MS-PINPOINT · Running now

Multiple sclerosis is unpredictable. This project is built to change that.

MS-PINPOINT is a multi-center project developing advanced artificial intelligence tools to choose the right treatment for the right person at the right time, to delay disability, improve the quality of life of those living with MS and their families, and eventually save costs for the healthcare systems (including the NHS in the UK).

Eight axial slices through the MNI152 brain template, ascending from the cerebellum to the vertex

The brief

More than fifteen treatments, and no reliable way to know which one is yours.

Multiple sclerosis is incurable and disabling, and costs the UK approximately £3 billion annually. The treatments we have can only moderately slow disability worsening — and choosing the right one for the right patient at the right time is so difficult that most people with MS will switch treatment at some point.

Data providers
12hospitalsHospitals contributing routine MRI and electronic health records to the study.
Archive depth
10–20yearsHow far back into hospital archives we reach, so the data reflects everyone living with MS.
Approved for MS
15+treatmentsThey can moderately slow disability worsening, but none of them can halt it.

NHS hospitals have gathered large data sets over the past few decades, which are used for patient care but not for research to help patients. MS-PINPOINT goes back to those archives so the tools we build are exposed to the full diversity of people living with MS, including under-represented patients.

What the study uses

The scans and records hospitals already hold.

We are using electronic health records and pictures taken from brain and spinal cord (MRI scans) of people living with multiple sclerosis to predict who will respond to which treatment.

Input 01

Electronic health records

Medications, characteristics and the clinical history of people living with MS — the record of what was actually prescribed, and what happened next.

Input 02

Brain and spinal cord MRI

Ordinary clinical scans, taken as part of routine care rather than for a trial, measured at a scale no single hospital could reach on its own.

Input 03

The link between them

Linking records to images is what makes the rest possible: it connects age, ethnicity and self-reported sex to what the scan shows.

What it predicts

Who will respond to which treatment.

Computers use artificial intelligence to make sense of enormous data sets and provide personalised recommendations. Three questions matter most, and each one is answerable only at this scale.

Prognosis

The future course of MS

How MS is likely to change for one person, instead of what happens to an average patient in a trial.

Subtypes

MS types you can see

Grouping people by what their brain and spinal cord images actually show, into types that are informative of treatment effect.

Treatment

Who responds to what

Which treatment a particular person is most likely to respond to — earlier, and with fewer adverse events.

Getting this right means prescribing the right treatments sooner, delaying disability, keeping people with MS employed for longer and saving costs for the NHS.

Read the methods

Patients and the public

Anonymised inside the hospital. Simple to opt out of.

Data for research is anonymised in the hospitals, so the possibility of reidentifying people with MS is extremely low. No data from different hospitals is centralised or transferred out of the hospital setting, and every NHS number registered in the National Data Opt-Out is excluded before the data flows.

Funding and governance

Funded by the National Institute for Health and Care Research.

Funded by the National Institute for Health and Care ResearchMS-PINPOINT

The principal investigator is Dr Arman Eshaghi, a National Institute for Health and Care Research (NIHR) Advanced Fellow at University College London. He holds — or will hold — an honorary contract with the participating hospital in this research in order to access data. This study lays the basis for a future prospective clinical trial, which will consent patients to acquire data.