Serviceeinschränkungen vom 12.-22.02.2026 - weitere Infos auf der UB-Homepage

Treffer: Time series modeling of pathogen-specific disease probabilities with subsampled data.

Title:
Time series modeling of pathogen-specific disease probabilities with subsampled data.
Authors:
Fisher L; Department of Biostatistics, University of Washington, Seattle, Washington, U.S.A., Wakefield J; Department of Biostatistics, University of Washington, Seattle, Washington, U.S.A.; Department of Statistics, University of Washington, Seattle, Washington, U.S.A., Bauer C; Department of Biostatistics, Brown University, Providence, Rhode Island, U.S.A., Self S; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, U.S.A.
Source:
Biometrics [Biometrics] 2017 Mar; Vol. 73 (1), pp. 283-293. Date of Electronic Publication: 2016 Jul 05.
Publication Type:
Journal Article; Research Support, N.I.H., Extramural
Language:
English
Journal Info:
Publisher: Oxford University Press Country of Publication: England NLM ID: 0370625 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1541-0420 (Electronic) Linking ISSN: 0006341X NLM ISO Abbreviation: Biometrics Subsets: MEDLINE
Imprint Name(s):
Publication: March 2024- : [Oxford] : Oxford University Press
Original Publication: Alexandria Va : Biometric Society
References:
J Infect. 2007 Jun;54(6):530-8. (PMID: 17097147)
Am J Epidemiol. 2006 Jan 15;163(2):181-7. (PMID: 16319291)
J Am Stat Assoc. 2012;107(500):1410-1426. (PMID: 37583443)
PLoS One. 2012;7(10):e46845. (PMID: 23071650)
Epidemiology. 2011 Nov;22(6):781-92. (PMID: 21968769)
PLoS One. 2011;6(9):e25287. (PMID: 21980416)
Glob Health Action. 2014 Aug 05;7:24664. (PMID: 25098727)
Biometrics. 2006 Dec;62(4):1170-7. (PMID: 17156292)
Sci Total Environ. 2011 Dec 1;410-411:119-25. (PMID: 22014509)
BMC Infect Dis. 2013 Mar 13;13:134. (PMID: 23497074)
Epidemiol Infect. 2013 Oct;141(10):2196-204. (PMID: 23217849)
PLoS Comput Biol. 2011 Aug;7(8):e1002136. (PMID: 21901082)
Epidemiol Infect. 2010 Dec;138(12):1779-88. (PMID: 20875200)
Proc Natl Acad Sci U S A. 2006 Dec 5;103(49):18438-43. (PMID: 17121996)
Grant Information:
R01 CA095994 United States CA NCI NIH HHS; R21 AI119773 United States AI NIAID NIH HHS
Contributed Indexing:
Keywords: Empirical Bayes; Generalized additive models; Infectious disease modeling; Subsampled data
Entry Date(s):
Date Created: 20160706 Date Completed: 20170927 Latest Revision: 20240324
Update Code:
20250114
PubMed Central ID:
PMC5224700
DOI:
10.1111/biom.12560
PMID:
27378138
Database:
MEDLINE

Weitere Informationen

Many diseases arise due to exposure to one of multiple possible pathogens. We consider the situation in which disease counts are available over time from a study region, along with a measure of clinical disease severity, for example, mild or severe. In addition, we suppose a subset of the cases are lab tested in order to determine the pathogen responsible for disease. In such a context, we focus interest on modeling the probabilities of disease incidence given pathogen type. The time course of these probabilities is of great interest as is the association with time-varying covariates such as meteorological variables. In this set up, a natural Bayesian approach would be based on imputation of the unsampled pathogen information using Markov Chain Monte Carlo but this is computationally challenging. We describe a practical approach to inference that is easy to implement. We use an empirical Bayes procedure in a first step to estimate summary statistics. We then treat these summary statistics as the observed data and develop a Bayesian generalized additive model. We analyze data on hand, foot, and mouth disease (HFMD) in China in which there are two pathogens of primary interest, enterovirus 71 (EV71) and Coxackie A16 (CA16). We find that both EV71 and CA16 are associated with temperature, relative humidity, and wind speed, with reasonably similar functional forms for both pathogens. The important issue of confounding by time is modeled using a penalized B-spline model with a random effects representation. The level of smoothing is addressed by a careful choice of the prior on the tuning variance.
(© 2016, The International Biometric Society.)