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Commonly Asked Questions

Are soy foods high in Aluminium?
Should people with kidney failure avoid soy foods?
Is soy beneficial for brain (cognitive) function?
Does tofu cause dementia?
Could the isoflavones in soy infant formula cause long-term reproductive problems or infertility for human infants?
Does soy infant formula cause thyroid disease in healthy infants?
Have soy beans been genetically modified?
Are non-GM soy foods and ingredients available in Australia and New Zealand?
Are soy foods harmful to thyroid function?
Will consuming soy foods reduce fertility in men?
Will consuming soy foods reduce fertility in women?
Can I consume soy during pregnancy?
Can I consume soy while breastfeeding?
NIEHS review of genistein and soy infant formula - what's the latest?
Are soy foods safe and how much should we eat?

 

1. Are soy foods high in Aluminium?

Aluminium is a naturally occurring element present in abundant levels in soil (in fact, it is the third most abundant element in the earth's crust), and is therefore naturally present in most plant foods, including soybeans.

In soy drinks, the tiny amount of aluminium present comes from the soybeans, via the soil in which they grow. It is useful to compare levels of aluminium in soy products with those of other common foods.

Table 1: Aluminium Content of Some Typical Foods as Consumed 1,2,3
mg per 100g mg per serving
Yogurt, plain 0.112mg 0.224mg /200g
Cheese, American 41.100mg 12.3mg / 30g
Cheese, Swiss 1.9mg 0.57mg / 30g
Beef, minced, cooked 0.019mg 0.019mg / 100g
Frankfurter, boiled 0.247mg 0.124mg / 50g
Peanut Butter 0.576mg 0.173mg / 30g
Asparagus, boiled 0.141mg 0.141mg / 100g
Pinto Beans, boiled 0.252mg 0.252mg / 100g
Spinach, boiled 2.500mg 2.500mg / 100g
Potato, baked 2.600mg 2.600mg / 100g
Muffins, blueberry 12.800mg 6.4mg / 50g
1/4 Hamburger (fast food) 2.040mg 4.080mg / 200g
Tea 0.446mg 1..12mg / 250mL
Stringy bark (dark) honey - Australia 5.77mg 0.289mg / 5g
White clover (light) honey - Australia 0.47mg 0.024mg / 5g
Dairy based infant formula, 0-6 months, made up2 0.098mg 0.9mg / recommended total daily intake
Soy based infant formula, made up2 0.587mg 5.5mg / recommended total daily intake
So Good® soy milk3 0.030mg 0.075mg / 250mL

In a recent report from the Water Services Association of Australia4 the average weekly aluminium intake is the equivalent of 35mg for a 70kg male and 30mg for a 60kg female (0.5mg/kg body weight). In Australian children, the average weekly intake of aluminium was 1.4mg / kg body weight. These figures are well below the Food and Agricultural Organisation/World Health Organisation (FAO/WHO) provisional tolerable intake of 7mg / kg body weight per week (which correlates to 490mg aluminium / week for average males and 420mg aluminium / week for average females).

In 1992, the Australia New Zealand Food Authority (ANZFA, now called Food Standards Australia New Zealand, FSANZ), measured the aluminium intakes of Australian infants as part of the Australian Market Basket Survey (which is now known as the Total Diet Survey ). It was found that although soy based infant formulas contained higher levels of aluminium than other formulas or breast milk, the estimated aluminium intake was still well below estimated safe levels2. Interestingly, the Total Diet Survey no longer includes aluminium intakes as part of the survey, which is conducted to monitor dietary intakes of pesticides and other toxic components, such as cadmium, mercury and lead.

Aluminium is not an essential nutrient in the diet, and the body has highly effective barriers to limit its uptake. Only a very small percentage of what is ingested is absorbed by the stomach and intestines, and almost all of what is absorbed is passed through the kidneys and eliminated as waste.

Dr. Gruskin, the chairman of the Department of Pediatrics, Wayne State University, Michigan5 recently stated that he had not been able to find any data to suggest or prove that the quantities of aluminum fed to full-term infants with normal renal function are either harmful or accumulate in tissues. Also of interest is that aluminum is virtually non-detectable in bone obtained from normal adults.

1The Total Diet Survey monitors the levels of pesticides and contaminants in foods and the Australian public's dietary exposure to these compounds. Foods that are representative of a balanced diet, that are commonly consumed and/or of particular interest from a pesticide or contaminant viewpoint are included in the survey. The results are used as background information for developing food standards and as part of the registration process for agricultural chemicals10.

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2. Should people with kidney failure avoid soy foods?

In recent years, a concern about aluminum has developed in regard to individuals with kidney failure6-9. As a result of malfunctioning kidneys, aluminum accumulates in body tissues. Most of this is thought to originate from dialysis fluids and/or intravenous feeding. There is no evidence that dietary intake of aluminium is a major contributor. Individuals with impaired renal function should always consult with their physician and dietitian before changing their diet.

