Colour-Coded Reaction-Time Images Predict Multiple Sclerosis Disability Progression Better Than Summary Scores

A picture built from how fast someone presses a screen
Each participant's repeated reaction-time results became a colour image used to estimate disability risk.
Mark

Why turn reaction times into pictures at all?

Mimi

Because summaries like an average throw away the shape of the data. Each person's image keeps every month and every response, so the model can see patterns over time.

Mark

What are the colours doing?

Mimi

Red, green and blue each stand for one task: simple reaction, attention and working memory. Each row of pixels is one month.

Luke

And the result? How much better is better?

Mimi

The paper says it outperformed summary-based methods. The material I have doesn't give the figures.

Luke

Then I'd hold the claim loosely. We know the direction, not the size.

Mark

Who was in the study?

Mimi

746 people with relapsing-remitting MS from four Australian clinics, recruited from 2016 to 2019, tested about every six months, with optional home tests.

Luke

That's one country's clinics and one MS type. Whether it works elsewhere isn't established here.

Mark

Does the funding matter?

Mimi

It's disclosed in detail. Biogen and Novartis part-funded the original cohort, but the authors say the funders played no role in this analysis.

Luke

Fair, though it's worth knowing. And the claims about trial selection and earlier review are possibilities the authors raise, not things they showed.

  • A string of short, low-burden screen tests, some taken at home, is quietly tracking how quickly people with MS respond, and those patterns are flagging who may be heading toward worsening disability.
  • Researchers found that summary scores were throwing away useful signal, so they rebuilt each participant's testing history into colored images and let a transformer-based AI read the patterns.
  • Across 746 participants from four Australian MS clinics, the image-based approach predicted confirmed disability progression better than the conventional summary measures.
  • The result could mean earlier clinical review and sharper selection of people for trials, but the method must still be validated beyond this cohort before it reaches routine care.

In a quiet way, the body's slow changes often arrive before anyone can name them, and this study asks whether the speed of a fingertip on a screen can tell us what the nerves are about to do. Across four Australian clinics, 746 people with relapsing-remitting multiple sclerosis tapped and responded to simple tasks again and again, and a team led by Chao Zhu and Xing Zhang, reporting in PLOS Digital Health, turned that long record into colored images read by an artificial intelligence. Their finding is that keeping every fragment of the record, rather than reducing it to a single average, gave a clearer sense of who would worsen over time. It is an early and careful step, still awaiting proof beyond its own cohort.

Each of the 746 people in this study ended up with a picture of their own. It was not a brain scan. It was a small image built from how quickly they pressed a screen, test after test, over months and years. The colors of that image, red, green and blue, carried a pattern that turned out to hint at whether their multiple sclerosis would worsen.

The work, published in PLOS Digital Health, comes from a team led by Chao Zhu and Xing Zhang. People with relapsing-remitting MS often show shifts in thinking speed, attention and memory well before physical disability becomes obvious. Digital tests can catch those shifts repeatedly, even at home, but they produce so much data that it is usually reduced to summary scores, and those scores can discard what matters.

Participants were recruited from four Australian MS clinics between 2016 and 2019 and used MSReactor, a web-based set of three reaction-time tasks covering psychomotor speed, attention and working memory. Each session took about five minutes. Progression was judged on the standard EDSS disability scale, confirmed at two later visits, with scores near relapses set aside to avoid mistaking a passing dip for a real change.

The key move was in how the data were handled. Results were organized by month, with one row of pixels per month and each task given its own color, and a neural network read these images to estimate each person's risk over time. Keeping the full detail from each test outperformed the summary approaches. The authors suggest this could support earlier review and better trial selection, and perhaps other forms of digital health data. The next step is testing it beyond this group of patients.

Each of the 746 people in this study ended up with a picture of their own. It was not a scan of the brain. It was a small image built from how quickly they pressed a screen, test after test, over months and years. The pixels were red, green and blue, and the pattern those colours made turned out to say something about whether their multiple sclerosis would worsen.

The work, published in PLOS Digital Health on 25 September 2026, comes from a team led by Chao Zhu and Xing Zhang, with senior contributors including Anneke van der Walt, Bruce Taylor, Mastura Monif and Tomas Kalincik. The study asks a practical question. People with relapsing-remitting MS often show changes in thinking speed, attention and memory, sometimes years before physical disability is clear. Digital tests can capture those changes repeatedly, even at home, but they generate a lot of data, and that data is usually boiled down into summary scores that can discard useful information.

The participants were recruited from four tertiary MS clinics in Australia between March 2016 and December 2019. They used MSReactor, a web-based battery of three reaction-time tasks: simple reaction time for psychomotor function, choice reaction time for attention, and a one-back task for working memory. Participants responded to on-screen stimuli as fast as they could, and the system logged speed in milliseconds along with accuracy. Each task continued until at least 30 correct responses were recorded, and a full session typically took about five minutes.

Testing happened at clinic visits roughly every six months, on iPads supplied by each site. Participants could also test at home on their own tablet or computer, as often as they liked, with monthly testing suggested. People with upper-limb, visual or cognitive deficits that prevented touchscreen use were excluded, as were those who completed fewer than three tests or were enrolled for less than 180 days.

The outcome the researchers tried to predict was confirmed disability progression on the EDSS, the standard clinical disability scale. The size of the required increase depended on the starting score, and it had to be confirmed at two later assessments at least six months apart. To avoid mistaking a temporary dip for a baseline, they excluded EDSS scores recorded within 30 days of a relapse.

The core innovation is how the test data were handled. The team organised each person's results by month, keeping only the last test if there were several in one month and carrying forward the last observation to fill gaps. They then encoded each person's history as an image. Red, green and blue stood for the three tasks. The horizontal axis held 30 responses per task, and each row of pixels represented one month. A convolutional neural network extracted features from these images, and a transformer-based survival model, which the authors call MS-TranSurv, estimated each person's risk of progression over time.

Keeping the detail from each test paid off. The approach outperformed methods that rely on summary measures of performance. The authors conclude that repeated, low-burden cognitive testing can help identify people at higher risk of worsening disability, and that this could support earlier clinical review and better selection of participants for clinical trials. They also suggest the image-based method might be adapted to other kinds of digital health data.

The disclosures are extensive. Several authors report ties to MS drug makers including Biogen, Novartis, Roche and Merck, and the original MSReactor cohort was part-funded by Biogen and Novartis Australia through unrestricted funding. The authors state that the funders had no role in this study's design, analysis or publication. Patient-level data cannot be shared publicly, though qualified researchers can request access through MSBase. The next step is validation beyond this cohort.

Repeated, low-burden cognitive testing can help identify people with MS at higher risk of worsening disability.
— Zhu et al., PLOS Digital Health (paraphrased)
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