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dc.contributor.advisorGoodreau, Steven Men_US
dc.contributor.authorKhanna, Adityaen_US
dc.date.accessioned2013-04-17T17:58:29Z
dc.date.available2013-10-15T11:06:14Z
dc.date.issued2013-04-17
dc.date.submitted2012en_US
dc.identifier.otherKhanna_washington_0250E_11079.pdfen_US
dc.identifier.urihttp://hdl.handle.net/1773/22461
dc.descriptionThesis (Ph.D.)--University of Washington, 2012en_US
dc.description.abstract<italic>Background</italic>: In this dissertation, I model HIV transmission in two different populations: circular migrants in South Africa, and men who have sex with men (MSM) in Southern California. <italic>Objectives</italic>: One objective of the circular migrations (Chapter 2) project is to compare compartmental and network models in how they explain the dynamics of a system in which some individuals engage in circular migrations. Another goal is to understand the role such movement patterns play in HIV transmission, given the critical interaction between acute infection and rate of movement. In the population of MSM in Southern California, I model post-diagnosis behavior change (PDBC). The objective in Chapter 3 is to quantify the population-level effects of individual-level PDBC. A second objective (Chapter 4) is to compare various strategies for early diagnosis in terms of how many new infections they produce over a 10-year period. <italic>Methods</italic>: The compartmental models in Chapter \ref{chap:migrations} are developed using ordinary differential equations (ODE's) and the network models are derived from the exponential random graph models (ERGM's). Epidemiological studies on circular migrations in the KwaZulu-Natal province conducted over the past decade provide the necessary motivation. The models on PDBC in Chapters 3 and 4 are based on ERGMs. The behavioral components of these models are parameterized primarily using the Acute Infection and Early Disease Research Program (AIEDRP). Several other studies are used to model the various biological and demographic components of these models (details in Appendix F). <italic>Results</italic>: In Chapter 2, I find that compartmental models do not show any impact of the frequency of migrations on HIV prevalence. Under suitable assumptions, network models show that ``frequent'' migrations (that take place at intervals shorter than the window of acute infection) produce a larger epidemic than infrequent migrations. In Chapter 3, I find that if there were no PDBC, HIV prevalence in Southern California MSM would be higher by about a third. In Chapter 4, I find that individual testing strategies where people test based on the number of partners or time since last test work better than other strategies I consider. <italic>Discussion</italic>: Chapter 2 is a largely theoretical study, parameterized by qualitative descriptions of data. While the question of the precise impact of circular migrations on HIV transmission is still an open one, and likely contingent upon specific behavioral components in particular populations where circular migrations are practiced. However, our %%my? work demonstrates that we need to network models to understand this connection. We also demonstrate the potential impact of acute infection and its interaction with frequency of migration, and the effect of delayed path-acceleration. In Chapters 3 and 4, I focus on behavioral interventions to prevent HIV infections. I do not consider ``treatment as prevention'' type strategies; though such considerations are suitable for future work and may act in synergy with the behavioral interventions I consider here.en_US
dc.format.mimetypeapplication/pdfen_US
dc.language.isoen_USen_US
dc.rightsCopyright is held by the individual authors.en_US
dc.subjectBioBehavioral HIV Modeling; Circular Migrations; Compartmental Modeling; Exponential Random Graph Models; MSM; Network Modelingen_US
dc.subject.otherApplied mathematicsen_US
dc.subject.otherStatisticsen_US
dc.subject.otherEpidemiologyen_US
dc.subject.otherquantitative ecology and resource managementen_US
dc.titleBio-Behavioral Models for HIV Preventionen_US
dc.typeThesisen_US
dc.embargo.termsDelay release for 6 months -- then make Open Accessen_US


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