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About BMDS

Background Information

Prior to the 1990's, RfDs and RfCs had been determined from no-observed-adverse-effect levels (NOAELs), which represent the highest experimental dose for which no statistically significant adverse health effects were reported or, in the absence of a NOAEL, the lowest-observed-adverse-effect levels (LOAEL). In 1995, EPA's Risk Assessment Forum published guidance on the benchmark dose (BMD) approach in the assessment of noncancer health risk (U.S. EPA, 1995) which listed several advantages of the BMD approach over use of NOAELs and LOAELs. In 1995, EPA's National Center for Environmental Assessment (NCEA) initiated a project to develop benchmark dose software to assist Agency risk assessors in deriving benchmark dose values for use in Agency risk assessments.

This latest version (2.0) contains twenty five (25) different models that are appropriate for the analysis of dichotomous (quantal) data (Gamma, Hill, Logistic, Log-Logistic, Multistage, Probit, Log-Probit, Quantal-Linear, Quantal-Quadratic, Weibull and Multistage-Cancer), continuous data (Linear, Polynomial, Power, Hill and Exponential) and nested developmental toxicology data (NLogistic, NCTR, and Rai & Van Ryzin).

Use of BMD methods involve fitting mathematical models to dose-response data and using the different results to select a BMD that is associated with a predetermined benchmark response (BMR), such as a 10% increase in the incidence of a particular lesion or a 10% decrease in body weight gain. BMDS facilitates these operations by providing simple data-management tools and an easy-to-use interface to run multiple models on the same dose-response data set.

Results from all models include a reiteration of the model formula and model run options chosen by the user, goodness-of-fit information, the BMD, and the estimate of the lower-bound confidence limit on the BMD (BMDL). Model results are presented in textual and graphical output files which can be printed or saved and incorporated into other documents

History of BMDS

September 30, 2008 - EPA is making version 2.1 of BMDS available at this time for public beta testing. Version 2.1 includes a beta (external peer review) version of a new time-dependent toxicodiffusion model for continuous outcomes (Zhu et al., 2005), incorporates graphical plots for the continuous exponential models and allows for the use of individual animal continuous response data. The BMDS toxicodiffusion model was developed by the USEPA National Center for Environmental Assessment (NCEA), through partnerships with the USEPA Neurotoxicology Division (NTD) and the University of South Florida, to characterize toxic effects (e.g., neurotoxicity) that potentially evolve along critical time points. It does this by:

In addition, EPA is distributing and external review (beta) version of a concentration-time (CxT) model originally programmed by Wil ten Berge. The EPA ten Berge model implements an approach to evaluating the CxT relationships for effects associated with chemical exposures. The EPA's version 1.0 implementation of this model is being distributed along with associated documentation and comments on the model received from external peer reviewers.

Finally, EPA has updated this website to offer new online and hands-on training opportunities. The online training tutorial has been updated for the 2.x versions of BMDS. A new web page has been added that details upcoming training opportinities.

July 10, 2008 - BMDS Version 2.0 final is now available. Released on July 10, 2008, it replaces BMDS 1.4.1c as the official BMDS software. BMDS 2.0 employs a new graphical user interface and makes it easy to run a number of models on a data set and compare the results. BMDS 2.0 also has a new set of quantal models with alternative background (i.e., background additive to dose) and asymptote (i.e., Hill model) parameters, as well as a Beta Exponential set of models.

November 9, 2007 - BMDS version 1.4.1c is now available. This version updates dichotomous models that were already included on BMDS version 1.4.1b. The updates primarily improve the handling of parameter specifications, particularly in situations where the user may wish to specify the background parameter to be zero.

October 10, 2007 - BMDS 2.0 beta - Build 19 released on October 10, 2007 replaces the first BMDS 2.0 beta release of September 28, 2007 (Build 13). The new Build 19 has important changes and enhancements as a result of additional testing and user exposure and should be downloaded and used instead of Build 13. Enhancements include the ability to better run a number of the BMD models and also added flexibility and fixes for user interface features. Changes include the designation of the new Dichotomous models as Alternate Dichotomous to better reflect their production status.

September 28, 2007 - EPA released BMDS Version 2.0 beta for review and testing. BMDS 2.0 beta employs a new graphical user interface and makes it easy to run a number of models for one data set and compare the results. BMDS 2.0 beta also has a new set of quantal models with alternative background (i.e., background additive to dose) and asymptote (i.e., Hill model) parameters.

