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Grant: Project Grant

University of Manitoba

$566,100.00

Perinatal nutrition strategy with omega-3 docosahexaenoic acid to protect brain in fetal alcohol spectrum disorders

EF 2022-23

Résumé
Drinking alcohol during pregnancy can lead to many problems for the developing baby, resulting in fetal alcohol spectrum disorders (FASD). FASD damages the fetus by limiting its physical and neurological growth, and may cause facial deformities. These effects lead to life-long physical and developmental problems. Among these issues, brain dysfunction is considered the most serious, particularly as it causes deficits in learning and memory. It is estimated that 4% of North Americans are affected by FASD and 10.7% of Canadian women report some alcohol intake while pregnant. While the current strategy to reduce FASD is counselling pregnant women to abstain from alcohol, the rate of FASD is rising. Despite this, there is no effective measure to prevent FASD, nor is there a standard treatment or cure for these disorders. Proper nutrition during pregnancy has shown to alleviate several underlying issues, specifically the omega-3 fatty acid docosahexaenoic acid (DHA). Many health professional societies promote DHA as a brain super food, and recommend the adequate intake of DHA during pregnancy to support fetal brain development. A DHA deficiency results in impaired brain development by altering the structure of brain cells. Prenatal alcohol exposure is known to decrease the maternal DHA status and reduces the transfer of DHA to the fetus and disturb normal brain function. Thus, it is plausible that maternal DHA supplementation may alleviate the deleterious effects of alcohol on the fetal brain. The overall objective of this study is to determine whether DHA provision during pregnancy or lactation is a simple and effective nutrition strategy to prevent or treat FASD by reducing brain inflammation and preserving memory function. The outcomes of this study may provide scientific evidence for the use of DHA supplementation to enhance the health of mothers who are at risk of having children with FASD and cannot stop drinking during pregnancy.
Programme
Project Grant
Emplacement
Manitoba, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
469139
Name
Suh Miyoung
Region
Manitoba
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Nutrition, Metabolism and Diabetes
Theme2
Biomedical
Prcname2
Nutrition, Food & Health
Projecttitle
Perinatal nutrition strategy with omega-3 docosahexaenoic acid to protect brain in fetal alcohol spectrum disorders
Programtype2
Operating Grants
Orgnameinp2
University of Manitoba
Cihramount2
$566,100
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Alcohol Toxicity; Birth Outcomes; Fetal Alcohol Spectrum Disorders; Fetal Brain Development; Lipid Metabolism; Maternal And Infant Nutrition
Abstract
Drinking alcohol during pregnancy can lead to many problems for the developing baby, resulting in fetal alcohol spectrum disorders (FASD). FASD damages the fetus by limiting its physical and neurological growth, and may cause facial deformities. These effects lead to life-long physical and developmental problems. Among these issues, brain dysfunction is considered the most serious, particularly as it causes deficits in learning and memory. It is estimated that 4% of North Americans are affected by FASD and 10.7% of Canadian women report some alcohol intake while pregnant. While the current strategy to reduce FASD is counselling pregnant women to abstain from alcohol, the rate of FASD is rising. Despite this, there is no effective measure to prevent FASD, nor is there a standard treatment or cure for these disorders. Proper nutrition during pregnancy has shown to alleviate several underlying issues, specifically the omega-3 fatty acid docosahexaenoic acid (DHA). Many health professional societies promote DHA as a brain super food, and recommend the adequate intake of DHA during pregnancy to support fetal brain development. A DHA deficiency results in impaired brain development by altering the structure of brain cells. Prenatal alcohol exposure is known to decrease the maternal DHA status and reduces the transfer of DHA to the fetus and disturb normal brain function. Thus, it is plausible that maternal DHA supplementation may alleviate the deleterious effects of alcohol on the fetal brain. The overall objective of this study is to determine whether DHA provision during pregnancy or lactation is a simple and effective nutrition strategy to prevent or treat FASD by reducing brain inflammation and preserving memory function. The outcomes of this study may provide scientific evidence for the use of DHA supplementation to enhance the health of mothers who are at risk of having children with FASD and cannot stop drinking during pregnancy.
Competitiondate
202209
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Suh, Miyoung
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $566,100~ $0~