Evidence map›Paper›PMID 30171436›Full record

ArticleMedical & biological engineering & computing2019

Physiological study of pulmonary involvement in adults with cystic fibrosis through simulated modeling of different clinical scenarios.

Antonio Alberto Rodríguez Sousa, Jesús M Barandica Fernández, Jonathan Miller, Matías Mir-Montejano

Abstract read
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In one paragraph

Article in Medical & biological engineering & computing, 2019. 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
–field-weighted citation impact, top 85% 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, 1 citations in OpenAlex.

  1. Article
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 3 institutions in 1 country.

Antonio Alberto Rodríguez SousaBiological Sciences Faculty, University Complutense of Madrid, C/ José Antonio Nováis 2, 28040, Madrid, Spain. antonr05@ucm.es.ORCID http://orcid.org/0000-0002-6292-1425
Jesús M Barandica FernándezBiological Sciences Faculty, University Complutense of Madrid, C/ José Antonio Nováis 2, 28040, Madrid, Spain.
Jonathan MillerNational Museum of Natural Sciences-Superior Council of Scientific Investigations, C/ José Gutiérrez Abascal 2, 28006, Madrid, Spain.
Matías Mir-MontejanoMadrid Health Service, Mar Báltico Health Center, C/ Mar Báltico 2, 28033, Madrid, Spain.
Universidad Complutense de Madrid · ESMadrid Health Service · ESMuseo Nacional de Ciencias Naturales · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cystic fibrosis is an inherited disorder of the cystic fibrosis transmembrane conductance regulator gene (CFTR) that affects the respiratory system. Current treatment is palliative, but there is a gene therapy under investigation which involves inserting a functional CFTR gene into affected cells. Given the clinical variety of the disease, it is necessary to characterize key indicators in its evolution (e.g., the number of functional alveolar sacs and its relationship with a healthy lung function), to anticipate its advancement. A dynamic model was used to evaluate the evolution of cystic fibrosis over time. We considered the application of conventional medical treatments and evaluated the benefits of the application of an experimental gene therapy that would reverse lung damage. Without treatment the life expectancy of the patient is low, but it is increased with the application of conventional treatments, being the progressive loss of the lung function inevitable. Simulating the application of a gene therapy, the life expectancy of patients would not be limited, given the recovery of all altered cellular processes. With this model we can make predictions that demonstrate the need for a curative treatment, in addition to presenting the evolution of pathology in a specific clinical setting. Graphical abstract Graphic representation of the analysis performed in the present work on simulation of different clinical situations regarding patients with cystic fibrosis of pulmonary involvement.

Indexed as

AdultCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorGenetic TherapyHumansRespiratory Physiological PhenomenaRespiratory SystemCystic Fibrosis Transmembrane Conductance RegulatorCFTR protein (cystic fibrosis transmembrane conductance regulator)Dynamic modelingGenetic therapyPulmonary functionRespiratory physiology

Identifiers

PMID30171436
OpenAlexW2889255575

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.