August 29, 2007 - BMDS Version 1.4.1b has been added to replace version 1.4.1. This version contains an update to the BMDS help file.

February 5, 2007 - EPA released BMDS Version 1.4.1 so that all models were recompiled to improve speed, stability and compatibility with the latest version of the Windows operating system. Improvements were made to the model output format for all models. A Multistage-Cancer model was added which calculates and reports a cancer slope factor and plots the linear extrapolation from the BMDL to the background response estimate per EPA's 2005 cancer guidelines. Unlike the Multistage model, the Multistage Cancer model does not estimate added risk, nor does it allow beta coefficients to be restricted. The Quantal-Quadratic model was removed from Dichotomous model choices (note: the user can still run this model by specifying the power term of the Weibull model to be 2, but this model is not retained in the BMDS dichotomous model listings)

Issues in the continuous models that caused occasional errors in degrees of freedom assignments which impacted continuous model test results have been resolved. Acceptance criteria for Tests 2, 3 and 4 was changed from p>=0.05 to p>=0.1 and default risk type changed to "Std. Dev." for all continuous models to be consistent with EPA's draft BMD technical guidance (EPA, 2000). Issues with the Hill model have been fixed, including memory problems which were causing some operating systems to crash. Parameter standard error estimates and Chi-squared residual calculations in all the continuous models were checked and corrected if in error. Model A3 of the continuous model testing procedures has been modified so that it always uses the user-specified value for the parameter rho, including the constant-variance case where rho = 0. When rho = 0, model A3 is the same as model A1, and it is reported explicitly in the constant-variance runs. As a consequence, all model runs report the entire set of models (A1, A2, A3, R and the fitted model) and all four hypothesis tests.

Issues in the Nested models that caused occasional errors in degrees of freedom assignments have been resolved. Memory problems which were causing problems for some NCTR model runs have been fixed.

May 23, 2003 - EPA released BMDS Version 1.3.2 which contained revised polynomial (poly.exe) and nested logistic (nlogist.exe) models that are compatible with Windows 2000.

November 13, 2002 - EPA released a new polynomial model (Version 2.2) that fixed the previous incompatibility with Windows 2000.

January 22, 2002 - EPA released BMDS Version 1.3.1 which contained a revised help manual and user interface, including a revision to the interface that allows the Multistage model to calculate BMD and BMDL values for very low (below E-5) benchmark response (BMR) levels.

March 22, 2001 - EPA released BMDS Version 1.3 which contained new continuous Polynomial (v2.1), Power (v2.1) and Hill (v2.1) models, new dichotomous Multistage (v2.1), Weibull (v2.1) and Gamma (v2.2) models, and an improved user interface.  The new models are more compact and stable (will converge on BMD and BMDL solutions more often).  The user interface upgrades are described in the new help manual for version 1.3 and the readme.txt file that is distributed with the upgrade.

February 20, 2001 - EPA released BMDS Version 1.2.1 zip files containing source code, along with instructions for compiling them. If you are a programmer and wish to revise the code, please do not distribute the revised code as EPA software.

November 16, 2000 -EPA posted the report from the Discussion Materials for External Peer Review of the Draft Benchmark Dose Technical Guidance Document, Peer Review Documents for Workshop, December 7-8, 2000. 

October 25, 2000 - EPA released BMDS Version 1.2.1 which contained new versions of the continuous Polynomial (version 2.1) and Hill (version 2.1) models.  These new versions of the polynomial and Hill models fix problems associated with running the model on Windows NT/2000 operating systems, provide improved model fit for certain unique data sets and improve upon the rate of convergence on a BMD and BMDL.

September 2, 2000 - EPA released BMDS Version 1.2 to fix some problems with installation of BMDS on certain Windows 98 configurations.  This upgrade merely simplifies the installation process and corrects some problems that did not allow BMDS to install to certain computer hardware/software configurations. (This version of the software is no longer being made available as there are newer versions now available which fix problems that were being encountered on newer operating systems. See above.)

1999 - EPA hosted a Public and External Review of BMDS version 1.1b for feedback and comments. Link to the BMDS Peer Review Workshop Documents.

1995 - EPA's National Center for Environmental Assessment (NCEA) Division in RTP, NC begins the development of the EPA's benchmark dose software (BMDS) application.

1995 - EPA's Risk Assessment Forum(RAF) publishes the initial guidelines on the use of the BMD approach in the assessment of noncancer health risk.

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