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 281 - 290 of 318

Investigator:Serge Gauthier


Title:Neurobiological Markers of Suicide Vulnerability in Alzheimer?s Disease Patients

Date of Request:9/3/2015

ID:DIAN-D1513




Aim 1:to characterize neurobiological markers (socio-demographic, clinical, neuropsychological, and biological profile) of asymptomatic ADAD mutation carriers and symptomatic ADAD mutation carriers with suicidal ideations (suicidal patients).




Aim 2:to compare neurobiological markers (socio-demographic, clinical, neuropsychological, and biological) in a) asymptomatic ADAD mutation carriers suicidal patients, b) symptomatic ADAD mutation carriers suicidal patients, c) asymptomatic non-mutation carrier non-suicidal controls, and to d) symptomatic







Investigator:NA


Title:Examining the relationship between exercise, Aβ accumulation, brain atrophy and age at onset: A study of autosomal-dominant Alzheimer?s disease mutation carriers

Date of Request:11/3/2015

ID:DIAN-D1514




Aim 1:1. Examine the rates of brain Aβ accumulation between exercising and sedentary asymptomatic mutation carriers, versus aged matched non-mutation carriers.




Aim 2:2. Examine rates of hippocampal and prefrontal cortex atrophy between exercising and sedentary asymptomatic mutation carriers, versus aged matched non-mutation carriers.




Aim 3:3. Examine the relationship between baseline exercise levels and age at onset in symptomatic mutation carriers.




Investigator:John Ringman/JJ Wang


Title:Microhemorrhages and vascular compliance

Date of Request:11/9/2015

ID:DIAN-D1515




Aim 1:To relate number of micro hemorrhages to cerebrovascular compliance for UCLA DIAN subjects










Investigator:Prof. Dr. Adrian Danek


Title:Frequency of seizures in the DIAN cohort: A comparison between mutation carriers and non-carriers

Date of Request:11/23/2015

ID:DIAN-D1516




Aim 1:Our specific aim for our proposed work with the DIAN data set is to find out whether there is a difference in frequency of seizures in mutation carriers of familial Alzheimer?s disease in comparison to non-carriers.




Aim 2:Furthermore we are planning to follow an enhanced approach by querying the NACC data base for a comparison of frequency of seizures between patients with sporadic Alzheimer?s disease, mutation carriers for the familial Alzheimer?s disease and non-carriers.




Aim 3:A further possibility is to additionally include patients with frontotemporal lobar degeneration for comparison of frequency of seizures.




Investigator:Randall J Bateman


Title:DIAN-TU NexGen Trial Design Manuscript

Date of Request:12/29/2015

ID:DIAN-D1517




Aim 1:Disseminate DIAN-TU NexGen trial design analyses




Aim 2:Optimize DIAN-TU cognitive composite for the primary endpoint




Aim 3:Develop a desease progression model for autosomal dominant Alzheimer's disease




Aim 4Evaluate the benefits of run-in data to enhance trial statistical power and identify a drug effect

Investigator:Karch


Title:Clinical and Molecular Characterization of Novel PSEN1 Mutation

Date of Request:1/8/2016

Status:Pending

ID:DIAN-D1601




Aim 1:To describe the biomarker (fluid and imaging) profile for research participants from a family with a novel PSEN1 mutation










Investigator:NA


Title:State space modeling of the clinical and biomarker changes in Dominantly Inherited Alzheimer?s Disease

Date of Request:1/15/2016

ID:DIAN-D1602




Aim 1:Apply state space model to DIAN data to estimate the clinical and biomarker changes in Dominantly Inherited Alzheimer's Disease




Aim 2:Compare the results from state space model with the result from the mixed model




Aim 3:Simulate Alzheimer's disease clinical trials based on the DIAN data and to propose statistical test methods for efficacy




Investigator:Dawn Matthews


Title:Multimodality Imaging Diagnostic for Preclinical and Prodromal AD

Date of Request:1/25/2016

ID:DIAN-D1603




Aim 1:Further refine and validate our use of early frame amyloid data as a marker of disease and predictor of functional change




Aim 2:Refine and validate PET and structural MRI classifiers in differentiating amyloid positive and negative populations and predicting rate of clinical decline.




Aim 3:Optimize processing and classification approaches to functional MRI data as available to characterize disease state and progression




Aim 4Compare imaging markers of disease progression in the DIAN population to Late Onset populations

Investigator:Eric McDade


Title:Task Based Functional MRI in Preclinical Autosomal Dominant Alzheimer Dementia

Date of Request:1/27/2016

ID:DIAN-D1604




Aim 1:To identify differences in neuronal network function during working memory and learning in preclinical ADAD




Aim 2:To explore the association of task-based functional MRI activity in preclinical mutation carriers with imaging and CSF based AD pathology.




Aim 3:To explore task-based function MRI activity with longitudinal PET amyloid deposition.




Investigator:John M. Ringman, M.D., M.S.


Title:Description of a novel pathogenic PSEN1 mutation (S230N)

Date of Request:1/31/2016

ID:DIAN-D1605




Aim 1:We want to write a manuscript presenting the comprehensive descriptions of 3 persons from a family featuring a novel PSEN1 mutation, including PiB scans, quantification of MRI and CSF variables.