Evidence map›Paper›PMID 36926064›Full record

ArticleFrontiers in network physiology2022

A Personalized Spring Network Representation of Emphysematous Lungs From CT Images.

Ziwen Yuan, Jacob Herrmann, Samhita Murthy, Kevin Peters, Sarah E Gerard, Hadi T Nia, Kenneth R Lutchen, Béla Suki

Open access · goldFull text read
In one paragraph

Article in Frontiers in network physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

8 authors at 2 institutions in 1 country.

Ziwen YuanDepartment of Biomedical Engineering, Boston University, Boston, MA, United States.
Jacob HerrmannDepartment of Biomedical Engineering, Boston University, Boston, MA, United States.
Samhita MurthyDepartment of Biomedical Engineering, Boston University, Boston, MA, United States.
Kevin PetersDepartment of Biomedical Engineering, Boston University, Boston, MA, United States.
Sarah E GerardDepartment of Radiology, University of Iowa, Iowa City, IA, United States.
Hadi T NiaDepartment of Biomedical Engineering, Boston University, Boston, MA, United States.
Kenneth R LutchenDepartment of Biomedical Engineering, Boston University, Boston, MA, United States.
Béla SukiDepartment of Biomedical Engineering, Boston University, Boston, MA, United States.
Boston University · USUniversity of Iowa · US

Funding

A multi-scale computational model of the extracellular matrix of the lungU01HL139466 · NHLBI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI SUKI, BELA · 2018 to 2022
$3.9M
NHLBI NIH HHS U01 HL139466
6 · The paper itself

Abstract

Emphysema is a progressive disease characterized by irreversible tissue destruction and airspace enlargement, which manifest as low attenuation area (LAA) on CT images. Previous studies have shown that inflammation, protease imbalance, extracellular matrix remodeling and mechanical forces collectively influence the progression of emphysema. Elastic spring network models incorporating force-based mechanical failure have been applied to investigate the pathogenesis and progression of emphysema. However, these models were general without considering the patient-specific information on lung structure available in CT images. The aim of this work was to develop a novel approach that provides an optimal spring network representation of emphysematous lungs based on the apparent density in CT images, allowing the construction of personalized networks. The proposed method takes into account the size and curvature of LAA clusters on the CT images that correspond to a pre-stressed condition of the lung as opposed to a naïve method that excludes the effects of pre-stress. The main findings of this study are that networks constructed by the new method 1) better preserve LAA cluster sizes and their distribution than the naïve method; and 2) predict different course of emphysema progression compared to the naïve method. We conclude that our new method has the potential to predict patient-specific emphysema progression which needs verification using clinical data.

Indexed as

average symmetric surface distanceclustersemphysemalow attenuation areamechanical failure

Identifiers

PMID36926064
PMCPMC10013051
OpenAlexW4220978351

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read9
table measurements read1
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.