A genetic mutation that can lead to haemorrhagic stroke has been identified by scientists along with a drug to potentially treat it.
Research published in journal Human Molecular Genetics highlights a mutation in the gene COL4a2 that causes bleeding in the brain.
COL4a2 is a protein that is expressed by the gene of the same name, which forms a structure outside the cell called a basement membrane.
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Importantly, the scientists have also identified a cure to treat this disease by using a drug which has been approved for human patients and the results highlight its potential future therapeutic use for stroke.
Haemorrhagic stroke accounts for half of all stroke cases in children and currently there is no treatment, said, Tom Van Agtmel of the Institute of Cardiovascular and Medical Sciences at the University of Glasgow who led the study.
Although it is expected that only a small number of patients will have defects in this membrane, this research gives us a better understanding of how this type of stroke develops, he said, adding, importantly it has identified how we might treat it in some cases.
"However, this is just one genetic mutation we have identified and analysed so there is still a long way to go, but it s a start", said Agtmel.
The researchers obtained their results by analysing skin biopsies from a father a son with a family history of porencephaly, a cavity in the brain caused by perinatal haemorrhagic bleeding which can result in seizures and paralysis.
Both father and son carried the genetic mutation but only the son displayed the accumulation of the mutant protein inside the cell.
The next stage will be to see if the drug treatment works in an animal model.
If it does then this is a first step towards investigating its potential in human patients with this type of stroke using the pre-existing, approved drug.
The study was funded by the Medical Research Council, Wellcome Trust and a Research Councils UK fellowship.