Evidence map›Paper›PMID 37000171›Full record

ArticleThe Journal of general physiology2023

Machine learning meets Monte Carlo methods for models of muscle's molecular machinery to classify mutations.

Anthony Asencio, Sage Malingen, Kristina B Kooiker, Joseph D Powers, Jennifer Davis, Thomas Daniel, Farid Moussavi-Harami

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of general physiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. How can AI accelerate advances in physiology?The Journal of general physiology · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Anthony AsencioDepartment of Biology, University of Washington , Seattle, WA, USA.ORCID 0000-0002-8147-0180
Sage MalingenDepartment of Bioengineering, University of Washington , Seattle, WA, USA.ORCID 0000-0003-0407-0498
Kristina B KooikerDivision of Cardiology, University of Washington , Seattle, WA, USA.ORCID 0000-0003-1817-9080
Joseph D PowersDepartment of Bioengineering, University of California, San Diego , San Diego, CA, USA.ORCID 0000-0001-7841-2337
Jennifer DavisDepartment of Bioengineering, University of Washington , Seattle, WA, USA.ORCID 0000-0003-2380-1321
Thomas DanielDepartment of Biology, University of Washington , Seattle, WA, USA.ORCID 0000-0002-5706-1096
Farid Moussavi-HaramiDivision of Cardiology, University of Washington , Seattle, WA, USA.ORCID 0000-0002-0189-7214
University of Washington · USUniversity of California San Diego · US

Funding

UW Center for Translational Muscle Research (Overall Application)P30AR074990 · NIAMS · UNIVERSITY OF WASHINGTON · PI Jennifer Michelle Davis, DANIEL RAFTERY · 2019 to 2026
$7.5M
Integrating Transcriptome Reprogramming Into Cardiac Plasticity Regulatory MechanismsR01HL141187 · NHLBI · UNIVERSITY OF WASHINGTON · PI Jennifer Michelle Davis · 2018 to 2026
$4.0M
Uncovering The Mechanogenomic Basis For Cardiac PlasticityR01HL142624 · NHLBI · UNIVERSITY OF WASHINGTON · PI Jennifer Michelle Davis · 2018 to 2026
$3.8M
Experimental and Computational Studies in Genetic CardiomyopathiesR01HL157169 · NHLBI · UNIVERSITY OF WASHINGTON · PI Farid Moussavi-Harami · 2022 to 2026
$3.3M
Regulators of Myofibroblast State Stability & Fibrotic Responsiveness of the HeartR01HL162229 · NHLBI · UNIVERSITY OF WASHINGTON · PI DAVIS, JENNIFER MICHELLE · 2022 to 2025
$2.5M
NHLBI NIH HHS R01 HL141187NHLBI NIH HHS R01 HL142624NHLBI NIH HHS R01 HL157169NHLBI NIH HHS R01 HL162229NIAMS NIH HHS P30 AR074990
6 · The paper itself

Abstract

The timing and magnitude of force generation by a muscle depend on complex interactions in a compliant, contractile filament lattice. Perturbations in these interactions can result in cardiac muscle diseases. In this study, we address the fundamental challenge of connecting the temporal features of cardiac twitches to underlying rate constants and their perturbations associated with genetic cardiomyopathies. Current state-of-the-art metrics for characterizing the mechanical consequence of cardiac muscle disease do not utilize information embedded in the complete time course of twitch force. We pair dimension reduction techniques and machine learning methods to classify underlying perturbations that shape the timing of twitch force. To do this, we created a large twitch dataset using a spatially explicit Monte Carlo model of muscle contraction. Uniquely, we modified the rate constants of this model in line with mouse models of cardiac muscle disease and varied mutation penetrance. Ultimately, the results of this study show that machine learning models combined with biologically informed dimension reduction techniques can yield excellent classification accuracy of underlying muscle perturbations.

Indexed as

Muscle ContractionMuscle, SkeletalAnimalsMiceMutation

Identifiers

PMID37000171
PMCPMC10067704
OpenAlexW4362194813

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.