GM Free Cymru

Company Research on GM Foods is Systematically Rigged

Nov 21 2007
responsibletechnology.org,
http://www.gmwatch.org/archive2.asp?arcid=8520
http://foodconsumer.org/7777/8888/T_echnologies_40/
112107022007_Company_Research_on_Genetically_Modified_Foods_is_Rigged.shtml
GM Free Cymru has been campaigning for years against the decline in ethical standards in GM science, linked in part to the rise in corporate control over the research agenda, and in part to feeble regulatory bodies that place the “politics of convenience” and commercial interests above scientific integrity and respect for the truth.
This is an extract from an article by Jeffrey Smith, in which he exposes some of the common practices of those who have set themselves the goal of demonstrating that GM crops and foods are safe and environmentally harmless – come hell or high water.
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SECRET, INADEQUATE, AND FLAWED

THE UNPUBLISHED INDUSTRY STUDIES SUBMITTED TO REGULATORS ARE TYPICALLY KEPT SECRET BASED ON THE CLAIM THAT IT IS 'CONFIDENTIAL BUSINESS INFORMATION.' THE ROYAL SOCIETY OF CANADA IS ONE OF MANY ORGANIZATIONS THAT CONDEMN THIS PRACTICE. THEY WROTE:
'IN THE JUDGMENT OF THE EXPERT PANEL, THE MORE REGULATORY AGENCIES LIMIT FREE ACCESS TO THE DATA UPON WHICH THEIR DECISIONS ARE BASED, THE MORE COMPROMISED BECOMES THE CLAIM THAT THE REGULATORY PROCESS IS 'SCIENCE BASED.' THIS IS DUE TO A SIMPLE BUT WELL-UNDERSTOOD REQUIREMENT OF THE SCIENTIFIC METHOD ITSELF - THAT IT BE AN OPEN, COMPLETELY TRANSPARENT ENTERPRISE IN WHICH ANY AND ALL ASPECTS OF SCIENTIFIC RESEARCH ARE OPEN TO FULL REVIEW BY SCIENTIFIC PEERS. PEER REVIEW AND INDEPENDENT CORROBORATION OF RESEARCH FINDINGS ARE AXIOMS OF THE SCIENTIFIC METHOD, AND PART OF THE VERY MEANING OF THE OBJECTIVITY AND NEUTRALITY OF SCIENCE.' [7]
Whenever private submissions are made public through lawsuits or Freedom of Information Act Requests, it becomes clear why companies benefit from secrecy. The quality of their research is often miserable, incompetent, and unacceptable for peer-review. In 2000, for example, after the potentially allergenic StarLink corn was discovered in the food supply, Aventis CropScience presented wholly inadequate safety data to the EPA's scientific advisory panel. One frustrated panel member, Dean Metcalfe, MD, - the government's top allergist - said during a hearing, 'Most of us review for a lot of journals. And if this were presented for publication in the journals that I review for, it would be sent back to the authors with all of these questions. It would be rejected.' [8]
Submissions to the US Food and Drug Administraion (FDA) may be worse than in other countries, since the agency doesn’t actually require any data. Their policy - overseen by Monsanto;s former attorney who later became the company's vice president - says that biotech companies can determine if their own foods are safe. Anything submitted is voluntary and, according to former Environmental Protection Agency scientist Doug Gurian-Sherman, 'often lack[s] sufficient detail, such as necessary statistical analyses needed for an adequate safety evaluation.' Using Freedom of Information Requests, Gurian-Sherman analyzed more than a fourth of the data summaries (14 of 53) of GM crops reviewed by the FDA. He says, 'Our evaluation found that the biotechnology companies provide inadequate data to ensure their products are safe.' [9]

