A flexible generative algorithm for growing in silico placentas

The placenta is crucial for a successful pregnancy, facilitating oxygen exchange and nutrient transport between mother and fetus. Complications like fetal growth restriction and pre-eclampsia are linked to placental vascular structure abnormalities, highlighting the need for early detection of placental health issues. Computational modelling offers insights into how vascular architecture correlates with flow and oxygenation in both healthy and dysfunctional placentas. These models use synthetic networks to represent the multiscale feto-placental vasculature, but current methods lack direct control over key morphological parameters like branching angles, essential for predicting placental dysfunction. We introduce a novel generative algorithm for creating in silico placentas, allowing user-controlled customisation of feto-placental vasculatures, both as individual components (placental shape, chorionic vessels, placentone) and as a complete structure. The algorithm is physiologically underpinned, following branching laws (i.e. Murray's Law), and is defined by four key morphometric statistics: vessel diameter, vessel length, branching angle and asymmetry. Our algorithm produces structures consistent with in vivo measurements and ex vivo observations. Our sensitivity analysis highlights how vessel length variations and branching angles play a pivotal role in defining the architecture of the placental vascular network. Moreover, our approach is stochastic in nature, yielding vascular structures with different topological metrics when imposing the same input settings. Unlike previous volume-filling algorithms, our approach allows direct control over key morphological parameters, generating vascular structures that closely resemble real vascular densities and allowing for the investigation of the impact of morphological parameters on placental function in upcoming studies.

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Publication Details

Journal
PLoS Computational Biology
Published
2024-10-07
DOI
https://doi.org/10.1371/journal.pcbi.1012470
Citations
2
Primary Topic
Pregnancy and preeclampsia studies
Type
article
Field-Weighted Citation Impact
1.17

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article

A flexible generative algorithm for growing in silico placentas

Rebecca J. Shipley, Daniel C. Alexander, Diana Oliveira, Paddy J. Slator et al.
2 citations
PLoS Computational Biology
Pregnancy and preeclampsia studies
1.17
article

A flexible generative algorithm for growing in silico placentas

Rebecca J. Shipley, Daniel C. Alexander, Diana Oliveira, Paddy J. Slator, Jana Hutter, Kelly Payette, Joseph V. Hajnal, Lisa Story, Hani Cheikh Sleiman
article en
2 citations

Abstract

The placenta is crucial for a successful pregnancy, facilitating oxygen exchange and nutrient transport between mother and fetus. Complications like fetal growth restriction and pre-eclampsia are linked to placental vascular structure abnormalities, highlighting the need for early detection of placental health issues. Computational modelling offers insights into how vascular architecture correlates with flow and oxygenation in both healthy and dysfunctional placentas. These models use synthetic networks to represent the multiscale feto-placental vasculature, but current methods lack direct control over key morphological parameters like branching angles, essential for predicting placental dysfunction. We introduce a novel generative algorithm for creating in silico placentas, allowing user-controlled customisation of feto-placental vasculatures, both as individual components (placental shape, chorionic vessels, placentone) and as a complete structure. The algorithm is physiologically underpinned, following branching laws (i.e. Murray's Law), and is defined by four key morphometric statistics: vessel diameter, vessel length, branching angle and asymmetry. Our algorithm produces structures consistent with in vivo measurements and ex vivo observations. Our sensitivity analysis highlights how vessel length variations and branching angles play a pivotal role in defining the architecture of the placental vascular network. Moreover, our approach is stochastic in nature, yielding vascular structures with different topological metrics when imposing the same input settings. Unlike previous volume-filling algorithms, our approach allows direct control over key morphological parameters, generating vascular structures that closely resemble real vascular densities and allowing for the investigation of the impact of morphological parameters on placental function in upcoming studies.

PLoS Computational BiologyVol. 20(10)
King's College London (GB), Universitätsklinikum Erlangen (DE), University College London (GB), Cardiff University (GB)
Wellcome Trust, UK Research and Innovation, Cancer Research UK, National Institute for Health and Care Research, Deutsche Forschungsgemeinschaft, University College London Hospitals NHS Foundation Trust, Engineering and Physical Sciences Research Council, UCLH Biomedical Research Centre, Centre For Medical Engineering, King’s College London
Good health and well-being
Openalex Percentile: Top 19%
Pregnancy and preeclampsia studies
1.17
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