Today, U.S. Sen. David Vitter (R-La.), top Republican on the Environment and Public Works Committee, sent a letter to Jim Jones, Assistant Administrator of the Office of Chemical Safety and Pollution Prevention (OCSPP) of the U.S. Environmental Protection Agency (EPA), regarding the Agency's Final Toxicological Review of Methanol (Non-Cancer) that was released on September 30th. Vitter attests that the EPA fails to use the best available science in their final review, and that the Agency goes so far as to intentionally ignore their own peer reviewers.

"I cannot fathom why EPA continues to ignore implementing the reform principals that the National Academy of Sciences has said are necessary. The Agency is taking creative liberties while using dubious rhetorical arguments, which only undermine their product for chemical management," said Vitter. "The most disappointing aspect is that this is not the first time, nor do I expect it to be the last time, that EPA chooses its ‘science-based' conclusions in a manner that is devoid of recognizing the weight of the scientific evidence."

In January 2012, Vitter, along with Sen. James Inhofe (R-Okla.) and Reps. Paul Broun (R-Ga.) and Andy Harris (R-Md.), wrote to the Director of the National Toxicology Program and the Assistant Administrator of the Office of Research and Development of the EPA, expressing concern that EPA continued to fail the transparency test and persisted in using faulty data from the Ramazzini Institute in Italy to come to predetermined conclusions. The Members' bicameral oversight and inquiry lead to the EPA withdrawing use of work from the Ramazzini Institute for multiple assessments, and led the Agency to claim they would move forward using "the soundest possible science" in future EPA Assessments. Click here to read more.

The assessment released on September 30, 2013 ignores that commitment.

Text of today's letter is below. Click here for the PDF version.


October 9, 2013

The Honorable Jim Jones
Assistant Administrator
U.S. Environmental Protection Agency
Office of Chemical Safety and Pollution Prevention (OCSPP)
1200 Pennsylvania Avenue, NW
Washington, D.C. 20460

Dear Mr. Jones:

On September 30th, the EPA released its final Toxicological Review of Methanol (Non-Cancer) in support of the web posting of summary information for the Integrated Risk Information System, including a set of Appendices with the Agency's response to comments from its External Peer Review Panel as well as public comments. This is one of the first IRIS assessments to be finalized following the 2011 National Academy of Sciences series of recommendations for IRIS improvements. While this final assessment does make some important cosmetic improvements that provide for a more concise and readable report, the scientific rigor of the analysis fails to address the concerns raised by the NAS and members of Congress.

Strikingly, the Agency has chosen to ignore public comments and the criticism of its own external peer review panel. In particular, the external peer review panel raised concern that the assessment employs "Uncertainty Factors" that systematically lead to conclusions that are overly conservative by several orders of magnitude. In its insufficient response to comments, the assessment employs dubious rhetorical arguments such as referring to "unquantifiable effects of uncertain adversity" to justify its rejection of suggested higher "safe" exposure levels. Further, the assessment fails to address a fundamental criticism that external exposures at the oral reference dose and inhalation reference concentration result in methanol levels in humans that are well within normal background levels from dietary exposures.

The final methanol (non-cancer) assessment fails to use the "best available science" on several fronts:

1. Toxic effects are caused by internal levels of methanol in cells, in this case estimated by blood methanol concentration. When there are both internal and external sources of a chemical at play, it is more difficult to determine the individual effect of each on human health. EPA's job - via the IRIS assessment process - is to recommend levels of external exposure which, when combined with internal exposure levels, will not result in adverse effects on human health. Unfortunately, this assessment does not determine a blood level of methanol that is likely to be without toxic effects. Rather, the assessment focuses on whether an oral exposure at the RfD combined with inhalation exposure at the RfC results in a blood methanol level that is "distinguishable" for a non-externally exposed person with average endogenous blood methanol levels. All three external peer reviewers and public commenters disagreed with the EPA that EPA's suggested RfD and RfC would lead to a "distinguishable" effect. What is more, by the EPA's own estimates only 20% of the population would show a measurable increase in blood methanol exposure to the Agency's proposed RfD/RfC.

2. On the one hand, the assessment finds that a primate study in the literature is not reliable enough to be used as a basis for establishing the reference concentration, while at the same time the Agency uses the same study to justify their proposed RfD and RfC values. This monkey study suggested methanol effects, but the differences from control groups were not statistically significant. EPA justifies their suggested RfD and RfC values on the basis that if those "uncertain, but potentially adverse effects" in monkeys were real, and the study had been used to derive the RfC and RfD, then the higher values recommended by the external peer review panel could potentially reach these levels associated with uncertain effects. A convoluted argument at best.

3. The assessment used this data to increase the literature database Uncertainty Factor (UF) from "1" to "3," and the same data to raise the animal to human UF from "3" to "10." Both the external peer reviewers and the public commenters recommended against this double counting. The choice of specific Uncertainty Factors appears to result from a desire on the part of the Agency to establish the lowest RfC and RfD that produce blood levels distinguishable from the endogenous background levels. The assessment acknowledges that the database for methanol is extensive, but then assigns a "3" UF for the literature database because there is inconclusive monkey data, even though monkey data is seldom available. The assessment provides extensive PBPK analysis to set pharmacokinetic (PK) animal to human comparison of methanol levels; thus the UF should have been no more than "3" to account for pharmacodynamic (PD) differences. They used a value of "10" (3 for PK and 3 for PD), again, because the monkey data are not fully understood.

This assessment of the non-cancer health effects of methanol by the EPA systematically ratchets down the "safe" exposure levels by providing overly conservative assumptions and uncertainty factors to the point where it provides questionable utility for risk assessment or risk management. The assessment fails to address a fundamental criticism, that exposures at the RfC and RfD result in methanol levels in humans that are well within normal background levels from dietary exposures.


David Vitter
Ranking Member
Environment and Public Works Committee