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Deformable brain templates are an important tool in many neuroimaging analyses. Conditional templates (e.g., age-specific templates) have advantages over single population templates by enabling improved registration accuracy and capturing common processes in brain development and degeneration. Conventional methods require large, evenly spread cohorts to develop conditional templates, limiting their ability to create templates that could reflect richer combinations of clinical and demographic variables. More recent deep-learning methods, which can infer relationships in very high-dimensional spaces, open up the possibility of producing conditional templates that are jointly optimised for these richer sets of conditioning parameters. We have built on recent deep-learning template generation approaches using a diffeomorphic (topology-preserving) framework to create a purely geometric method of conditional template construction that learns diffeomorphisms between: (i) a global or group template and conditional templates, and (ii) conditional templates and individual brain scans. We evaluated our method, as well as other recent deep-learning approaches, on a data set of cognitively normal (CN) participants from the Alzheimer's Disease Neuroimaging Initiative (ADNI), using age as the conditioning parameter of interest. We assessed the effectiveness of these networks at capturing age-dependent anatomical differences. Our results demonstrate that while the assessed deep-learning methods have a number of strengths, they require further refinement to capture morphological changes in ageing brains with an acceptable degree of accuracy. The volumetric output of our method, and other recent deep-learning approaches, across four brain structures (grey matter, white matter, the lateral ventricles and the hippocampus), was measured and showed that although each of the methods captured some changes well, each method was unable to accurately track changes in all of the volumes. However, as our method is purely geometric, it was able to produce T1-weighted conditional templates with high spatial fidelity and with consistent topology as age varies, making these conditional templates advantageous for spatial registrations. The use of diffeomorphisms in these deep-learning methods represents an important strength of these approaches, as they can produce conditional templates that can be explicitly linked, geometrically, across age as well as to fixed, unconditional templates or brain atlases. The use of deep learning in conditional template generation provides a framework for creating templates for more complex sets of conditioning parameters, such as pathologies and demographic variables, in order to facilitate a broader application of conditional brain templates in neuroimaging studies. This can aid researchers and clinicians in their understanding of how brain structure changes over time and under various interventions, with the ultimate goal of improving the calibration of treatments and interventions in personalised medicine. The code to implement our conditional brain template network is available at: github.com/lwhitbread/deep-diff.
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http://dx.doi.org/10.1002/hbm.70229 | DOI Listing |
Commun Biol
May 2025
Xianghu Laboratory, Zhejiang Academy of Agricultural Sciences, Hangzhou, 310021, China.
The rapid advancement of artificial intelligence (AI) has enabled de novo design of functional proteins, circumventing the reliance on natural templates or sequencing databases. However, current protein design models are ineffective in generating proteins without stable structures, such as antimicrobial peptides (AMPs), which are short and structurally flexible yet play critical biological roles. To address this challenge, we present AMPGen, an evolutionary information-reserved and diffusion-driven generative model for de novo design of target-specific AMPs.
View Article and Find Full Text PDFHum Brain Mapp
June 2025
Australian Institute for Machine Learning (AIML), The University of Adelaide, Adelaide, Australia.
Deformable brain templates are an important tool in many neuroimaging analyses. Conditional templates (e.g.
View Article and Find Full Text PDFbioRxiv
March 2025
Department of Global Health, University of Washington, Seattle, WA, USA.
Unlabelled: The malaria parasite has a complex lifecycle involving various host cell environments in both human and mosquito hosts. The parasite must tightly regulate gene expression at each stage in order to adapt to its current environment while continuing development. However, it is challenging to study gene function and regulation of essential genes across the parasite's multi-host lifecycle.
View Article and Find Full Text PDFNephrol Dial Transplant
March 2025
Department of Pediatric Nephrology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Background And Hypothesis: In search for controlled access to expensive innovative orphan drugs, a national access route called "Orphan Drug Access Protocol" (ODAP) was developed and piloted with lumasiran, a new drug for patients with primary hyperoxaluria type 1 (PH1). Here, we present a two-year evaluation of this pilot study.
Methods: Specialists from the Dutch PH1 Expert Centre and the national ODAP steering group developed a protocol for controlled and conditional treatment of children and adults with PH1 with lumasiran.