The Lililwan Project: Prevalence Of Fetal Alcohol Spectrum Disorders In The Fitzroy Valley
Funder
National Health and Medical Research Council
Funding Amount
$777,758.00
Summary
Alcohol use in pregnancy is widespread in Australia. Alchohol may cause physical and developmental problems in the developing child including the Fetal Alcohol Spectrum Disorders (FASD). This collaborative project, initiated and led by Aboriginal leaders in the Fitzroy Valley in the remote East Kimberley, WA, will establish the prevalence of FASD, health and developmental problems in a population of primary school-aged, predominantly Aboriginal children and develop strategies for service deliver ....Alcohol use in pregnancy is widespread in Australia. Alchohol may cause physical and developmental problems in the developing child including the Fetal Alcohol Spectrum Disorders (FASD). This collaborative project, initiated and led by Aboriginal leaders in the Fitzroy Valley in the remote East Kimberley, WA, will establish the prevalence of FASD, health and developmental problems in a population of primary school-aged, predominantly Aboriginal children and develop strategies for service delivery, prevention and education.Read moreRead less
Improving The Neonatal Transition In Infants With A Congenital Diaphragmatic Hernia
Funder
National Health and Medical Research Council
Funding Amount
$551,644.00
Summary
Congenital diaphragmatic hernia is a common congenital abnormality and occurs when the diaphragm fails to separate the abdominal and thoracic compartments before birth. This prevents the lung from growing properly and so at birth, the lung is unable to take over the role of gas exchange without considerable assistance. As a result, these infants are at high risk of death or significant disability and this application is focused on improving care and reducing morbidity in these infants.
Improving The Prediction And Detection Of Contributors To Term Stillbirth
Funder
National Health and Medical Research Council
Funding Amount
$570,358.00
Summary
Stillbirths are a global human tragedy, with 1 in 130 of all pregnancies in Australia ending in stillbirth. We propose to use ultrasound and blood markers to improve the detection of babies who are not growing well, a leading risk factor for stillbirth. Sleep position has also been associated with stillbirth, so we will study fetal heart rate responses during an overnight sleep study to see if breathing events overnight may be an important contributor to stillbirth in growth restricted fetuses.
Asking QUestions About Alcohol In Pregnancy (AQUA): Longitudinal Cohort Study Of The Effects Of Low And Moderate Doses Of Alcohol Exposure On The Fetus
Funder
National Health and Medical Research Council
Funding Amount
$1,368,294.00
Summary
National alcohol guidelines advise women to have no alcohol in pregnancy. However, many find they are unexpectedly pregnant and have been drinking, leading to considerable anxiety. While evidence is clear that heavy drinking is bad for the unborn baby, no-one knows for sure if low or even moderate levels of alcohol in pregnancy are harmful. We will study this important public health problem, following a group of pregnant women through their pregnancy and until their child is two years.
Genetic Autopsy Of Perinatal Death: Diagnosis And Discovery By Genome Sequencing
Funder
National Health and Medical Research Council
Funding Amount
$989,332.00
Summary
Stillbirth, miscarriage and genetic termination of pregnancy are common and traumatic events. Despite medical investigation, many of the causes of these events are unexplained. This project plans to employ the latest in whole genome sequencing and functional modelling to explain these occurrences as well as lead to an increase in knowledge of genetics and development.
Contrary to traditional belief few cases of cerebral palsy are due to problems at birth. Most have earlier origins. Sophisticated new methods have found that many developmental brain disorders e.g. autism, intellectual disability and epilepsy are associated with submicroscopic but genetically large alterations in the genetic code of these children. This novel study will seek these alterations in a large group of Australian cerebral palsy families. The pilot data show novel and exciting findings.
Intergenerational Determinants Of Fetal Growth In Aboriginal Western Australians
Funder
National Health and Medical Research Council
Funding Amount
$399,179.00
Summary
We will study birth and disease records over 3 generations of Aboriginal families to investigate how a mother’s birth weight and her diseases in pregnancy influence both her reproductive health and her risk of chronic diseases (eg heart disease and diabetes) later in life. This world-first study will guide effective prevention of chronic disease in Aboriginal Australians; it may suggest that prevention needs to start with grand-mothers rather than in later generations.
Measuring Hypoxia Induced MRNA In Maternal Blood To Monitor Wellbeing Of Growth-restricted Fetuses
Funder
National Health and Medical Research Council
Funding Amount
$421,358.00
Summary
Severely growth restricted fetuses are at peril of stillbirth from low oxygenation. While ultrasound monitoring improves outcomes, babies are still lost. Better ways to monitor the health the unborn baby are needed. We have recently discovered fetuses’ starved of oxygen leak RNA into mother's blood. Thus, measuring RNA molecules in blood could be used to assess fetal health. We will examine whether measuring mRNA in maternal blood could be used to monitor wellbeing of growth-restricted fetuses.
Mechanisms Of PTEN Regulation By Ndfip1 And Their Biological Consequences For Neuron Survival During Brain Injury
Funder
National Health and Medical Research Council
Funding Amount
$686,640.00
Summary
We have discovered a new protein (Ndfip1) that protects brain cells from death after brain injury from trauma and stroke. We will investigate why this protein is activated only in some, but not in other, brain cells after injury. In this application, we will study the mechanisms behind neuron protection, and use this information to explore how to increase the number of brain cells activating Ndfip1.
This study investigates how much an individual's genes and environment account for the wide variation in brain structure and function. Using brain imaging we examine in what way the connectivity of the brain of identical and non-identical twins is the same or different from that of their co-twin, and carry out analysis of their DNA to identify some of the genes involved. This will provide fundamental information on genetic mechanisms influencing variation in brain structure and function.