REFERENCES:
  1. Pennington JAT, Aluminium content of foods and diets, Food Additives and Contaminants, 1987: 5;161-232.
  2. National Food Authority, The 1992 Australian Market Basket Survey.
  3. Sanitarium Health Food Company, Aluminium and So Good Product Information Sheet, 2001.
  4. Allen JL, Cumming FJ, Aluminium in the Food and Water Supply: An Australian Perspective, UWRAA Research Report No. 202, November 1998.
  5. Gruskin AB, Aluminium toxicity in infants and children, In: Trace Elements in Nutrition of Children-II, Nestle Nutrition Workshop Series, Chandra RK Ed., Raven Press, NY, p15-26, 1991.
  6. Alfrey AC, LeGendre GR, Kaehny WD, The dialysis encephaopathy syndrome. Possible aluminium intoxidcation, New Engl J Med 1976;294:184-188.
  7. Alfrey AC, Hegg A, Craswell P, Metabolism and toxicity of aluminium in renal failure, Am J Clin Nutr 1980;33:1059-1516.
  8. Sedman AB, Klein GL, Merritt RJ, et al., Evidence of aluminium loading in infants receiving intravenous therapy, New Engl J Med 1985;312:1337-1343.
  9. Polinksy MS, Gruskin AB, Baluarte HJ, et al., Aluminum in chronic renal failure: a pediatric perspective, In: Pediatric Nephrology, Vol. 6, (Strauss, J., Ed.), New York. Plenum Press, p 315-333, 1981.
  10. Australia New Zealand Food Authority, About the Australian Market Basket Survey 1996, www.anzfa.gov.au/documents/pub10_99.asp, accessed March 2001, now www.foodstandards.gov.au

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3. Is soy beneficial for brain (cognitive) function?

The hormone oestrogen is thought to be beneficial for maintaining cognitive function (and reducing the risk for dementia) in older age. Some population studies have linked the use of oestrogen in post-menopausal women with a reduced risk of Alzheimer's disease in later life1. As a result, researchers have questioned whether soy isoflavones may be effective in helping to maintain brain function in later life since these natural compounds share similarities to oestrogen, although they are not identical.

While there are no studies in humans especially designed to establish whether consuming soy foods or soy isoflavones can prevent or reduce the risk of dementia, several population studies have found that certain groups of people, that are known to habitually consume soy foods, have lower rates of dementia.

Researchers at the Australian National University recently analysed 23 studies comparing the incidence of dementia and Alzheimer's disease in different countries. They found that people in East Asian countries, where soy is a staple in the diet, have a significantly lower incidence of dementia and also tend towards a lower incidence of Alzheimer's disease compared to people from European countries2.

Results from a study of Seventh-day Adventists3, who have been shown in a number of studies to live a healthier lifestyle than the general population, indicated that the meat eaters were more than twice as likely to develop dementia compared to the vegetarians (who consume soy regularly). There was also a trend towards delayed onset of dementia in the vegetarians.

Studies in animals are underway to determine the potential benefits of soy in cognitive function. In a study from the University of Alabama4, Dr Helen Kim investigated the effect of dietary soy protein with naturally occurring isoflavones in aged monkeys for three years. She measured levels of a protein in the brain that is specifically related to Alzheimer's disease and found that the level of this protein, called tau protein was suppressed in the brains of the monkeys who had been given the soy protein with natural levels of isoflavones. This indicates that regular consumption of soy protein with naturally occurring isoflavones may protect against the accumulation of Alzheimer's disease-related proteins in the brain.

Researchers from Wake Forest University in the USA looked at the effect of soy isoflavones compared to oestrogen on cognitive function in rats5. Markers of memory, using approved radial arm maze tests, were measured after eight weeks of oestrogen treatment or soy isoflavone consumption. Both oestrogen and soy isoflavones improved the levels of the memory markers, however the effect of soy isoflavones on some markers was lower than oestrogen.

The role of soy protein and soy isoflavones in mediating brain (cognitive) function is an emerging area of research. More studies are needed, particularly in humans, before conclusions regarding the effect of soy on brain function can be made.

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4. Does tofu cause dementia?

One study reported a link between tofu consumption during mid-life and early brain aging in a group of American-Japanese men living on the Island of Oahu in Hawaii6. In this observational study, the men who consumed two or more servings of tofu per week during their middle years were found to have lower scores on tests of brain function (cognitive performance), and a lower brain weight in later life. Interestingly, miso soup consumption was also measured. However consumption of this food was not related to poorer brain function scores. Miso is a fermented soy product containing significant levels of isoflavones7.

The principal investigator of this study, Dr Lon White and his colleagues concluded that education level, age and a history of prior strokes were the three most important predictors of cognitive functioning. These factors explained over one quarter (27.8%) of the differences in test scores of brain function in these Japanese-American men. Tofu intake accounted for less than 1% of the difference in test scores of brain function. This study does not provide evidence that soy foods in general, nor isoflavones specifically, are related to an increased risk of dementia. Further, it is contrary to the epidemiological evidence that indicates populations who consume soy as a staple in the diet have a lower incidence of dementia, compared to Western populations2.

REFERENCES:
  1. Miller MM, Franklin KB, Theoretical basis for the benefit of postmenopausal estrogen substitution, Exp Gerontol 1999;34:587-604.
  2. Jorm AF and Jolley D, The incidence of dementia: a meta-analysis, Neurology 1998;51:728-33.
  3. Giem P, Beeson WL, Fraser GE, The incidence of dementia and intake of animal products: preliminary findings from the Adventist Health Study, Neuroepidemiology 1993;12: 28-36.
  4. Kim H, Xia H, Li L, et al., Modulation of neurodegeneration markers by dietary soy in a primate model of menopause, Abstract, Third International Symposium on the Role of Soy in Preventing and Treating Chronic Disease, Washington, 1999. P27.
  5. Pan Y, Anthony M, Clarkson T, Soy, Estradiol and cognitive function: Effects on biomarkers and learning/memory performance of estrogen-deficient rats, Abstract, Third International Symposium on the Role of Soy in Preventing and Treating Chronic Disease, Washington, 1999. P27.
  6. White L, Petrovitch H, Ross W, et al., Brain aging and midlife tofu consumption, J Am Coll Nutr 2000;19:242-255.
  7. Wakai K, Egami I, Kato, K, et al., Dietary intake and sources of isoflavones among Japanese, Nutr Cancer 1999;33:139-45.

