Trans fat regulation: Difference between revisions

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Hydrogenation is a [[catalysis|catalytic]] reaction, meaning that another atom is temporarily bonded into the fatty acid during the conversion process and then released. The other elements used (the [[catalyst]]s) are finely divided [[nickel]], [[palladium]], [[platinum]] or [[cobalt]].
Hydrogenation is a [[catalysis|catalytic]] reaction, meaning that another atom is temporarily bonded into the fatty acid during the conversion process and then released. The other elements used (the [[catalyst]]s) are finely divided [[nickel]], [[palladium]], [[platinum]] or [[cobalt]].


Keeping in mind that the goal of hydrogenation is to add hydrogen (rather than produce ''cis'' to ''trans'' reconformation), it has been noted that the amount of trans fat in the product is dependent on reaction conditions. Increasing the [[pressure]] at which an oil is hydrogenated reduces trans fat formation. Researchers at the [[United States Department of Agriculture]] applied 1400&nbsp;[[kPa]] (200&nbsp;[[psi]]) of pressure to soybean oil in a 2&nbsp;litre vessel while heating it to between 140&nbsp;°C and 170&nbsp;°C. The standard 140&nbsp;kPa (20&nbsp;psi) process of hydrogenation produces a product of about 40% trans fatty acid by weight, compared to about 17% using the high pressure method. Blended with unhydrogenated liquid soybean oil, the high pressure processed oil produced margarine containing 5 to 6% trans fat which could qualify for a label of zero grams of trans fat.<ref>{{cite journal | author=FJ Eller | title=Preparation of spread oils meeting U.S. Food and Drug Administration Labeling requirements for trans fatty acids via pressure-controlled hydrogenation | journal=Journal of Agricultural and Food Chemistry | year=2005 | volume=53 | issue=15 | pages= 5982&ndash;5984 | url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=16028984 | id=PMID 16028984}}</ref>
Keeping in mind that the goal of hydrogenation is to add hydrogen (rather than produce ''cis'' to ''trans'' reconformation), it has been noted that the amount of trans fat in the product is dependent on reaction conditions. Increasing the [[pressure]] at which an oil is hydrogenated reduces trans fat formation. Researchers at the [[United States Department of Agriculture]] applied 1400&nbsp;[[Pascal (unit)|kPa]] (200&nbsp;[[pound-force per square inch|psi]]) of pressure to soybean oil in a 2&nbsp;litre vessel while heating it to between 140&nbsp;°C and 170&nbsp;°C. The standard 140&nbsp;kPa (20&nbsp;psi) process of hydrogenation produces a product of about 40% trans fatty acid by weight, compared to about 17% using the high pressure method. Blended with unhydrogenated liquid soybean oil, the high pressure processed oil produced margarine containing 5 to 6% trans fat which could qualify for a label of zero grams of trans fat.<ref>{{cite journal | author=FJ Eller | title=Preparation of spread oils meeting U.S. Food and Drug Administration Labeling requirements for trans fatty acids via pressure-controlled hydrogenation | journal=Journal of Agricultural and Food Chemistry | year=2005 | volume=53 | issue=15 | pages= 5982&ndash;5984 | url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=16028984 | id=PMID 16028984}}</ref>


==Health effects==
==Health effects==

Revision as of 23:33, 11 November 2006

Trans fatty acids (commonly termed trans fats) are a type of unsaturated fat (and may be monounsaturated or polyunsaturated).

Trans fats occur naturally, in small quantities, in meat and dairy products from ruminants. Most trans fats consumed today, however, are industrially created through partial hydrogenation of plant oils and animal fats — a chemical process developed in the early 1900s and first commercialized as Crisco in 1911.

Unlike other fats, trans fats are neither required nor beneficial for health.[1] Eating trans fat increases the risk of coronary heart disease.[2] For these reasons, health authorities worldwide recommend that consumption of trans fat be reduced to trace amounts. Trans fats from partially hydrogenated oils are generally considered to be worse than those occurring naturally.[3]

Trans fats are increasingly being linked to chronic health conditions (see below), are tightly regulated in a few countries, are mandatory on product labels in many others, and are the central issue in several ongoing lawsuits (particularly against fast food outlets). Many companies are voluntarily removing trans fats from their products, or establishing trans-free product lines.

