
What is it?
Conjugated linoleic acid (CLA) is a slightly altered form of the essential fatty acid
linoleic acid.
Preliminary animal and test tube research suggests that CLA might reduce the risk of cancers at several sites, including breast,
prostate, colorectal, lung, skin, and
stomach.1 2 3 4 One preliminary study in humans
suggests that increasing CLA intake may reduce the risk of colorectal cancer.5
In a double-blind study, volunteers participating in an exercise programme received 600 mg
of CLA or a placebo three times per day for 12 weeks. Compared with placebo, CLA significantly
reduced percent body fat, but did not significantly reduce body weight.6 In a
double-blind study of obese men, supplementation with 4.2 grams of CLA per day for four weeks
produced a small but statistically significant reduction in waist size. However, compared with
the placebo, CLA did not promote weight loss.7 At present, there is not sufficient
evidence to support the use of CLA as a treatment for obesity.
Animal research suggests an effect of CLA supplementation on reducing body fat.8 9 Limited controlled
human research found 5.6-7.2 grams per day of CLA produced nonsignificant gains in muscle size
and strength in experienced10 and inexperienced11 weight-training
men.
Animal research also suggests an effect of CLA supplementation on limiting food allergy reactions,12 preventing atherosclerosis,13 14 and
improving glucose tolerance.15 As with the cancer research, the effects of CLA on
these conditions in humans remains unclear.
Where is it found?
CLA is found mainly in dairy products and also in beef and poultry, eggs, and corn oil.
Bacteria that live in the intestine of humans can produce CLA from linoleic acid, but
supplementation of a rich source of linoleic acid did not produce increases in blood levels of
CLA in one human study.16 CLA is available as a supplement.
CLA has been used in
connection with the following conditions (refer to the individual
health concern for complete information):
Who is likely to be deficient?
No deficiencies of CLA are reported or believed to occur, since it is not an essential
nutrient.
How much is usually taken?
Animal research uses very large amounts, equivalent to several grams per day for humans.
Until human research is conducted with CLA, the appropriate amount to take of this nutrient
remains unclear.
Are there any side effects or interactions?
Overweight volunteers who took 4.5 grams of
CLA per day for one year had an increase in their blood levels of lipoprotein(a), a risk
factor for heart disease.17 In a double-blind study of human volunteers,
supplementation with 4.2 grams per day of a mixture of cis-9,trans-11 CLA and trans-10,cis-12
CLA for three months increased the concentration of C-reactive protein, another risk factor
for heart disease.18 In a study of healthy volunteers, supplementing with 4.5 grams
of CLA per day for 12 weeks caused an impairment of blood vessel function (endothelial
dysfunction), which is believed to be associated with an increased risk of heart
disease.19 Taken together, these findings suggest that long-term use of CLA could
increase the risk of developing heart
disease.
In a double-blind study of people with type 2
diabetes, supplementing with 3 grams of CLA per day for eight weeks significantly
increased blood glucose levels by 6.3% and decreased insulin sensitivity.20 A
reduction in insulin sensitivity was also seen in a study of overweight men without diabetes
after treatment with 3 grams of CLA per day for three months,21 although in a study
of young sedentary men, 4 grams of CLA per day for eight weeks improved insulin
sensitivity.22 Thus, although the studies are conflicting, CLA may be harmful for
some people who have, or are at risk of developing, diabetes. One unpublished human trial
reported isolated cases of gastrointestinal upset.23
At the time of writing, there were no well-known drug interactions
with conjugated linoleic acid.
References
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1. Cesano A, Visonneau S, Scimeca JA, et al. Opposite effects of linoleic
acid and conjugated linoleic acid on human prostatic cancer in SCID mice. Anticancer
Res 1998;18:1429-34.
2. Thompson H, Zhu Z, Banni S, et al. Morphological and biochemical
status of the mammary gland as influenced by conjugated linoleic acid: implication for a
reduction in mammary cancer risk. Cancer Res 1997;57:5067-72.
3. Ip C. Review of the effects of trans fatty acids, oleic acid,
n-3 polyunsaturated fatty acids, and conjugated linoleic acid on mammary carcinogenesis in
animals. Am J Clin Nutr 1997;66(suppl):1523S-29S [review].
4. Parodi PW. Cows’ milk fat components as potential
anticarcinogenic agents. J Nutr 1997;127:1055-60 [review].
