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Ottar Bjornstad Center for Infectious Disease Dynamics, Penn State University

Some challenges to make current data-driven (‘statistical’) models even more relevant to public health. Ottar Bjornstad Center for Infectious Disease Dynamics, Penn State University. Focus on time series analysis of incidence analysis. 400k. 0-1y. 5-10y. 1-3y. 10-15y. 350k. 3-5y. 15- y.

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Ottar Bjornstad Center for Infectious Disease Dynamics, Penn State University

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  1. Some challenges to make current data-driven (‘statistical’) models even more relevant to public health Ottar Bjornstad Center for Infectious Disease Dynamics, Penn State University

  2. Focus on time series analysis of incidence analysis 400k 0-1y 5-10y 1-3y 10-15y 350k 3-5y 15- y 300k 250k 200k 150k 100k 50k 0 ‘44 ‘55 Quarterly measles incidence 44-55

  3. Outline: ~ 1993 then –> now current challenges mostly anecdotal personal reflections

  4. ~ 1993

  5. ~1993 maturing* mathematical formalism incorporating: (cf yesterdays talks by Mick and Val) • Seasonal forcing • Age-structure & non-homogenous mixing • Spatial diffusion & metapopulation dynamics • Plausible scenarios of scaling of transmission with pop size • Stochasticity But, early days w.r.t. letting these general models loose on data … * for directly transmitted persistent (SI), fully immunizing (SIR) or fully non-immunizing (SIS)

  6. ~1993 Early days w.r.t. letting these general models loose on data … … because of many challenges The obvious: • Absence of data on key state variables (eg susceptible) • Disparity between key state variables and observed quantities (eg incidence is not prevalence) The less obvious: • Weariness regarding whether a detailed quantitative match to data should be a critical characteristic of mathematical models

  7. then –> now

  8. Today’s expectation for match (1) eg TSIR forecast for E&W measles (E&W) Incidence TSIR forecast

  9. TSIR: Discrete time ‘piecewise constant’ B-D process (cf Chain-binomial) If l is small relative to S, then the chain can be approximated by an unconstrained B-D process; The conditional distribution of It+1 is the sum of It Geometric distributions -> NegBin with clumping It Host dynamics Transmission dynamics Stochasticity S - Susceptibles, B - Births , I - Infected and Infective,  - epidemic intensity,  - correction for time discretization, β - seasonal transmission rate

  10. Today’s expectation for match (2) eg age-structured TSIR forecast for rubella (South Africa) * * difference in heat intensity is due to underreporting Metcalf et al 2013

  11. Yesteryear’s expectations Kot and Schaffer (1985) JTB: “One way of resolving the problem is to view the motion in phase space, i.e. in a vector space whose axes are the state independent variables. However, for most real world ecological and epidemiological systems, this requirement is not easily met. It is often difficult even to enumerate all of the state variables, much less to follow their magnitudes over time. Put another way, the variables studied in nature are generally embedded in more complex systems. As a practical matter, it is unlikely that population dynamicists will ever be able to write down the complete governing equations for any natural system.” ID complexities: age-structured mixing, age-specific seasonality in transmission, spatial heterogeneity, heterogeneities in susceptibility, etc, etc

  12. Journey from there to here (1) -> Many ‘Obvious’ challenges were painstakingly resolved along the way

  13. Journey from there to here (1) -> Many ‘Obvious’ challenges were painstakingly resolved along the way 1) Perhaps models may have some qualitative relevance? - Nonparametric forecasting to distinguish cycles from chaos (Suigihara &c). - Nonparametric Lyapunov exponent estimators (Ellner &c).

  14. Journey from there to here (1) -> Many ‘Obvious’ challenges were painstakingly resolved along the way 1) Perhaps models may have some qualitative relevance? - Nonparametric forecasting to distinguish cycles from chaos (Suigihara &c). - Nonparametric Lyapunov exponent estimators (Ellner &c). 2) If we can somehow reconstruct the unobserved susceptible class, would it be egregiously ambitious to compare model simulations and data? - Semiparametric models with smart embedding (Ellner &c) - Susceptible reconstruction (Bobashev &c; Finkenstadt &c)

  15. Journey from there to here (1) -> Many ‘Obvious’ challenges were painstakingly resolved along the way 1) Perhaps models may have some qualitative relevance? - Nonparametric forecasting to distinguish cycles from chaos (Suigihara &c). - Nonparametric Lyapunov exponent estimators (Ellner &c). 2) If we can somehow reconstruct the unobserved susceptible class, would it be egregiously ambitious to compare model simulations and data? - Semiparametric models with smart embedding (Ellner &c) - Susceptible reconstruction (Bobashev &c; Finkenstadt &c) 3) A seasonal chain-binomial model can in fact be recast as a non-autonomous autoregressive regression: I dear you! - Time-series SIR ver 1 (Finkenstadt & Grenfell) and TSIR ver 2

