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This article was published 2/12/2012 (1635 days ago), so information in it may no longer be current.
NEW YORK -- In October, the office of the inspector general of the U.S. Department of Health and Human Services issued two reports underscoring the need for improved oversight of the marketing of dietary supplements and improved surveillance of their effects. The reports add to a mounting body of evidence documenting a serious public-health problem.
Use of dietary and herbal supplements has grown dramatically in recent years in the United States. In 2007, according to the National Center for Complementary and Alternative Medicine, $14.8 billion was spent on non-vitamin, non-mineral natural products, such as fish oil, glucosamine and echinacea -- equivalent to approximately one-third of total out-of-pocket spending on prescription drugs in the U.S.
Of that total, $4.4 billion was spent on herbal supplements. Data from the National Health and Nutrition Survey for 2003 to 2006 indicate one-half of American adults use dietary supplements and 20 per cent use a supplement with at least one botanical ingredient.
Many people think because herbs are natural, and because they are being marketed and sold legally, they must be safe and effective. Furthermore, surveys of the public indicate most people believe these products are regulated by the U.S. Food and Drug Administration. In fact, both assumptions are mistaken.
In 1994, Congress passed the Dietary Supplement Health and Education Act, with heavy backing from the dietary-supplements industry. By defining herbal supplements and botanicals as dietary supplements, the act exempted them from the more rigorous standards used by the FDA in regulating food, drugs and medical devices -- essentially leaving it up to the industry to regulate itself. This piece of legislation opened the floodgates to a rapid expansion in the sale of dietary supplements.
Between 1994 and 2008, the number of dietary-supplement products on the market increased from 4,000 to 75,000. In the first 10 months of 2008, the FDA received nearly 600 reports of serious adverse events (including hospitalization, disability and death) from these products and 350 reports of moderate or mild adverse events. The FDA believes, however, these reports are drastically under-reported and estimates 50,000 annual adverse events.
Two highly respected physician-scientists, Donald Marcus of Baylor College of Medicine and Arthur Grollman of Stony Brook University, have been drawing attention to the dangers of herbal supplements for more than a decade.
In a recent article in the Archives of Internal Medicine, they noted that, "Even when the agency (the FDA) identifies an unsafe product, it lacks authority to mandate its removal from the market because it must meet the very high legal requirement to demonstrate a 'significant or unreasonable' risk. That is why it took the FDA more than 10 years to remove from the market ephedra-containing herbal weight-loss products that had caused hundreds of deaths and thousands of adverse events."
Marcus and Grollman point to major deficiencies in the regulation of herbal supplements: There is a lack of standardization to guard against adulteration and ensure a consistent level of the active ingredients. Herbal supplements can interact adversely with prescribed drugs. Herbal supplements do not need to be tested before marketing, as is required for prescription and over-the-counter drugs. Producers of dietary supplements engage in deceptive marketing and do not adequately label products to inform consumers about their nature and regulation. Finally, there is no requirement to report all adverse effects promptly.
This lack of safeguards creates a situation in which unwitting consumers are exposed to herbal products that in most cases have no proven effectiveness but often have serious toxicities. Though we tend to equate natural with healthy, plants have developed toxins to protect themselves against predators.
The perception that herbal supplements and botanicals are inherently safe is belied by extensive evidence of the danger posed by such products, including kava, ephedra, comfrey and aristolochic acid. Intensive advertising by the dietary-supplements industry, however, exploits and reinforces the illusion plant products are beneficial and harmless.
The most dramatic instance of the potential for harm occurred in Brussels, Belgium. Women attending a weight-loss clinic participated in a program that involved taking a combination of Chinese herbs. The program had been in operation for 15 years with no ill effects. In the early 1990s, however, the company that supplied the herbs substituted Aristolochia for another, benign, herb with a similar-sounding name in Chinese. Aristolochia has been widely used in herbal medicine, but it contains aristolochic acid -- a powerful kidney toxin and a carcinogen.
As a result of including Aristolochia in the regimen (for a period of two years), 105 women attending the clinic developed rapidly progressing kidney failure and had to go on dialysis or have kidney transplants. Many of the women went on to develop cancer of the upper urinary tract. Cases of kidney failure have also been reported in the United States, Europe and Asia. This dramatic case led the FDA to issue a warning regarding products containing aristolochic acid. What is essential to realize is the effects of Aristolochia were identified only thanks to the large cluster of cases of kidney failure occurring in young women who had attended the same spa. It is much more likely isolated cases will go unnoticed.
People failed to recognize the nephrotoxic effects of Aristolochia in spite of its use in many cultures worldwide over thousands of years. In an interview, Grollman explained why: "The reason, of course, is quite simple. It's painless, and the damage happens much later, so you don't put together the fact that you took this medicine and four years later, you have kidney failure. It's been part of Ayurvedic, European, Chinese and South American medicine for centuries. All of the great civilizations have used it. And not one reported its toxicity until the Belgians did 20 years ago. There are certain things that tradition can't tell you."
All the more reason why dietary and herbal supplements ought to be subject to at least as rigorous safeguards as those that apply to prescription and over-the-counter medications.
Geoffrey Kabat is a cancer epidemiologist at the Albert Einstein College of Medicine and the author of Hyping Health Risks: Environmental Hazards in Daily Life and the Science of Epidemiology.