UNSCIENTIFIC ASSUMPTIONS ARE THE BASIS OF APPROVALS

'Most or all of the conclusions of food safety for individual GM crops are based on inferences and assumptions, rather than on actual testing,' says Professor E. Ann Clark, who analyzed submissions to Canadian regulators. For example, rather than actually testing to see if the amino acid sequence produced by their inserted gene is correct, 'the standard practice,' according to research analyst William Freese, 'is to sequence just 5 to 25 amino acids, even if the protein has more than 600 in total. If the short sample matches what is expected, they assume that the rest are also fine. If they are wrong, however, a rearranged protein could be quite dangerous.'
Monsanto's submission to Australian regulators on their high lysine GM corn provides several examples of optimistic assumptions used in place of science. The GM protein produced in the corn is also found in soil. The company claimed that since people consume small residues of soil on fruits and vegetables, the protein has a history of safe consumption. An independent calculation by the Centre for Integrated Research on Biosafety (INBI), however, reveals the weakness of this argument. Based on the amount of GM corn protein an average US citizen would consume (if all their corn were Monsanto's variety), 'for equivalent exposure' of the protein from soil 'people would have to eat between 80-800 million (males) or 60-700 million (females) kilograms of soil each day, or nearly as much as 10,000kg/second 24 hours a day seven days a week.' INBI estimated that the normal exposure to the protein from soil residues was actually 'about 30 billion-4 trillion times less than exposure through [high lysine] corn.' [10]
In addition, certain nutritional components of this GM variety (i.e. protein content, total dietary fiber, acid detergent fiber, and neutral detergent fiber) lie far outside the normal range for corn. Instead of comparing their corn to normal controls, which would reveal this disparity, Monsanto compared it to obscure corn varieties that were also substantially outside the normal range on precisely these values.
Epidemiologist Judy Carman points out that GM 'experiments used some very unusual animal models for human health, such as chickens, cows and trout. Some of the measurements taken from these animals are also unusual measures of human health, such as abdominal fat pad weight, total de-boned breast meat yield, and milk production.' In her examination of the full range of submittals to authorities in Australia and New Zealand, she says that there was no proper evaluation of 'biochemistry, immunology, tissue pathology, and gut, liver and kidney function.' [11] Writing on behalf of the Public Health Association of Australia, Carman says, 'The effects of feeding people high concentrations of the new protein over tens of years cannot be determined by feeding 20 mice a single oral gavage of a given high concentration of the protein and taking very basic data for 13-14 days . . .The acute toxicity testing proposed as adequate would simply not pick up cancer, teratology [birth defects] or the long-tem effects of nutrient deficiencies or increases in anti-nutrients.' [12]

