scholarly journals Assessing the performance of the generalized propensity score for estimating the effect of quantitative or continuous exposures on survival or time-to-event outcomes

2018 ◽  
Vol 28 (8) ◽  
pp. 2348-2367
Author(s):  
Peter C Austin

Propensity score methods are frequently used to estimate the effects of interventions using observational data. The propensity score was originally developed for use with binary exposures. The generalized propensity score (GPS) is an extension of the propensity score for use with quantitative or continuous exposures (e.g. pack-years of cigarettes smoked, dose of medication, or years of education). We describe how the GPS can be used to estimate the effect of continuous exposures on survival or time-to-event outcomes. To do so we modified the concept of the dose–response function for use with time-to-event outcomes. We used Monte Carlo simulations to examine the performance of different methods of using the GPS to estimate the effect of quantitative exposures on survival or time-to-event outcomes. We examined covariate adjustment using the GPS and weighting using weights based on the inverse of the GPS. The use of methods based on the GPS was compared with the use of conventional G-computation and weighted G-computation. Conventional G-computation resulted in estimates of the dose–response function that displayed the lowest bias and the lowest variability. Amongst the two GPS-based methods, covariate adjustment using the GPS tended to have the better performance. We illustrate the application of these methods by estimating the effect of average neighbourhood income on the probability of survival following hospitalization for an acute myocardial infarction.

2020 ◽  
Vol 29 (3) ◽  
pp. 709-727
Author(s):  
Shandong Zhao ◽  
David A van Dyk ◽  
Kosuke Imai

Propensity score methods are a part of the standard toolkit for applied researchers who wish to ascertain causal effects from observational data. While they were originally developed for binary treatments, several researchers have proposed generalizations of the propensity score methodology for non-binary treatment regimes. Such extensions have widened the applicability of propensity score methods and are indeed becoming increasingly popular themselves. In this article, we closely examine two methods that generalize propensity scores in this direction, namely, the propensity function (PF), and the generalized propensity score (GPS), along with two extensions of the GPS that aim to improve its robustness. We compare the assumptions, theoretical properties, and empirical performance of these methods. On a theoretical level, the GPS and its extensions are advantageous in that they are designed to estimate the full dose response function rather than the average treatment effect that is estimated with the PF. We compare GPS with a new PF method, both of which estimate the dose response function. We illustrate our findings and proposals through simulation studies, including one based on an empirical study about the effect of smoking on healthcare costs. While our proposed PF-based estimator preforms well, we generally advise caution in that all available methods can be biased by model misspecification and extrapolation.


2020 ◽  
Vol 375 (1800) ◽  
pp. 20190271 ◽  
Author(s):  
Jasper H. B. de Groot ◽  
Peter A. Kirk ◽  
Jay A. Gottfried

Humans, like other animals, have an excellent sense of smell that can serve social communication. Although ample research has shown that body odours can convey transient emotions like fear, these studies have exclusively treated emotions as categorical , neglecting the question whether emotion quantity can be expressed chemically. Using a unique combination of methods and techniques, we explored a dose–response function: Can experienced fear intensity be encoded in fear sweat? Specifically, fear experience was quantified using multivariate pattern classification (combining physiological data and subjective feelings with partial least-squares-discriminant analysis), whereas a photo-ionization detector quantified volatile molecules in sweat. Thirty-six male participants donated sweat while watching scary film clips and control (calming) film clips. Both traditional univariate and novel multivariate analysis (100% classification accuracy; Q 2 : 0.76; R 2 : 0.79) underlined effective fear induction. Using their regression-weighted scores, participants were assigned significantly above chance (83% > 33%) to fear intensity categories (low–medium–high). Notably, the high fear group ( n = 12) produced higher doses of armpit sweat, and greater doses of fear sweat emitted more volatile molecules ( n = 3). This study brings new evidence to show that fear intensity is encoded in sweat (dose–response function), opening a field that examines intensity coding and decoding of other chemically communicable states/traits. This article is part of the Theo Murphy meeting issue ‘Olfactory communication in humans’.


Atmósfera ◽  
2017 ◽  
Vol 30 (1) ◽  
pp. 53-61 ◽  
Author(s):  
John Fredy Ríos Rojas ◽  
◽  
David Aperador Rodríguez ◽  
Edwin Arbey Hernández García ◽  
Carlos Enrique Arroyave Posada ◽  
...  

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