Evidence map›Paper›PMID 23438430›Full record

ArticleEpidemics2013

Detectable signals of episodic risk effects on acute HIV transmission: strategies for analyzing transmission systems using genetic data.

Shah Jamal Alam, Xinyu Zhang, Ethan Obie Romero-Severson, Christopher Henry, Lin Zhong, Erik M Volz, Bluma G Brenner, James S Koopman

Abstract read
In one paragraph

Article in Epidemics, 2013. 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
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Prospects of elimination of HIV with test-and-treat strategy.Proceedings of the National Academy of Sciences of the United States of America · 2013
    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

8 authors.

Shah Jamal AlamUniversity of Michigan, School of Public Health, 109 Observatory Street, Ann Arbor, MI 48109, USA. sjalam@umich.edu
Xinyu Zhang
Ethan Obie Romero-Severson
Christopher Henry
Lin Zhong
Erik M Volz
Bluma G Brenner
James S Koopman

Funding

HIV Risk Dynamics, Genetic Patterns, and ControlR01AI078752 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KOOPMAN, JAMES STEPHEN · 2008 to 2012
$2.7M
Estimation of HIV Transmission Dynamics Using Genetic Sequences of VirusK01AI091440 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI VOLZ, ERIK MCCULLOUGH · 2010 to 2013
$521k
Medical Research Council MR/K010174/1NIAID NIH HHS 5-K01-AI-091440-03NIAID NIH HHS K01 AI091440NIAID NIH HHS R01 AI078752NIAID NIH HHS R01AI078752
6 · The paper itself

Abstract

Episodic high-risk sexual behavior is common and can have a profound effect on HIV transmission. In a model of HIV transmission among men who have sex with men (MSM), changing the frequency, duration and contact rates of high-risk episodes can take endemic prevalence from zero to 50% and more than double transmissions during acute HIV infection (AHI). Undirected test and treat could be inefficient in the presence of strong episodic risk effects. Partner services approaches that use a variety of control options will be likely to have better effects under these conditions, but the question remains: What data will reveal if a population is experiencing episodic risk effects? HIV sequence data from Montreal reveals genetic clusters whose size distribution stabilizes over time and reflects the size distribution of acute infection outbreaks (AIOs). Surveillance provides complementary behavioral data. In order to use both types of data efficiently, it is essential to examine aspects of models that affect both the episodic risk effects and the shape of transmission trees. As a demonstration, we use a deterministic compartmental model of episodic risk to explore the determinants of the fraction of transmissions during acute HIV infection (AHI) at the endemic equilibrium. We use a corresponding individual-based model to observe AIO size distributions and patterns of transmission within AIO. Episodic risk parameters determining whether AHI transmission trees had longer chains, more clustered transmissions from single individuals, or different mixes of these were explored. Encouragingly for parameter estimation, AIO size distributions reflected the frequency of transmissions from acute infection across divergent parameter sets. Our results show that episodic risk dynamics influence both the size and duration of acute infection outbreaks, thus providing a possible link between genetic cluster size distributions and episodic risk dynamics.

Indexed as

Homosexuality, MaleModels, GeneticAcute DiseaseAdultCanadaCluster AnalysisComputer SimulationGenetic VariationHIV InfectionsHumansMalePopulation SurveillancePrevalenceRiskSexual BehaviorSexual Partners

Identifiers

PMID23438430
PMCPMC3748724

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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.