About this trial
Study background
High blood pressure during pregnancy is a worldwide health problem that can be dangerous to mothers and commonly causes premature birth and small babies. There is also growing evidence that mothers who suffer from high blood pressure in pregnancy, and their babies, have a higher risk of high blood pressure and cardiovascular disease later in life. Previous studies have revealed detrimental changes in the structure and function of the heart and blood vessels of mothers, and their babies, who experience this common complication. These changes may explain their increased risk of later disease. The investigators have also learned through previous studies that tetrahydrobiopterin (BH4), a molecule that has a role in blood vessel health, plays an important role in stabilising blood vessel function. Lower levels of BH4 are evident in both the placenta and the umbilical cord from mothers with high blood pressure. We, therefore, want to investigate how closely BH4 levels are related to clinical features of pre-eclampsia and whether altering levels of BH4, using a nutritional supplement, improves features of the disease such as blood vessel function. To do this, the investigators need to compare the levels of BH4 between mothers with pre-eclampsia, those taking the supplement and those without pre-eclampsia. The investigators also compare how the heart and blood vessels look and function in these groups using ultrasound methods, including echocardiography and fetal sonography.
Study objectives
CAREFOL-HT will assess how levels of BH4 differ in pregnant women with high blood pressure and if this is reflected in functional changes in the heart and blood vessels of these women. The investigators will also determine whether changing levels of BH4, using a tetrahydrofolate supplement (5-MTHF), changes blood vessel function.
Eligibility criteria
Qualifiers
Diagnosed with preeclampsia, as defined in Section 8.1, at <34 weeks' gestation within the last 48 hours and with no delivery planned within the next week
Receiving antenatal care in the John Radcliffe Hospital
Participant is willing and able to give informed consent for participation in the study
Age >18 and ≤45 years
Disqualifiers
History of cardiac impairments including uncontrolled arrhythmia, unstable angina, decompensated congestive heart failure or valve disease
History of preexisting chronic renal disease
Contraindication to taking folate related supplements
Folate supplementation in excess of 400mcg in the third trimester
Trial design
Treatments tested in this trial
- Arcofolin® 5-Methyltetrahydrofolate
- Arcofolin® Placebo
Treatment groups
Locations
2Sponsors and collaborators
University of Oxford
Lead sponsor
National Institute for Health Research, United Kingdom
Collaborator
British Heart Foundation
Collaborator
Merck & Cie
Collaborator