Millions of NHS patients will get a free personalised health report based on their DNA to help them live longer, the Government has announced.
The Department of Health and Social Care said the move will flag which conditions people are at risk of getting before any symptoms appear.
This will then allow people to take preventative measures to stay healthier for longer, reducing the pressure on the NHS, ministers said.
The move is the latest in a string of projects announced as part of Health Secretary Matt Hancock’s planned digital revolution.
Mr Hancock has said the use of better tech ‘will make the NHS the best in the world’, having previously accused it of falling behind Tesco.
Five million volunteers will give their DNA to the Accelerating Detection of Disease (ADD) programme to receive a free personalised health report
Leading charities such as Cancer Research UK, the British Heart Foundation and Alzheimer’s Research UK are all funding the programme.
However, it is likely to fuel concerns about data safety, considering hackers have attempted to steal data from previous NHS genome projects.
Advancement in technology mean it is possible to combine genetic information into polygenic risk scores (PRS), which spot warning signs of disease.
Five million volunteers will give their DNA for the project, but it won’t be revealed until the autumn how they will be recruited.
They will have their genome analysed to identify risk of developing diseases like cancer or heart disease.
This could allow them to make lifestyle changes that will help prevent the disease diagnosis or reduce its severity.
The ‘fully anonymised’ data will then be used for research, expected to finish by by 2024, in order to develop a new wave of personalised treatments.
Professor Sir John Bell is leading the programme, named Accelerating Detection of Disease (ADD).
He said: ‘The ability to identify people at risk or suffering from early forms of disease with greater precision will have a profound impact on how we develop diagnostics and new ways to treat disease.’
Health Minister Nicola Blackwood said: ‘Prioritising life-saving research and innovation means we can unlock solutions to deadly conditions like cancer, dementia and heart disease – saving lives and securing the health of the next generation.
‘To achieve this we must harness the power of technology, so I am delighted with today’s investment from businesses and charities – a huge boost for healthcare innovation which will help patients lead longer, happier lives.’
ADD will receive investment worth up to £160million from charities, alongside a £79million from the Government.
Hilary Evans, chief executive of Alzheimer’s Research UK, said: ‘Alzheimer’s Research UK is delighted to play a part in this landmark cohort and harness this incredible resource to make breakthroughs possible for people with dementia.
‘Today, we diagnose dementia causing diseases after symptoms show, but to ensure people get the greatest benefit from future treatments, we must be able to diagnose them as soon as possible.
‘Alzheimer’s Research UK is working to revolutionise how diseases like Alzheimer’s are identified and uniting the best minds in digital data and technology to draw on the full potential of the Accelerating Detection of Disease cohort.’
Genome sequencing found its way into the public eye when, in December 2018, Genomics England completed their 100,000 Genomes Project.
Over the past six years, researchers have sequenced the DNA of 85,000 patients who had been diagnosed with either cancer or a rare disease.
Although everyone involved in the study was known to have an illness, around one in four people found out about other conditions they didn’t know about.
But foreign hackers have made multiple attempts to steal the genetic details, which are said to be guarded at a top-security military base.
It comes after health chiefs announced every sick child in England with mysterious conditions will have the chance to have their entire DNA mapped as of next year.
All youngsters admitted to intensive care in England with an unknown disorder will be offered a genome analysis from January.
The NHS will be the first in the world to offer the screening, also an option given to the parents of children, carried out via a blood sample.
There are fears that patients will regret learning they have or are likely to develop a terminal illness, and that the information could be misused by insurance companies.