Literature DB >> 22295167

An advanced stochastic model for mucociliary particle clearance in cystic fibrosis lungs.

Robert Sturm1.   

Abstract

BACKGROUND: A mathematical model describing mucociliary clearance in cystic fibrosis (CF) patients and its development with progressing course of the disease was developed. The approach should support the prediction of the disease state on the basis of measured bronchial clearance efficiencies.
METHODS: The approach is based on the assumption of a steady-state steady-flow mucus transport through the tracheobronchial tree which enables the determination of airway generation-specific mucus velocities by using a measured tracheal mucus velocity and a realistic morphometric dataset of the human lung. Architecture of the tracheobronchial tree was approximated by a stochastic model, reflecting the intra-subject variability of geometric parameters within a given lung generation.
RESULTS: As predicted by the appropriately validated mathematical approach, mucociliary clearance efficiency in CF patients is partly significantly decreased with respect to healthy controls. 24-h retention of patients with mild CF (FEV(1) >70% of predicted) is reduced by 10% compared to healthy subjects, whilst 24-h retention of patients with moderate to severe CF (FEV(1) <70% of predicted) differs by 25% from that of the healthy controls. These discrepancies are further enhanced with continuation of the clearance process.
CONCLUSIONS: The theoretical results lead to the conclusion that CF patients have a higher risk of inhaled particle accumulation and related particle overload in specific lung compartments than healthy subjects.

Entities:  

Keywords:  24-h retention; Clearance model; mucociliary clearance; stochastic lung structure

Year:  2012        PMID: 22295167      PMCID: PMC3256542          DOI: 10.3978/j.issn.2072-1439.2011.09.09

Source DB:  PubMed          Journal:  J Thorac Dis        ISSN: 2072-1439            Impact factor:   2.895


  27 in total

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Authors:  Michael R Knowles; Richard C Boucher
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Authors:  Robert Sturm; W Hofmann
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Authors:  R C Boucher
Journal:  Adv Drug Deliv Rev       Date:  2002-12-05       Impact factor: 15.470

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Journal:  Chest       Date:  1993-05       Impact factor: 9.410

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Journal:  Cell       Date:  1996-04-19       Impact factor: 41.582

10.  The relative roles of passive surface forces and active ion transport in the modulation of airway surface liquid volume and composition.

Authors:  R Tarran; B R Grubb; J T Gatzy; C W Davis; R C Boucher
Journal:  J Gen Physiol       Date:  2001-08       Impact factor: 4.086

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  7 in total

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Review 3.  Translational Research in Cystic Fibrosis: From Bench to Beside.

Authors:  Laura de Castro E Garcia; Lucas Montiel Petry; Pedro Augusto Van Der Sand Germani; Luiza Fernandes Xavier; Paula Barros de Barros; Amanda da Silva Meneses; Laura Menestrino Prestes; Luana Braga Bittencourt; Marina Puerari Pieta; Frederico Friedrich; Leonardo Araújo Pinto
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4.  Local lung deposition of ultrafine particles in healthy adults: experimental results and theoretical predictions.

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5.  A physiologically-motivated compartment-based model of the effect of inhaled hypertonic saline on mucociliary clearance and liquid transport in cystic fibrosis.

Authors:  Matthew R Markovetz; Timothy E Corcoran; Landon W Locke; Michael M Myerburg; Joseph M Pilewski; Robert S Parker
Journal:  PLoS One       Date:  2014-11-10       Impact factor: 3.240

6.  Scoring tools to monitor risk of disease progression in patients with cystic fibrosis.

Authors:  Márcio Vinícius Fagundes Donadio; Fernanda Maria Vendrusculo; Margarita Pérez-Ruiz
Journal:  J Thorac Dis       Date:  2020-08       Impact factor: 2.895

Review 7.  Systems Medicine for Lung Diseases: Phenotypes and Precision Medicine in Cancer, Infection, and Allergy.

Authors:  Bernd Schmeck; Wilhelm Bertrams; Xin Lai; Julio Vera
Journal:  Methods Mol Biol       Date:  2016
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