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Grant: Travel Awards - Institute Community Support

University of Alberta

$1,000.00

Sex-specific changes in neonatal cardiac mitochondrial function in response to perinatal iron deficiency

FY 2019-20

Summary
After birth, the hardworking newborn heart needs an efficient power plant to satisfy its energy needs. If the proper components are unavailable to produce energy, the heart may develop improperly and impart a vulnerability to health complications in later life. Within the powerhouse of the cell - the mitochondria - iron is essential for energy production. Pregnant women have a high risk of developing iron deficiency (ID). The heart has high energy needs to support both growth and blood pumping, making it particularly vulnerable to negative changes caused by ID. We found that male, but not female, newborn hearts adapt to perinatal ID by producing more mitochondria to compensate for reduced efficiency. This research will be important in identifying targets for new treatments in pregnancy that reduce or prevent chronic disease susceptibility due to ID and illuminating sex differences in disease development and progression.
Program
Travel Awards - Institute Community Support
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
412245
Name
Holody Claudia D
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Human Development, Child and Youth Health
Theme2
Biomedical
Prcname2
Institute of Human Development, Child and Youth Health
Projecttitle
Sex-specific changes in neonatal cardiac mitochondrial function in response to perinatal iron deficiency
Programtype2
Undefined
Orgnameinp2
University of Alberta
Cihramount2
$1,000
Cihrequipment2
$0
Programname2
Travel Awards - Institute Community Support
Keyworddelim
Ics Travel Awards
Abstract
After birth, the hardworking newborn heart needs an efficient power plant to satisfy its energy needs. If the proper components are unavailable to produce energy, the heart may develop improperly and impart a vulnerability to health complications in later life. Within the powerhouse of the cell - the mitochondria - iron is essential for energy production. Pregnant women have a high risk of developing iron deficiency (ID). The heart has high energy needs to support both growth and blood pumping, making it particularly vulnerable to negative changes caused by ID. We found that male, but not female, newborn hearts adapt to perinatal ID by producing more mitochondria to compensate for reduced efficiency. This research will be important in identifying targets for new treatments in pregnancy that reduce or prevent chronic disease susceptibility due to ID and illuminating sex differences in disease development and progression.
Competitiondate
201909
Approvedterm2
1 yr 0 mth
Pinamesdelim
Holody, Claudia D
Approvedterm
1 an 0 mois
Cihrcontribution2
Inst of Human Dev &Child &Yth~ $1,000~ $0~