Chemically, trans fats are made of the same building blocks as non-trans fats, but have a different shape. In trans fat molecules, the double bonds between carbon atoms (characteristic of all unsaturated fats) are in the trans rather than the cis configuration, resulting in a more straight rather than a kinked shape. As a result, trans fats are less fluid and have a higher melting point than the equivalent cis fats.

Presence in food

Salers Cow. Milk and meat from cows and other ruminants contains naturally occurring trans fats in small quantities.

Trans fats occur naturally in the milk and body fat of ruminants (such as cows and sheep) at a level of 2-5% of total fat.[4] They originate in the rumens of these animals. Animal-based fats were once the only trans fats consumed, but by far the largest amount of trans fat consumed today is created by the processed food industry by partially hydrogenating unsaturated plant fats (generally vegetable oils). These have displaced natural solid fats and liquid oils in many areas, notably in the fast food, snack food, fried food and baked good industries. Vegetable shortenings are primarily trans fats packaged for home use, and some margarines contain a large proportion of them. Foods containing artificial trans fats formed by partially hydrogenating plant fats may contain up to 45% trans fat compared to their total fat.[4]

Benefits of hydrogenating plant-based fats for food manufacturers include an increased product shelf life and decreased refrigeration requirement. Partial hydrogenation raises the melting point of fat, producing a semi-solid material, which is much more desirable than liquid oils for use in baking. Plant-based hydrogenated vegetable oils are much less expensive than the animal fats traditionally favored by bakers, such as butter or lard, and may be more readily available or less expensive than semi-solid plant fats such as palm oil.

Because partial hydrogenation of plant oils can replace animal fats, the resulting products can be consumed (barring other ingredient and preparation violations) by adherents to Kashrut (kosher) and Halal, as well as by adherents to vegetarianism in Buddhism, ahimsa in Jainism and Hinduism, veganism, and other forms of vegetarianism.

It has been established that trans fats in human milk fluctuate with maternal consumption of trans fat, and that the amount of trans fats in the bloodstream of breastfed infants fluctuates with the amounts found in their milk. Reported percentages of trans (compared to total fats) in human milk range from 1% in Spain, 2% in France and 4% in Germany to 7% in Canada.[5]

Nutritional guidelines

The National Academy of Sciences (NAS) advises the United States and Canadian governments on nutritional science for use in public policy and product labelling programs. Their 2002 Dietary reference intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids [6] contains their findings and recommendations regarding consumption of Trans fat (summary).

Their recommendations are based on two key facts. First, "trans fatty acids are not essential and provide no known benefit to human health",[1] whether of animal or plant origin.[7] Second, while both saturated and trans fats increase levels of LDL cholesterol (so-called "bad" cholesterol), trans fats also lower levels of HDL cholesterol (so-called "good" cholesterol) [2]; this increases the risk of coronary heart disease (CHD). The NAS is concerned "that dietary trans fatty acids are more deleterious with respect to CHD than saturated fatty acids".[2] This analysis is supported by a 2006 New England Journal of Medicine (NEJM) scientific review that states "from a nutritional standpoint, the consumption of trans fatty acids results in considerable potential harm but no apparent benefit."[3]

Because of these facts and concerns, the NAS has concluded there is no safe level of trans fat consumption. There is no adequate level, recommended daily amount or tolerable upper limit for trans fats. This is because any incremental increase in trans fat intake increases the risk of coronary heart disease.[2]

Despite this concern, the NAS dietary recommendations have not recommended the elimination of trans fat from the diet. This is because trans fat is naturally present in many animal foods, and therefore in most non-vegan diets; its removal from ordinary diets might introduce undesirable side effects and nutritional imbalances if proper nutritional planning is not undertaken. The NAS has therefore "recommended that trans fatty acid consumption be as low as possible while consuming a nutritionally adequate diet".[8] Like the NAS, the World Health Organization has tried to balance public health goals with a practical level of trans fat consumption, recommending in 2003 that trans fats be limited to less than 1% of overall energy intake.[4]

