Evidence map›Paper›PMID 35908812›Full record

ArticleStatistics in medicine2022

Classification of disease recurrence using transition likelihoods with expectation-maximization algorithm.

Huijun Jiang, Quefeng Li, Jessica T Lin, Feng-Chang Lin

Abstract read
In one paragraph

Article in Statistics in medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Huijun JiangDepartment of Biostatistics, University of North Carolina, Chapel Hill, North Carolina, USA.ORCID 0000-0002-7918-8805
Quefeng LiDepartment of Biostatistics, University of North Carolina, Chapel Hill, North Carolina, USA.ORCID 0000-0003-0707-2763
Jessica T LinDivision of Infectious Disease, School of Medicine, University of North Carolina, Chapel Hill, North Carolina, USA.ORCID 0000-0002-4516-723X
Feng-Chang LinDepartment of Biostatistics, University of North Carolina, Chapel Hill, North Carolina, USA.ORCID 0000-0002-2638-1775

Funding

Re-Entry Supplement: Investigation of Oral Microbial Enzymes for the Detection and Treatment of Periodontal DiseaseUL1TR002489 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BUSE, JOHN BERNARD, SHAHEEN, NICHOLAS J · 2018 to 2022
$48.6M
Statistical Methods for Integrative Analysis of Large Scale Neuroimaging DataR01AG073259 · NIA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LI, QUEFENG · 2021 to 2025
$1.8M
Genetic determinants of Plasmodium vivax relapseK08AI110651 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIN, JESSICA · 2014 to 2018
$869k
Plasmodium ovale hypnozoite development and relapse: a coordinated in vivo in vitro studyR21AI152260 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ADAMS, JOHN H, LIN, JESSICA · 2021 to 2022
$418k
NCATS NIH HHS UL1 TR002489NCATS NIH HHS UL1TR002489NIAID NIH HHS K08 AI110651NIAID NIH HHS K08AI110651NIAID NIH HHS R21 AI152260NIA NIH HHS R01 AG073259NIA NIH HHS R01AG073259
6 · The paper itself

Abstract

When an infectious disease recurs, it may be due to treatment failure or a new infection. Being able to distinguish and classify these two different outcomes is critical in effective disease control. A multi-state model based on Markov processes is a typical approach to estimating the transition probability between the disease states. However, it can perform poorly when the disease state is unknown. This article aims to demonstrate that the transition likelihoods of baseline covariates can distinguish one cause from another with high accuracy in infectious diseases such as malaria. A more general model for disease progression can be constructed to allow for additional disease outcomes. We start from a multinomial logit model to estimate the disease transition probabilities and then utilize the baseline covariate's transition information to provide a more accurate classification result. We apply the expectation-maximization (EM) algorithm to estimate unknown parameters, including the marginal probabilities of disease outcomes. A simulation study comparing our classifier to the existing two-stage method shows that our classifier has better accuracy, especially when the sample size is small. The proposed method is applied to determining relapse vs reinfection outcomes in two Plasmodium vivax treatment studies from Cambodia that used different genotyping approaches to demonstrate its practical use.

Indexed as

AlgorithmsMotivationHumansMarkov ChainsProbabilityRecurrenceclassificationEM algorithminfectious diseasesmalariatransition likelihood

Identifiers

PMID35908812
PMCPMC9489660

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.