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Effect of black tea drinking on blood lipids, blood pressure and aspects of bowel habit

Published online by Cambridge University Press:  09 March 2007

S. A. Bingham
Affiliation:
1Medical Research Council, Dunn Clinical Nutrition Centre, Hills Road, Cambridge CB2 2DH
H. Vorster
Affiliation:
Department of Nutrition, Potchefstroom University for Christian Higher Education, Potchefstroom, South Africa
J. C. Jerling
Affiliation:
Department of Nutrition, Potchefstroom University for Christian Higher Education, Potchefstroom, South Africa
E. Magee
Affiliation:
1Medical Research Council, Dunn Clinical Nutrition Centre, Hills Road, Cambridge CB2 2DH
A. Mulligan
Affiliation:
1Medical Research Council, Dunn Clinical Nutrition Centre, Hills Road, Cambridge CB2 2DH
S. A. Runswick
Affiliation:
Department of Nutrition, Potchefstroom University for Christian Higher Education, Potchefstroom, South Africa
J. H. Cummings
Affiliation:
1Medical Research Council, Dunn Clinical Nutrition Centre, Hills Road, Cambridge CB2 2DH
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Abstract

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Thirty-one men (47 (SD 14) years) and thirty-four women (35 (SD 13) years) took part in a 4-week randomized cross-over trial to compare the effect of six mugs of black tea daily v. placebo (water, caffeine, milk and sugar) on blood lipids, bowel habit and blood pressure, measured during a run-in period and at the end of weeks 2, 3 and 4 of the test periods. Compliance was established by adding a known amount of p–aminobenzoic acid (PABA) to selected tea bags, and then measuring its excretion in urine. Mean serum cholesterol values during run-in, placebo and on tea drinking were 5·67 (SD 1·05), 5·76 (SD 1·11) and 5·69 (SD 1·09)mmol/l (P=0·16). There were also no significant changes in diet, LDL-cholesterol, HDL-cholesterol, triacylglycerols, and blood pressure in the tea intervention period compared with placebo. Compared with placebo, stool consistency was softened with tea (P=0·04), and no other differences were found in bowel habit. Results were unchanged when fifteen ‘non-compliers’, whose PABA excretion indicated that fewer than six tea bags had been used, were excluded from the analysis, and when differences between run-in and tea periods were considered separately for those who were given tea first or second.

Type
Human and Clinical Nutrition
Copyright
Copyright © The Nutrition Society 1997