  16. Journey from there to here (1) -> Many ‘Obvious’ challenges were painstakingly resolved along the way 1) Perhaps models may have some qualitative relevance? - Nonparametric forecasting to distinguish cycles from chaos (Suigihara &c). - Nonparametric Lyapunov exponent estimators (Ellner &c). 2) If we can somehow reconstruct the unobserved susceptible class, would it be egregiously ambitious to compare model simulations and data? - Semiparametric models with smart embedding (Ellner &c) - Susceptible reconstruction (Bobashev &c; Finkenstadt &c) 3) A seasonal chain-binomial model can in fact be recast as a non-autonomous autoregressive regression: I dear you! - Time-series SIR ver 1 (Finkenstadt & Grenfell) and TSIR ver 2 4) Why in the world does the TSIR seem to fit measles in E&W? - ‘Emergent simplicity’ (Grenfell); Dynamic homogeneity (Earn &c)

  17. Journey from there to here (2) 5) We believe! Real dynamics can be predicted by simple mechanistic models (that incorporates key idiosyncrasies) - POMP et al (King &c) - Hierarchical models with observation process (Cauchemez &c). - Age-structured TSIR (Metcalf &c). ….. (cf Simon’s talk)

  18. Journey from there to here (2) 5) We believe! Real dynamics can be predicted by simple mechanistic models (that incorporates key idiosyncrasies) - POMP et al (King &c) - Hierarchical models with observation process (Cauchemez &c). - Age-structured TSIR (Metcalf &c). ….. (cf Simon’s talk) Lessons from last 20 years: - ‘All models are wrong …’ Some much less than we expected. - Emergent simplicity once key idiosyncrasies are identified - ?Tactical/strategical? models may be more relevant than we expected. [The prevailing notion that computation was the important driver in the field is wrong (Cambridge MRCs BUGS has been around since 20 years)]

  19. Some current challenges

  20. Some critical issues are: • (i) use nonlinear stochastic modeling to identify all potentially undesirable • side effects of intervention-induced reduction in circulation. • Rubella and CRS (cf Jess’ talk) • Chikenpox vaccine and increased shingles incidence • Whooping cough and the role of natural antigen circulation in maintaining immune memory. The possibility of long-term vaccine failure. • More case law!

  21. Mass-vaccination introduced in most rich countries in mid ‘40s - early ’50s Vaccine introduced The first decades of vaccine induced control was extremely successful …

  22. Mass-vaccination introduced in most rich countries in mid ‘40s - early ’50s Vaccine introduced The first decades of vaccine induced control was extremely successful … … Then even in very high cover areas throughout the developed world (e.g. Massachusetts with consistent >95% cover) the disease re-emerged!

  23. Massachusets age-incidence patterns Re-emergence is associated with a completely different core group Lavine, King and Bjornstad. 2011. PNAS

  24. The ‘anamnestic’ 4 compartment SIR model – re-exposure helps maintain immune memory  - force of infection  - boosting coeffiecient  - recovery rate • - rate of loss of immunity  - rate of loss of immunity S – suceptible I – Infected R – Highly immune W – Waning: resistant to infection and will get boosted or loose immunity depending on competing rates Lavine, King and Bjornstad. 2011. PNAS

  25. As long as the anamnestic response is at least 10x greater than the naïve response: Pre-vaccination prediction Age

  26. Post-vaccination prediction: Lavine, King and Bjornstad. 2011. PNAS

  27. Natural immune boosting in pertussis dynamics and the potential for long-term vaccine failure      Incidence ‘SIS’ ‘SIR’ Vaccine coverage

  28. Predicted public health consequences of a booster vaccine at age 15 … … The booster may push circulation towards adults of childbearing age and increase perinatal infection and increase severe disease. (cf CRS but different mechanism)

  29. Some critical issues are: • (ii) robust forecasting in the face of rapidly changing demographies and • vaccination schedules

  30. (ii) robust forecasting in the face of rapidly changing demographies and • vaccination schedules e.g. Measles Incidence in China: 3 provinces From Matt Ferrari

  31. (ii) robust forecasting in the face of rapidly changing demographies and • vaccination schedules; * * Perreti et al PNAS 2013 110:5253-5257 (‘Model-free forecasting outperforms the correct mechanistic model for simulated and experimental data’) is not the way to go

  32. (iii) probabilistically projecting possible/probable build-up of ‘susceptible pockets’ in the face of imperfect vaccination programs

  33. (iii) probabilistically projecting possible/probable build-up of ‘susceptible pockets’ in the face of imperfect vaccination programs Eg Measles (from Matt Ferrari) Sao Paolo: 1997 Burkina Faso: 2009 France, 2011 • Malawi: 2010 • >135,000 cases following 10 years of low incidence

  34. (iv) Important challenge: We need accurate parametric anchoring of mechanistic models Log-likelihood • Inference for mechanistic models usually reveal severe multicollinearity among parameters: • Various parameter combinations can fit observed data equally well, • but will not make the same out of sample predictions Interstage β Intrastage β Eg 2-stage PDV model (cf Klepac et al. 2009)

  35. - ‘All models are wrong …’ Some much less than we expected. - Emergent simplicity once key idiosyncrasies are identified. • ?Tactical/strategical? models may be more relevant than we expected. - We have an enormous arsenal of model fitting tools. - Multicollinearity makes anchoring of estimates a critical challenge. Current modeling challenges: - Study unanticipated Public health consequences - Consequences of rapidly changing demographics - Understand build-up of susceptible pockets Thank you!

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