香港六合彩

The study, published today in Science Translational Medicine, builds on recent evidence by the same research team, which found that a novel blood test can predict the onset and track the progression of the disease in people who carry the gene responsible for the incurable and fatal brain disorder.

In conducting this latest study, the team developed a tool kit to guide measurement of two early biomarkers of Huntington鈥檚 disease found in blood and brain fluid, for use in clinical trials that seek to find the first disease-altering treatment for Huntington鈥檚.

鈥淢any people who develop Huntington鈥檚 report subtle signs such as with mood or coordination, in what鈥檚 called the prodromal stage before any changes can be detected by brain scans. We鈥檝e found that blood testing could help identify groups of people with very early neurodegeneration to help us run clinical trials of drugs to prevent symptoms,鈥� said lead author Dr Ed Wild of the 香港六合彩 Huntington鈥檚 Disease Centre, 香港六合彩 Institute of Neurology. 鈥淲e were surprised to find the blood tests could pick up signs even before any evidence of neurodegeneration could be seen in brain scans.鈥�

The researchers caution that the blood test is not yet helpful for individual patients.

鈥淢ore research is needed to clarify the clinical potential of this test. We hope it can help to develop the first drugs to slow Huntington鈥檚, and if they become available, then hopefully this test could help guide decisions on when to begin treatment,鈥� said first author Lauren Byrne (香港六合彩 Institute of Neurology).

Huntington鈥檚 disease is caused by a single known genetic mutation, and each child of a mutation carrier has a 50% chance of inheriting the disease. While most people with the mutation start to show symptoms between 30 to 50 years of age, the onset of the disease can happen at any age.聽

The study involved 40 people with Huntington鈥檚 disease who were at different stages of the disease, 20 people who carried the genetic mutation but had not yet been diagnosed with Huntington鈥檚, and 20 healthy control subjects, recruited through the National Hospital for Neurology and Neurosurgery.

The researchers took samples of blood plasma and cerebrospinal (brain) fluid, and tested them for both neurofilament light (NfL) protein, which is often a product of nerve cell damage, and for concentration of the mutant huntingtin (mHTT) protein that causes the disease. They then compared these results to clinical measures such as brain area volumes from MRI scans, and a few motor and cognitive tests.

They found that measures of NfL in blood were most strongly associated with all clinical measures.

The research team used the data to model what stage of the disease or of pre-Huntington鈥檚 each person was in. From their modelling, supported by a comparison with a much larger cohort of patients, they could determine that the first identifiable changes are the quantity of the mutant gene in brain fluid, and of NfL in blood and brain fluid.

The researchers say their findings could be vital for clinical trials such as an upcoming trial to determine whether the drug RG6042 (formerly IONIS-HTTRx) can slow the progression of the disease.

鈥淲e are living in a time of incredible advancement in the field of neurodegeneration, and research in Huntington鈥檚 disease is paving the way towards interventions that can change people鈥檚 lives. Developing tools to track biological and clinical changes, and identify candidates to participate in clinical trials, is vital for the success of such trials,鈥� said co-author Dr Filipe Brogueira Rodrigues (香港六合彩 Institute of Neurology).

The study was conducted by researchers at 香港六合彩 Institute of Neurology, 香港六合彩 Centre for Medical Image Computing and the National Hospital for Neurology and Neurosurgery and funded by the Medical Research Council UK (MRC), the CHDI Foundation, Wellcome, Engineering and Physical Sciences Research Council (EPSRC) and Hoffman La Roche, with support from the National Institute for Health Research University College London Hospitals Biomedical Research Centre, the UK Dementia Research Institute, and the Horizon 2020 Framework Programme.

More about Huntington鈥檚 disease

Huntington鈥檚 disease is a fatal genetic neurological disease. It usually develops in adulthood and causes abnormal involuntary movements, psychiatric symptoms and dementia. Approximately 10,000 people in the UK have HD with around 25,000 at risk. It is incurable, and no effective treatments exist to slow it down. Patients usually die within 20 years of the start of symptoms.

Links

• Byrne, et al. .Science Translational Medicine聽 12 Sep 2018: Vol. 10, Issue 458, eaat7108. DOI: 10.1126/scitranslmed.aat7108

Image

• Source: National Eye Institute on聽