Evidence map›Paper›PMID 39117222›Full record

ArticleThe Science of the total environment2024

Robust identification of environmental exposures and community characteristics predictive of rapid lung disease progression.

Clayton J Peterson, Marepalli B Rao, Anushka Palipana, Erika Rasnick Manning, Andrew Vancil, Patrick Ryan, Cole Brokamp, Elizabeth Kramer, Rhonda D Szczesniak, Emrah Gecili

Abstract read
In one paragraph

Article in The Science of the total environment, 2024. 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
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. 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

10 authors.

Clayton J PetersonDivision of Biostatistics and Bioinformatics, Environmental & Public Health Sciences, University of Cincinnati College of Medicine, CARE/Crawley Building, Suite E-870 3230, Eden Ave, Cincinnati, OH 45267, USA; Division of Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center, MLC 5041, Cincinnati, OH 45229, USA.
Marepalli B RaoDivision of Biostatistics and Bioinformatics, Environmental & Public Health Sciences, University of Cincinnati College of Medicine, CARE/Crawley Building, Suite E-870 3230, Eden Ave, Cincinnati, OH 45267, USA.
Anushka PalipanaDivision of Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center, MLC 5041, Cincinnati, OH 45229, USA; School of Nursing, Duke University, 307 Trent Dr., Durham, NC 27710, USA.
Erika Rasnick ManningDivision of Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center, MLC 5041, Cincinnati, OH 45229, USA.
Andrew VancilDivision of Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center, MLC 5041, Cincinnati, OH 45229, USA.
Patrick RyanDivision of Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center, MLC 5041, Cincinnati, OH 45229, USA; Department of Pediatrics, University of Cincinnati College of Medicine, 2600 Clifton Ave, Cincinnati, OH 45221, USA.
Cole BrokampDivision of Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center, MLC 5041, Cincinnati, OH 45229, USA; Department of Pediatrics, University of Cincinnati College of Medicine, 2600 Clifton Ave, Cincinnati, OH 45221, USA.
Elizabeth KramerDepartment of Pediatrics, University of Cincinnati College of Medicine, 2600 Clifton Ave, Cincinnati, OH 45221, USA; Division of Pulmonary Medicine, Cincinnati Children's Hospital Medical Center, MLC 5041, Cincinnati, OH 45229, USA.
Rhonda D SzczesniakDivision of Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center, MLC 5041, Cincinnati, OH 45229, USA; Department of Pediatrics, University of Cincinnati College of Medicine, 2600 Clifton Ave, Cincinnati, OH 45221, USA; Division of Pulmonary Medicine, Cincinnati Children's Hospital Medical Center, MLC 5041, Cincinnati, OH 45229, USA.
Emrah GeciliDivision of Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center, MLC 5041, Cincinnati, OH 45229, USA; Department of Pediatrics, University of Cincinnati College of Medicine, 2600 Clifton Ave, Cincinnati, OH 45221, USA. Electronic address: emrah.gecili@cchmc.org.

Funding

R01- Mapping environmental contributions to rapid lung disease progression in cystic fibrosisR01HL141286 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI SZCZESNIAK, RHONDA · 2019 to 2023
$2.3M
NHLBI NIH HHS R01 HL141286
6 · The paper itself

Abstract

Environmental exposures and community characteristics have been linked to accelerated lung function decline in people with cystic fibrosis (CF), but geomarkers, the measurements of these exposures, have not been comprehensively evaluated in a single study. To determine which geomarkers have the greatest predictive potential for lung function decline and pulmonary exacerbation (PEx), a retrospective longitudinal cohort study was performed using novel Bayesian joint covariate selection methods, which were compared with respect to PEx predictive accuracy. Non-stationary Gaussian linear mixed effects models were fitted to data from 151 CF patients aged 6-20 receiving care at a CF Center in the midwestern US (2007-2017). The outcome was forced expiratory volume in 1 s of percent predicted (FEV1pp). Target functions were used to predict PEx from established criteria. Covariates included 11 routinely collected clinical/demographic characteristics and 45 geomarkers comprising 8 categories. Unique covariate selections via four Bayesian penalized regression models (elastic-net, adaptive lasso, ridge, and lasso) were evaluated at both 95 % and 90 % credible intervals (CIs). Resultant models included one to 6 geomarkers (air temperature, percentage of tertiary roads outside urban areas, percentage of impervious nonroad outside urban areas, fine atmospheric particulate matter, fraction achieving high school graduation, and motor vehicle theft) representing weather, impervious descriptor, air pollution, socioeconomic status, and crime categories. Adaptive lasso had the lowest information criteria. For PEx predictive accuracy, covariate selection from the 95 % CI elastic-net had the highest area under the receiver-operating characteristic curve (mean ± standard deviation; 0.780 ± 0.026) along with the 95 % CI ridge and lasso methods (0.780 ± 0.027). The 95 % CI elastic-net had the highest sensitivity (0.773 ± 0.083) while the 95 % CI adaptive lasso had the highest specificity (0.691 ± 0.087), suggesting the need for different geomarker sets depending on monitoring goals. Surveillance of certain geomarkers embedded in prediction algorithms can be used in real-time warning systems for PEx onset.

Indexed as

Bayes TheoremEnvironmental ExposureAdolescentAir PollutantsAir PollutionChildCystic FibrosisDisease ProgressionFemaleHumansLongitudinal StudiesLung DiseasesMaleRetrospective StudiesYoung AdultAir PollutantsChemical stressorsChronic disease managementCystic fibrosisLung functionMedical monitoringPulmonary exacerbationSocial determinants of health

Identifiers

PMID39117222
PMCPMC11349456

What OpenQuestion holds

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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.