Sabine Tricon
University of Reading
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Proceedings of the Nutrition Society | 2005
Sabine Tricon; Graham C. Burdge; Christine M. Williams; Philip C. Calder; Parveen Yaqoob
Conjugated linoleic acid (CLA) is a collective term for a mixture of positional and geometric isomers of conjugated dienoic derivatives of linoleic acid. CLA has received considerable attention as a result of animal experiments that report anti-carcinogenic, anti-atherogenic and anti-diabetic properties, and modulation of body composition and immune function. Several studies of CLA supplementation in human subjects have now been published, but in contrast to animal studies there has been marked variation between reports on the health-related outcomes. The consensus from seventeen published studies in human subjects is that CLA does not affect body weight or body composition. Some detrimental effects of the trans-10,cis-12 CLA isomer have also been reported in terms of altered blood lipid composition and impaired insulin sensitivity. Finally, CLA has only limited effects on immune functions in man. However, there have been reports of some interesting isomer-specific effects of CLA on the blood lipid profile, but not on immune function. These isomer-specific effects need further investigation. Until more is known, CLA supplementation in man should be considered with caution.
British Journal of Nutrition | 2005
Graham C. Burdge; Sabine Tricon; R. Morgan; Kirsty E. Kliem; Caroline E. Childs; Emma L Jones; Jennifer J. Russell; Robert F. Grimble; Christine M. Williams; Parveen Yaqoob; P. C. Calder
The present study investigated whether consuming dairy products naturally enriched in cis-9, trans-11 (c9,t11) conjugated linoleic acid (CLA) by modification of cattle feed increases the concentration of this isomer in plasma and cellular lipids in healthy men. The study had a double-blind cross-over design. Subjects aged 34-60 years consumed dairy products available from food retailers for 1 week and then either control (0.17 g c9,t11 CLA/d; 0.31 g trans-vaccenic acid (tVA)/d) or CLA-enriched (1.43 g c9,t11 CLA/d; 4.71 g tVA/d) dairy products for 6 weeks. After 7 weeks washout, this was repeated with the alternate products. c9,t11 CLA concentration in plasma lipids was lower after consuming the control products, which may reflect the two-fold greater c9,t11 CLA content of the commercial products. Consuming the CLA-enriched dairy products increased the c9,t11 CLA concentration in plasma phosphatidylcholine (PC) (38 %; P = 0.035), triacylglycerol (TAG) (22 %; P < 0.0001) and cholesteryl esters (205 %; P < 0.0001), and in peripheral blood mononuclear cells (PBMC) (238 %; P < 0.0001), while tVA concentration was greater in plasma PC (65 %; P = 0.035), TAG (98 %; P = 0.001) and PBMC (84 %; P = 0.004). Overall, the present study shows that consumption of naturally enriched dairy products in amounts similar to habitual intakes of these foods increased the c9,t11 CLA content of plasma and cellular lipids.
Atherosclerosis | 2012
Bettina M. Kofler; Elizabeth A. Miles; Peter Curtis; Christopher K. Armah; Sabine Tricon; Jilly P Grew; Frances L. Napper; Leslie Farrell; Georg Lietz; Christopher J. Packard; Muriel J. Caslake; John C. Mathers; Christine M. Williams; Philip C. Calder; Anne Marie Minihane
Here the impact of APOE genotype on CHD risk in UK adults is reported, along with an analysis of APOE genotype × BMI/age/sex interactions. APOE genotype had a significant impact on fasting total:LDL-cholesterol (TC:LDL-C) ratio, triglycerides, % HDL3, and the Framingham 10-year CVD risk score (P<0.05), with an overall trend towards lower and higher risk in E2- and E4-carriers, respectively, relative to the wild-type E3/E3 genotype. A greater impact of genotype on TC:HDL-C was observed in females, which explained 16% of the variability in this outcome versus 6% in males. APOE genotype was also associated with plasma C-reactive protein and adhesion molecule concentrations (P<0.05), with significant genotype × BMI interactions observed. Our observations indicate that the association between the APOE genotype and CHD risk is unlikely to be homogenous and highlights the risk of inaccurate estimations of genotype-phenotype associations in population subgroups without appropriate stratification for sex and adiposity.
Improving the Fat Content of Foods | 2006
Parveen Yaqoob; Sabine Tricon; Graham C. Burdge; Philip C. Calder
Publisher Summary Conjugated Linoleic Acid [“CLA”] is a collective term for a mixture of positional and geometric isomers of linoleic acid in which the two double bonds are conjugated, that is, contiguous, unlike the double bonds in linoleic acid, which are separated by a methylene group. Although diet is the major source of CLA in humans, there is no systematic database for the CLA content of foods and limited data are available on the isomeric distribution of CLA isomers in food, owing to the difficulties in the chromatographic separation of the individual isomers. More controlled studies in specific populations with purified isomers of CLA are needed and should be used to define the beneficial and detrimental effects of each individual CLA isomer in humans. The development of dairy products naturally enriched with CLA should be considered with caution, given the associated increase in trans fatty acids, which might counteract any beneficial effects to health. Therefore, strategies to enrich milk with cis-9 , trans -11 CLA without the accompanying increase in Trans Vaccenic Acid [“TVA”] are likely to be important for the future development of CLA-enriched dairy products.
The American Journal of Clinical Nutrition | 2004
Sabine Tricon; Graham C. Burdge; Samantha Kew; Tapati Banerjee; Jennifer J. Russell; Emma L Jones; Robert F. Grimble; Christine M. Williams; Parveen Yaqoob; Philip C. Calder
The American Journal of Clinical Nutrition | 2004
Samantha Kew; María Dolores Mesa; Sabine Tricon; Richard Buckley; Anne Marie Minihane; Parveen Yaqoob
The American Journal of Clinical Nutrition | 2006
Sabine Tricon; Graham C. Burdge; Emma L Jones; Jennifer J. Russell; Soraya El-Khazen; Emmanuelle Moretti; Wendy L. Hall; Andrew B. Gerry; David S. Leake; Robert F. Grimble; Christine M. Williams; Philip C. Calder; Parveen Yaqoob
The American Journal of Clinical Nutrition | 2004
Sabine Tricon; Graham C. Burdge; Samantha Kew; Tapati Banerjee; Jennifer J. Russell; Robert F. Grimble; Christine M. Williams; Philip C. Calder; Parveen Yaqoob
Clinical & Experimental Allergy | 2006
Sabine Tricon; S. Willers; H. A. Smit; Peter Burney; Graham Devereux; Anthony J. Frew; S. Halken; Arne Høst; Michael Nelson; Seif O. Shaheen; J. O. Warner; Philip C. Calder
Journal of Lipid Research | 2004
Graham C. Burdge; Berit Lupoli; Jennifer J. Russell; Sabine Tricon; Samantha Kew; Tapati Banerjee; Kevin J. Shingfield; D.E. Beever; Robert F. Grimble; Christine M. Williams; Parveen Yaqoob; Philip C. Calder