Completed Pregnancy, Children & Inherited Conditions Bones, Joints & Muscles

Assessment of Potential Therapies for Pre-eclampsia and Fetal Growth Restriction using Murine Models

In plain English

AI plain-English summary

Every year in the UK, up to 5 women and 600 babies die because of pre-eclampsia, and fetal growth restriction causes 1 in 4 stillbirths. These complications affect up to 1 in 10 pregnancies, yet no drugs exist to treat them. Women with severe cases must deliver prematurely, risking chronic illness or death for the baby. Survivors face higher risks of cerebral palsy, heart disease, diabetes, and mental health problems later in life. The NHS spends around £420 million annually on intensive care for growth-restricted babies, who occupy 20% of all intensive care cots. This project tests existing, already-safe drugs on specially-bred mouse strains that show signs of pre-eclampsia and fetal growth restriction during pregnancy. The goal is to identify which treatments relieve symptoms effectively. Promising candidates will then be tested on blood vessels from donated human placentas and women after childbirth. These experiments will provide the evidence needed to design clinical trials for pregnant women. If successful, this research could lead to the first drug treatments for these conditions, reducing deaths, premature births, and long-term health burdens on families and the NHS.

View original technical description
Pre-eclampsia and fetal growth restriction (babies born smaller than they should be) are complications that affect up to 1 in 10 pregnancies and are responsible for grave illness in affected mothers and babies. Each year in the UK, up to 5 women and 600 babies die because of pre-eclampsia; 1 in 4 stillbirths are caused by fetal growth restriction and this is responsible for 1 in 6 sudden infant deaths. Babies who survive these complications are at greater risk of cerebral palsy and, later on in life as children and adults, they are at higher risk of suffering heart disease, diabetes, bone disease and mental health problems. Babies born of pregnancies complicated by pre-eclampsia and fetal growth restriction place a heavy burden on the NHS, with 20% of all intensive care baby cots being occupied by babies from pre-eclampsia pregnancies and around #420m being spent each year on intensive care of growth restricted babies. In addition, looking after children with illnesses related to pre-eclampsia and fetal growth restriction places a heavy burden on families, the NHS and social services. Unfortunately, there are no cures for either pre-eclampsia or fetal growth restriction and women suffering from severe problems have to undergo premature delivery of their baby, which also carries great risks of chronic illness and death. Although there have been no drugs specially designed to treat these illnesses, there are a number of possible treatments that are used to treat other illnesses and that have already been shown to be safe in people who are not pregnant. These treatments cannot be tested on pregnant women without first establishing whether they are effective and safe in treating symptoms of pre-eclampsia and fetal growth restriction in animals. We would like to test a number of existing drugs to see if they are useful at treating the symptoms of these diseases in a number of specially-bred mouse strains that display signs of pre-eclampsia and fetal growth restriction when pregnant. Once we have found which treatments have the greatest potential for treatment in mice, we will use them on blood vessels taken from human placentas and women (with informed written consent) after they have given birth to test whether they might be effective in human pregnancy. Such experiments will provide information on how to design clinical trials for the development of these treatments in pregnant women suffering from pre-eclampsia or fetal growth restriction.

View the original record at the funder ↗

Researchers

Colin Sibley (Principal Investigator)Mark Wareing (Co-Investigator)Miguel Constancia (Co-Investigator)Philip Baker (Co-Investigator)Stephen Brown (Co-Investigator)Susan Greenwood (Co-Investigator)

Related Research

Grants with similar aims, by meaning.

Developing personalized nanotherapies to target placental abnormalities causing fetal growth restriction
Regulation of uteroplacental vascular remodelling by maternal endothelial cell tetrahydrobiopterin: Role in pre-eclampsia and programmed cardiovascular risk in mothers and offspring
MICA: MRC EVERREST: A Pre-clinical Efficacy Study for FGR
Is kynurenine pathway manipulation a novel therapeutic strategy for ameliorating features of pre-eclampsia?
Mouse models to study novel anti-inflammatory approaches to prevention of preterm labour and neonatal handicap.

Original classification

Research Grant

Plain English summaries and category classifications on this site are generated by AI and may not perfectly reflect the original research.