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5. Could the isoflavones in soy infant formula cause long-term reproductive problems or infertility for human infants?

Dr. Kenneth Setchell from the Children's Hospital Medical Center, Cincinnati, USA, first reported that soy infant formulas contained high levels of naturally occurring isoflavones1, confirming observations made 13 years ago2. Despite these high levels, there have never been any case reports in the medical and scientific literature that isoflavones cause later infertility in human infants.

Recent questions regarding the levels of isoflavones in soy-based infant formulas have been raised. The negative effects of extremely high doses of isoflavones on the fertility and development in animals such as sheep3 and cheetah4 have been known for many years and extensively investigated. In these cases, blood levels were 100-500 times higher than what we see in infants fed soy infant formula. However, there are large species differences in how phytoestrogens are handled, and in their effects. Animals such as monkeys5, rats6, mares and cattle7 do not experience reproductive problems when fed a diet containing soy protein or isoflavones.

With regard to humans, the Australia New Zealand Food Authority (ANZFA, now called Food Standards Australia New Zealand, FSANZ) conducted a safety review and found no evidence that exposure of healthy infants to soy-based infant formula over some 30 years of use has been associated with any demonstrated harm8. A retrospective study by Dr. Strom and his colleagues from the University of Iowa, USA, did not find any delayed negative effects in young men and women, who had been fed soy-based infant formula as infants. There were no statistically significant differences between those adults who were fed milk-based formula versus soy-based formula, with many variables being studied including adult height, usual weight, body mass index, indices of precocity, and a large number of other non-reproductive and reproductive outcomes such as cancer and infertility9.

There is a long history of safe and effective use of commercially available soy-based infant formulas10. There are also no reports that Asian populations, which ingest high quantities of soy from early life, have impaired sexual development or higher rates of infertility later in life.

If more recent studies using suitable animal models can be extrapolated to humans, the early introduction of soy and its isoflavones, even for short periods of time, may lead to a decreased risk of breast cancer later in life11. The soy isoflavones appear to cause beneficial changes to the architecture of the breast making it more resistant to cancer. This is an area of great research interest at present.

NIEHS review of genistein and soy infant formula - what's the latest?

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6. Does soy infant formula cause thyroid disease in healthy infants?

Prior to the 1960's soy formula was made from soy flour and was deficient in iodine12. Iodine deficiency is known to cause goiter (an enlarged thyroid gland). Worldwide, however, there were only a small number of case reports (comprising 12 individuals) linking thyroid abnormalities in infants to this early type of soy-based infant formula13,14,15,16. Since iodine supplementation was introduced in 1959, only one case has been reported in the medical literature, associating the consumption of soy protein with thyroid abnormality17.

All modern infant formulas, including soy-based infant formula, are designed to provide a nutritionally balanced diet when used as the sole source of nutrition for an infant. While experts agree that breast milk is the best choice of food for infants, soy infant formulas are a suitable alternative to breast milk or cow's milk formula for healthy term infants.

The New Zealand Ministry of Health recommends that clinicians who are treating infants with hypothyroidism (by replacing thyroxine - a thyroid hormone), closely monitor those infants fed soy-based formula or consuming large amounts of soy-containing infant foods, as they may require higher levels of thyroxine18.

REFERENCES:
  1. Setchell KDR, Zimmer-Nechemias L, Cai J, et al., Exposure of infants to phytoestrogens from soy-based infant formulas. Lancet, 1997;350, 23-27.
  2. Setchell KDR, Welsh MB & Lim CK, High-performance liquid chromatographic analysis of phytoestrogens in soy protein preparations with ultraviolet, electrochemical, and thermospray mass spectrometric detection, J Chromatogr 1987;386:315-323.
  3. Bennetts HW, Underwood EJ, Shier FL, A specific breeding problem of sheep on subterranean clover pastures in western Australia, Aust Vet J 1946;22:2-12.
  4. Setchell KDR, Gosselin SJ, Welsh MB et al., Dietary estrogens - a probably cause of infertility and liver disease in captive cheetahs, Gastroenterology 1987;93:225-33.
  5. Anthony MS, Clarkson TB, Hughes CL, et al., Soybean isoflavones improve cardiovascular risk factors without affecting the reproductive system of peripubertal rhesus monkeys, J Nutr 1996;126:43-50.
  6. Thigpen JE, Setchell KDR, Ahlmark KB, et al., The phytoestrogen content of purified, open and closed formula laboratory animal diets, Journal of Animal Laboratory Science (in press), 1999.
  7. Kurzer MS, Xu X, Dietary phytoestrogens, Annu Rev Nutr 1997;17:353-81.
  8. Australia New Zealand Food Authority, Phytoestrogens - an assessment of the potential risks to infants associated with exposure to soy-based infant formula, March 1999.
  9. Strom BL, Schinnar R, Ziegler EE, et al., Follow-up study of a cohort fed soy-based formula during infancy, Experimental Biology Late Breaking Abstracts (program addendum) 2000;LB39:7.
  10. Strom BL et al, Exposure to soy-based formula in infancy and endocrinological and reproductive outcomes in young adulthood, JAMA 2001;286:807-14.
  11. Lamartiniere CA, Moore JB, Holland M, et al., Neonatal genistein chemo prevents mammary cancer, Proc Soc Exp Biol Med 1995;208:120-123.
  12. American Academy of Pediatrics Committee on Nutrition, Soy protein-based formulas: recommendations for use in infant feeding, Pediatrics 1998;101:148-153.
  13. Hydovitz JD, Occurrence of goiter in an infant fed on a soy diet, NEJM 1959;262:351-3.
  14. Van Wyk JJ, Arnold MB, Wynn J et al., The effects of a soybean product on thyroid function in humans, Pediatrics 1959;24:752-60.
  15. Shepard TH, Pyne GE, Kirschvink JF, et al., Soybean goiter, NEJM 1960;22:1099-1103.
  16. Pinchera A, MacGillivray MH, Crawford JD, et al., Thyroid refractoriness in an athyreotic cretin fed soybean formula, 1965:273:83-87.
  17. Labib M, Gama R, Wright J, et al., Dietary maladvice as a cause of hypothyroidism and short stature, Br Med J 1989;298:232-3.
  18. Ministry of Health, Soy-based infant formula, New Zealand 1998.