The US National Dairy Council has asserted that the trans fats present in animal foods are of a different type than those in partially hydrogenated oils, and do not appear to exhibit the same negative effects.[9] While a recent scientific review agrees with the conclusion (stating that "the sum of the current evidence suggests that the public health implications of consuming trans fats from ruminant products are relatively limited") it cautions that this may be due to the relatively low consumption of trans fats from animal sources compared to artificial ones.[3]

History

Wilhelm Normann patented the hydrogenation of liquid oils

Nobel laureate Paul Sabatier worked in the 1890s to develop the chemistry of hydrogenation which enabled the margarine, oil hydrogenation, and synthetic methanol industries.[10] While Sabatier only considered hydrogenation of vapours, the German chemist Wilhelm Normann showed in 1901 that liquid oils could be hydrogenated and patented the process in 1902.[11] In 1909, Procter & Gamble acquired the US rights to the Normann patent[12]; in 1911, they began marketing the first hydrogenated shortening, Crisco (composed largely of partially hydrogenated cottonseed oil). Further success came from the marketing technique of giving away free cookbooks with every recipe calling for Crisco. Hydrogenation strongly stimulated whaling, as it made it possible to stabilize whale oil for human consumption.

Production of trans fats increased steadily until the 1960s as artificially created trans fats replaced saturated animal fats in the US and other western countries. At first, the argument was a financial one due to lower costs, however, advocates also said that the trans fats of margarine were healthier than the saturated fats of butter.[13]

There were suggestions in the scientific literature as early as 1988 that trans fats could be a cause of the large increase in coronary artery disease.[13][14] In 1994, it was estimated that trans fats caused 30,000 deaths annually in the US from heart disease.[15]

The Center for Science in the Public Interest (CSPI) campaigned against fast foods using saturated fats starting in 1984. When fast food companies replaced the saturated fat with trans fat, CSPI's campaign against them ended. CSPI defended trans fats in their 1987 Nutrition Action newsletter. However, by 1992, CSPI began to speak against trans fats and is currently strongly against their use.[16]

Chemistry

From a chemical perspective, fats are large E-shaped molecules that support three fatty acids on a backbone. What is commonly termed a trans fat is more accurately described as a trans fatty acid. Fatty acid molecules consist of a backbone of carbon atoms surrounded by hydrogen atoms (as well as a carboxyl group — located at the end of the molecule — that we will not be concerned with in this discussion). Fatty acids are characterized as saturated or unsaturated based on the number of hydrogen atoms in the acid. If the molecule contains the maximum possible number of hydrogen atoms then it is saturated; otherwise, it is unsaturated.

Carbon atoms are tetravalent, forming four covalent bonds with other atoms, while hydrogen atoms bond with only one other atom. In saturated fatty acids, each carbon atom is connected to its two neighbour carbon atoms as well as two hydrogen atoms (see structure diagram, below). In unsaturated fatty acids the carbon atoms that are short hydrogen atoms are joined by double bonds rather than single bonds (see structure graphic below) so that each carbon atom participates in four bonds.

Hydrogenation of an unsaturated fatty acid refers to the addition of hydrogen atoms to the acid, causing double bonds to become single ones as carbon atoms acquire new hydrogen partners (to maintain four bonds per carbon atom). Full hydrogenation results in a molecule containing the maximum amount of hydrogen (in other words the conversion of an unsaturated fatty acid into a saturated one). Partial hydrogenation results in the addition of hydrogen atoms at some of the empty positions, with a corresponding reduction in the number of double bonds.

In most naturally occuring unsaturated fatty acids, the hydrogen atoms are on the same side of the double bonds of the carbon chain (cis configuration). However, partial hydrogenation reconfigures most of the double bonds that do not become chemically saturated, twisting them so that the hydrogen atoms end up on different sides of the chain. This type of configuration is called trans, which means "across" in Latin.

