TY - JOUR
T1 - Processus à haut degré d'intégration pour l’étude de troubles cardiovasculaires
T2 - exemples de médecine de précision appliquée à la maladie d'Alzheimer et à la dissection aortique
AU - Vardakis, J. C.
AU - Bonfanti, M.
AU - Franzetti, G.
AU - Guo, L.
AU - Lassila, T.
AU - Mitolo, M.
AU - Hoz de Vila, M.
AU - Greenwood, J. P.
AU - Maritati, G.
AU - Chou, Danny
AU - Taylor, Z. A.
AU - Venneri, A.
AU - Homer-Vanniasinkam, S.
AU - Balabani, S.
AU - Frangi, A. F.
AU - Ventikos, Y.
AU - Diaz-Zuccarini, V.
N1 - Funding Information:
The consolidated pipeline allied to the Alzheimer's Disease study was supported by the European Commission FP7 project VPH-DARE@IT (FP7-ICT-2011-9-601055) , and partially by the EPSRC-funded projects OCEAN (EP/M006328/1) and EPSRC-NIHR HTC Partnership Award ‘Plus’: Medical Image Analysis Network (EP/N026993/1) . MB is supported by the European Union's Horizon 2020 research and innovation programme (Marie Sklodowska-Curie GA No. 642612, http://www.vph-case.eu) ; MB and VDZ are supported by the Wellcome/EPSRC Centre for Interventional and Surgical Sciences (WEISS) (203145Z/16/Z) ; VDZ is supported by the Leverhulme Trust (Senior Research Fellowship No. RF-2015-482) .
Funding Information:
The consolidated pipeline allied to the Alzheimer's Disease study was supported by the European Commission FP7 project VPH-DARE@IT (FP7-ICT-2011-9-601055), and partially by the EPSRC-funded projects OCEAN (EP/M006328/1) and EPSRC-NIHR HTC Partnership Award ‘Plus’: Medical Image Analysis Network (EP/N026993/1). MB is supported by the European Union's Horizon 2020 research and innovation programme (Marie Sklodowska-Curie GA No. 642612, http://www.vph-case.eu); MB and VDZ are supported by the Wellcome/EPSRC Centre for Interventional and Surgical Sciences (WEISS) (203145Z/16/Z); VDZ is supported by the Leverhulme Trust (Senior Research Fellowship No. RF-2015-482). This is a summary of independent research carried out at the National Institute for Health Research (NIHR) Sheffield Biomedical Research Centre (Translational Neuroscience). The views expressed are those of AV and the remaining authors, and not necessarily those of the NIHR or the Department of Health.
Publisher Copyright:
© 2019 Elsevier Masson SAS
PY - 2019/12
Y1 - 2019/12
N2 - For precision medicine to be implemented through the lens of in silico technology, it is imperative that biophysical research workflows offer insight into treatments that are specific to a particular illness and to a particular subject. The boundaries of precision medicine can be extended using multiscale, biophysics-centred workflows that consider the fundamental underpinnings of the constituents of cells and tissues and their dynamic environments. Utilising numerical techniques that can capture the broad spectrum of biological flows within complex, deformable and permeable organs and tissues is of paramount importance when considering the core prerequisites of any state-of-the-art precision medicine pipeline. In this work, a succinct breakdown of two precision medicine pipelines developed within two Virtual Physiological Human (VPH) projects are given. The first workflow is targeted on the trajectory of Alzheimer's Disease, and caters for novel hypothesis testing through a multicompartmental poroelastic model which is integrated with a high throughput imaging workflow and subject-specific blood flow variability model. The second workflow gives rise to the patient specific exploration of Aortic Dissections via a multi-scale and compliant model, harnessing imaging, computational fluid-dynamics (CFD) and dynamic boundary conditions. Results relating to the first workflow include some core outputs of the multiporoelastic modelling framework, and the representation of peri-arterial swelling and peri-venous drainage solution fields. The latter solution fields were statistically analysed for a cohort of thirty-five subjects (stratified with respect to disease status, gender and activity level). The second workflow allowed for a better understanding of complex aortic dissection cases utilising both a rigid-wall model informed by minimal and clinically common datasets as well as a moving-wall model informed by rich datasets.
AB - For precision medicine to be implemented through the lens of in silico technology, it is imperative that biophysical research workflows offer insight into treatments that are specific to a particular illness and to a particular subject. The boundaries of precision medicine can be extended using multiscale, biophysics-centred workflows that consider the fundamental underpinnings of the constituents of cells and tissues and their dynamic environments. Utilising numerical techniques that can capture the broad spectrum of biological flows within complex, deformable and permeable organs and tissues is of paramount importance when considering the core prerequisites of any state-of-the-art precision medicine pipeline. In this work, a succinct breakdown of two precision medicine pipelines developed within two Virtual Physiological Human (VPH) projects are given. The first workflow is targeted on the trajectory of Alzheimer's Disease, and caters for novel hypothesis testing through a multicompartmental poroelastic model which is integrated with a high throughput imaging workflow and subject-specific blood flow variability model. The second workflow gives rise to the patient specific exploration of Aortic Dissections via a multi-scale and compliant model, harnessing imaging, computational fluid-dynamics (CFD) and dynamic boundary conditions. Results relating to the first workflow include some core outputs of the multiporoelastic modelling framework, and the representation of peri-arterial swelling and peri-venous drainage solution fields. The latter solution fields were statistically analysed for a cohort of thirty-five subjects (stratified with respect to disease status, gender and activity level). The second workflow allowed for a better understanding of complex aortic dissection cases utilising both a rigid-wall model informed by minimal and clinically common datasets as well as a moving-wall model informed by rich datasets.
KW - Alzheimer's Disease
KW - Aortic Dissection
KW - Computational Fluid Dynamics
KW - Dementia
KW - Glymphatic system
KW - Haemodynamics
KW - Multiple-Network Poroelastic Theory
KW - Virtual Physiological Human (VPH)
UR - https://www.scopus.com/pages/publications/85075788327
U2 - 10.1016/j.morpho.2019.10.045
DO - 10.1016/j.morpho.2019.10.045
M3 - Article
C2 - 31786098
AN - SCOPUS:85075788327
SN - 1286-0115
VL - 103
SP - 148
EP - 160
JO - Morphologie
JF - Morphologie
IS - 343
ER -