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Distributions of Autocorrelated First-Order Kinetic Outcomes: Illness Severity

Many complex systems produce outcomes having recurring, power law-like distributions over wide ranges. However, the form necessarily breaks down at extremes, whereas the Weibull distribution has been demonstrated over the full observed range. Here the Weibull distribution is derived as the asymptoti...

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Autor principal: Englehardt, James D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4465627/
https://www.ncbi.nlm.nih.gov/pubmed/26061263
http://dx.doi.org/10.1371/journal.pone.0129042
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author Englehardt, James D.
author_facet Englehardt, James D.
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description Many complex systems produce outcomes having recurring, power law-like distributions over wide ranges. However, the form necessarily breaks down at extremes, whereas the Weibull distribution has been demonstrated over the full observed range. Here the Weibull distribution is derived as the asymptotic distribution of generalized first-order kinetic processes, with convergence driven by autocorrelation, and entropy maximization subject to finite positive mean, of the incremental compounding rates. Process increments represent multiplicative causes. In particular, illness severities are modeled as such, occurring in proportion to products of, e.g., chronic toxicant fractions passed by organs along a pathway, or rates of interacting oncogenic mutations. The Weibull form is also argued theoretically and by simulation to be robust to the onset of saturation kinetics. The Weibull exponential parameter is shown to indicate the number and widths of the first-order compounding increments, the extent of rate autocorrelation, and the degree to which process increments are distributed exponential. In contrast with the Gaussian result in linear independent systems, the form is driven not by independence and multiplicity of process increments, but by increment autocorrelation and entropy. In some physical systems the form may be attracting, due to multiplicative evolution of outcome magnitudes towards extreme values potentially much larger and smaller than control mechanisms can contain. The Weibull distribution is demonstrated in preference to the lognormal and Pareto I for illness severities versus (a) toxicokinetic models, (b) biologically-based network models, (c) scholastic and psychological test score data for children with prenatal mercury exposure, and (d) time-to-tumor data of the ED(01) study.
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spelling pubmed-44656272015-06-25 Distributions of Autocorrelated First-Order Kinetic Outcomes: Illness Severity Englehardt, James D. PLoS One Research Article Many complex systems produce outcomes having recurring, power law-like distributions over wide ranges. However, the form necessarily breaks down at extremes, whereas the Weibull distribution has been demonstrated over the full observed range. Here the Weibull distribution is derived as the asymptotic distribution of generalized first-order kinetic processes, with convergence driven by autocorrelation, and entropy maximization subject to finite positive mean, of the incremental compounding rates. Process increments represent multiplicative causes. In particular, illness severities are modeled as such, occurring in proportion to products of, e.g., chronic toxicant fractions passed by organs along a pathway, or rates of interacting oncogenic mutations. The Weibull form is also argued theoretically and by simulation to be robust to the onset of saturation kinetics. The Weibull exponential parameter is shown to indicate the number and widths of the first-order compounding increments, the extent of rate autocorrelation, and the degree to which process increments are distributed exponential. In contrast with the Gaussian result in linear independent systems, the form is driven not by independence and multiplicity of process increments, but by increment autocorrelation and entropy. In some physical systems the form may be attracting, due to multiplicative evolution of outcome magnitudes towards extreme values potentially much larger and smaller than control mechanisms can contain. The Weibull distribution is demonstrated in preference to the lognormal and Pareto I for illness severities versus (a) toxicokinetic models, (b) biologically-based network models, (c) scholastic and psychological test score data for children with prenatal mercury exposure, and (d) time-to-tumor data of the ED(01) study. Public Library of Science 2015-06-10 /pmc/articles/PMC4465627/ /pubmed/26061263 http://dx.doi.org/10.1371/journal.pone.0129042 Text en © 2015 James D. Englehardt http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Englehardt, James D.
Distributions of Autocorrelated First-Order Kinetic Outcomes: Illness Severity
title Distributions of Autocorrelated First-Order Kinetic Outcomes: Illness Severity
title_full Distributions of Autocorrelated First-Order Kinetic Outcomes: Illness Severity
title_fullStr Distributions of Autocorrelated First-Order Kinetic Outcomes: Illness Severity
title_full_unstemmed Distributions of Autocorrelated First-Order Kinetic Outcomes: Illness Severity
title_short Distributions of Autocorrelated First-Order Kinetic Outcomes: Illness Severity
title_sort distributions of autocorrelated first-order kinetic outcomes: illness severity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4465627/
https://www.ncbi.nlm.nih.gov/pubmed/26061263
http://dx.doi.org/10.1371/journal.pone.0129042
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