Had cognitive impairment on testing
- Not ethnically matched to any of the target case cohorts
Unaffected Siblings of enrolled Alzheimer's patients
A sibling of an Alzheimer's patient was eligible for inclusion in this study only if all of the following criteria apply:
- Is 65 years of age or older
- Same as Control
Affected Biological (Blood) Relatives of enrolled Alzheimer's patients
Where feasible, affected biological relatives of up to third degree relationship were recruited and follow the protocol as per a case (see above criteria for Alzheimer's patients).
For GenADA LONG:
Cases or Patients with Alzheimer's Disease (AD)
An Alzheimer's patient was eligible for inclusion in GenADA LONG only if all of the following criteria applied:
- An informed and signed consent by self and/or appropriate representative.
- They participated in the previous GenADA study. (The patients at this second time-point may have now progressed to an atypical form of dementia and/or may not fulfill the inclusion criteria from the previous study.)
- They have a Global Deterioration Scale (GDS) score of 3, 4 or 5 at the time of their GenADA visit
- OR they have a GDS of 6 AND an Mini Mental State Examination (MMSE) of greater than or equal to 10 at the time of their GenADA visit
An Alzheimer's patient was not eligible for inclusion in GenADA LONG if any of the following criteria applied:
- Was currently in a Major Depressive episode, psychosis (excluding psychosis related to dementia), acute manic depressive episode of Bipolar disorder.
- In the investigator's opinion, was not able to be followed up (due to behaviour, ability to re-test, co-morbidities, etc)
Controls and Unaffected Biological Siblings
A control was eligible for inclusion in GenADA LONG if any of the following criteria applied:
- They participated in the previous GenADA study.
- They voluntarily provide an informed consent.
- Controls were matched at site for age (+ 5 years) and gender or if assessed show signs of cognitive decline
A control was not eligible for inclusion in GenADA LONG if any of the following criteria applied:
- Was currently in a Major Depressive episode, psychosis, acute manic depressive episode of Bipolar disorder
A control with change in cognitive status was eligible for inclusion into GenADA LONG if their DRS2 score has declined ≥10% since their GenADA visit. These subjects were considered "controls with change in cognitive status".
Affected Biological (Blood) Relatives of enrolled Alzheimer patients
Where feasible, biological relatives with AD and who were recruited into the original GenADA were recalled for inclusion into this longitudinal part. These study participants fall under the same study criteria as those for Cases or Patients with Alzheimer's.
For GenADA Imaging:
Cases and Controls Inclusion Criteria:
All participants from the original GenADA study who met the inclusion criteria below were invited to take part in this optional sub-study.
- All participants must have satisfied the minimum study inclusion of an informed and signed consent by self and/or appropriate representative.
- The participant must have been able to provide an adequate baseline scan acquisition. Two T1W scans were taken on first baseline visit, with a repeat visit if necessary due to inadequate scan quality. If the scan was not fit for purpose, participant was excluded from the study.
- Patients with probable AD were eligible for inclusion in this study if they participated in the previous GenADA study as a case and were also participating in the GenADA LONG component. The patients at this second time-point may have presented with a dementia which makes the diagnosis of probable AD less certain. These patients may have show significant vascular pathology (e.g. > 25% white matter lesions), or have evolved clinical features suggestive of an alternative diagnosis. They were included in the imaging study, but the change in diagnostic certainty were recorded for the purpose of differential analysis.
- All cases were at least mild to moderate at first scan as defined by a Global Deterioration Score (GDS) of 3-5 and a Mini-Mental Status Examination (MMSE) greater than 15 out of 30.
Exclusion criteria for all participants:
- Inability to tolerate MRI scanning or any contraindication to scanning such as pacemaker, certain ferrous metal implant, claustrophobia.
- Participant suffers from uncontrolled epilepsy, seizures or blackouts etc.
- Failure to obtain adequate baseline acquisition after 2 separate baseline visits.
- Molecular Data
Type Source Platform Number of Oligos/SNPs SNP Batch Id Comment Whole Genome Genotyping Affymetrix Mapping250K_Nsp 262264 33767 Affymetrix 500K Set comprises Mapping250K_Nsp and Mapping250K_Sty Arrays Whole Genome Genotyping Affymetrix Mapping250K_Sty 238304 33766 Affymetrix 500K Set comprises Mapping250K_Nsp and Mapping250K_Sty Arrays
- Selected publications
- Diseases/Traits Related to Study (MeSH terms)
- Primary Phenotype: Alzheimer Disease
- Links to Related Resources
- Authorized Data Access Requests
- Study Attribution
- Luis Fornazzari. Memory Clinic, St. Michaels Hospital, Toronto, Canada.
- Serge Gauthier. McGill Centre for Studies in Aging, Alzheimer's Disease Research Unit, Verdun, Quebec.
- Peter H. St. George-Hyslop. University of Toronto, Center for Research in Neurodegenerative Diseases, Toronto, Ontario.
- Howard Feldman. Vancouver Hospital and Health Sciences Centre, Vancouver, British Columbia.
- Anthony Guzman. Clinical Trial Unit, SCO Health Service, Ottawa, Ontario.
- Michael Borrie. Parkwood Hospital, London, Ontario.
- Andrew Kertesz. St. Joseph's Hospital, London, Ontario.
- Richard Delisle. Clinique de Neurologie, Trois-Riviéres, Quebec.
- John Wherrett. University Health Network, Toronto, Ontario.
- Ron Keren. University Health Network, Toronto, Ontario.
- Inge Loy-English. Clinical Trial Unit, SCO Health Service, Ottawa, Ontario.
- Ging-Yuek Hsiung. University of British Columbia, Vancouver, British Columbia.
- GlaxoSmithKline, Inc. Translational Medicine & Genetics, Clinical Imaging Center, R&D Alliances, and Worldwide Epidemiology.
- Principal Investigators