Grant: Travel Awards - Institute Community Support
Université Laval
$1,000.00
Temporal lobe atrophy in MCI adults with or without depressive symptoms and in patients with late-life depression
FY 2016-17
Summary
Individuals with mild cognitive impairment (MCI) or late-life depression (LLD) are known to be at risk for Alzheimer's disease (AD). However, it is unclear as to which clinical characteristics predict the occurrence of AD for each condition. Although MCI and LLD have been rigorously described individually, few studies have investigated the characteristics shared by both conditions. Nonetheless, there are many overlaps in the brain regions affected in MCI and LLD. These brain lesions have otherwise been associated with cognitive decline and progression towards AD. Furthermore, both conditions frequently coexist, as it is when patients with MCI also present depressive symptoms (MCI/D+), which is true for a great proportion of patients. This project aims to identify and compare the common and specific characteristics (e.g., brain lesions) amongst different groups of at risk participants. We recruited a cohort of participants presenting either MCI, MCI/D+, or LLD. All participants had a brain scan at baseline in order to locate and quantify the lesions. Subsequent analyses compared the lesions between the three groups. The results revealed that overall, MCI/D+ participants had more severe lesions in many brain regions but that these lesions were significantly more important than those in MCI participants in one region: the hippocampus. The results also revealed there was no difference between the LLD participants and the two other groups in those same regions. These findings contribute to better understanding the clinical differences between diverse at risk groups of patients. Further research should investigate the impact of such differences on future risk of progression towards AD.
Department
Program
Travel Awards - Institute Community Support
Recipient
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
364734
Name
Parent Camille
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Clinical
Prcname2
Institute of Aging
Projecttitle
Temporal lobe atrophy in MCI adults with or without depressive symptoms and in patients with late-life depression
Programtype2
Undefined
Orgnameinp2
Université Laval
Cihramount2
$1,000
Cihrequipment2
$0
Programname2
Travel Awards - Institute Community Support
Keyworddelim
Bourses De Voyage D'Aci
Abstract
Individuals with mild cognitive impairment (MCI) or late-life depression (LLD) are known to be at risk for Alzheimer's disease (AD). However, it is unclear as to which clinical characteristics predict the occurrence of AD for each condition. Although MCI and LLD have been rigorously described individually, few studies have investigated the characteristics shared by both conditions. Nonetheless, there are many overlaps in the brain regions affected in MCI and LLD. These brain lesions have otherwise been associated with cognitive decline and progression towards AD. Furthermore, both conditions frequently coexist, as it is when patients with MCI also present depressive symptoms (MCI/D+), which is true for a great proportion of patients. This project aims to identify and compare the common and specific characteristics (e.g., brain lesions) amongst different groups of at risk participants. We recruited a cohort of participants presenting either MCI, MCI/D+, or LLD. All participants had a brain scan at baseline in order to locate and quantify the lesions. Subsequent analyses compared the lesions between the three groups. The results revealed that overall, MCI/D+ participants had more severe lesions in many brain regions but that these lesions were significantly more important than those in MCI participants in one region: the hippocampus. The results also revealed there was no difference between the LLD participants and the two other groups in those same regions. These findings contribute to better understanding the clinical differences between diverse at risk groups of patients. Further research should investigate the impact of such differences on future risk of progression towards AD.
Competitiondate
201701
Approvedterm2
1 yr 0 mth
Pinamesdelim
Parent, Camille
Approvedterm
1 an 0 mois
Cihrcontribution2
Institute of Aging~ $1,000~ $0~