Evidence map›Paper›PMID 37794364›Full record

ArticleBMC infectious diseases2023

Modeling homophily in dynamic networks with application to HIV molecular surveillance.

Victor DeGruttola, Masato Nakazawa, Tuo Lin, Jinyuan Liu, Ravi Goyal, Susan Little, Xin Tu, Sanjay Mehta

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 86% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. 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 at 5 institutions in 1 country.

Victor DeGruttolaDivision of Biostatistics and Bioinformatics Herbert Wertheim School of Public Health and Human Longevity Science, University of California, 9500 Gilman Dr., 92093-0628, San Diego, La Jolla, CA, USA. degrut@hsph.harvard.edu.
Masato NakazawaPacira Biosciences, San Diego, CA, USA.
Tuo LinDivision of Biostatistics and Bioinformatics Herbert Wertheim School of Public Health and Human Longevity Science, University of California, 9500 Gilman Dr., 92093-0628, San Diego, La Jolla, CA, USA.
Jinyuan LiuVanderbilt University, Department of Medicine, Nashville, USA.
Ravi GoyalDivision of Infectious Diseases and Global Public Health, University of California San Diego, La Jolla, CA, USA.
Susan LittleDivision of Infectious Diseases and Global Public Health, University of California San Diego, La Jolla, CA, USA.
Xin Tu *Division of Biostatistics and Bioinformatics Herbert Wertheim School of Public Health and Human Longevity Science, University of California, 9500 Gilman Dr., 92093-0628, San Diego, La Jolla, CA, USA.
Sanjay Mehta *Veterans Affairs, San Diego Healthcare System, San Diego, CA, USA.
Human Longevity (United States) · USUniversity of California, San Diego · USPacira (United States) · USVanderbilt University · USVA San Diego Healthcare System · US

Funding

UC San Diego Clinical and Translational Research InstituteUL1TR001442 · NCATS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FIRESTEIN, GARY S, HOGARTH, MICHAEL · 2015 to 2024
$88.3M
VirologyP30AI036214 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI David Mitchell Smith · 1994 to 2026
$78.4M
Primary Infection Resource Consortium (PIRC)R24AI106039 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LITTLE, SUSAN JANET · 2013 to 2021
$23.1M
Methods to Advance the HIV Prevention Research AgendaR37AI051164 · NIAID · HARVARD SCHOOL OF PUBLIC HEALTH · PI DEGRUTTOLA, VICTOR GERARD · 2012 to 2019
$3.3M
Modeling and simulation tools for optimizing design of network-informed clinical trials of combination HIV prevention interventionsR01AI147441 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GOYAL, RAVI · 2019 to 2022
$2.1M
NCATS NIH HHS UL1 TR001442NIAID NIH HHS P30 AI036214NIAID NIH HHS R01 AI147441NIAID NIH HHS R24 AI106039NIAID NIH HHS R37 AI051164
6 · The paper itself

Abstract

backgroundEfforts to control the HIV epidemic can benefit from knowledge of the relationships between the characteristics of people who have transmitted HIV and those who became infected by them. Investigation of this relationship is facilitated by the use of HIV genetic linkage analyses, which allows inference about possible transmission events among people with HIV infection. Two persons with HIV (PWH) are considered linked if the genetic distance between their HIV sequences is less than a given threshold, which implies proximity in a transmission network. The tendency of pairs of nodes (in our case PWH) that share (or differ in) certain attributes to be linked is denoted homophily. Below, we describe a novel approach to modeling homophily with application to analyses of HIV viral genetic sequences from clinical series of participants followed in San Diego. Over the 22-year period of follow-up, increases in cluster size results from HIV transmissions to new people from those already in the cluster-either directly or through intermediaries.

methodsOur analytical approach makes use of a logistic model to describe homophily with regard to demographic, clinical, and behavioral characteristics-that is we investigate whether similarities (or differences) between PWH in these characteristics are associated with their sequences being linked. To investigate the performance of our methods, we conducted on a simulation study for which data sets were generated in a way that reproduced the structure of the observed database.

resultsOur results demonstrated strong positive homophily associated with hispanic ethnicity, and strong negative homophily, with birth year difference. The second result implies that the larger the difference between the age of a newly-infected PWH and the average age for an available cluster, the lower the odds of a newly infected person joining that cluster. We did not observe homophily associated with prior diagnosis of sexually transmitted diseases. Our simulation studies demonstrated the validity of our approach for modeling homophily, by showing that the estimates it produced matched the specified values of the statistical network generating model.

conclusionsOur novel methods provide a simple and flexible statistical network-based approach for modeling the growth of viral (or other microbial) genetic clusters from linkage to new infections based on genetic distance.

Indexed as

HIV InfectionsSexually Transmitted DiseasesEthnicityHispanic or LatinoHumansModels, StatisticalDynamic networksHomophilyViral genetic linkage

Identifiers

PMID37794364
PMCPMC10548762
OpenAlexW4387337419

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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.