Evidence map›Paper›PMID 41874390›Full record

ArticleThe Journal of physiology2026

A constitutive modelling framework for applications to in vivo longitudinal data: Evaluation in a 60-day head-down bed rest study on arterial function.

Alessandro Giudici, Karen Barchetti, Umit Gencer, Hakim Khettab, Elie Mousseaux, Carole Leguy, Tammo Delhaas, Rosa Maria Bruno, Bart Spronck, Pierre Boutouyrie

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Article in The Journal of physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Alessandro GiudiciDepartment of Biomedical Engineering, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, The Netherlands.
Karen BarchettiUniversité Paris Cité, INSERM U970, Paris Cardiovascular Research Centre - PARCC, Paris, France.
Umit GencerUniversité Paris Cité, INSERM U970, Paris Cardiovascular Research Centre - PARCC, Paris, France.
Hakim KhettabUniversité Paris Cité, INSERM U970, Paris Cardiovascular Research Centre - PARCC, Paris, France.
Elie MousseauxUniversité Paris Cité, INSERM U970, Paris Cardiovascular Research Centre - PARCC, Paris, France.
Carole LeguyDepartment of Cardiovascular Engineering, Institute of Applied Medical Engineering, Helmholtz Institute, Medical Faculty, RWTH Aachen University, Aachen, Germany.
Tammo DelhaasDepartment of Biomedical Engineering, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, The Netherlands.
Rosa Maria BrunoUniversité Paris Cité, INSERM U970, Paris Cardiovascular Research Centre - PARCC, Paris, France.
Bart SpronckDepartment of Biomedical Engineering, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, The Netherlands.
Pierre BoutouyrieUniversité Paris Cité, INSERM U970, Paris Cardiovascular Research Centre - PARCC, Paris, France.

Funding

European Union's Horizon Europe Research and Innovation Programme (AG, BS, RMB, and PB) 101136728French Centre d'Etudes Spatiales (CNES) NCT03594799Short Term Scientific Mission grant of the European Union COST Action VascAgeNet (Network for Research in Vascular Ageing) to AG 18216
6 · The paper itself

Abstract

Vascular cells continuously remodel the arterial wall (micro)structure in response to changes in their biomechanical/biochemical environment. Although the functional effects of arterial remodelling can be easily measured, assessing the underlying microstructural mechanisms is complex in vivo. Constitutive modelling is a computational technique that allows for linking whole-organ function to tissue constituent-level mechanics. However, the need for comprehensive biomechanical data for model parametrisation hampers its clinical applicability. In the present study, we propose a novel constitutive modelling framework that addresses this limitation by leveraging longitudinal acquisitions of pressure-diameter relationships at different arterial beds to aid model parametrisation. We applied our constitutive framework to data from a study on the effect of 60 days head-down bed rest (HDBR) on arterial function, where pressure-diameter relationships of three arteries (carotid, femoral and popliteal) were measured at baseline, during HDBR (two time points) and during a 30-day recovery (two time points). We modelled the arterial wall as a constrained mixture of elastin, collagen and vascular smooth muscle cells (VSMCs). The dimensionality of the parameterisation problem was reduced through assumptions on (i) the time evolution of the behaviour of individual constituents and (ii) consistency in intrinsic constituent mechanical properties across different arterial beds. Overall, the proposed framework captured well the in vivo data (R

Indexed as

ArteriesBed RestHead-Down TiltModels, CardiovascularAdultCarotid ArteriesCollagenFemaleFemoral ArteryHumansLongitudinal StudiesMaleMuscle, Smooth, VascularPopliteal ArteryVascular RemodelingCollagenarterial biomechanical homeostasisarterial computational constitutive modellingarterial remodellingarterial stiffnesshead‐down bed rest

Identifiers

PMID41874390
PMCPMC13628561

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.