| Literature DB >> 25161995 |
Abstract
A new concept of within-individual epidemiology termed "myEpi" is introduced. It is argued that traditional epidemiological methods, which are usually applied to populations of humans, can be applicable to a single individual and thus used for self-monitoring and forecasting of "epidemic" outbreaks within an individual. Traditional epidemiology requires that results be generalizable to a predefined population. The key component of myEpi is that a single individual may be viewed as an entire population of events and thus, the analysis should be generalizable to this population. Applications of myEpi are aimed for, but not limited to, the analysis of data collected by individuals with the help of wearable sensors and digital diaries. These data can include physiological measures and records of healthy and risky behaviors (e.g., exercise, sleep, smoking, food consumption, alcohol, and drug use). Although many examples of within-individual epidemiology exist, there is a pressing need for systematic guidance to the analysis and interpretation of intensive individual-level data. myEpi serves this need by adapting statistical methods (e.g., regressions, hierarchical models, survival analysis, agent-based models) to individual-level data.Entities:
Keywords: data science; epidemiology; evidence-based practice; mobile health; myEpi; self-care; statistics; wearable devices
Year: 2014 PMID: 25161995 PMCID: PMC4129497 DOI: 10.3389/fpubh.2014.00097
Source DB: PubMed Journal: Front Public Health ISSN: 2296-2565
Figure 1An illustration of inferring to an individual form the population-level and individual-level data. The green “myEpi” oval denotes within-person data which could be also combined with information about blood relatives, social networks, as well as the entire population and the environment. The purpose of the analysis, however, is the individual-level inference.
Figure 2A “moving windows” method to identify patterns of alcohol use trajectories. Distributional properties of sliding windows Wt and W+−1 are compared to each other. The point when the distributions become significantly different signifies the change in patterns. We illustrate the point at which the pattern switched from type 5 to 7 as the number of drinks increases. The figure is reproduced with permission from Ref. (8).
Figure 3Survival curves for staying HIV negative for a female with a male HIV-positive partner in a latent HIV stage, assuming two unprotected vaginal intercourses per week. Model details and parameters are described in detail in Ref. (7).