Search DIAN Data Resource Requests

In order to avoid the situation where two investigators study the same research question, please search our database to determine if your topic has already been studied. If you find that your topic or a related topic has already been submitted, you may wish to contact the investigator to inquire about his/her findings to determine how you might proceed. You may wish to collaborate or modify your request to avoid overlap. The results below reflect requests made since online requests have been accepted. As such, not all fields will have data as certain information, such as aims, were not collected until recently. If an entry has been assigned an ID # (e.g. DIAN-D1004), the full request has been submitted and is either approved, disapproved or in process.

Displaying 291 - 294 of 294

Investigator:Elena Rodriguez-Vieitez


Title:Early hypermetabolism in Alzheimer?s disease? Investigating longitudinal multivariate associations between in vivo metabolism, pathophysiology, cognition and genotype

Date of Request:12/23/2016

ID:DIAN-D1703




Aim 1:Test the hypothesis of early hypermetabolism in autosomal dominant AD, and investigate longitudinal multivariate associations between in vivo metabolism, pathophysiology and cognition.




Aim 2:Test how cognitive reserve may modulate the longitudinal associations between in vivo biomarkers and cognition investigated in Aim 1.




Aim 3:Investigate the effect of genotype (familial gene type, mutation type, APOE) on the longitudinal associations investigated in Aims 1 and 2.




Investigator:Mathias Jucker, Johannes Levin, Igor Yakushev


Title:Regional pattern of longitudinal A� accumulation in autosomal dominant Alzheimer's disease

Date of Request:12/31/2016

ID:DIAN-D1701




Aim 1:To investigate regional patterns of longitudinal Aβ accumulation in autosomal dominant AD




Aim 2:To establish a set of target brain regions for antiamyloid clinical trials such as the DIAN-TU







Investigator:Andrew McKenzie


Title:The role of PSEN1 coding mutations on white matter neuroimaging volumes

Date of Request:1/5/2017

ID:DIAN-D1702




Aim 1:Test the hypothesis that individuals with PSEN1 FAD-causative mutations have alterations in their white matter volume sizes compared to individuals without PSEN1 FAD-causative mutations.










Investigator:Josephine Barnes


Title:Baseline volumes and rates of WMH accrual in familial AD: relationships with brain atrophy and cognitive measures

Date of Request:1/26/2017

ID:-




Aim 1:to quantify WMH accrual in FAD using our longitudinal WMH measurement tool




Aim 2:to assess whether WMH accrual is related to concurrent atrophy of the brain and hippocampus, estimated using the boundary shift integral, and also to change in cognition.




Aim 3:to investigate whether any potential relationships from aims 1) and 2) differ according to genetic status (APP vs. PSEN1 vs. PSEN2).




Aim 4to investigate whether any potential relationships from aims 1) and 2) are materially altered by adjustment for APOE e4 status