Restriction or ban of Ephedra supported by first comparitive herbal study
The first comparative study to examine the risk of taking ephedra with that of taking other commonly used herbs calls into question the herbal stimulant’s current standing as an unrestricted dietary supplement.
Researchers found that products containing ephedra accounted for less than 1 percent of the herbal supplement sales in the United States in 2001. These products, however, were responsible for 62 percent of all herbal-related reports made to poison control centers nationwide that year, according to the study by researchers at the San Francisco VA Medical Center (SFVAMC).
“The argument has always been that ephedra is safe because it is natural and has been used for thousands of years. Our study shows that ephedra is hundreds of times riskier than other commonly used herbs,” said the study’s lead author, Stephen Bent, MD, staff physician at SFVAMC and an assistant professor of medicine at UCSF.
The study will appear in the March 18 issue of the Annals of Internal Medicine and becomes available online February 3. The findings prompted its authors to call for more stringent regulation or banning of the substance by the U.S. Food and Drug Administration.
Products containing ephedra, also known as ma-huang, often claim to promote weight-loss and boost energy. However, the herb and its extract are known to cause certainevere side-effects including anxiety, insomnia, increases in blood pressure and heart rate, and have been associated with many more serious reactions, including heart attacks and strokes that can lead to death.
In the current study, researchers used data gathered by the American Association of Poison Control Centers and published in its “Toxic Event Surveillance System Database Annual Report 2001.” An estimated 80 percent of the calls received by poison control centers come from the general public, as opposed to health care providers.
The researchers used the call data in conducting a statistical analysis commonly employed to monitor the relative safety of prescription drugs. “We looked at the number of adverse events among ephedra users versus the number of adverse events among users of other herbs,” said Bent, also a researcher with UCSF’s Osher Center for Integrative Medicine.
Taking into account the volume of sales for each product, the researchers calculated that the use of ephedra poses a risk 200 times greater than the risks posed by all other herbal supplements combined. Individual comparisons ranged from a relative risk compared to kava of 100 times greater to 720 times greater when compared to Ginkgo biloba.
“The markedly elevated relative risks observed with ephedra-containing products were stable over a wide range of estimates of ephedra sales,” Bent said
The study’s senior author, Michael Shlipak, MD, MPH, said ephedra has stimulant properties that have been well described. “Our study shows that ephedra is unsafe for routine and unsupervised use,” said Shlipak, a SFVAMC researcher and an assistant professor of medicine and epidemiology and biostatistics at UCSF.
Shlipak said: “The regulation of ephedra is an important issue that currently has the attention of the US Congress and the Bush administration, and we hope that our study will inform that decision.”
Additional authors on the study include Thomas N. Tiedt, PhD of the Med-Tox Group of Longboat Key, Florida and Michelle Odden, BS of the San Francisco VA Medical Center.
Bent’s research is supported by a career development award from the National Center for Complementary and Alternative Medicine, a component of the National Institutes of Health.
Shlipak’s research is supported by a career development award from the Health Services Research and Development division of the Veterans Affairs.
Source: University Of California - San Francisco. February 3, 2003.
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