Molecular structure of different fatty acids
Saturated fat Cis-unsaturated fatty acid Trans-unsaturated fatty acid
saturated carbon atoms (each with 2 hydrogens) joined by a single bond unsaturated carbon atoms (each with 1 hydrogen) joined by a double bond. Cis configuration. unsaturated carbon atoms (each with 1 hydrogen) joined by a double bond. Trans configuration.

The same molecule, containing the same number of atoms, with the double bond in the same location, can be either a trans or a cis fatty acid depending on the conformation of the double bond. For example, oleic acid and elaidic acid are both unsaturated fatty acids with the chemical formula C18H34O2. They both have a double bond 9 carbon atoms from the end of the molecule. It is the conformation of this bond that sets them apart. The conformation has an implication for the orientation of the rest of the molecule. The trans configuration is straighter, while the cis configuration is noticeably kinked as can be seen from the following three-dimensional representation.

Oleic acid Elaidic acid
Oleic acid is a cis unsaturated fatty acid that comprises 55-80% of olive oil. Elaidic acid is a trans unsaturated fatty acid often found in hydrogenated vegetable oils.
These fatty acids are geometric isomers (chemically identical except for the arrangement of the double bond).

The trans fatty acid elaidic acid has different chemical properties owing to the slightly different bond configuration. Notably, it has a much higher melting point, 46.5 °C rather than oleic acid's 13.5 °C.

Generally, the goal is not to simply change the configuration of double bonds while maintaining the same ratios of hydrogen to carbon, but rather to decrease the number of double bonds and increase the amount of hydrogen in the fatty acid. This changes the consistency of the fatty acid and makes it less prone to rancidity (in which free radicals attack double bonds).

Commercial hydrogenation is typically only partial in order to get a malleable fat that is solid at room temperature, but melts upon baking (or consumption). A notable exception is The J.M. Smucker Company's new Crisco formulation made from solid fully hydrogenated palm oil cut with soybean oil and sunflower oil.[17] This is blended with liquid vegetable oils to yield a shortening much like the previous partially hydrogenated Crisco which was made from partially hydrogenated vegetable oil.

Hydrogenation is a catalytic reaction, meaning that another atom is temporarily bonded into the fatty acid during the conversion process and then released. The other elements used (the catalysts) are finely divided nickel, palladium, platinum or cobalt.

Keeping in mind that the goal of hydrogenation is to add hydrogen (rather than produce cis to trans reconformation), it has been noted that the amount of trans fat in the product is dependent on reaction conditions. Increasing the pressure at which an oil is hydrogenated reduces trans fat formation. Researchers at the United States Department of Agriculture applied 1400 kPa (200 psi) of pressure to soybean oil in a 2 litre vessel while heating it to between 140 °C and 170 °C. The standard 140 kPa (20 psi) process of hydrogenation produces a product of about 40% trans fatty acid by weight, compared to about 17% using the high pressure method. Blended with unhydrogenated liquid soybean oil, the high pressure processed oil produced margarine containing 5 to 6% trans fat which could qualify for a label of zero grams of trans fat.[18]

Health effects

Partially hydrogenated vegetable oils have been a significant part of the human diet for just over 100 years, and some deleterious effects of trans fat consumption are scientifically accepted, forming the basis of the health guidelines discussed above.

The exact biochemical methods by which trans fats produce specific health problems are a topic of continuing research. For example, the mechanisms through which trans fats contribute to coronary heart disease are fairly well understood, while the mechanism for trans fat's effect on diabetes is under investigation.

Coronary heart disease

The primary health risk identified for trans fat consumption is an elevated risk of coronary heart disease (CHD).[19] A comprehensive review of studies of trans fats was published in 2006 in the New England Journal of Medicine that concludes that there is a strong and reliable connection between trans fats and CHD.[3]

The major evidence for the effect of trans fat on CHD comes from the Nurses' Health Study (NHS) — a cohort study that has been following 120,000 female nurses since its inception in 1976.