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7. Have soy beans been genetically modified?

Soybeans have been identified as one of several crops that have genetically modified analogs with improved growing characteristics and yields. Other crops with genetically modified analogues include corn, cotton and canola.

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8. Are non-GM soy foods and ingredients available in Australia and New Zealand?

Not all soy-containing foods and food ingredients used in Australia and New Zealand are derived from genetically modified soybeans.

Some companies use non-GM soy that is grown under an Identity Preservation (IP) system. This follows soy production from non-GM soybean seed, right through to the food manufacturer. Each element in the chain is documented with the whole system being independently audited.

Since December 8, 2001, all GM ingredients within a food which contain novel DNA or protein, will be identified in the ingredient panel of the label, or on the front of the pack for single ingredient products such as soy beans. Some products carry what is known as a 'negative' label, indicating that their ingredients have been sourced from non-GM soybeans.

Consumers interested in which soy products in the supermarket contain non-GM soy should check on the label of the particular product or alternatively contact the manufacturer directly.

For further information on GM food labelling, visit www.foodstandards.gov.au

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9. Are soy foods harmful to thyroid function?

There is no scientific evidence showing a correlation between soy consumption and thyroid disorders in humans. A number of clinical studies have also failed to note clinically significant changes in thyroid hormones in either men or women consuming soy protein or isoflavones 1-4.

Recent studies in test tubes have shown that, under certain experimental conditions, the principle isoflavones in soy, genistein and daidzein, can inhibit the enzyme thyroid peroxidase (TPO)5. This enzyme is responsible for the conversion of thyroglobulin to thyroid hormone.

It must be emphasised, however, that this occurs only with large amounts of soy isoflavones (more than an adult could typically consume as part of a normal diet), and/or when the diet is low in iodine. The inhibition of this enzyme can be completely abolished in the presence of iodine5.

Further, soy isoflavones are not the only natural dietary constituents that inhibit TPO. A variety of other closely related flavonoids have been shown to be even more potent in inhibiting the activity of this enzyme. These flavonoids are present in a number of plant based foods, including cabbage, broccoli and cauliflower6, and would be consumed at relatively high levels by vegetarians, yet these individuals do not have a significant increased incidence of goitre. In addition, flavonoid consumption has been associated with significantly reducing the risk of coronary heart disease7.

If people have any questions regarding soy and thyroid function, they should consult their health care practitioner.

REFERENCES:
  1. Ham JO, Chapman KM, Essex-Sorlie D, et al, Endocrinological response to soy protein and fiber in mildly hypercholesterolemic men, Nutr Res 1993;13: 873-884.
  2. Duncan AM, Merz BE, Xu X, et al., Soy isoflavones exert modest hormonal effects in premenopausal women, J Clin Endocrinol Metab 1999a;84:192-197.
  3. Duncan AM, Underhill KE, Xu X, et al., Modest hormonal effects of soy isoflavones in postmenopausal women, J Clin Endocrinol Metab 1999b;84:3479-3484.
  4. Mackey R, Ekangaki A, Eden JA, The effects of soy protein in women and men with elevated plasma lipids, BioFactors 2000;12:251-257.
  5. Divi RL, Chang HC, Doerge DR, Anti-thyroid isoflavones from soybean, Biochem. Pharmacol 1997;54:1087-1096.
  6. Divi RL and Doerge DR, Inhibition of thyroid peroxidase by dietary flavonoids, Chem Res Toxicol 1996;9:16-23.
  7. Hertog MGL, Feskens EJM, Hollman PCH, et al., Dietary antioxidant flavonoids and risk of coronary heart disease: the Zutphen Elderly Study, The Lancet 1993;342:1007-11.

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10. Will consuming soy foods reduce fertility in men?

There has been concern raised that sperm counts in men are falling, and that exposure to synthetic estrogens may be a contributing factor1. Some people have also speculated that phytoestrogens - the natural phytonutrients found in soy foods - might be implicated. However, there is no evidence that fertility is affected when humans eat soy foods as part of their regular diet.

In a comprehensive review of soy based infant formulas, Food Standards Australia New Zealand (our food regulatory body), concluded that there is no evidence that exposure of healthy infants to soy-based infant formula has been associated with any demonstrated harm or that it reduces fertility2. In addition, there is no evidence suggesting that sperm quality or fertility is adversely affected in men from Asian countries who traditionally consume soy foods frequently in their diet.

