Evidence map›Paper›PMID 16093514›Full record

ReviewAnnals of the New York Academy of Sciences2005

Multiscale modeling of cardiac cellular energetics.

James B Bassingthwaighte, Howard J Chizeck, Les E Atlas, Hong Qian

Open access · greenAbstract readReview
In one paragraph

Review in Annals of the New York Academy of Sciences, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 29% of its field
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

7 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Multi-scale modeling in biology: how to bridge the gaps between scales?Progress in biophysics and molecular biology · 2011
    Review
  4. Article
  5. Article
  6. Multi-scale computational modelling in biology and physiology.Progress in biophysics and molecular biology
    Review
  7. Multiscale models of angiogenesis.IEEE engineering in medicine and biology magazine : the quarterly magazine of the Engineering in Medicine & Biology Society
    Review
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

4 authors at 1 institution in 1 country.

James B BassingthwaighteBioengineering Department, University of Washington, Box 357962, Seattle, WA 98195-7962, USA. jbb@bioeng.washington.edu
Howard J Chizeck
Les E Atlas
Hong Qian
University of Washington · US

Funding

3D IMAGING &COMPUTER MODEL OF THE RESPIRATORY TRACTR01HL073598 · NHLBI · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI CORLEY, RICHARD A · 2004 to 2014
$17.6M
Simulation Resource in Circulatory Mass TransportR01EB001973 · NIBIB · UNIVERSITY OF WASHINGTON · PI BASSINGTHWAIGHTE, JAMES B · 2003 to 2006
$1.8M
NHLBI NIH HHS HL 073598-1NHLBI NIH HHS R01 HL073598NIBIB NIH HHS EB 1973-24NIBIB NIH HHS R01 EB001973
6 · The paper itself

Abstract

Multiscale modeling is essential to integrating knowledge of human physiology starting from genomics, molecular biology, and the environment through the levels of cells, tissues, and organs all the way to integrated systems behavior. The lowest levels concern biophysical and biochemical events. The higher levels of organization in tissues, organs, and organism are complex, representing the dynamically varying behavior of billions of cells interacting together. Models integrating cellular events into tissue and organ behavior are forced to resort to simplifications to minimize computational complexity, thus reducing the model's ability to respond correctly to dynamic changes in external conditions. Adjustments at protein and gene regulatory levels shortchange the simplified higher-level representations. Our cell primitive is composed of a set of subcellular modules, each defining an intracellular function (action potential, tricarboxylic acid cycle, oxidative phosphorylation, glycolysis, calcium cycling, contraction, etc.), composing what we call the "eternal cell," which assumes that there is neither proteolysis nor protein synthesis. Within the modules are elements describing each particular component (i.e., enzymatic reactions of assorted types, transporters, ionic channels, binding sites, etc.). Cell subregions are stirred tanks, linked by diffusional or transporter-mediated exchange. The modeling uses ordinary differential equations rather than stochastic or partial differential equations. This basic model is regarded as a primitive upon which to build models encompassing gene regulation, signaling, and long-term adaptations in structure and function. During simulation, simpler forms of the model are used, when possible, to reduce computation. However, when this results in error, the more complex and detailed modules and elements need to be employed to improve model realism. The processes of error recognition and of mapping between different levels of model form complexity are challenging but are essential for successful modeling of large-scale systems in reasonable time. Currently there is to this end no established methodology from computational sciences.

Indexed as

Computer SimulationEnergy MetabolismModels, CardiovascularAlgorithmsAnimalsExerciseHumansMyocardiumReproducibility of Results

Identifiers

PMID16093514
PMCPMC2864600
OpenAlexW1983402806

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.