Evidence map›Paper›PMID 36469509›Full record

ArticlePLoS computational biology2022

Using genetic data to identify transmission risk factors: Statistical assessment and application to tuberculosis transmission.

Isaac H Goldstein, Damon Bayer, Ivan Barilar, Balladiah Kizito, Ogopotse Matsiri, Chawangwa Modongo, Nicola M Zetola, Stefan Niemann, Volodymyr M Minin, Sanghyuk S Shin

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 23% of its field
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

9 citing papers in PubMed, 11 citations in OpenAlex.

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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 at 3 institutions in 2 countries.

Isaac H GoldsteinDepartment of Statistics, University of California, Irvine, California, United States of America.
Damon BayerDepartment of Statistics, University of California, Irvine, California, United States of America.ORCID 0000-0003-2819-7645
Ivan BarilarGerman Center for Infection Research, Research Center Borstel, Borstel, Germany.ORCID 0000-0002-4789-2777
Balladiah KizitoVictus Global Botswana Organisation, Gaborone, Botswana.ORCID 0000-0002-9905-9322
Ogopotse MatsiriVictus Global Botswana Organisation, Gaborone, Botswana.
Chawangwa ModongoVictus Global Botswana Organisation, Gaborone, Botswana.
Nicola M ZetolaAugusta University, Augusta, Georgia, United States of America.
Stefan NiemannGerman Center for Infection Research, Research Center Borstel, Borstel, Germany.
Volodymyr M MininDepartment of Statistics, University of California, Irvine, California, United States of America.ORCID 0000-0002-1917-9288
Sanghyuk S ShinSue & Bill Gross School of Nursing, University of California, Irvine, California, United States of America.ORCID 0000-0001-9982-4373
University of California, Irvine · USGerman Center for Infection Research · DEAugusta University · US

Funding

Improved understanding of TB transmission by accounting for within-host heterogeneity of M. tuberculosis: A population-based molecular epidemiology study in a high HIV prevalent settingR01AI147336 · NIAID · UNIVERSITY OF CALIFORNIA-IRVINE · PI SHIN, SANGHYUK SAM · 2020 to 2024
$3.3M
Dynamics of TB and MDR TB transmission in areas with high HIV prevalenceR01AI097045 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ZETOLA, NICOLA MARIO · 2011 to 2015
$2.9M
NIAID NIH HHS R01 AI097045NIAID NIH HHS R01 AI147336
6 · The paper itself

Abstract

Identifying host factors that influence infectious disease transmission is an important step toward developing interventions to reduce disease incidence. Recent advances in methods for reconstructing infectious disease transmission events using pathogen genomic and epidemiological data open the door for investigation of host factors that affect onward transmission. While most transmission reconstruction methods are designed to work with densely sampled outbreaks, these methods are making their way into surveillance studies, where the fraction of sampled cases with sequenced pathogens could be relatively low. Surveillance studies that use transmission event reconstruction then use the reconstructed events as response variables (i.e., infection source status of each sampled case) and use host characteristics as predictors (e.g., presence of HIV infection) in regression models. We use simulations to study estimation of the effect of a host factor on probability of being an infection source via this multi-step inferential procedure. Using TransPhylo-a widely-used method for Bayesian estimation of infectious disease transmission events-and logistic regression, we find that low sensitivity of identifying infection sources leads to dilution of the signal, biasing logistic regression coefficients toward zero. We show that increasing the proportion of sampled cases improves sensitivity and some, but not all properties of the logistic regression inference. Application of these approaches to real world data from a population-based TB study in Botswana fails to detect an association between HIV infection and probability of being a TB infection source. We conclude that application of a pipeline, where one first uses TransPhylo and sparsely sampled surveillance data to infer transmission events and then estimates effects of host characteristics on probabilities of these events, should be accompanied by a realistic simulation study to better understand biases stemming from imprecise transmission event inference.

Indexed as

HIV InfectionsTuberculosisBayes TheoremComputer SimulationDisease OutbreaksHumans

Identifiers

PMID36469509
PMCPMC9754595
OpenAlexW4311621214

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.