Evidence map›Paper›PMID 25533437›Full record

ArticleJournal of biomedical informatics2015

Sparse modeling of spatial environmental variables associated with asthma.

Timothy S Chang, Ronald E Gangnon, C David Page, William R Buckingham, Aman Tandias, Kelly J Cowan, Carrie D Tomasallo, Brian G Arndt, Lawrence P Hanrahan, Theresa W Guilbert

Abstract read
In one paragraph

Article in Journal of biomedical informatics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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

10 authors.

Timothy S ChangDepartment of Biostatistics and Medical Informatics, School of Medicine and Public Health, University of Wisconsin, 5795 Medical Sciences Center, 1300 University Ave, Madison, WI 53706, USA. Electronic address: tschang3@uwalumni.com.
Ronald E GangnonDepartment of Biostatistics and Medical Informatics, School of Medicine and Public Health, University of Wisconsin, 603 Warf Office Building, 610 Walnut St, Madison, WI 53706, USA. Electronic address: ronald@biostat.wisc.edu.
C David PageDepartment of Biostatistics and Medical Informatics, School of Medicine and Public Health, University of Wisconsin, 6743 Medical Sciences Center, 1300 University Ave, Madison, WI 53706, USA. Electronic address: page@biostat.wisc.edu.
William R BuckinghamApplied Population Laboratory, Department of Rural Sociology, University of Wisconsin, 308b Agricultural Hall, 1450 Linden Dr, Madison, WI 53706, USA. Electronic address: wrbuckin@wisc.edu.
Aman TandiasDepartment of Family Medicine, School of Medicine and Public Health, University of Wisconsin, 1100 Delaplaine Ct, Madison, WI 53715, USA. Electronic address: aman.tandias@fammed.wisc.edu.
Kelly J CowanDepartment of Pediatrics, School of Medicine and Public Health, University of Wisconsin, Madison, WI 53706, USA. Electronic address: kelly.cowan@vtmednet.org.
Carrie D TomasalloDivision of Public Health, Bureau of Environmental and Occupational Health, Wisconsin Department of Health Services, Room 150, 1 West Wilson Street, Madison, WI 53703, USA. Electronic address: carrie.tomasallo@dhs.wisconsin.gov.
Brian G ArndtDepartment of Family Medicine, School of Medicine and Public Health, University of Wisconsin, 1100 Delaplaine Ct, Madison, WI 53715, USA. Electronic address: brian.arndt@fammed.wisc.edu.
Lawrence P HanrahanDepartment of Family Medicine, School of Medicine and Public Health, University of Wisconsin, 1100 Delaplaine Ct, Madison, WI 53715, USA. Electronic address: larry.hanrahan@fammed.wisc.edu.
Theresa W GuilbertDepartment of Pediatrics, School of Medicine and Public Health, University of Wisconsin, Madison, WI 53706, USA. Electronic address: theresa.guilbert@cchmc.org.

Funding

Institutional Clinical and Translational Science AwardUL1TR000427 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$32.2M
INSTITUTIONAL CTSA (UW-MADISON): CLINICAL TRIALSUL1RR025011 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2007 to 2011
$29.5M
INTEGRATED TRAINING FOR PHYSICIAN-SCIENTISTST32GM008692 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI BURKARD, MARK E · 1998 to 2020
$10.3M
Institutional Clinical and Translational Science AwardTL1TR000429 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$1.5M
Clustering to identify novel phenotypes in childhood asthmaF30HL112491 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI CHANG, TIMOTHY S · 2012 to 2013
$68k
NCATS NIH HHS 9U54TR000021NCATS NIH HHS TL1 TR000429NCATS NIH HHS UL1 TR000427NCEH CDC HHS U38 EH000951NCRR NIH HHS 1UL1RR025011NCRR NIH HHS UL1 RR025011NHLBI NIH HHS F30 HL112491NHLBI NIH HHS F30HL112491NIGMS NIH HHS T32 GM008692ODCDC CDC HHS U58 CD001316
6 · The paper itself

Abstract

Geographically distributed environmental factors influence the burden of diseases such as asthma. Our objective was to identify sparse environmental variables associated with asthma diagnosis gathered from a large electronic health record (EHR) dataset while controlling for spatial variation. An EHR dataset from the University of Wisconsin's Family Medicine, Internal Medicine and Pediatrics Departments was obtained for 199,220 patients aged 5-50years over a three-year period. Each patient's home address was geocoded to one of 3456 geographic census block groups. Over one thousand block group variables were obtained from a commercial database. We developed a Sparse Spatial Environmental Analysis (SASEA). Using this method, the environmental variables were first dimensionally reduced with sparse principal component analysis. Logistic thin plate regression spline modeling was then used to identify block group variables associated with asthma from sparse principal components. The addresses of patients from the EHR dataset were distributed throughout the majority of Wisconsin's geography. Logistic thin plate regression spline modeling captured spatial variation of asthma. Four sparse principal components identified via model selection consisted of food at home, dog ownership, household size, and disposable income variables. In rural areas, dog ownership and renter occupied housing units from significant sparse principal components were associated with asthma. Our main contribution is the incorporation of sparsity in spatial modeling. SASEA sequentially added sparse principal components to Logistic thin plate regression spline modeling. This method allowed association of geographically distributed environmental factors with asthma using EHR and environmental datasets. SASEA can be applied to other diseases with environmental risk factors.

Indexed as

EnvironmentAdolescentAdultAlgorithmsAnimalsAsthmaChildChild, PreschoolData CollectionDogsElectronic Health RecordsFemaleGeographic Information SystemsGeographyHousingHumansAsthmaElectronic health recordEnvironmental variablesSparsitySpatial statistics

Identifiers

PMID25533437
PMCPMC4355087

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.