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Plappert, F.

Publications and source records attributed to Plappert, F..

2 recordsLinked to original sources

Representing Sex in Cardiovascular Models: Calibrating Reference Parameters from Healthy Cohorts

Reduced-order models are increasingly used to study cardiac physiology and inform patient-specific therapies. However, a model's prediction is only as reliable as its underlying parameters: representative model parameterization is essential to reflect the physiology of the populations these models are meant to represent, including biological sex. Most current models are parameterized from male or sex-agnostic data and/or focus on specific pathologies. Therefore, the goal of this work is to establish a formal parameter estimation pipeline for deriving reduced-order cardiovascular model parameter ranges that are physiologically representative of healthy women and men. We calibrated a closed-loop reduced order model of the heart and circulation separately for healthy female and male populations, using data pooled from eleven healthy cohorts. To account for parameter sensitivity and identifiability, we employed a three-stage parameter subset reduction pipeline: global sensitivity analysis (Sobol's method), collinearity screening (Fisher information matrix), and profile-likelihood identifiability analysis. Sex-specific distributions of parameters that were deemed sensitive and identifiable for each sex, ten for women and 9 for men, were obtained by Hamiltonian Monte Carlo. All the calibrated parameters showed less than 80% overlap between sexes, with the smallest overlap observed in some of the most influential parameters, such as stressed blood volume. Comparing simulations of the calibrated models against allometrically size-matched simulations showed that body size explained some, but not all, of the sex differences. The resulting parameter distributions provide reference ranges usable in future mechanistic and patient-specific simulations to contribute to more inclusive cardiovascular modeling.

bioengineering↗

A computational model to study hemodynamics during atrial fibrillation

Atrial fibrillation (AF) is associated with reduced cardiac output, which is correlated with increased symptomatic burden and declined quality of life. Predicting hemodynamic effects of AF remains challenging due to the complex interplay of multiple contributing mechanisms. Computational modeling offers a valuable tool for simulating hemodynamics. However, existing models are lacking the capabilities to both replicate beat-to-beat hemodynamic variations during AF while being well suited for fitting to clinical data. In this study, we present a computational model comprising: 1) an electrical subsystem that generates uncoordinated atrial and irregular ventricular activation times characteristic of AF, and 2) a mechanical subsystem that simulates hemodynamics using a reduced order model. The model was fitted to replicate individual hemodynamic measurements from 17 patients in the SMURF study during both normal sinus rhythm (NSR) and AF. The fitted model matched a large majority (75%) of blood pressure and intracardiac pressure measurements in both NSR and AF with absolute simulation errors well below 10 mmHg. Furthermore, a large majority of left atrial and left ventricular ejection fraction measurements during NSR were matched with absolute simulation errors well below 10%. The model consistently underestimated right ventricular diastolic pressure during NSR while overestimating right ventricular systolic and mean left atrial pressures during AF. The presented approach of modeling atrial activity in AF as uncoordinated atrial contractions, rather than no atrial contraction, achieved lower overall absolute simulation errors when fitting to individual patients. This computationally efficient model provides a platform for future investigations of patient-specific hemodynamics during AF.

bioengineering↗