Hu and colleagues analyzed data from 900 coronary events from the NHS population during 14 years of followup. He determined that a nurse's CHD risk roughly doubled (relative risk of 1.94) for each 2% increase in trans fat calories consumed (instead of carbohydrate calories). By contrast, it takes more than a 15% increase in saturated fat calories (instead of carbohydrate calories) to produce a similar increase in risk. Eating non-trans unsaturated fats instead of carbohydrates reduces the risk of CHD rather than increasing it.[20]

Hu also reports on the benefits of reducing trans fat consumption. Replacing 2% of food energy from trans fat with non-trans unsaturated fats more than halves the risk of CHD (53%). By comparison, replacing a larger 5% of food energy from saturated fat with non-trans unsatured fats reduces the risk of CHD by 43%.[20]

There are two accepted measures of risk for coronary heart disease, both blood tests. The first considers ratios of two types of cholesterol, the other the amount a cell-signalling cytokine called C-reactive protein. The ratio test is more accepted, while the cytokine test may be more powerful but is still being studied.[19] The effect of trans fat consumption has been documented on each as follows:

  • Cholesterol ratio: This ratio compares the levels of LDL (so-called "bad" cholesterol) to HDL (so-called "good" cholesterol). Trans fat behaves like saturated fat by raising the level of LDL, but unlike saturated fat it has the additional effect of decreasing levels of HDL. The net increase in LDL/HDL ratio with trans fat is approximately double that due to saturated fat.[21] (Higher ratios are worse.)
  • C-reactive protein (CRP): A study of over 700 nurses showed that those in the highest quartile of trans fat consumption had blood levels of CRP that was 73% higher than those in the lowest quartile.[22]

Another study considered deaths due to CHD, with consumption of trans fats being linked to an increase in mortality, and consumption of polyunsaturated fats being linked to a decrease in mortality.[19][23]

Other effects

There has been suggestion that the negative consequences of trans fat consumption go beyond the cardiovascular risk. In general, there is much less scientific consensus that eating trans fat specifically increases the risk of other chronic health problems:

  • Cancer: There is no scientific consensus that consumption of trans fats significantly increases cancer risks across the board.[19] The American Cancer Society states that a relationship between trans fats and cancer "has not been determined."[24] However, one recent study has found connections between trans fat and prostate cancer.[25]
  • Diabetes: There is a growing concern that the risk of type 2 diabetes increases with trans fat consumption.[19] However, consensus has not been reached.[3] For example, one study found that risk is higher for those in the highest quartile of trans fat consumption.[26] Another study has found no diabetes risk once other factors such as total fat intake and BMI were accounted for.[27]
  • Obesity: Research indicates that trans fat may increase weight gain and abdominal fat, despite a similar caloric intake.[28] A 6-year experiment revealed that monkeys fed a trans-fat diet gained 7.2% of their body weight, as compared to 1.8% for monkeys on a mono-unsaturated fat diet. Although obesity is frequently linked to trans fat in the popular media,[29] this is generally in the context of eating too many calories; there is no scientific consensus connecting trans fat and obesity.
  • Liver Dysfunction: Trans fats are metabolized differently by the liver than other fats and interfere with delta 6 desaturase. Delta 6 desaturase is an enzyme involved in converting essential fatty acids to arachidonic acid and prostaglandins, both of which are important to the functioning of cells.[30]

Public response and regulation

The lengthy political process of balancing the public health versus private profit from the public sale of processed foods containing artificially hydrogenated oils and fats continues today. Some countries are considering a complete ban against artificial hydrogenation products in food.