THE SCIENCE OF RIGGING STUDIES

When independent researchers published a study in July 1999 showing that GM soy contains 12%-14% less cancer-fighting phytoestrogens, Monsanto responded with its own study, concluding that soy’s phytoestrogen levels vary too much to even carry out a statistical analysis. Researchers failed to disclose, however, that they had instructed the laboratory to use an obsolete method of detection—one that had been prone to highly variable results. [13]
WHEN AVENTIS PREPARED SAMPLES TO SEE IF THE POTENTIAL ALLERGEN IN STARLINK CORN REMAINED INTACT AFTER COOKING, INSTEAD OF USING THE STANDARD 30-MINUTE TREATMENT, THEY HEATED CORN FOR TWO HOURS.
TO SHOW THAT PASTEURIZATION DESTROYED BOVINE GROWTH HORMONE IN MILK FROM COWS TREATED WITH RBGH, THEY PASTEURIZED THE MILK 120 TIMES LONGER THAN NORMAL. UNABLE TO DESTROY MORE THAN 19%, THEY THEN SPIKED THE MILK WITH A HUGE AMOUNT OF THE HORMONE AND REPEATED THE LONG PASTEURIZATION, DESTROYING 90%. (THE FDA REPORTED THAT PASTEURIZATION DESTROYS 90% OF THE HORMONE.)
TO DEMONSTRATE THAT INJECTIONS OF RBGH DID NOT INTERFERE WITH COW’S FERTILITY, MONSANTO APPARENTLY ADDED COWS TO THE STUDY THAT WERE PREGNANT PRIOR TO INJECTION.
AND IN ORDER TO PROVE THAT THE PROTEIN FROM THEIR GM CROPS BREAKS DOWN QUICKLY DURING SIMULATED DIGESTION, BIOTECH COMPANIES USED THOUSANDS OF TIMES THE AMOUNT OF DIGESTIVE ENZYMES AND A MUCH STRONGER ACID COMPARED TO THAT RECOMMENDED BY THE WORLD HEALTH ORGANIZATION.
METHODS USED TO HIDE PROBLEMS ARE VARIED AND PLENTIFUL. FOR EXAMPLE, RESEARCHERS:
*USE HIGHLY VARIABLE ANIMAL STARTING WEIGHTS TO HINDER DETECTION OF FOOD-RELATED CHANGES
*KEEP FEEDING STUDIES SHORT TO MISS LONG-TERM IMPACTS
*TEST EFFECTS OF ROUNDUP READY SOYBEANS THAT HAVE NOT BEEN SPRAYED WITH ROUNDUP
*AVOID FEEDING ANIMALS THE ACTUAL GM CROP, BUT GIVE THEM INSTEAD A SINGLE DOSE OF THE GM PROTEIN THAT WAS PRODUCED INSIDE GM BACTERIA
*USE TOO FEW SUBJECTS TO DERIVE STATISTICALLY SIGNIFICANT RESULTS
*USE POOR STATISTICAL METHODS OR SIMPLY LEAVE OUT ESSENTIAL METHODS, DATA, OR STATISTICS
*USE RIGGED OR IRRELEVANT CONTROL GROUPS, AND EMPLOY INSENSITIVE OR OBSOLETE EVALUATION TECHNIQUES
Monsanto’s 1996 Journal of Nutrition study [14] , [15] provides plenty of examples of scientific transgressions. Roundup Ready soybeans are engineered to withstand the normally fatal effects of Monsanto’s herbicide called Roundup. Monsanto scientists published a feeding study that purported to test their soybeans’ effect on rats, catfish, chickens, and cows. The study has been used often by the industry as validation for safety claims. According to Dr. Arpad Pusztai, however, 'It was obvious that the study had been designed to avoid finding any problems. Everybody in our consortium knew this.' Pusztai was commissioned at the time by the UK government to develop rigorous testing protocols on GM foods—protocols that were never implemented. Pusztai, who had published several studies in that same nutrition journal, said the Monsanto paper was 'not really up to the normal journal standards.' Pusztai says that if he had been asked to referee the paper for publication, 'it would never have passed.' He's confident that even his graduate assistants would have taken the study apart in short order. Some of the flaws include:
Researchers tested GM soy on mature animals, not young ones. Young animals use protein to build their muscles, tissues, and organs. Problems with GM food could therefore show up in organ and body weight. But adult animals use the protein for tissue renewal and energy. 'With a nutritional study on mature animals,' says Pusztai, 'you would never see any difference in organ weights even if the food turned out to be anti-nutritional. The animals would have to be emaciated or poisoned to show anything.'