Researchers at the Rowett Research Institute in Scotland also showed that there is no difference in the reproductive health of young, healthy adult males consuming 40mg of isoflavones per day as a supplement. Isoflavones are the main type of phytoestrogens found in soy3. After two months of consuming an isoflavone supplement, no differences were seen in semen quality (including sperm concentrations and sperm motility), testicular volume, testosterone and other hormone levels (such as estrogen). A recent review of several scientific studies concluded that there is no evidence to suggest that consuming isoflavones has adverse effects on sperm quality in men4.

REFERENCES:
  1. Sharpe RM, Skakkebaek NE, Are oestrogens involved in falling sperm counts and disorders of the male reproductive tract? The Lancet 1993;341:1392-1395.
  2. Australia New Zealand Food Authority, Phytoestrogens - an assessment of the potential risks to infants associated with exposure to soy-based infant formula, March 1999.
  3. Mitchell JH et al, Effect of a phytoestrogen food supplement on reproductive health in normal males, Clin Sc 2001;100:613-618.
  4. Kurzer MS, Hormonal effects of soy in premenopausal women and men, J Nutr 2002;132:570S-573S.

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11. Will consuming soy foods reduce fertility in women?

A concern has been raised that consuming soy may interfere with a woman's chance of falling pregnant. One unpublished study (which was presented in June 2005), found that combining genistein (one of the isoflavones in soybeans) and two other 'environmental estrogens' (chemicals from industrial products) in a test tube triggered sperm to undergo a reaction that could potentially reduce its ability to fertilise an egg . The authors speculated that it might therefore be best to avoid soy in case sperm also respond this way to genistein inside the body.

However, there is no evidence that fertility is affected in women consuming soy foods as part of a balanced diet. Even in Asian populations where soy foods have been consumed as a staple part of the diet for centuries, it has never been suggested that soy interferes with conception.

Genistein is one of several components in soy. However, people do not eat genistein, they eat soy foods. In common with how other nutrients work in isolation, an extract of pure genistein will behave differently in the body than genistein consumed as part of a food - in this case a soy food. In addition, a study conducted in test-tube studies does not reflect the complex nature of the human body.

Soy has been widely used as a protein source in the diets of laboratory animals . Consumption of these diets has not resulted in adverse effects on the reproductive ability of these animals. For example, researchers from the University of Arkansas conducted a multi-generation study in rats aimed at examining the long-term health consequences of early consumption of soy protein. The number of offspring, gender ratios, birth weights, birth lengths, health, and general appearance of soy-fed rats was no different to rats raised on animal proteins.

To date there have been no credible reports in medical and scientific journals of reproductive problems in humans who include soy foods as part of their regular diet.

REFERENCES:
  1. Fraser L, Presentation at the European Society of Human Reproduction and Embryology, June 2005
  2. Thigpen JE et al, Phytoestrogen content of purified, open- and closed- formula laboratory animal diets, Lab Anim Sci 1999;49(5):530-6.
  3. Badger TM et al, Developmental effects and health aspects of soy protein isolate, casein, and whey in male and female rats, Int J Toxicol 2001;20(3):165-74.

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12. Can I consume soy during pregnancy?

A hypothetical concern has been raised about consuming soy during pregnancy due to the presence of naturally occurring isoflavones in soy foods. Under certain circumstances, isoflavones can provide weak oestrogen-like effects according to animal studies and research in human adults. However, it is important to understand that these substances are not real 'oestrogens' and there is no evidence that babies born to mums who consume soy regularly during their pregnancy have increased health problems.

When a pregnant woman includes soy in her diet, isoflavones cross the placenta and reach the developing baby - in the same way as other nutrients do - according to studies on Japanese1 and Indonesian2 women who regularly eat soy foods. This transfer of isoflavones occurs in both animals and humans. However, to put this into context, during pregnancy a baby in the uterus is bathed in a sea of estrogens coming from the mother, which are much more powerful than the isoflavones derived from soy foods. To guard against too much exposure, the foetus has high levels of a protein called alpha-fetoprotein. This protein strongly binds oestrogens and isoflavones to reduce their hormonal potency and keep the foetus protected3.

Women in Asia, as well as many vegetarians in western countries, have been including soy foods in their diets for centuries. These women don't stop eating soy when they become pregnant and they give birth to healthy babies with good long-term health statistics.

It is important that women eat a wide variety of nutritious foods during pregnancy. Including legumes, such as soybeans and soy foods, is one way to provide a good source of protein, fibre and minerals.

There is no evidence that eating soy foods during pregnancy will result in any harm to a developing baby.

REFERENCES:
  1. Dalais FS, Meliala A, Wahlqvist ML, Maternal and cord blood phytoestrogen levels in Indonesian women, Third International Symposium on the Role of Soy in Preventing and Treating Chronic Disease, Oct 31-Nov 3, 1999, Washington, DC, USA.
  2. Adlercreutz H, Yamada T, Wahala K et al., Maternal and neonatal phytoestrogens in Japanese women during birth, Am J Obstet Gynecol 1999;180:737-743.

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13. Can I consume soy while breastfeeding?

It has been suggested that women should avoid soy foods while breastfeeding because their babies will be exposed to high levels of oestrogenic compounds (called isoflavones) from the soybeans.

While it is true that isoflavones can mimic the hormone oestrogen, they are much weaker in their effects. Paradoxically, isoflavones can also block oestrogens when the levels of oestrogen are too high in the body. In addition, isoflavones provide many other effects such as antioxidant benefits. An overwhelming number of studies suggest that a diet rich in isoflavones protects against many chronic diseases, such as heart disease and cancer1.

