Molecular Networks and Deep Learning for Targeted HIV Interventions among PWID
Molecular Networks and Deep Learning for Targeted HIV Interventions among PWID
批准号:
10469166
负责人:
Steven J. Clipman
金额:
$245.63万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2022
资助国家:
美国
项目状态:
未结题
起止时间:
2022-04-15 至 2026-03-31
关键词:
AIDS preventionAccountingAcquired Immunodeficiency SyndromeAddressCitiesCountryDataData CollectionDevelopmentDisease OutbreaksEpidemicFaceFutureHIVHIV InfectionsHeroinIncidenceIndiaIndividualInjecting drug userInjectionsInterruptionInterventionLeadMachine LearningModelingMolecularMonitorNetwork-basedOverdosePhylogenetic AnalysisPlayPopulationPrevention approachProxyPublic HealthResourcesRiskRoleScienceSocial NetworkUnited StatesViralbehavioral pharmacologycommunity transmissioncost efficientdeep learningexperiencehealth disparityinjection drug useinnovationlenslow and middle-income countriesmeetingsnetwork modelsopioid useprescription opioidprogramssocialsocial structuresubstance usetooltransmission process
中文摘要
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英文摘要
PROJECT SUMMARY
Meeting targets set to end AIDS by 2030 requires reaching all populations, particularly those with the highest
burden, such as people who inject drugs (PWID). PWID continue to experience some of the most explosive
HIV epidemics globally. Injection drug use is increasingly accounting for new HIV infections in both low- and
middle-income countries (LMICs) and countries that once saw notable declines in HIV incidence among PWID.
Even in countries with notable declines in HIV incidence among PWID, such as the United States, the rise of
prescription opioid use has resulted in increased heroin injection, increased overdose rates, and outbreaks of
HIV. Combating the HIV epidemic among hard-to-reach populations, such as PWID, requires targeted
approaches that consider multiple levels of risk that extend beyond individual-level factors alone. Looking at
HIV prevention through the lens of network science can allow us to study and address health disparities on a
social and structural level. Limited network studies among PWID have demonstrated that social and spatial
networks play a significant role in HIV transmission and may be further leveraged for targeted intervention
approaches. However, network data can be challenging to enumerate and analyze, and additional network
tools and analytic approaches are needed to take full advantage of the power of social networks for HIV
prevention efforts. Given the challenges of collecting data on social connections among PWID, by finding
proxies for network data or ways to impute networks we can harness these connections to interrupt HIV
transmission. Network-based interventions may not only be more effective at interrupting community
transmission than individual-level approaches but could represent the most cost-efficient approach as well –
which is crucial given the budgetary and resource constraints programs often face.
This study leverages a rare set of longitudinal social and spatial network data along with detailed individual-
level data and HIV sequences from over 2,500 PWID in New Delhi, India followed from 2016-21. It aims to
explore the use of machine learning and viral phylogenetics as a potential avenue to circumvent network
enumeration challenges and produce new analytical strategies to monitor epidemics and model the most
effective and resource-efficient intervention approach in a city. In practice, this affords the development of
network models that simulate the effect of various network-based intervention strategies on HIV incidence and
could be used to inform a wide array of social, behavioral, and pharmacologic interventions. Making network
data more accessible can lead to new HIV prevention approaches that guide officials in focusing limited
resources for the greatest impact and can provide a greater understanding of the epidemic dynamics.
期刊论文(3)
专著(0)
科研奖励(0)
会议论文
A hepatitis B virus (HBV) sequence variation graph improves sequence alignment and sample-specific consensus sequence construction for genetic analysis of HBV.
乙型肝炎病毒 (HBV) 序列变异图可改善 HBV 遗传分析的序列比对和样本特异性共有序列构建。
DOI:
10.1101/2023.01.11.523611
发表时间:
2023
期刊:
bioRxiv : the preprint server for biology
影响因子:
--
作者:
[Duchen,Dylan, Clipman,Steven, Vergara,Candelaria, Thio,ChloeL, Thomas,DavidL, Duggal,Priya, Wojcik,GenevieveL]
通讯作者:
Wojcik,GenevieveL
DOI:
10.1093/ofid/ofac481
发表时间:
2022-10
期刊:
Open forum infectious diseases
影响因子:
4.2
作者:
[]
通讯作者:
DOI:
10.1126/sciadv.abf0158
发表时间:
2022-10-21
期刊:
Science advances
影响因子:
13.6
作者:
[]
通讯作者:
Leveraging the plasma virome as a biological indicator of HIV risk and transmission networks among people who inject drugs
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批准号:10700415
-
项目类别:
-
资助金额:$62.48万
-
财政年份:2023
-
负责人:Steven J. Clipman
-
依托单位:
海外基金