Even if there were an organ development problem, the study wouldn’t have picked it up since the researchers didn’t weigh the organs.
In one of the trials, researchers substituted only one tenth of the natural protein with GM soy protein. In two others, they diluted their GM soy six- and twelve-fold. [16] Scientists Ian Pryme of Norway and Rolf Lembcke of Denmark wrote, the 'level of the GM soy was too low, and would probably ensure that any possible undesirable GM effects did not occur.'
Pryme and Lembcke, who published a paper in Nutrition and Health that analyzed all peer-reviewed feeding studies on GM foods as of 2003, also pointed out that the percentage of protein in the feed used in the Roundup Ready study was 'artificially too high.' This 'would almost certainly mask, or at least effectively reduce, any possible effect of the [GM soy].' They said it was 'highly likely that all GM effects would have been diluted out.' [17]
Proper compositional studies filter out effects of weather or geography by comparing plants grown at the same time in the same location. Monsanto, however, pooled data from several locations, which makes it difficult for differences to be statistically significant. Nonetheless, the data revealed significant differences in the ash, fat, and carbohydrate content. Roundup Ready soy meal also contained 27% more trypsin inhibitor, a potential allergen, which might explain the sudden jump in soy allergies in the UK beginning right after Roundup Ready soy was introduced. Also, cows fed GM soy produced milk with a higher fat content, demonstrating another disparity between the two types of soy.
One field trial, however, did grow GM and non-GM plants next to each other, but this data was not included in the paper. Years after the study appeared, medical writer Barbara Keeler discovered the data that had been omitted. It showed that Monsanto’s GM soy had significantly lower levels of protein, a fatty acid, and phenylalanine, an essential amino acid. Also, toasted GM soy meal contained nearly twice the amount of a lectin - one that may interfere with the body’s ability to assimilate other nutrients. And the amount of trypsin inhibitor in cooked GM soy was as much as seven times higher than a cooked non-GM control.
The study also omitted many details normally required for a published paper. According to Pryme and Lembcke, 'No data were given for most of the parameters.'
And when researchers tested the effects of Roundup Ready protein on animals, they didn’t extract the protein from the soybeans. Instead, they derived it from GM bacteria, claiming the two forms of protein were equivalent. There are numerous ways, however, in which the protein in the soy may be different. In fact, nine years after this study was published, another study showed that the gene inserted into the soybeans produced unintended aberrant RNA strands, meaning that the protein may be quite different than what was intended. [18]
In Pryme and Lembcke’s analysis, it came as no surprise that this Monsanto study, along with the other four peer-reviewed animal feeding studies that were 'performed more or less in collaboration with private companies,' reported no negative effects of the GM diet. 'On the other hand,' they wrote, 'adverse effects were reported (but not explained) in [the five] independent studies.' They added, 'It is remarkable that these effects have all been observed after feeding for only 10–14 days.' [19]