References

REFERENCES

Ali, M. & Afzal, M. (1987). A potent inhibitor of thrombin stimulated platelet thromboxane formation from unprocessed tea. Prostaglandins Leukotrienes and Medicine 27, 913.CrossRefGoogle ScholarPubMed
Armitage, P. & Berry, G. (1987). Statistical Methods in Medical Research, 2nd ed. Oxford: Blackwell Scientific Publications.Google Scholar
Bingham, S. A., Cassidy, A., Cole, T. J., Welch, A., Runswick, S. A., Black, A. E., Thurnham, D., Bates, C., Khaw, K. T., Key, T. J. A. & Day, N. E. (1995). Validation of weighed records and other methods of dietary assessment using the 24 h urine nitrogen technique and other biological markers. British Journal of Nutrition 73, 531550.CrossRefGoogle ScholarPubMed
Bingham, S. A. & Cummings, J. H. (1983). The use of 4-aminobenzoic acid as a marker to validate the completeness of 24 hour urine collections in man. Clinical Science 64, 629635.CrossRefGoogle Scholar
Bingham, S. A., Gill, C., Welch, A., Day, K., Cassidy, A., Khaw, K. T., Sneyd, M. J., Key, T. J. A., Roe, L. & Day, N. E. (1994). Comparison of dietary assessment methods in nutritional epidemiology. British Journal of Nutrition 72, 619643.CrossRefGoogle ScholarPubMed
Bingham, S. A., Pett, S. & Day, K. C. (1990). NSP intake of a random sample of British adults. Journal of Human Nutrition and Dietetics 3, 333337.CrossRefGoogle Scholar
Bingham, S., Williams, D. R. R., Cole, T. J., Price, C. P. & Cummings, J. H. (1988). Reference values for analytes of 24h urine collections. Annals of Clinical Biochemistry 25, 610619.CrossRefGoogle ScholarPubMed
Brown, C. A., Bolton-Smith, C., Woodward, M. & Tunstall-Pedoe, H. (1993). Coffee and tea consumption and the prevalence of CHD in men and women. Journal of Epidemiology and Community Health 47, 171175.CrossRefGoogle Scholar
Crawley, H. (1988). Food Portion Sizes. London: H. M. Stationery Office.Google Scholar
Gardner, M. J. & Heady, J. A. (1973). Some effects of within person variability in epidemiological studies. Journal of Chronic Diseases 26, 781795.CrossRefGoogle Scholar
Graham, G. (1992). Green tea composition, consumption and polyphenol chemistry Preventive Medicine 21, 334350.Google ScholarPubMed
Gregory, J., Foster, K., Tyler, H. & Wiseman, M. (1990). The Dietary and Nutritional Survey of British Adults. London: H. M. Stationery Office.Google Scholar
Hara, Y. (1992). The effects of tea polyphenols on cardiovascular diseases. Preventive Medicine 21, 333A.Google Scholar
Hertog, M. G., Feskens, E. J. M., Hollman, P. C. H., Katan, M. B. & Kromhout, D. (1993). Dietary antioxidants and risk of coronary heart disease. Lancet 342, 10071011.CrossRefGoogle ScholarPubMed
Hojgaard, L., Arffman, S., Jorgensen, M. & Krag, E. (1981). Tea consumption: a cause for constipation? British Medical Journal 282, 864.CrossRefGoogle ScholarPubMed
Holland, B., Unwin, I. D. & Buss, D. H. (1988). Cereals and Cereal Products: Supplement to the 4th Edition of The Composition of Foods. Cambridge: Royal Society of Chemistry.Google Scholar
Holland, B., Unwin, I. D. & Buss, D. H. (1989). Milk Products and Eggs: Supplement to the 4th Edition of the Composition of Foods. Cambridge: Royal Society of Chemistry.Google Scholar
Holland, B., Welch, A., Unwin, I. D., Buss, D. H., Paul, A. & Southgate, D. A. T. (1991). McCance and Widdowson's The Composition of Foods, 5th ed. Cambridge: Royal Society of Chemistry.Google Scholar
Holme, I. (1990). An analysis of randomised trials on the effect of cholesterol reduction on total mortality and CHD incidence. Circulation 82, 19161924.CrossRefGoogle Scholar
Ikeda, I., Imasato, Y., Sasaki, E., Nakayama, M., Nagao, H., Takeo, T., Yayabe, F. & Sugano, M. (1992). Tea catechins decrease micellar solubility and intestinal absorption of cholesterol in rats. Biochimica et Biophysica Acta 1127, 141146.CrossRefGoogle ScholarPubMed
Imai, K. & Nakachi, K. (1995). Cross sectional study of effects on drinking green tea on cardiovascular and liver diseases. British Medical Journal 310, 693–496.CrossRefGoogle ScholarPubMed
Kark, J. D., Freidlander, Y., Kaufmann, N. A. & Stein, Y. (1985). Coffee, tea and plasma cholesterol: the Jerusalem Lipid Research Clinic Prevalence Study. British Medical Journal 291, 699704.CrossRefGoogle ScholarPubMed
Laughton, M. J., Evans, P. J., Moroney, M. A., Hoult, J. R. D. S. & Halliwell, B. N. A. (1991). Inhibition of mammalian 5-lipoxygenase and cyclooxygenase by flavonoids and phenolic dietary additives. Biochemical Pharmacology 42, 16731681.CrossRefGoogle ScholarPubMed
Lawson, M., Fredricks, S. & Johnson, A. (1991). The Hawksley random zero sphygmomanometer: unbiased assessment of blood pressure in clinical trials? British Journal of Pharmacology 32, 647650.Google Scholar
Lou, F. Q., Zhang, M. F., Zhang, X. G., Liu, J. M. & Yaun, W. L. (1989). A study on tea pigment in prevention of atherosclerosis. Chinese Medical Journal 102, 579583.Google Scholar
Magee, E. (1993). The effect of tea on bowel habit, measured by a diary and retrospective questionnaire. Industrial Placement Dissertation, University of Ulster, Coleraine.Google Scholar
Matsuda, H., Chisaka, T., Kubomura, Y., Yamahar, J., Sawada, T., Fujimura, H. & Kimura, H. (1986). Effects of crude tea on experimental hypercholesterolaemia. Journal Of Ethnopharmacology 17, 213224.Google Scholar
Mulligan, E. (1993). p–Amino benzoic acid as a monitor of compliance in intervention studies. Industrial Placement Dissertation, University of Ulster, Coleraine.Google Scholar
Muramatsu, K., Fukuyo, M. & Hara, Y. (1986). Effect of green tea catechins on plasma cholesterol level in cholesterol fed rats. Journal of Nutrition Science and Vitaminology 32, 613622.CrossRefGoogle ScholarPubMed
O'Brien, E., Mee, F., Atkins, N. & O'Malley, K. (1990). Inaccuracy of the Hawksley random zero sphygmomanometer. Lancet 336, 14651468.CrossRefGoogle ScholarPubMed
Paul, A. A. & Southgate, D. A. T. (1978). McCance and Widdowson's The Composition of Foods, 4th ed. London: H. M. Stationery Office.Google Scholar
Serafini, M., Ghiselli, A. & FerroLuzzi, A. N. A. (1996). In vivo antioxidant effect of green and black tea in man. European Journal of Clinical Nutrition 50, 2832.Google ScholarPubMed
Silverman, K., Evans, S. M., Strain, E. C. & Griffiths, R. R. (1992). Withdrawal symptoms after the double blind cessation of caffeine comsumption. New England Journal of Medicine 327, 11091114.CrossRefGoogle Scholar
Steinberg, D., Parthasarathy, S., Carew, T. E. & Witztum, D. (1989). Beyond cholesterol: modifications of LDL that increase in atherogenicity. New England Journal of Medicine 320, 915924.Google ScholarPubMed
Stensvold, I., Tverdal, A., Solvoll, K. & Foss, O. P. (1992). Tea consumption: relationship to cholesterol, blood pressure and coronary and total mortality. Preventive Medicine 21, 546553.CrossRefGoogle ScholarPubMed
Systat (19901992). Systat 5.2. Evanston, IL: Systat.Google Scholar
Vorster, H., Jerling, J., Oosthuizen, W., Cummings, J., Bingham, S., Magee, L., Mulligan, A. & Runswick, S. (1996). Tea drinking and haemostasis: a randomised, placebo controlled, cross over study in free living subjects. Haemostasis 26, 5864.Google ScholarPubMed
Wiles, S. J., Nettleton, P. A., Black, A. E. & Paul, A. A. (1980). The nutrient content of some cooked dishes eaten in Britain: a supplementary food table. Journal of Human Nutrition 34, 189223.Google Scholar
Yang, C. S. & Wang, Z. (1993). Tea and cancer. Journal of the National Cancer Institute 85, 10381049.CrossRefGoogle ScholarPubMed