Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Prediction Intervals01:03

Prediction Intervals

2.4K
The interval estimate of any variable is known as the prediction interval. It helps decide if a point estimate is dependable.
However, the point estimate is most likely not the exact value of the population parameter, but close to it. After calculating point estimates, we construct interval estimates, called confidence intervals or prediction intervals. This prediction interval comprises a range of values unlike the point estimate and is a better predictor of the observed sample value, y. 
2.4K
Model Approaches for Pharmacokinetic Data: Distributed Parameter Models01:06

Model Approaches for Pharmacokinetic Data: Distributed Parameter Models

143
Pharmacokinetic models are mathematical constructs that represent and predict the time course of drug concentrations in the body, providing meaningful pharmacokinetic parameters. These models are categorized into compartment, physiological, and distributed parameter models.
The distributed parameter models are specifically designed to account for variations and differences in some drug classes. This model is particularly useful for assessing regional concentrations of anticancer or...
143
Multicompartment Models: Overview01:14

Multicompartment Models: Overview

287
Multicompartment models are mathematical constructs that depict how drugs are distributed and eliminated within the body. They segment the body into several compartments, symbolizing various physiological or anatomical areas connected through drug transfer processes such as absorption, metabolism, distribution, and elimination.
These models offer a more comprehensive representation of drug behavior in the body than one-compartment models. They accommodate the complexity of drug distribution,...
287
Mechanistic Models: Compartment Models in Individual and Population Analysis01:23

Mechanistic Models: Compartment Models in Individual and Population Analysis

103
Mechanistic models are utilized in individual analysis using single-source data, but imperfections arise due to data collection errors, preventing perfect prediction of observed data. The mathematical equation involves known values (Xi), observed concentrations (Ci), measurement errors (εi), model parameters (ϕj), and the related function (ƒi) for i number of values. Different least-squares metrics quantify differences between predicted and observed values. The ordinary least...
103
End Point Prediction: Gran Plot01:07

End Point Prediction: Gran Plot

681
A Gran plot is used to predict the equivalence volume or endpoint of a potentiometric or acid-base titration without reaching the endpoint. Typically, titration data is collected as a function of the titrant's volume up to a point less than the equivalence volume and then transformed into a linear format. The straight line is extended to the x-axis, indicating the necessary titrant volume to achieve the equivalence point.
For potentiometric titration, the Gran plot is created by plotting...
681
Per-Unit Sequence Models01:26

Per-Unit Sequence Models

146
An ideal Y-Y transformer, grounded through neutral impedances, displays per-unit sequence networks akin to those of a single-phase ideal transformer when subjected to balanced positive- or negative-sequence currents. These currents do not produce neutral currents, and their associated voltage drops.
Zero-sequence currents, which are identical in magnitude and phase, generate a neutral current, resulting in voltage drops across the neutral impedance and the low-voltage winding. If the...
146

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

The Triple Functions of D2 Silencing in Treatment of Periapical Disease.

Journal of endodontics·2017
Same author

Excellent Thermoelectric Properties in monolayer WSe<sub>2</sub> Nanoribbons due to Ultralow Phonon Thermal Conductivity.

Scientific reports·2017
Same author

Activation of Akt by SC79 protects myocardiocytes from oxygen and glucose deprivation (OGD)/re-oxygenation.

Oncotarget·2017
Same author

ColorSketch: A Drawing Assistant for Generating Color Sketches from Photos.

IEEE computer graphics and applications·2017
Same author

Enclosure Transform for Interest Point Detection From Speckle Imagery.

IEEE transactions on medical imaging·2017
Same author

Altered brain structural networks in attention deficit/hyperactivity disorder children revealed by cortical thickness.

Oncotarget·2017

Related Experiment Video

Updated: Oct 9, 2025

A Method of Trigonometric Modelling of Seasonal Variation Demonstrated with Multiple Sclerosis Relapse Data
10:46

A Method of Trigonometric Modelling of Seasonal Variation Demonstrated with Multiple Sclerosis Relapse Data

Published on: December 9, 2015

10.8K

Dynamic prediction using joint models of longitudinal and recurrent event data: A Bayesian perspective.

Xuehan Ren1, Jue Wang2, Sheng Luo1,2

  • 1Xuehan Ren, Ph.D. Candidate, Department of Biostatistics, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.

Biostatistics & Epidemiology
|December 20, 2021
PubMed
Summary

This study introduces a new joint model for predicting recurrent cardiovascular events using longitudinal data. The Bayesian approach with parallel MCMC enhances personalized risk prediction for better clinical decisions.

Keywords:
ALLHAT studycardiovascular diseaseparallel EP-MCMCpersonalized prediction

More Related Videos

Using Eye Movements Recorded in the Visual World Paradigm to Explore the Online Processing of Spoken Language
09:27

Using Eye Movements Recorded in the Visual World Paradigm to Explore the Online Processing of Spoken Language

Published on: October 13, 2018

10.2K
Development of an Individual-Tree Basal Area Increment Model using a Linear Mixed-Effects Approach
04:35

Development of an Individual-Tree Basal Area Increment Model using a Linear Mixed-Effects Approach

Published on: July 3, 2020

3.5K

Related Experiment Videos

Last Updated: Oct 9, 2025

A Method of Trigonometric Modelling of Seasonal Variation Demonstrated with Multiple Sclerosis Relapse Data
10:46

A Method of Trigonometric Modelling of Seasonal Variation Demonstrated with Multiple Sclerosis Relapse Data

Published on: December 9, 2015

10.8K
Using Eye Movements Recorded in the Visual World Paradigm to Explore the Online Processing of Spoken Language
09:27

Using Eye Movements Recorded in the Visual World Paradigm to Explore the Online Processing of Spoken Language

Published on: October 13, 2018

10.2K
Development of an Individual-Tree Basal Area Increment Model using a Linear Mixed-Effects Approach
04:35

Development of an Individual-Tree Basal Area Increment Model using a Linear Mixed-Effects Approach

Published on: July 3, 2020

3.5K

Area of Science:

  • Biostatistics
  • Cardiovascular Disease Research
  • Clinical Epidemiology

Background:

  • Cardiovascular disease (CVD) studies often involve recurrent events, where individuals experience multiple occurrences.
  • Longitudinal measurements collected during follow-up are crucial predictors of these recurrent events.
  • Personalized prediction of recurrent events is vital for informed clinical decision-making.

Purpose of the Study:

  • To propose a novel joint model for analyzing longitudinal and recurrent event data in CVD studies.
  • To develop a Bayesian inference approach and a dynamic prediction framework for personalized risk assessment.
  • To enable accurate prediction of future outcome trajectories and the risk of subsequent recurrent events.

Main Methods:

  • Development of a joint model integrating longitudinal measurements and recurrent event data.
  • Application of a Bayesian approach for robust model inference.
  • Utilization of an embarrassingly parallel Markov Chain Monte Carlo (EP-MCMC) method for computational efficiency, involving data partitioning and random partition trees.

Main Results:

  • The proposed joint model effectively integrates longitudinal data with recurrent event processes.
  • The dynamic prediction framework allows for real-time risk assessment based on individual patient data.
  • The EP-MCMC method significantly improves computational efficiency for large datasets.

Conclusions:

  • The developed joint modeling framework provides a powerful tool for personalized risk prediction in cardiovascular disease.
  • This approach enhances clinical decision-making by offering dynamic and individualized predictions of recurrent events.
  • The study demonstrates the successful application of the method to the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT).