Active Brain & Nervous System Psychology & Behaviour

Biophysical Signal Prediction for Translation of Population Neuroimaging

In plain English

AI plain-English summary

A hospital MRI scanner and a UK Biobank research scanner produce images that cannot be directly compared, even of the same person. This fellowship aims to fix that mismatch. The problem is one of translation. Population-level brain imaging resources, such as UK Biobank, now contain detailed scans from hundreds of thousands of people, linked to their health records. These scans can reveal how an individual’s brain deviates from normal, potentially flagging early signs of disease. But the cutting-edge technology and protocols used in these research studies do not match the compromised, real-world equipment and faster protocols used in hospital scanners. Clinicians cannot currently apply population-level insights to individual patient scans. This project will build a biophysical framework that links the underlying biology of brain tissue to the physics of the imaging measurement. The researcher will identify which biological changes drive the variations seen in UK Biobank scans, then design new hospital-grade imaging sequences that are sensitive to the same biological signals. Finally, the team will create a harmonisation method that allows direct comparison between new clinical data and existing population norms. If successful, a routine hospital scan could be compared against a vast reference database, giving radiologists a quantitative, biologically grounded readout of whether a patient’s brain tissue is abnormal—without needing to upgrade every hospital scanner.

View original technical description
The past decade has seen the emergence of population-level brain imaging. For the first time, imaging can provide a rich, multi-faceted description of how an individual’s brain deviates from population norms, potentially informing about early pathology or susceptibility to disease. Studies with access to health records, like UK Biobank, enable that link to be explicitly identified. However, the imaging in these new population-health resources, which use cutting-edge imaging technology, does not match hospital-based patient imaging in the real world, which incurs compromises in technologies and protocols. We aim to address the deep challenges of information translation that currently prevent clinical imaging from taking advantage of population-level health data resources. This fellowship proposes to develop a biophysical approach to such translation. That is, linking the relevant biology to the physics of the imaging measurement. Core to this approach is a biophysical framework for phenotype prediction (WP1), which will enable us to: (i) identify and validate the biological source of variations in UKB-derived imaging markers (WP2) (ii) design new imaging acquisitions that are maximally sensitive to the same biological information as UKB imaging (WP3) (iii) establish biophysically-valid harmonisation to enable direct comparison of newly-acquired data with UKB imaging phenotypes (WP4)

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Researchers

Karla Miller (EPMC Awardee)

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Original classification

Senior Research Fellowship Renewal

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