Grant: CIHR Fellowship
University of Alberta
$135,000.00
Mechanisms underlying abnormal uteroplacental vascular adaptations in pregnancies complicated by advanced maternal age
EF 2019-20
Résumé
More women are having their first pregnancies at an older age. In Canada, 8% of women have their first child when they are over 35 years of age (also known as advanced maternal age). A woman's blood vessels need to go through large changes during pregnancy, so that the fetus can receive enough blood and nutrients to grow normally. If the blood vessels do not adapt well enough, this can cause problems during pregnancy such as poor fetal growth and preeclampsia. Advanced maternal age is a risk factor for both of these pregnancy problems. Unfortunately, advanced maternal age impacts on how well these blood vessels change in pregnant women. If we can find out exactly how advanced maternal age adversely affects these blood vessel changes in pregnancies in women at advanced maternal age, we can target these mechanisms for treatment. Our lab found that uterine arteries from aged pregnant rats did not function as well as the arteries from young pregnant rats. The differences that we found may explain the increased problems in advanced maternal age pregnancies. We thus need to know more about these poor functioning arteries and why they do not function well. To do this, we will assess the function of vessels from pregnant young (4 months old) and aged (9.5 months old, equivalent to ~35 years in humans) rats. We will test blood vessel function, and use specific drugs to identify how their function is different. We will also compare blood vessels from pregnant and non-pregnant young and old rats. This will allow us to test if the blood vessels from old rats adapt differently than in young rats. At the same time, we will assess this mechanism in vessels from human biopsies taken during caesarean deliveries from young and older pregnant women. Pregnancy affects the short- and long-term cardiovascular health of both mother and child. This will help develop new treatments for older pregnant women to improve pregnancy outcomes in this high-risk group.
Programme
CIHR Fellowship
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
412898
Name
Wooldridge Amy
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Human Development, Child and Youth Health
Theme2
Biomedical
Prcname2
Fellowships - Post-PhD
Projecttitle
Mechanisms underlying abnormal uteroplacental vascular adaptations in pregnancies complicated by advanced maternal age
Programtype2
Fellowship Programs
Orgnameinp2
University of Alberta
Cihramount2
$135,000
Cihrequipment2
$0
Programname2
CIHR Fellowship
Keyworddelim
Advanced Maternal Age; Myogenic Tone; Pressure Myography; Rat Model; Transient Vanilloid Potential Receptor 4; Vascular Function
Abstract
More women are having their first pregnancies at an older age. In Canada, 8% of women have their first child when they are over 35 years of age (also known as advanced maternal age). A woman's blood vessels need to go through large changes during pregnancy, so that the fetus can receive enough blood and nutrients to grow normally. If the blood vessels do not adapt well enough, this can cause problems during pregnancy such as poor fetal growth and preeclampsia. Advanced maternal age is a risk factor for both of these pregnancy problems. Unfortunately, advanced maternal age impacts on how well these blood vessels change in pregnant women. If we can find out exactly how advanced maternal age adversely affects these blood vessel changes in pregnancies in women at advanced maternal age, we can target these mechanisms for treatment. Our lab found that uterine arteries from aged pregnant rats did not function as well as the arteries from young pregnant rats. The differences that we found may explain the increased problems in advanced maternal age pregnancies. We thus need to know more about these poor functioning arteries and why they do not function well. To do this, we will assess the function of vessels from pregnant young (4 months old) and aged (9.5 months old, equivalent to ~35 years in humans) rats. We will test blood vessel function, and use specific drugs to identify how their function is different. We will also compare blood vessels from pregnant and non-pregnant young and old rats. This will allow us to test if the blood vessels from old rats adapt differently than in young rats. At the same time, we will assess this mechanism in vessels from human biopsies taken during caesarean deliveries from young and older pregnant women. Pregnancy affects the short- and long-term cardiovascular health of both mother and child. This will help develop new treatments for older pregnant women to improve pregnancy outcomes in this high-risk group.
Competitiondate
201910
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Wooldridge, Amy
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $135,000~ $0~