Evidence map›Paper›PMID 31237876›Full record

ArticlePLoS computational biology2019

A new framework for assessing subject-specific whole brain circulation and perfusion using MRI-based measurements and a multi-scale continuous flow model.

Erlend Hodneland, Erik Hanson, Ove Sævareid, Geir Nævdal, Arvid Lundervold, Veronika Šoltészová, Antonella Z Munthe-Kaas, Andreas Deistung, Jürgen R Reichenbach, Jan M Nordbotten

Abstract read
In one paragraph

Article in PLoS computational biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
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  8. Frontiers in neurology · 2020
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Erlend HodnelandNorwegian Research Centre, Bergen, Norway.ORCID 0000-0003-2828-1521
Erik HansonDepartment of Mathematics, University of Bergen, Bergen, Norway.
Ove SævareidNorwegian Research Centre, Bergen, Norway.
Geir NævdalNorwegian Research Centre, Bergen, Norway.ORCID 0000-0003-2497-198X
Arvid LundervoldMohn Medical Imaging and Visualization Centre, Department of Radiology, Haukeland Universitetssykehus, Bergen, Norway.
Veronika ŠoltészováNorwegian Research Centre, Bergen, Norway.
Antonella Z Munthe-KaasMohn Medical Imaging and Visualization Centre, Department of Radiology, Haukeland Universitetssykehus, Bergen, Norway.
Andreas DeistungMedical Physics Group, Institute of Diagnostic and Interventional Radiology, Jena University Hospital - Friedrich Schiller University Jena, Germany.
Jürgen R ReichenbachMedical Physics Group, Institute of Diagnostic and Interventional Radiology, Jena University Hospital - Friedrich Schiller University Jena, Germany.
Jan M NordbottenDepartment of Mathematics, University of Bergen, Bergen, Norway.ORCID 0000-0003-1455-5704

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A large variety of severe medical conditions involve alterations in microvascular circulation. Hence, measurements or simulation of circulation and perfusion has considerable clinical value and can be used for diagnostics, evaluation of treatment efficacy, and for surgical planning. However, the accuracy of traditional tracer kinetic one-compartment models is limited due to scale dependency. As a remedy, we propose a scale invariant mathematical framework for simulating whole brain perfusion. The suggested framework is based on a segmentation of anatomical geometry down to imaging voxel resolution. Large vessels in the arterial and venous network are identified from time-of-flight (ToF) and quantitative susceptibility mapping (QSM). Macro-scale flow in the large-vessel-network is accurately modelled using the Hagen-Poiseuille equation, whereas capillary flow is treated as two-compartment porous media flow. Macro-scale flow is coupled with micro-scale flow by a spatially distributing support function in the terminal endings. Perfusion is defined as the transition of fluid from the arterial to the venous compartment. We demonstrate a whole brain simulation of tracer propagation on a realistic geometric model of the human brain, where the model comprises distinct areas of grey and white matter, as well as large vessels in the arterial and venous vascular network. Our proposed framework is an accurate and viable alternative to traditional compartment models, with high relevance for simulation of brain perfusion and also for restoration of field parameters in clinical brain perfusion applications.

Indexed as

BrainModels, CardiovascularAdultAlgorithmsCerebrovascular CirculationComputational BiologyComputer SimulationHumansMagnetic Resonance ImagingMalePerfusion

Identifiers

PMID31237876
PMCPMC6613711

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Registered trials

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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.