Breast milk is not a good source of isoflavones, even if a woman eats a lot of soy each day. Research has shown that breast milk from mothers who regularly consume soy contains only 0.015-0.03 mg per litre2 - the daily amount consumed by a four month old infant. These are miniscule amounts! To put this into some perspective, one glass of soy milk provides around 15 mg, depending on the brand. Even vegetarian and Asian women, despite regularly including soy foods in their diet, don't produce isoflavone-rich breast milk.

On the other hand, in the first few days of lactation a baby will be exposed to high levels of oestrogens from breast milk that have accumulated in the breast during pregnancy3. But it is the environmental oestrogens - such as pesticides - that we should be concerned about as these also find their way into breast milk.

In conclusion, breast milk is a poor source of isoflavones, even if a nursing mother eats soy foods on a regular basis. There is no evidence that eating soy during breastfeeding is unsafe for the mother or infant.

REFERENCES:
  1. Radd S & Setchell K, Eat to Live, Hodder Headline 2002.
  2. Franke AA, Yu MC, Maskarinec G et al., Phytoestrogens in human biomatrices including breast milk, Biochem Soc Trans 1999;27:308-318.
  3. Sahlberg BL & Axelson M, Identification and quantitation of free and conjugated steroids in milk from lactating women, J Steroid Biochem 1986;25:379-391.
14. NIEHS review of genistein and soy infant formula - what's the latest?

"Expert panel expresses negligible concern for reproductive and developmental effects from exposure of adults [to genistein] in the general population" (Genistein and Soy Formula Expert Panel conclusions, March 2006).

This is one of 3 conclusions arising from the public meeting convened by the NIEHS on March 15-17, 2006 after discussions on the draft reports on soy infant formula and genistein. The panel also made the following conclusions -

"The expert panel expresses negligible concern for adverse effects in neonates and infants who may consume up to 0.01-0.08 mg/kg bw/day of genistein aglycone contained in soy formula", and
"There are insufficient human or experimental animal data available to permit a determination of the developmental or reproductive toxicity of soy infant formula". The conclusions of the expert panel are available at http://cerhr.niehs.nih.gov/chemicals/genistein-soy/genistein/pubcomm-genistein.html

International Soy Advisory Board member, Professor Ken Setchell, was recently invited by the editors Environmental Health Perspectives, to comment on the scientific issues related to genistein and soy infant formula. In his guest editorial, Professor Setchell reviews the limitations of many studies that have led to questions being raised over the risks and benefits of genistein and soy (Environmental Health Perspectives, June 2006;114(6):332-333). Click here to read Professor Setchell's guest editorial.

Who is the NIEHS?
The National Institute of Environmental Health Sciences (NIEHS) is a department of the National Institutes of Health in the United States. The NIEHS assembled a panel of toxicologists who reviewed scientific studies on the reproductive and developmental effects of genistein (one of the isoflavones in soybeans) and secondly, soy infant formula. The NIEHS convened a public meeting on March 15-17, 2006 to discuss the two reports and determine conclusions on the effects of genistein and soy infant formula, and identify future research needs.

The NIEHS accepted public comments on the reports, and those received to date are available on the NIEHS website at http://cerhr.niehs.nih.gov/chemicals/genistein-soy/genistein/pubcomm-genistein.html
Click here to read Professor Ken Setchell's submission to the NIEHS regarding the two draft reports.

Many studies reviewed in the reports involved feeding or directly injecting pure genistein into rats and mice. However, there are severe limitations in extrapolating the findings of these studies to the effects of consuming soy foods by healthy humans.

What are the limitations in relating some of the findings to healthy human infants and adults?
  1. Children raised on soy formula do not consume pure genistein - in fact genistein accounts for less than 2% of the isoflavone content of most western soy foods including soy infant formula and soy-milks 1,2.
  2. The levels of genistein injected into rodents are often much higher than what would be consumed naturally through the diet.
  3. When genistein is injected directly into an animal, the normal metabolism of isoflavones that usually occurs in the digestive system and liver after isoflavones are consumed naturally through the diet is bypassed. The result is a significant difference in the levels and types of isoflavones that circulate in the bloodstream3 compared to the effects of eating soy foods or formula. Basically, the animals end up being exposed to very high levels of the 'free' (or active) genistein - a situation to which the human body is not usually subjected.
  4. Genistein is just one of several components in soy. And, people do not eat pure genistein, they eat soy foods. In common with how other nutrients work in isolation, an extract of pure genistein will therefore behave differently in the body than genistein consumed as part of a food - in this case a soy food.
  5. For example, beta-carotene, an important dietary antioxidant, is one of several components found in naturally high levels in green leafy and orange vegetables. In research studies where men were given purified beta-carotene supplements, they experienced an unexpected increase in risk of lung cancer and cardiovascular disease4,5. However, scientists and nutritionists agree that it is not necessary for people to avoid orange and leafy green vegetables to minimise beta-carotene intakes, and on the contrary they recommend people consume more of these protective foods as numerous studies have demonstrated that higher intakes of these foods are associated with a lower rate of many cancers and heart disease. Supplements of beta-carotene however are discouraged.
  6. Soy protein has also been widely used as a protein source in the diets of laboratory animals6. Consumption of these diets has not resulted in adverse effects on the reproductive ability of these animals.
  7. Finally, newborn rodents are not an appropriate animal model to investigate the effects of isoflavones on development and reproduction. This is because newborn rodents are equivalent in development to a human foetus in the first three months of pregnancy and not a human baby.

