Public health in genetic spaces: a statistical framework to optimize cluster-based outbreak detection. Issue 1 (13th March 2020)

• Record Type: Journal Article
• Authors: Chato, Connor; Kalish, Marcia L; Poon, Art F Y
• Is Part Of: Virus evolution. Volume 6:Issue 1(2020)
• Publication Date: 2020-03-13
• Subjects: molecular epidemiology -- genetic clustering -- modifiable areal unit problem -- virus evolution -- HIV prevention; Viruses -- Evolution -- Periodicals; 579.2138
• DOI: 10.1093/ve/veaa011
• Languages: English
• ISSNs: 2057-1577

Abstract

Abstract: Genetic clustering is a popular method for characterizing variation in transmission rates for rapidly evolving viruses, and could potentially be used to detect outbreaks in 'near real time'. However, the statistical properties of clustering are poorly understood in this context, and there are no objective guidelines for setting clustering criteria. Here, we develop a new statistical framework to optimize a genetic clustering method based on the ability to forecast new cases. We analysed the pairwise Tamura-Nei (TN93) genetic distances for anonymized HIV-1 subtype B pol sequences from Seattle ( n = 1, 653) and Middle Tennessee, USA ( n = 2, 779), and northern Alberta, Canada ( n = 809). Under varying TN93 thresholds, we fit two models to the distributions of new cases relative to clusters of known cases: 1, a null model that assumes cluster growth is strictly proportional to cluster size, i.e. no variation in transmission rates among individuals; and 2, a weighted model that incorporates individual-level covariates, such as recency of diagnosis. The optimal threshold maximizes the difference in information loss between models, where covariates are used most effectively. Optimal TN93 thresholds varied substantially between data sets, e.g. 0.0104 in Alberta and 0.016 in Seattle and Tennessee, such that the optimum for one population would potentially misdirect prevention efforts in another. For a given population, the range of thresholds where the weighted model conferred greater predictive accuracy tended to be narrow (±0.005 units), and the optimal threshold tended to be stable over time. Our framework also indicated that variation in the recency of HIV diagnosis among clusters was significantly more predictive of new cases than sample collection dates (ΔAIC > 50). These results suggest that one cannot rely on historical precedence or convention to configure genetic clustering methods for public health applications, especially when translating methods between settings of low-level and generalized epidemics. Our framework not only enables investigators to calibrate a clustering method to a specific public health setting, but also provides a variable selection procedure to evaluate different predictive models of cluster growth.