Evidence map›Paper›PMID 30980869›Full record

ArticleJournal of theoretical biology2019

The problem of detrending when analysing potential indicators of disease elimination.

Adjani Gama Dessavre, Emma Southall, Michael J Tildesley, Louise Dyson

Abstract read
In one paragraph

Article in Journal of theoretical biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
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  9. Early warning signals of infectious disease transitions: a review.Journal of the Royal Society, Interface · 2021
    Review
  10. 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.

Adjani Gama DessavreMathematics Institute, University of Warwick, Coventry, UK.
Emma SouthallMathematics Institute, University of Warwick, Coventry, UK.
Michael J TildesleyMathematics Institute, University of Warwick, Coventry, UK; School of Life Sciences, University of Warwick, Coventry, UK.
Louise DysonMathematics Institute, University of Warwick, Coventry, UK; School of Life Sciences, University of Warwick, Coventry, UK. Electronic address: l.dyson@warwick.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As we strive towards the elimination of many burdensome diseases, the question of when intervention efforts may cease is increasingly important. It can be very difficult to know when prevalences are low enough that the disease will die out without further intervention, particularly for diseases that lack accurate tests. The consequences of stopping an intervention prematurely can put back elimination efforts by decades. Critical slowing down theory predicts that as a dynamical system moves through a critical transition, deviations from the steady state return increasingly slowly. We study two potential indicators of disease elimination predicted by this theory, and investigate their response using a simple stochastic model. We compare our dynamical predictions to simulations of the fluctuation variance and coefficient of variation as the system moves through the transition to elimination. These comparisons demonstrate that the primary challenge facing the analysis of early warning signs in timeseries data is that of accurately 'detrending' the signal, in order to preserve the statistical properties of the fluctuations. We show here that detrending using the mean of even just four realisations of the process can give a significant improvement when compared to using a moving window average. Taking this idea further, we consider a 'metapopulation' model of an endemic disease, in which infection spreads in various separated areas with some movement between the subpopulations. We successfully predict the behaviour of both variance and the coefficient of variation in a metapopulation by using information from the other subpopulations to detrend the system.

Indexed as

Communicable Disease ControlCommunicable DiseasesModels, BiologicalHumans

Identifiers

PMID30980869
PMCPMC6859505

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Registered trials

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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.