How much research has been conducted on soy infant formula? It is important to consider that over 20 million infants worldwide have been raised on soy-based infant formula for more than 30 years with no scientific reports of adverse health conditions. A robust body of science has clearly demonstrated its safety and efficacy. In addition, the American Academy of Pediatrics (AAP)7, the Food and Drug Administration (FDA) and Food Standards Australia New Zealand (FSANZ)8 have concluded that soy-based infant formula is a safe and acceptable way to support the normal growth and development of healthy infants.

In addition, several studies suggest that eating a diet rich in soy early in life can enhance the overall health of adults and reduce the risk of heart disease and certain cancers. Recent studies in China and the United States show that groups of women who regularly consumed soy foods early in life had a lower risk of breast cancer in adulthood.9,10

  1. Setchell KDR, Zimmer-Nechemias L, Cai J et al, Exposure of infants to phyto- oestrogens from soy-based infant formula. Lancet 1997;350:23-7.
  2. Setchell KDR, Zimmer-Nechemias L, Cai J et al, Isoflavone content of infant formulas and the metabolic fate of these phytoestrogens in early life. Am J Clin Nutr 1998;68:1453S-1461S.
  3. Brown NM, Setchell KDR, Efficient transplacental passage of isoflavones, Abstract, 5th International symposium on the role of soy in preventing and treating chronic disease, September 2003.
  4. ATBC Cancer Prevention Group, The effect of vitamin E and beta carotene on the incidence of lung cancer and other cancers in male smokers, N Eng J Med 1994;330:1029-1035.
  5. Omenn GS, Goodman GE, Thornquist MD et al, Effects of a combination of beta carotene and vitamin A on lung cancer and cardiovascular disease, N Eng J Med 1996;334:1150-1155.
  6. Thigpen JE et al, Phytoestrogen content of purified, open- and closed- formula laboratory animal diets, Lab Anim Sci 1999;49(5):530-6.
  7. American Academy of Pediatrics Committee on Nutrition. Soy protein-based formulas: Recommendations for use in infant feeding. Pediatrics 1998;101:148-153.
  8. Australia New Zealand Food Authority (now FSANZ), Phytoestrogens - an assessment of the potential risks to infants associated with exposure to soy-based infant formula, March 1999
  9. Shu XO; Jin F; Dai Q; et all, Soyfood intake during adolescence and subsequent risk of breast cancer among Chinese women, Cancer Epidemiol Biomarkers Prev 2001;10:483-8
  10. Wu AH et al, Adolescent and adult soy intake and risk of breast cancer in Asian-Americans, Carcinogenesis 2002;23(9):1491-1496.
15. Are soy foods safe and how much should we eat?

Recently a few media stories have suggested that consuming soy products can have a negative effect on health. Unfortunately, this has created mixed messages and confusion about soy foods.

Concerns expressed in the media by the Cancer Council (NSW) related to the use of high doses of phytoestrogen supplements for people with cancer. Their concerns did not relate to the consumption of soy foods among healthy people.

Are soy foods safe?
  • Soy is one of the most widely studied foods. There are now over 3,000 research papers on the subject and the weight of evidence indicates, no negative health effects in humans from consuming soy foods as part of a balanced diet.
  • Enjoying soy foods at normal dietary levels, such as soymilk on your cereal, soy and linseed bread in your sandwich and tofu in your stir-fry, is safe for people including those with breast and prostate cancer.
  • Soy is one of nature’s superfoods rich in important nutrients:
    • High quality protein.
    • No cholesterol or animal fat and low in saturated fat.
    • High in fibre and carbohydrate.
    • Contains a large number of important micronutrients.
    • Contains natural protective phytoestrogens (which are also found richly in linseeds and sprouts and a diet based on whole plant foods).
  • Soy foods and beverages are a nutritious addition to the diet and offer a range of potential health benefits, such as lower blood cholesterol1-5 and blood pressure5-8, improved bone density9-15, protection against breast, prostate and bowel cancer16-25 and reduced symptoms of menopause7,26-29.
  • The safety of consuming high dose, purified phytoestrogen supplements (as well as some other high dose nutrient supplements) has not been established, and we therefore recommend you contact your health care professional for advice.

Our conclusion, along with leading world health authorities, doctors, nutritionists and research scientists who have particular expertise in the field of soy is very clear; soy foods, as a part of a balanced diet, are safe and offer significant health benefits.

How much soy can we eat?
  • Experts agree that one to four servings of soy foods each day29-31 is safe and will provide long-term health benefits.
    Why not try:
    • Soy milk on your cereal for breakfast
    • Soy and linseed bread for lunch
    • Tofu in your evening meal
    • Soy yoghurt or roasted soy nuts as a snack

Sanitarium believes it is not only safe, but also beneficial to enjoy soy foods as part of a healthy diet based on a wide variety of colourful and minimally refined plant foods.

