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

Causality in Epidemiology01:21

Causality in Epidemiology

1.0K
Causality or causation is a fundamental concept in epidemiology, vital for understanding the relationships between various factors and health outcomes. Despite its importance, there's no single, universally accepted definition of causality within the discipline. Drawing from a systematic review, causality in epidemiology encompasses several definitions, including production, necessary and sufficient, sufficient-component, counterfactual, and probabilistic models. Each has its strengths and...
1.0K
Criteria for Causality: Bradford Hill Criteria - II01:28

Criteria for Causality: Bradford Hill Criteria - II

751
The Bradford Hill criteria serve as guidelines for establishing causative links in epidemiological research. Beyond Strength, Consistency, Specificity, and Temporality, key criteria also include Biological Gradient, Plausibility, Coherence, Experiment, and Analogy. These principles assist scientists in assessing the likelihood of causation in complex biological contexts. Below is a summary of these concepts:
751
Censoring Survival Data01:09

Censoring Survival Data

274
Survival analysis is a statistical method used to analyze time-to-event data, often employed in fields such as medicine, engineering, and social sciences. One of the key challenges in survival analysis is dealing with incomplete data, a phenomenon known as "censoring." Censoring occurs when the event of interest (such as death, relapse, or system failure) has not occurred for some individuals by the end of the study period or is otherwise unobservable, and it might have many different...
274
Assumptions of Survival Analysis01:15

Assumptions of Survival Analysis

215
Survival models analyze the time until one or more events occur, such as death in biological organisms or failure in mechanical systems. These models are widely used across fields like medicine, biology, engineering, and public health to study time-to-event phenomena. To ensure accurate results, survival analysis relies on key assumptions and careful study design.
215
Comparing the Survival Analysis of Two or More Groups01:20

Comparing the Survival Analysis of Two or More Groups

336
Survival analysis is a cornerstone of medical research, used to evaluate the time until an event of interest occurs, such as death, disease recurrence, or recovery. Unlike standard statistical methods, survival analysis is particularly adept at handling censored data—instances where the event has not occurred for some participants by the end of the study or remains unobserved. To address these unique challenges, specialized techniques like the Kaplan-Meier estimator, log-rank test, and...
336
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches01:23

Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches

193
Biopharmaceutical studies constitute a vital field aiming to enhance drug delivery methods and refine therapeutic approaches, drawing upon diverse interdisciplinary knowledge. In research methodologies, the choice between controlled and non-controlled studies significantly influences the study's reliability and accuracy.
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast,...
193

You might also read

Related Articles

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

Sort by
Same author

An Overview and Recent Developments in the Analysis of Multistate Processes.

Statistics in medicine·2026
Same author

Clarifying the 'set to zero' approach for time-varying prenatal exposures.

International journal of epidemiology·2026
Same author

Rejoinder to the discussion on 'Causal inference with misspecified network interference structure'.

Biometrics·2026
Same author

Causal inference with misspecified network interference structure.

Biometrics·2026
Same author

Mastering rare event analysis: subsample-size determination in Cox and logistic regressions.

Biometrics·2025
Same author

Cumulative incidence function estimation using population-based biobank data.

Biometrics·2025
Same journal

Towards optimal environmental policies: policy learning under arbitrary bipartite network interference.

Biostatistics (Oxford, England)·2026
Same journal

Multilevel functional quantile principal component analysis.

Biostatistics (Oxford, England)·2026
Same journal

Adaptive transfer learning for time-to-event modeling with applications in disease risk assessment.

Biostatistics (Oxford, England)·2026
Same journal

High-dimensional test for one-sided hypotheses.

Biostatistics (Oxford, England)·2026
Same journal

NBSR: a Negative Binomial Softmax Regression model for microRNA-seq data analysis.

Biostatistics (Oxford, England)·2026
Same journal

Addressing the influence of unmeasured confounding in observational studies with time-to-event outcomes: a semiparametric sensitivity analysis approach.

Biostatistics (Oxford, England)·2026
See all related articles

Related Experiment Video

Updated: Oct 8, 2025

Establishing a Competing Risk Regression Nomogram Model for Survival Data
04:57

Establishing a Competing Risk Regression Nomogram Model for Survival Data

Published on: October 23, 2020

10.4K

Causal inference for semi-competing risks data.

Daniel Nevo1, Malka Gorfine1

  • 1Department of Statistics and Operations Research, Tel Aviv University, Tel Aviv, Israel.

Biostatistics (Oxford, England)
|December 30, 2021
PubMed
Summary
This summary is machine-generated.

The Apolipoprotein E epsilon4 allele (APOE) influences Alzheimer's disease (AD) and mortality. This study uses semi-competing risks to analyze APOE's complex causal effects on AD diagnosis and death.

Keywords:
Alzheimer’s diseaseBoundsFrailty modelIllness-death modelPrincipal stratification

More Related Videos

An R-Based Landscape Validation of a Competing Risk Model
05:37

An R-Based Landscape Validation of a Competing Risk Model

Published on: September 16, 2022

2.2K
Inverse Probability of Treatment Weighting Propensity Score using the Military Health System Data Repository and National Death Index
06:55

Inverse Probability of Treatment Weighting Propensity Score using the Military Health System Data Repository and National Death Index

Published on: January 8, 2020

14.7K

Related Experiment Videos

Last Updated: Oct 8, 2025

Establishing a Competing Risk Regression Nomogram Model for Survival Data
04:57

Establishing a Competing Risk Regression Nomogram Model for Survival Data

Published on: October 23, 2020

10.4K
An R-Based Landscape Validation of a Competing Risk Model
05:37

An R-Based Landscape Validation of a Competing Risk Model

Published on: September 16, 2022

2.2K
Inverse Probability of Treatment Weighting Propensity Score using the Military Health System Data Repository and National Death Index
06:55

Inverse Probability of Treatment Weighting Propensity Score using the Military Health System Data Repository and National Death Index

Published on: January 8, 2020

14.7K

Area of Science:

  • Biostatistics
  • Epidemiology
  • Genetics

Background:

  • The Apolipoprotein E epsilon4 allele (APOE) is a significant genetic risk factor for late-onset Alzheimer's disease (AD).
  • Defining the causal impact of APOE on both AD onset and mortality is challenging due to the interplay between these two events.
  • AD occurrence can influence the age of death, complicating direct causal inference.

Purpose of the Study:

  • To propose novel statistical methods for estimating the causal effects of APOE on both Alzheimer's disease diagnosis and death.
  • To address the complexities arising from the semi-competing risks nature of these dual outcomes.
  • To develop a framework that accounts for the order of AD diagnosis and death.

Main Methods:

  • Utilizing a semi-competing risks framework for time-to-event data analysis.
  • Proposing new estimands stratified by the order of AD diagnosis and death.
  • Introducing a novel assumption leveraging time-to-event data properties, offering more flexibility than traditional monotonicity assumptions.
  • Developing and implementing nonparametric and semiparametric estimation methods.

Main Results:

  • Derivation of results on partial identifiability of causal effects.
  • Development of a sensitivity analysis approach to assess the impact of assumption violations.
  • Identification of conditions under which full identification of causal effects is achievable.
  • Presentation of estimation methods for right-censored semi-competing risks data.

Conclusions:

  • The proposed semi-competing risks framework provides a robust method for disentangling the complex causal relationships between APOE, Alzheimer's disease, and mortality.
  • The novel estimands and assumptions offer a more nuanced understanding of genetic risk factors in the presence of competing events.
  • The developed statistical methods facilitate more accurate causal inference in complex epidemiological and genetic studies.