Canada

Canada is one of the largest consumers of trans fats in the world.[31] In November 2004, an opposition day motion seeking a ban similar to Denmark's was introduced by Jack Layton of the New Democratic Party, and passed through the House of Commons by an overwhelming 193-73 vote.[32]

Since December 2005, Health Canada has required that food labels list the amount of trans fat in the nutrition facts section for most foods. Products with less than 0.1 grams of trans fat per serving are considered to be free of trans fats and may be labelled as such (although this leads to questions of serving sizes). In Canada, trans fat quantities on labels include naturally occurring trans fats from animal sources.[33]

In June 2006, a task force co-chaired by Health Canada and the Heart and Stroke Foundation of Canada recommended a limit of 5% trans fat (to total fat) ratio in all products sold to consumers in Canada (2% for tub margarines and spreads).[4] The amount was selected such that "most of the industrially produced trans fats would be removed from the Canadian diet, and about half of the remaining trans fat intake would be of naturally occurring trans fats". This recommendation has been endorsed by the Canadian Restaurant and Foodservices Association[34] and the Food and Consumer Products of Canada has congratulated the task force on the report.[35]

Denmark

Denmark became the first country to introduce laws strictly regulating the sale of many foods containing trans fats in March 2003, a move which effectively bans partially hydrogenated oils. Naturally present trace amounts of trans fats in dairy and meat products are unaffected by these bills. The UK campaigning body tfX offers an English translation on its Denmark's trans fat law page.

European Union

The European Food Safety Authority was asked to produce a scientific opinion on trans fats.[36]

United Kingdom

In October 2005, the Food Standards Agency (FSA) asked for better labelling in the UK.[37] In the 29 July 2006 edition of the British Medical Journal, an editorial also called for better labelling.[38][39]

United States

File:Nyc-trans-poster.gif
Poster from New York City's board of health encouraging consumers to limit trans fat consumption.

Before 2006, consumers in the United States could not directly determine the presence (or quantity) of trans fats in food products. This information could be inferred from the ingredient list, notably from the hydrogenated ingredients.

On July 11, 2003, the Food and Drug Administration (FDA) issued a regulation[40] requiring manufacturers to list trans fat on the Nutrition Facts panel of foods and some dietary supplements.[41] The new labeling rule allowed for immediate voluntary compliance with mandatory compliance by January 1, 2006 (although companies may petition for an extension to January 1, 2008). The regulation allows trans fat levels of less than 0.5 grams per serving to be labeled as 0 grams per serving, or trans fat free. (In this case, manufacturers may use the synonyms "free", "without," "no" and "zero" in their packaging claims.) This can be compared to Canada in which the threshold is 0.1 grams. (It should be noted that trans fats consumed may be significant, if many small servings are eaten together.) The FDA defines trans fats as containing one or more trans linkages that are not in a conjugated system. This is an important distinction, as it distinguishes non-conjugated synthetic trans fats from naturally occurring fatty acids with conjugated trans double bonds, such as conjugated linoleic acid.

The FDA estimates that by 2009, trans fat labeling will have prevented from 600 to 1,200 cases of coronary heart disease and 250 to 500 deaths each year. This benefit is expected to result from consumers choosing alternative foods lower in trans fats as well as manufacturers reducing the amount of trans fats in their products.

Some US cities are acting to reduce consumption of trans fats. In May 2005, Tiburon, California, became the first American city where all restaurants voluntarily cook with trans fat-free oils.[42]

New York City has embarked on a campaign to reduce consumption of trans fats, noting that heart disease is the primary cause of resident deaths. This has included a public education campaign (see trans fat pamphlet) and a request to restaurant owners to voluntarily eliminate trans fat from their offerings.[43] Finding that the voluntary program was not successful, New York City's Board of Health has solicited public comments on a proposal to ban artificial trans fats in restaurants.[44] A final vote by the board is planned for December. If approved, this would make New York the first large US city to strictly limit trans fats in restaurants.

Chicago is considering a ban on oils containing trans fats for large chain restaurants.[45]

Food industry response

Some major food chains have chosen to remove or reduce trans fats from their products. In some cases large processed food vendors have been targeted by legal action, and these cases have generated a lot of media attention. In May 2003, BanTransFats.com Inc., a U.S. non-profit corporation, filed a lawsuit against the food manufacturer Kraft Foods in an attempt to force Kraft to remove trans fats from the Oreo cookie. The lawsuit was withdrawn when Kraft agreed to work on ways to find a substitute for the trans fat in the Oreo.

