Two men in a computer hall.

Mika Gustafsson, professor, and David Martínez, PhD student at Linköping University.

Artificial intelligence, AI, which finds patterns in complex biological data could eventually contribute to the development of individually tailored healthcare. Researchers at Linköping University in Sweden have developed an AI-based method applicable to various medical and biological issues. Their models can for instance accurately estimate people’s chronological age and determine whether they have been smokers or not.

There are many factors that can affect which out of all our genes are used at any given point in time. Smoking, dietary habits and environmental pollution are some such factors. This regulation of gene activity can be likened to a power switch determining which genes are switched on or off, witout altering the actual genes, and is called epigenetics.

Researchers at Linköping University (LiU) have used data with epigenetic information from more than 75,000 human samples to train a large number of AI neural network models. They hope that such AI-based models could eventually be used in precision medicine to develop treatments and preventive strategies tailored to the individual. Their models are of the autoencoder type, that self-organises the information and finds interrelation patterns in the large amount of data.

To test their model, the LiU researchers compared it with existing models. There are already existing models of the effects of smoking on the body, building on the fact that specific epigenetic changes reflect the effect of smoking on the functioning of the lungs. These traces remain in the DNA long after a person has quit smoking, and this type of model can identify whether someone is a current, former or never smoker. Other models can, based on epigenetic markers, estimate the chronological age of an individual, or group individuals according to whether they have a disease or are healthy.

The LiU researchers trained their autoencoder and then used the result to answer three different queries: age determination, smoker status and diagnosing the disease systemic lupus erythematosus, SLE. Although the existing models rely on selected epigenetic markers known to be associated with the condition they aim to classify. However, it turned out that the LiU researchers’ autoencoders functioned better or equally well.

‚ÄúOur models not only enable us to classify individuals based on their epigenetic data. We found that our models can identify previously known epigenetic markers used in other models, but also new markers associated with the condition we‚Äôre examining. One example of this is that our model for smoking identifies markers associated with respiratory diseases, such as lung cancer, and DNA damage,‚ÄĚ says David Mart√≠nez, PhD student at Link√∂ping University.

The objective of the autoencoder models is to enable compression of extremely complex biological data into a representation of the most relevant characteristics and patterns in data.

‚ÄúWe didn‚Äôt steer the model and had no hypotheses based on existing biological knowledge, but let the data speak for itself. When subsequently looking at what was happening in the autoencoder, we saw that data self-organised in a way similar to how it works in the body,‚ÄĚ says Mika Gustafsson, professor of translational bioinformatics at Link√∂ping University, who led the study now published in Briefings in Bioinformatics.

In the next step, the researchers can use the most important characteristics found by the autoencoder to create models able to classify for a large amount of environment-related, individual-specific factors where there is not enough training data to train more complex AI models on.

Certain types of AI are sometimes likened to a black box that provides answers, but humans cannot see how the AI arrived at the answer. Mika Gustafsson and his colleagues however strive to create interpretable AI models that, so to speak, let the researchers peek under the lid of the ‚Äúblack box‚ÄĚ to understand what is going on inside.

‚ÄúWe want to be able to understand what the model shows us about the biology behind disease and other conditions. Then we‚Äôll see not only whether someone is ill or not, but, by interpreting data, we‚Äôll also have a chance to learn why,‚ÄĚ says Mika Gustafsson.

This research was funded by, among others, the Swedish Research Council, the Wallenberg AI, Autonomous Systems and Software Program (WASP) and the SciLifeLab & Wallenberg National Program for Data-Driven Life Science (DDLS).

 Article: NCAE: data-driven representations using a deep network-coherent DNA methylation autoencoder identify robust disease and risk factor signatures, David Martínez-Enguita, Sanjiv K. Dwivedi, Rebecka Jörnsten and Mika Gustafsson, (2023), Briefings in Bioinformatics, published online 16 August 2023, doi: https://doi.org/10.1093/bib/bbad293

 

For more information, please contact:

Mika Gustafsson, professor, mika.gustafsson@liu.se, +46 13 282138

David Martínez, doctoral student, david.martinez@liu.se, +46 13 282931

Karin Söderlund Leifler, press information officer, karin.soderlund.leifler@liu.se, +46 13 28 13 95

High-resolution press photos of the researchers can be downloaded from Linköping University media library.

Karin Söderlund Leifler

Press information officer
+46 13 28 13 95
Karin.soderlund.leifler@liu.se

Mika Gustafsson och David Martinez -2023-LiU-low Mika Gustafsson, professor, och David Martínez, doktorand vid Linköpings universitet. / Mika Gustafsson, professor, and David Martínez, PhD student at Linköping University.