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

Dose Response Curve: Conventional Versus Nonmonotonic01:21

Dose Response Curve: Conventional Versus Nonmonotonic

The correlation between a drug's dosage and its impact on a biological system is a cornerstone of pharmacology and toxicology. Conventional dose–response curves, which include graded and quantal relationships, are key to this understanding. Graded dose–response curves depict the spectrum of a biological reaction to different doses within an individual, indicating that as the drug dosage increases, so does the intensity of the response. On the other hand, quantal dose–response relationships...
Toxicity Testing in Animals01:23

Toxicity Testing in Animals

Toxicity tests in animals are grounded on two main assumptions: first, the effects observed in laboratory animals can be extrapolated to humans, especially when adjusted for body surface area; second, high-dose exposure in animals is essential to identify potential human hazards from lower doses. This is based on the quantal dose-response concept, which faces the challenge of extrapolating results from relatively few test animals to much larger human populations. For example, a 0.01% incidence...
Two-Compartment Open Model: Extravascular Administration01:12

Two-Compartment Open Model: Extravascular Administration

The two-compartment model for extravascular administration represents a drug's absorption and distribution process. It features a central compartment, where the drug is first absorbed, and a peripheral compartment, which illustrates the drug's distribution throughout the body. The rate of change in drug concentration in the central compartment is calculated by three exponents: absorption, distribution, and elimination.
The absorption exponent (ka) indicates the speed at which the drug is...
Drug Toxicity: Dose-Dependent Reactions01:24

Drug Toxicity: Dose-Dependent Reactions

Drug toxicities can be stratified into pharmacological, pathological, or genotoxic based on their mechanisms. The incidence and severity of these toxicities generally increase with the drug's concentration in the body and exposure time.Pharmacological toxicity is evident when the therapeutic effects of drugs overshoot into adverse reactions in a predictable, dose-dependent manner. Central nervous system (CNS) depression from barbiturates is a classic example, with effects escalating from...
Drug Toxicity: Risk factors01:24

Drug Toxicity: Risk factors

Adverse Drug Reactions (ADRs) are potential complications that arise during pharmacotherapy, influenced by multiple risk factors. Age plays a significant role; both neonates and the elderly are at heightened risk due to their respective immature and diminished metabolic and elimination processes. Gender also impacts ADRs, with females experiencing a 1.5 to 1.7-fold greater risk than males, which may be linked to pharmacokinetic, pharmacodynamic, and hormonal differences. Notably, neonates, the...
Three-Compartment Open Model01:06

Three-Compartment Open Model

The three-compartment open model is a pharmacokinetic model used to describe the distribution and elimination of drugs following extravascular administration. It comprises a central compartment representing the plasma and two peripheral compartments. The highly perfused peripheral compartment represents organs and tissues with a rich blood supply, such as the liver, kidneys, and lungs. The scarcely perfused peripheral compartment represents tissues with lower blood supply, such as adipose...

You might also read

Related Articles

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

Sort by
Same author

Bclaf1 drives heart failure by recruiting Srsf2 to enhance Hand2 pre-mRNA splicing and pathological hypertrophy.

Nature communications·2026
Same author

Efficient semi-supervised estimation of optimal individualized treatment regimes with survival outcome.

Statistical methods in medical research·2026
Same author

MXene/RGO/Si Schottky Junction for a High-Performance Self-Powered Broadband Photodetector.

Langmuir : the ACS journal of surfaces and colloids·2026
Same author

Hippocampal GFAP in aging: Associations with AD and LATE-NC pathologies and cognitive decline in older adults.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026
Same author

Preoperative dermatomal somatosensory evoked potentials in risk prediction of early postoperative neurological deterioration after thoracic spine surgery: a retrospective cohort study.

Journal of orthopaedic surgery and research·2026
Same author

Synergistic Design of ZnCo-MnO@NPC Cathode and ZIF-8@Zn Anode for High-Performance Aqueous Zinc-Ion Batteries.

Molecules (Basel, Switzerland)·2026

Related Experiment Video

Updated: Jun 11, 2026

Diffuse Optical Spectroscopy for the Quantitative Assessment of Acute Ionizing Radiation Induced Skin Toxicity Using a Mouse Model
06:21

Diffuse Optical Spectroscopy for the Quantitative Assessment of Acute Ionizing Radiation Induced Skin Toxicity Using a Mouse Model

Published on: May 27, 2016

Two-dimensional toxic dose and multivariate logistic regression, with application to decompression sickness.

Jialiang Li1, Weng Kee Wong

  • 1Department of Statistics & Applied Probability, Duke-NUS Graduate Medical School, National University of Singapore, Singapore 117546. stalj@nus.edu.sg

Biostatistics (Oxford, England)
|July 7, 2010
PubMed
Summary
This summary is machine-generated.

This study introduces a new statistical method for analyzing multiple dichotomous outcomes in toxicology, specifically for estimating toxic doses in decompression sickness (DCS) studies. The Gumbel-type logistic regression model helps determine risk factor ranges for a fixed DCS probability.

More Related Videos

In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox
05:47

In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox

Published on: August 28, 2019

Related Experiment Videos

Last Updated: Jun 11, 2026

Diffuse Optical Spectroscopy for the Quantitative Assessment of Acute Ionizing Radiation Induced Skin Toxicity Using a Mouse Model
06:21

Diffuse Optical Spectroscopy for the Quantitative Assessment of Acute Ionizing Radiation Induced Skin Toxicity Using a Mouse Model

Published on: May 27, 2016

In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox
05:47

In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox

Published on: August 28, 2019

Area of Science:

  • Toxicology and Biostatistics
  • Risk Assessment and Dose-Response Modeling

Background:

  • Multivariate statistical methods for continuous toxicological data are well-established.
  • Multivariate techniques for dichotomous response variables, crucial in many toxicological studies, are less developed.
  • Decompression sickness (DCS) studies often involve multiple, simultaneous dichotomous outcomes requiring advanced statistical analysis.

Purpose of the Study:

  • To develop and present a novel statistical methodology for analyzing multiple dichotomous toxicological outcomes.
  • To address the challenge of estimating a 2D toxic dose corresponding to a fixed risk for multiple DCS types.
  • To provide a robust method for risk factor analysis in toxicological experiments with binary endpoints.

Main Methods:

  • Proposed a Gumbel-type generalization of logistic regression tailored for multiple dichotomous variables.
  • Employed maximum likelihood estimation (MLE) to fit the proposed statistical model.
  • Demonstrated the application of the method using real-world data from a Wisconsin sheep DCS study.

Main Results:

  • Successfully fitted the Gumbel-type generalized logistic regression model to the toxicological data.
  • The fitted model enables the estimation of a 2D toxic dose based on a fixed probability of developing DCS.
  • The methodology provides a quantitative approach to understanding the relationship between risk factors and multiple adverse outcomes.

Conclusions:

  • The proposed Gumbel-type generalized logistic regression offers a viable statistical solution for analyzing multiple dichotomous toxicological endpoints.
  • This method advances the field of dose-response modeling for complex toxicological outcomes.
  • The approach is particularly useful for studies like DCS where multiple binary outcomes and risk factors are of interest.