Similarly, in 2006, the Center for Science in the Public Interest sued KFC over its use of trans fats in fried foods.[46][47] KFC reviewed alternative oil options, saying "there are a number of factors to consider including maintaining KFC's unique taste and flavor of Colonel Sanders' Original Recipe."[48] On October 30, 2006, KFC announced that it will replace the partially hydrogenated soybean oil it currently uses with a trans-fat free low linolenic soybean oil in all restaurants in the US by April 2007, although its biscuits will still contain trans-fats.[49][50] Despite the lawsuit targeting KFC in the US, KFC is making changes outside of the US as well; in Canada, KFC's brand owner is switching to trans-fat free Canadian canola oil by early 2007.[51]

The Walt Disney Company will begin getting rid of trans fats in meals at domestic theme parks (Disneyland, Walt Disney World, etc.) by the end of 2007. They will also be stopping the inclusion of trans fats in licensed or promotional products by 2008.[52]

Other restaurants and food vendors have announced removal of trans fats — or reductions in trans fat levels — in their core products:

References

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  4. ^ a b c d Health Canada / Santé Canada TRANSforming the Food Supply
  5. ^ Innis, Sheila M and King, D Janette (1999). "trans Fatty acids in human milk are inversely associated with concentrations of essential all-cis n-6 and n-3 fatty acids and determine trans, but not n-6 and n-3, fatty acids in plasma lipids of breast-fed infants". American Journal of Clinical Nutrition. 70 (3): 383–390.{{cite journal}}: CS1 maint: multiple names: authors list (link)
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  7. ^ Nat' Academies Press, Dietary Reference Intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids (Macronutrients) (2005) page 447
  8. ^ Nat' Academies Press, Dietary Reference Intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids (Macronutrients) (2005) page 424
  9. ^ National Dairy Council letter
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  11. ^ HBW Patterson (2001) "Hydrogenation" SCI Lectures Paper Series
  12. ^ History of Soybeans and Soyfoods: 1100 B.C. to the 1980s. Unpublished manuscript by William Shurtleff and Akiko Aoyagi
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  15. ^ Willett WC, Ascherio A (1995). "Trans fatty acids: are the effects only marginal?". American Journal of Public Health. 85 (3): 411–412. PMID 8179036
  16. ^ Mary G. Enig, PhD. "The Tragic Legacy of Center for Science in the Public Interest (CSPI)". Retrieved 2006-05-02.
  17. ^ Crisco nutritional facts
  18. ^ FJ Eller (2005). "Preparation of spread oils meeting U.S. Food and Drug Administration Labeling requirements for trans fatty acids via pressure-controlled hydrogenation". Journal of Agricultural and Food Chemistry. 53 (15): 5982–5984. PMID 16028984.
  19. ^ a b c d e TRANSforming the food supply, Appendix 9iiiConsultation on the health implications of alternatives to trans fatty acids: Summary of Responses from Experts
  20. ^ a b Hu, FB (1997). "Dietary fat intake and the risk of coronary heart disease in women". New England Journal of Medicine. 337 (21): 1491–1499. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help) PMID 9366580. Online Copy (free with registration).
  21. ^ A Ascherio (1999). "Trans fatty acids and coronary heart disease". New England Journal of Medicine. 340 (25): 1994–1998.
  22. ^ Esther Lopez-Garcia (2005). "Consumption of Trans Fatty Acids Is Related to Plasma Biomarkers of Inflammation and Endothelial Dysfunction". The Journal of Nutrition. 135 (3): 562–566. PMID 15735094.
  23. ^ Oh, K (2005). "Dietary fat intake and risk of coronary heart disease in women: 20 years of follow-up of the nurses' health study". American Journal of Epidemiology. 161 (7): 672–679. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help) PMID 15781956