5. Larsson SC, Bergkvist L, Wolk A. High-fat dairy food and conjugated
linoleic acid intakes in relation to colorectal cancer incidence in the Swedish Mammography
Cohort. Am J Clin Nutr 2005;82:894–900.
6. Thom E, Wadstein J, Gudmundsen O. Conjugated linoleic acid reduces
body fat in healthy exercising humans. J Int Med Res 2001;29:392-6.
7. Riserus U, Berglund L, Vessby B. Conjugated linoleic acid (CLA)
reduced abdominal adipose tissue in obese middle-aged men with signs of the metabolic
syndrome: a randomised controlled trial. Int J Obes 2001;25:1129-35.
8. West DB, Delany JP, Camet PM, et al. Effects of conjugated linoleic
acid on body fat and energy metabolism in the mouse. Am J Physiol
1998;275:R667-72.
9. Park Y, Albright KJ, Liu W, et al. Effect of conjugated linoleic acid
on body composition in mice. Lipids 1997;32:853-8.
10. Ferreira M, Krieder R, Wilson M. Effects of CLA supplementation
during resistance training on body composition and strength. J Strength Conditioning
Res 1998;11:280.
11. Lowery LM, Appicelli PA, Lemon PWR. Conjugated linoleic acid enhances
muscle size and strength gains in novice bodybuilders. Med Sci Sports Exerc
1998;30:S182 [abstract]
12. Sugano M, Tsujita A, Yamasaki M, et al. Conjugated linoleic acid
modulates tissue levels of chemical mediators and immunoglobulins in rats. Lipids
1998;33:521-7.
13. Nicolosi RJ, Rogers EJ, Kritchevsky D, et al. Dietary conjugated
linoleic acid reduces plasma lipoproteins and early aortic atherosclerosis in
hypercholesterolemic hamsters. Artery 1997;22:266-77.
14. Lee KN, Kritchevsky D, Pariza MW, et al. Conjugated linoleic acid and
atherosclerosis in rabbits. Atherosclerosis 1994;108:19-25.
15. Houseknecht KL, Vanden Heuvel JP, Moya-Camarena SY, et al. Dietary
conjugated linoleic acid normalizes impaired glucose tolerance in the Zucker diabetic fatty
fa/fa rat. Biochem Biophys Res Commun 1998;244:678-82.
16. Herbel BK, McGuire MK, McGuire MA, et al. Safflower oil consumption
does not increase plasma conjugated linoleic acid concentrations in humans. Am J Clin
Nutr 1998;67:332–7.
17. Gaullier JM, Halse J, Hoye K, et al. Conjugated linoleic acid
supplementation for 1 y reduces body fat mass in healthy overweight humans. Am J Clin
Nutr 2004;79:1118–25.
18. Smedman A, Basu S, Jovinge S, Fredrikson GN, Vessby B. Conjugated
linoleic acid increased C-reactive protein in human subjects. Br J Nutr
2005;94:791–5.
19. Taylor JS, Williams SR, Rhys R, et al. Conjugated linoleic acid
impairs endothelial function. Arterioscler Thromb Vasc Biol 2006;26:307–12.
20. Moloney F, Yeow TP, Mullen A, et al. Conjugated linoleic acid
supplementation, insulin sensitivity, and lipoprotein metabolism in patients with type 2
diabetes mellitus. Am J Clin Nutr 2004;80:887-95.
21. Riserus U, Vessby B, Arnlov J, Basu S. Effects of cis-9,trans-11
conjugated linoleic acid supplementation on insulin sensitivity, lipid peroxidation, and
proinflammatory markers in obese men. Am J Clin Nutr 2004;80:279–83.
22. Eyjolfson V, Spriet LL, Dyck DJ. Conjugated linoleic acid improves
insulin sensitivity in young, sedentary humans. Med Sci Sports Exerc
2004;36:814–20.
23. Thom E. A pilot study with the aim of studying the efficacy and
tolerability of Tonalin CLA on the body composition in humans. Lillestrom, Norway: Medstat
Research Ltd., July 1997 [unpublished].
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The information presented in Healthnotes is for informational purposes
only. It is based on scientific studies (human, animal, or in vitro), clinical
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making any changes in prescribed medications. Information expires March 2007.