Abstract
Most diffusion magnetic resonance imaging studies of disease rely on statistical comparisons between large groups of patients and healthy participants to infer altered tissue states in the brain; however, clinical heterogeneity can greatly challenge their discriminative power. There is currently an unmet need to move away from the current approach of group-wise comparisons to methods with the sensitivity to detect altered tissue states at the individual level. This would ultimately enable the early detection and interpretation of microstructural abnormalities in individual patients, an important step towards personalized medicine in translational imaging. To this end, Detect was developed to advance diffusion magnetic resonance imaging tractometry towards single-patient analysis. By operating on the manifold of white-matter pathways and learning normative microstructural features, our framework captures idiosyncrasies in patterns along white-matter pathways. Our approach paves the way from traditional group-based comparisons to true personalized radiology, taking microstructural imaging from the bench to the bedside.
| Original language | English |
|---|---|
| Pages (from-to) | 598-606 |
| Number of pages | 9 |
| Journal | Nature Computational Science |
| Volume | 1 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - Sept 2021 |
| Externally published | Yes |
Bibliographical note
Funding Information:This work was supported by a Wellcome Trust Investigator Award (grant no. 096646/Z/11/Z), a Wellcome Trust Strategic Award (grant no. 104943/Z/14/Z), and an EPSRC equipment grant (no. EP/M029778/1) to D.K.J., a Sir Henry Wellcome Fellowship (grant no. 215944/Z/19/Z) and VENI grant (no. 17331) from the Dutch Research Council (NWO) to C.M.W.T., a Wellcome Trust GW4-CAT Fellowship (grant no. 220537/Z/20/Z) to D.S., a Wellcome Trust Fellowship (grant no. 102003/Z/13/Z) to J.D. and an NIH NICDH fellowship (grant no. 1F32HD103313-01) to EPR. This study is also supported by the Brain Repair and Intracranial Neurotherapeutics (BRAIN) Unit, funded by Welsh Government through Health and Care Research Wales. M.C. was in part supported by the Radboud Excellence Initiative Fellowship. The authors thank M. Descoteaux and J.-C. Houde (Sherbrooke Connectivity Imaging Laboratory) for their useful discussions and code sharing.
Funding
This work was supported by a Wellcome Trust Investigator Award (grant no. 096646/Z/11/Z), a Wellcome Trust Strategic Award (grant no. 104943/Z/14/Z), and an EPSRC equipment grant (no. EP/M029778/1) to D.K.J., a Sir Henry Wellcome Fellowship (grant no. 215944/Z/19/Z) and VENI grant (no. 17331) from the Dutch Research Council (NWO) to C.M.W.T., a Wellcome Trust GW4-CAT Fellowship (grant no. 220537/Z/20/Z) to D.S., a Wellcome Trust Fellowship (grant no. 102003/Z/13/Z) to J.D. and an NIH NICDH fellowship (grant no. 1F32HD103313-01) to EPR. This study is also supported by the Brain Repair and Intracranial Neurotherapeutics (BRAIN) Unit, funded by Welsh Government through Health and Care Research Wales. M.C. was in part supported by the Radboud Excellence Initiative Fellowship. The authors thank M. Descoteaux and J.-C. Houde (Sherbrooke Connectivity Imaging Laboratory) for their useful discussions and code sharing. This work was supported by a Wellcome Trust Investigator Award (grant no. 096646/Z/11/Z), a Wellcome Trust Strategic Award (grant no. 104943/Z/14/Z), and an EPSRC equipment grant (no. EP/M029778/1) to D.K.J., a Sir Henry Wellcome Fellowship (grant no. 215944/Z/19/Z) and VENI grant (no. 17331) from the Dutch Research Council (NWO) to C.M.W.T., a Wellcome Trust GW4-CAT Fellowship (grant no. 220537/Z/20/Z) to D.S., a Wellcome Trust Fellowship (grant no. 102003/Z/13/Z) to J.D. and an NIH NICDH fellowship (grant no. 1F32HD103313-01) to EPR. This study is also supported by the Brain Repair and Intracranial Neurotherapeutics (BRAIN) Unit, funded by Welsh Government through Health and Care Research Wales. M.C. was in part supported by the Radboud Excellence Initiative Fellowship. The authors thank M. Descoteaux and J.-C. Houde (Sherbrooke Connectivity Imaging Laboratory) for their useful discussions and code sharing.
| Funders | Funder number |
|---|---|
| National Institutes of Health | 1F32HD103313-01 |
| Wellcome Trust | 096646/Z/11/Z, 104943/Z/14/Z |
| Engineering and Physical Sciences Research Council | 215944/Z/19/Z, EP/M029778/1, 17331 |
| Nederlandse Organisatie voor Wetenschappelijk Onderzoek | 102003/Z/13/Z, 220537/Z/20/Z |
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