  24. ^ Common questions about diet and cancer
  25. ^ Chavarro et al., "A prospective study of blood trans fatty acid levels and risk of prostate cancer," Proc. Amer. Assoc. Cancer Res., Volume 47, 2006 [1]
  26. ^ Hu, FB (2001). "Diet and risk of Type II diabetes: the role of types of fat and carbohydrate". Diabetologia. 44 (7): 805–817. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help) PMID 11508264
  27. ^ van Dam RM, Stampfer M, Willett WC, Hu FB, Rimm EB (2002). "Dietary fat and meat intake in relation to risk of type 2 diabetes in men". Diabetes care. 25 (3): 417–424.{{cite journal}}: CS1 maint: multiple names: authors list (link) PMID 11874924
  28. ^ Gosline, Anna Why fast foods are bad, even in moderation New Scientist 12 June 2006
  29. ^ e.g. Trans Fat Press Conference by Tommy G. Thompson, US Secretary of health and human services
  30. ^ M Mahfouz (1981). "Effect of dietary trans fatty acids on the delta 5, delta 6 and delta 9 desaturases of rat liver microsomes in vivo". Acta biologica et medica germanica. 40 (12): 1699–1705.
  31. ^ Health Canada Trans Fat
  32. ^ "Dosanjh snubs House, MP says". Retrieved 2006-05-02.
  33. ^ It's your health: Trans fat
  34. ^ Restaurant industry commits to Trans Fat Task Force recommendations
  35. ^ Food industry congratulates Trans Fat Task Force on report
  36. ^ European Food Safety Authority Opinion of the Scientific Panel on Dietetic Products, Nutrition and Allergies on a request from the Commission related to the presence of trans fatty acids in foods and the effect on human health of the consumption of trans fatty acids The EFSA Journal (2004) 81, 1-49
  37. ^ Gray, Richard (February 5, 2006). "Forced to own up to the killer fat in our food". Scotsman.com.
  38. ^ BBC 27 July 2006 Call to label hidden fats in food
  39. ^ Clarke, Robert; Lewington, Sarah Trans fatty acids and coronary heart disease British Medical Journal 2006;333:214 (29 July), doi:10.1136/bmj.333.7561.214
  40. ^ (21 CFR 101.9 (c)(2)(ii)): Trans Fatty Acids in Nutrition Labeling
  41. ^ "FDA Acts to Provide Better Information to Consumers on Trans Fats". Food and Drug Administration. Retrieved 2005-07-26.
  42. ^ Project Tiburon of Ban Trans Fats
  43. ^ City of New York press release: Health department asks restaurateurs and food suppliers to voluntarily make an oil change and eliminate artificial trans fat
  44. ^ Health department proposes two changes to city's health code for public comment
  45. ^ Burke Serves Up Another Trans Fat Plan Southwest News Herald article
  46. ^ KFC Sued for Fouling Chicken with Partially Hydrogenated Oil: Lawsuit Aimed at Eliminating, or Disclosing Use of Artery-Clogging Frying Oil
  47. ^ Class Action Complaint
  48. ^ The New York Times (Marian Burros) KFC Is Sued Over the Use of Trans Fats in Its Cooking 14 June 2006
  49. ^ KFC announces switch to zero trans fat cooking oil following two-year test for same great taste (press release)
  50. ^ BBC (Guto Harri) KFC cuts out unhealthy trans-fats 30 October 2006
  51. ^ KFC Canada phasing in zero grams trans fat menu in all 786 restaurants nationally early in the new year (press release)
  52. ^ Disney to serve healthier foods at parks Yahoo! news article on plans to eliminate trans fats in Disney's theme parks
  53. ^ Marks & Spencer To Remove Hydrogenated Fats From All Foods By Mid 2006
  54. ^ Latest on health: Hydrogenated vegetable oils Sainsbury's website announcement.
  55. ^ The Guardian (Sarah Hall) Supermarket chains to curb use of trans fats 3 August 2006
  56. ^ Waitrose - going trans-free
  57. ^ Wendy's Significantly Cuts Trans Fats — Switch to New Cooking Oil Under Way
  58. ^ Panera Bread® Product Nutrition Information

See also

External links