  1. Anderson J.W. Johnstone B.M. et al. Meta-analysis of the effects of soy protein intake on serum lipids. New England Journal of Medicine, 1995. 333:276-282.
  2. Weggemans RM and Trautwein EA. Relation between soy-associated isoflavones and LDL and HDL cholesterol concentrations in humans: a meta-analysis. European Journal of Clinical Nutrition, 2003. 57:940-946.
  3. Zhuo XG. Melby M.K. et al. Soy isoflavone intake lowers serum LDL cholesterol: A meta-analysis of 8 randomised controlled trials in humans. The Journal of Nutrition, 2004. 134:2395-2400.
  4. Reynolds K, Chin A. et al. A meta-analysis of the effect of soy protein supplementation on serum lipid. American Jounral of Cardiology. 2006. 98(5):633-40.
  5. Cassidy A and Hooper L. Phytoestrogens and cardiovascular disease. Journal of the British Menopause Society. 2006, Vol 12(2):49-56.
  6. Figtree GA, Griffiths H, Lu Y-Q et al, Plant-derived estrogens relax coronary arteries in vitro by a calcium antagonistic mechanism, J Am Coll Cardiol 2000;35:1977-1985.
  7. Washburn S, Burke GL, Morgan T, et al., Effect of soy protein supplementation on serum lipoproteins, blood pressure, and menopausal symptoms in perimenopausal women, Menopause 1999;6:7-13.
  8. Teede JH, Dalais FS, Kotsopoulos D, et al., Soy protein dietary supplementation improves lipid profiles and blood pressure: A double-blind, randomized, placebo-controlled study in men and postmenopausal women, (abstract p25) Third International Symposium on the Role of Soy in Preventing and Treating Chronic Disease, Oct 31-Nove 3, 1999, Washington, DC, USA.
  9. Scheiber MD, Liu JH, Subbiah MTR, et al., Dietary soy supplementation reduces LDL oxidation and bone turnover in healthy post-menopausal women, Menopause 2001 (in press).
  10. Arjmandi BH, Alekel L, Hollis BW, et al., Dietary soybean protein prevents bone loss in an ovariectomized rat model of osteoporosis, J Nutr 1996;126:161-167.
  11. Anderson JJG, Ambrose WW, Garner SC, Biphasic effects of genistein on bone tissue in the ovariectomized, lactating rat model, PSEBM 1998;217:345-350.
  12. Draper CR, Edel MJ, Dick IM, et al., Phytoestrogens reduce bone loss and bone resorption in oophorectomized rats, J Nutr 1997;127: 1795-1799.
  13. Potter SM, Baum J, Teng H, et al., Soy protein and isoflavones: their effects on blood lipids and bone density in postmenopausal women, AJCN 1998;68(suppl):1375S-9S.
  14. Alekel DL, St Germain A, Peterson CT, et al., Isoflavone-rich soy protein isolate attenuates bone loss in the lumbar spine of perimenopausal women, Am J Clin Nutr 2000;72:844-52.
  15. Dalais FS, Rice GE, Wahlqvist M, et al., Effects of dietary phytoestrogens in postmenopausal women, Climacteric 1998;1:124-129.
  16. Messina MJ, Persky V, Setchell KDR et al., Soy intake and cancer risk: A review of the in vitro and in v ivo data, Nutr Canc,1994;21:113-31.
  17. Badger TM, Ronis MJ, Simmen RC, Simmen FA. Soy protein isolate and protection against cancer. J Am Coll Nutr. 2005 Apr;24(2):146S-149S.
  18. Fournier DB, Erdman JW, Gordon GB, Soy, Its Components, and Cancer Prevention: A review of the in vitro, animal, and human data, Cancer Epidemiol, Biomarkers & Prev 1998;7:1055-65.
  19. Murkies A, Dalais, FS, Briganti EM, et al., Phytoestrogens and breast cancer in postmenopausal women: a case control study, Menopause 2000;7:289-96.
  20. Ingram D, Sanders K, Kolybaba M, et al., Case-control study of phytoestrogens and breast cancer, Lancet 1997;350:990-94.
  21. Gikas PD, Mokbel K. Phytoestrogens and the risk of breast cancer: a review of the literature. Int J Fertil Womens Med. 2005 Nov-Dec;50(6):250-8.
  22. Kolonel LN, Hankin JH, Whittemore AS, et al., Vegetables, fruits, legumes and prostate cancer: a multiethnic case-control study, Cancer Epidemiol Biomarkers Prev 2000;9:795-804.
  23. Strom SS, Yamamura Y, Duphorne CM, et al., Phytoestrogen intake and prostate cancer: a case-control study using a new database, Nutr Cancer 1999;33:20-5.
  24. Le Marchand L, Hankin JH, Wolkens LR, et al., Dietary fiber and colorectal cancer risk, Epidemiology 1997;8:658-65.
  25. Witte JS, Longnecker MP, Bird CL, et al., Relation of vegetable, fruit and grain consumption to colorectal adenomatous polyps, Am J Epidemiol 1996;144:1015-25.
  26. Murkies AL, Lombard C, Strauss BJG, et al., Dietary flour supplementation decreases post-menopausal hot flushes: Effect of soy and wheat, Maturitas 1995;21:189-195.
  27. Brzezinski A, Adlercreutz H, Shaoul R, et al., Short-term Effects of Phytoestrogen-rich Diet on Post-menopausal Women, Menopause 1997;4:89-94.
  28. Albertazzi P, Pansini F, Bonaccorsi G, et al., The effect of dietary soy supplementation on hot flashes, Obstet Gynecol 1998;91:6-11.
  29. Radd S., Setchell K. Eat to Live. (2002). Hodder books
  30. Food Labelling: health claims: soy protein and coronary heart disease. Food and Drug Administration, HHS: final rule: soy protein and coronary heart disease. Fed Reg. 1999;64:57700-57733.
  31. South African Health Information. Food Based Dietary Guidelines for South Africa, More legumes for overall health, background paper, 2001, SAJCN (supp), Vol 14(3).

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