Angular reproduction numbers improve estimates of transmissibility when disease generation times are misspecified or time-varying

Author:

Parag Kris V.12ORCID,Cowling Benjamin J.3ORCID,Lambert Ben C.45ORCID

Affiliation:

1. MRC Centre for Global Infectious Disease Analysis, Imperial College London, London, UK

2. NIHR Health Protection Research Unit in Behavioural Science and Evaluation, University of Bristol, Bristol, UK

3. WHO Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, The University of Hong Kong, Hong Kong Hong Kong

4. Department of Mathematics, College of Engineering, Mathematics and Physical Sciences, University of Exeter, Exeter, UK

5. Department of Statistics, University of Oxford, Oxford, UK

Abstract

We introduce theangular reproduction number Ω, which measures time-varying changes in epidemic transmissibility resulting from variations in both the effective reproduction numberR, and generation time distributionw. Predominant approaches for tracking pathogen spread infer eitherRor the epidemic growth rater. However,Ris biased by mismatches between the assumed and truew, whileris difficult to interpret in terms of the individual-level branching process underpinning transmission.Randrmay also disagree on the relative transmissibility of epidemics or variants (i.e.rA>rBdoes not implyRA>RBfor variantsAandB). We find thatΩresponds meaningfully to mismatches and time-variations inwwhile mostly maintaining the interpretability ofR. We prove thatΩ> 1 impliesR> 1 and thatΩagrees withron the relative transmissibility of pathogens. EstimatingΩis no more difficult than inferringR, uses existing software, and requires no generation time measurements. These advantages come at the expense of selecting one free parameter. We proposeΩas complementary statistic toRandrthat improves transmissibility estimates whenwis misspecified or time-varying and better reflects the impact of interventions, when those interventions concurrently changeRandwor alter the relative risk of co-circulating pathogens.

Funder

MRC Centre for Global Infectious Disease Analysis

Publisher

The Royal Society

Subject

General Agricultural and Biological Sciences,General Environmental Science,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference49 articles.

1. Anderson R Donnelly C Hollingsworth D Keeling M Vegvari C Baggaley R. 2020 Reproduction number ( R ) and growth rate ( r ) of the COVID-19 epidemic in the UK: methods of estimation data sources causes of heterogeneity. Royal Society technical report. See https://royalsociety.org/-/media/policy/projects/set-c/set-covid-19-R-estimates.pdf.

2. The temporal association of introducing and lifting non-pharmaceutical interventions with the time-varying reproduction number (R) of SARS-CoV-2: a modelling study across 131 countries

3. Assessing transmissibility of SARS-CoV-2 lineage B.1.1.7 in England

4. Are Epidemic Growth Rates More Informative than Reproduction Numbers?

5. A note on generation times in epidemic models

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