TY - JOUR
T1 - Bayesian inference of set-point viral load transmission models
AU - Libin, Pieter
AU - Hernalsteen, Laurens
AU - Theys, Kristof
AU - Gomes, Perpetua
AU - Abecasis, Ana
AU - Nowé, Ann
N1 - Publisher Copyright:
© 2018 University of Groningen. All rights reserved.
PY - 2018
Y1 - 2018
N2 - When modelling HIV epidemics, it is important to incorporate set-point viral load and its heritability. As set-point viral load distributions can differ significantly amongst epidemics, it is imperative to account for the observed local variation. This can be done by using a heritability model and fitting it to a local set-point viral load distribution. However, as the fitting procedure needs to take into account the actual transmission dynamics (i.e., social network, sexual behaviour), a complex model is required. Furthermore, in order to use the estimates in subsequent modelling analyses to inform prevention policies, it is important to assess parameter robustness. In order to fit set-point viral load models without the need to capture explicitly the transmission dynamics, we present a new protocol. Firstly, we approximate the transmission network from a phylogeny that was inferred from sequences collected in the local epidemic. Secondly, as this transmission network only comprises a single instance of the transmission network space, and our aim is to assess parameter robustness, we infer the transmission network distribution. Thirdly, we fit the parameters of the selected set-point viral load model on multiple samples from the transmission network distribution using approximate Bayesian inference. Our new protocol enables researchers to fit set-point viral load models in their local context, and diagnose the model parameter’s uncertainty. Such parameter estimates are essential to enable subsequent modelling analyses, and thus crucial to improve prevention policies.
AB - When modelling HIV epidemics, it is important to incorporate set-point viral load and its heritability. As set-point viral load distributions can differ significantly amongst epidemics, it is imperative to account for the observed local variation. This can be done by using a heritability model and fitting it to a local set-point viral load distribution. However, as the fitting procedure needs to take into account the actual transmission dynamics (i.e., social network, sexual behaviour), a complex model is required. Furthermore, in order to use the estimates in subsequent modelling analyses to inform prevention policies, it is important to assess parameter robustness. In order to fit set-point viral load models without the need to capture explicitly the transmission dynamics, we present a new protocol. Firstly, we approximate the transmission network from a phylogeny that was inferred from sequences collected in the local epidemic. Secondly, as this transmission network only comprises a single instance of the transmission network space, and our aim is to assess parameter robustness, we infer the transmission network distribution. Thirdly, we fit the parameters of the selected set-point viral load model on multiple samples from the transmission network distribution using approximate Bayesian inference. Our new protocol enables researchers to fit set-point viral load models in their local context, and diagnose the model parameter’s uncertainty. Such parameter estimates are essential to enable subsequent modelling analyses, and thus crucial to improve prevention policies.
KW - Approximate Bayesian Inference
KW - HIV epidemics
KW - HIV transmission networks
KW - Set-point viral load
UR - http://www.scopus.com/inward/record.url?scp=85072679433&partnerID=8YFLogxK
M3 - Conference article
AN - SCOPUS:85072679433
SN - 1568-7805
SP - 107
EP - 121
JO - Belgian/Netherlands Artificial Intelligence Conference
JF - Belgian/Netherlands Artificial Intelligence Conference
T2 - 30th Benelux Conference on Artificial Intelligence, BNAIC 2018
Y2 - 8 November 2018 through 9 November 2018
ER -