TOXIC GM FOODS COULD HAVE BEEN APPROVED

Two GM foods whose commercialization was stopped because of negative test results give a chilling example of what may be getting through. Rats fed GM potatoes had potentially precancerous cell growth in the stomach and intestines, less developed brains, livers, and testicles, partial atrophy of the liver, and damaged immune systems. [20] GM peas provoked an inflammatory response in mice, suggesting that the peas might trigger a deadly anaphylactic shock in allergic humans. [21] Both of these dangerous crops, however, could easily have been approved. The problems were only discovered because the researchers used advanced tests that were never applied to GM crops already on the market. Both would have passed the normal tests that companies typically use to get their products approved.
Ironically, when Monsanto was asked to comment on the pea study, their spokesperson said it demonstrated that the regulatory system works. He failed to disclose that none of the company’s GM crops had been put through such rigorous tests.
RAMPANT UNRELENTING INDUSTRY BIAS
Industry-funded research that favors the funders is not new. Bias has been identified across several industries. In pharmaceuticals, for example, positive results are four times more likely if the drug’s manufacturer funds the study. [22] When companies pay for the economic analyses of their own cancer drugs, the results are eight times more likely to be favorable. [23] Compared to drug research, the potential for industry manipulation in GM crop studies is considerably higher. Unlike pharmaceutical testing, GM research has no standardized procedures dictated by regulators. GM studies are not usually published in peer-reviewed journals and are typically kept secret by companies and governments. There is little money available for rigorous independent research, so company evidence usually goes unchallenged and unverified. Most importantly, whereas drugs can show serious side-effects and still be approved, GM food cannot. There is no tolerance for adverse reactions; feeding trials must show no problems.
Thus, when industry studies show problems (in spite of their efforts to avoid them), serious adverse reactions and even deaths among GM-fed animals are ignored or dismissed as 'not biologically significant' or due to 'natural variations.'
Numerous reports including peer-reviewed articles and part 3 of the book Genetic Roulette are replete with examples of rigged research. But making these public does not seem to curtail its practice. Consider the wormy corn of the British Food Journal. Not only has the editor refused to retract the paper, he has not even agreed to reconsider its Award for Excellence. A blatant propaganda exercise still stands validated as exemplary science.
In the critical arena of food safety research, where the health of society is caught in the balance, it is entirely unacceptable that the biotech industry is without accountability, standards, or peer-review. At our expense, they’ve got bad science down to a science.
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THIS ARTICLE (EDITED) IS BASED ON PART 3 OF THE BOOK, GENETIC ROULETTE: THE DOCUMENTED HEALTH RISKS OF GENETICALLY ENGINEERED FOODS, BY JEFFREY M. SMITH. www.GeneticRoulette.com.
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References [1] – [6] relate to the”wormy corn” fraud and are omitted here.
[7] 'Elements of Precaution: Recommendations for the Regulation of Food Biotechnology in Canada; An Expert Panel Report on the Future of Food Biotechnology prepared by The Royal Society of Canada at the request of Health Canada Canadian Food Inspection Agency and Environment Canada' The Royal Society of Canada, January 2001.
[8] FIFRA Scientific Advisory Panel (SAP), Open Meeting, July 17, 2001.
[9] Doug Gurian-Sherman, 'Holes in the Biotech Safety Net, FDA Policy Does Not Assure the Safety of Genetically Engineered Foods,' Center for Science in the Public Interest, http://www.cspinet.org/new/pdf /fda_report__final.pdf
[10] M. Cretenet, J. Goven, J. A. Heinemann, B. Moore, and C. Rodriguez-Beltran, 'Submission on the DAR for application A549 Food Derived from High-Lysine Corn LY038: to permit the use in food of high-lysine corn, 2006, www.inbi.canterbury.ac.nz
[11] Judy Carman, 'Is GM Food Safe to Eat?' in R. Hindmarsh, G. Lawrence, eds., Recoding Nature Critical Perspectives on Genetic Engineering (Sydney: UNSW Press, 2004): 82–93.
[12] FLRAG, 'Comments to ANZFA about Applications A346, A362 and A363,' http://www.iher.org.au/
[13] Marc Lappé and Britt Bailey, 'ASA Response,' June 25, 1999, http://cetos.org/articles /asaresponse.html
[14] S. R. Padgette, N. B.Taylor, D. L. Nida, M. R. Bailey, J. MacDonald, L. R. Holden, R. L. Fuchs, 'The composition of glyphosate-tolerant soybean seeds is equivalent to that of conventional soybeans,' J. Nutr. 126 (1996):702–716.
[15] B. G. Hammond, J. L. Vicini, G. F. Hartnell, M. W. Naylor, C. D. Knight, E. H. Robinson, R. L. Fuchs, and S. R. Padgette, 'The feeding value of soybeans fed to rats, chickens, catfish, and dairy cattle is not altered by genetic incorporation of glyphosate tolerance,' J. Nutr. 126 (1996): 717–727.
[16] A. Pusztai and S. Bardocz, 'GMO in animal nutrition: potential benefits and risks,' Chapter 17, Biology of Nutrition in Growing Animals (Elsevier, October 2005). earlier
[17] Ian F. Pryme and Rolf Lembcke, 'In Vivo Studies on Possible Health Consequences of Genetically Modified Food and Feed—with Particular Regard to Ingredients Consisting of Genetically Modified Plan Materials,' Nutrition and Health 17(2003): 1–8.
[18] Andreas Rang, et al, 'Detection of RNA variants transcribed from the transgene in Roundup Ready soybean,' Eur Food
Res Technol 220 (2005): 438–443.
[19] Ian F. Pryme and Rolf Lembcke, 'In Vivo Studies on Possible Health Consequences of Genetically Modified Food and Feed—with Particular Regard to Ingredients Consisting of Genetically Modified Plan Materials,' Nutrition and Health 17(2003): 1–8.
[20] Arpad Pusztai, 'Can science give us the tools for recognizing possible health risks of GM food,' Nutrition and Health, 2002, Vol 16 Pp 73-84; Stanley W. B. Ewen and Arpad Pusztai, 'Effect of diets containing genetically modified potatoes expressing Galanthus nivalis lectin on rat small intestine,' Lancet, 1999 Oct 16; 354 (9187): 1353-4; Arpad Pusztai, 'Genetically Modified Foods: Are They a Risk to Human/Animal Health?' June 2001 Action Bioscience http://www.actionbioscience .org/biotech/pusztai.html ; and A. Pusztai and S. Bardocz, 'GMO in animal nutrition: potential benefits and risks,' Chapter 17, Biology of Nutrition in Growing Animals, R. Mosenthin, J. Zentek and T. Zebrowska (Eds.) Elsevier, October 2005
[21] V. E. Prescott, et al, 'Transgenic Expression of Bean r-Amylase Inhibitor in Peas Results in Altered Structure and Immunogenicity,' Journal of Agricultural Food Chemistry (2005): 53.
[22] J. Lexchin, L. A. Bero, B. Djulbegovic, and O. Clark, 'Pharmaceutical industry sponsorship and research outcome and quality: systematic review,' BMJ 326 (2003):1167–1176.
[23] Mark Friedberg, et al, 'Evaluation of Conflict of Interest in Economic Analyses of New Drugs Used in Oncology,' JAMA 282