Grant: Project Grant
University of British Columbia
$884,186.00
Motherhood and brain aging: the effects of hormone therapy, immune and metabolic challenges later in life
FY 2019-20
Summary
Alzheimer's disease (AD) is a disease that results in the progressive loss of cells in the brain, in particular in an area important for the formation of new memories, called the hippocampus. Women are more likely to be diagnosed with AD and show greater brain pathology and memory loss with the disease than men. In addition, women are more likely to develop Alzheimer's disease especially when they have certain genes (APOEe4) and a previous history
of multiple pregnancies. This project aims to characterize the aging female brain and how is affected by reproductive experience (pregnancy) and genetics (APOEe4 status) under hormone therapy, immune, and metabolic (diet) challenges. Menopause is associated with dramatic changes in hormone levels and with cognitive decline and certain hormone therapies (HTs) positively affect cognition depending on timing and genotype. Our research shows that the sensitivity of the female brain to estrogens is altered with past parity to affect neuroplasticity and immune signalling. The goal of this proposal is to study the effects of parity and genetics on aging in the female brain exposed to hormone therapies, immune and metabolic challenges in preclinical models. This work will determine how physiological challenges faced by females during aging interact with motherhood and genetics can affect brain aging. It is clear that tailored treatment based on sex, genetics, and possibly reproductive history need to be developed to best treat individuals at risk to develop AD.
Department
Program
Project Grant
Recipient
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
419344
Name
Galea Liisa A
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Gender and Health
Theme2
Biomedical
Prcname2
Gender, Sex & Health
Projecttitle
Motherhood and brain aging: the effects of hormone therapy, immune and metabolic challenges later in life
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$884,186
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Aging; Alzheimer'S Disease; Apoe4; Cognition; Hippocampus; Metabolic Factors; Microglia; Neuroinflammation; Neuroplasticity; Parity
Abstract
Alzheimer's disease (AD) is a disease that results in the progressive loss of cells in the brain, in particular in an area important for the formation of new memories, called the hippocampus. Women are more likely to be diagnosed with AD and show greater brain pathology and memory loss with the disease than men. In addition, women are more likely to develop Alzheimer's disease especially when they have certain genes (APOEe4) and a previous history
of multiple pregnancies. This project aims to characterize the aging female brain and how is affected by reproductive experience (pregnancy) and genetics (APOEe4 status) under hormone therapy, immune, and metabolic (diet) challenges. Menopause is associated with dramatic changes in hormone levels and with cognitive decline and certain hormone therapies (HTs) positively affect cognition depending on timing and genotype. Our research shows that the sensitivity of the female brain to estrogens is altered with past parity to affect neuroplasticity and immune signalling. The goal of this proposal is to study the effects of parity and genetics on aging in the female brain exposed to hormone therapies, immune and metabolic challenges in preclinical models. This work will determine how physiological challenges faced by females during aging interact with motherhood and genetics can affect brain aging. It is clear that tailored treatment based on sex, genetics, and possibly reproductive history need to be developed to best treat individuals at risk to develop AD.
Competitiondate
202003
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Galea, Liisa A
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $884,186~ $0~