Hostname: page-component-cd9895bd7-q99xh Total loading time: 0 Render date: 2024-12-27T10:54:38.013Z Has data issue: false hasContentIssue false

The acute effects of different sources of dietary calcium on postprandial energy metabolism

Published online by Cambridge University Press:  08 March 2007

Nicola K. Cummings
Affiliation:
Program of Nutrition, Dietetics and Food Science, School of Public Health, Curtin University of Technology, GPO Box U1987, Perth, WA 6845, Australia
Anthony P. James
Affiliation:
Program of Nutrition, Dietetics and Food Science, School of Public Health, Curtin University of Technology, GPO Box U1987, Perth, WA 6845, Australia
Mario J. Soares*
Affiliation:
Program of Nutrition, Dietetics and Food Science, School of Public Health, Curtin University of Technology, GPO Box U1987, Perth, WA 6845, Australia
*
*Corresponding author: Dr Mario J. Soares, fax +61 8 9266 2958, email m.soares@curtin.edu.au
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Dairy Ca intake has been shown to be superior to elemental Ca in increasing the loss of body fat during energy restriction. We questioned whether the mechanisms involved an increase in postprandial energy expenditure, fat oxidation and/or a greater lipolysis. The acute effects of different sources of Ca were examined in eight subjects, aged 47–66 years and BMI 27·6–36·1kg/m2, in a three-way cross-over study. Subjects were randomly provided breakfast meals either low in dairy Ca and vitamin D (LD; control), high in non-dairy Ca (calcium citrate) but low in vitamin D (HC) or high in dairy Ca and vitamin D (HD). Diet-induced thermogenesis, fat oxidation rates (FOR), carbohydrate oxidation rates (COR), insulin, glucose, ΔNEFA and glycerol were measured hourly over a 6h postprandial period. Postprandial data were calculated as a change (Δ) from the fasting value. Results showed that ΔNEFA was significantly different between meals (LD −1·50 (sem 0·26), HC −1·22 (sem 0·32), HD −0·94 (sem 0·27) mmol/l×6h; P=0·035), with a lesser suppression following both high-Ca meals. ΔFOR was significantly higher following the two high-Ca meals (LD −6·5 (sem 2·2), HC 2·93 (sem 2·34), HD 3·3 (sem 2·5) g×6;h; P=0·005), while reciprocally ΔCOR was significantly lower. ΔGlycerol was less suppressed following the high-Ca meals but statistical significance was not achieved. No differences in diet-induced thermogenesis, insulin or glucose were observed. Regardless of source, Ca intake acutely stimulated postprandial fat oxidation; and there was a lesser suppression of NEFA following these meals.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2006

References

Australian Bureau of Statistics Nutrient intakes and physical measurements Canberra: Australian Bureau of Stastistics. 1998.Google Scholar
Bairaktari, E, Hatzidimou, K, Tzallas, C, Vini, M, Katsaraki, A, Tselepis, A, Elisaf, M, Tsolas, O, Estimation of LDL cholesterol based on the Friedewald formula and on apo B levels. Clin Biochem (2000) 33 549555.CrossRefGoogle ScholarPubMed
Coppack, SW, Jensen, MD, Miles, JM, In vivo regulation of lipolysis in humans. J Lipid Res (1994) 35 177193.CrossRefGoogle ScholarPubMed
Cummings, NK, Soares, MJCalcium bioavailability from dairy and non-dairy sources: possible suppression effect of paracetamol (Acetaminophen). Asia Pac J Clin Nutr (2005) 14 Suppl S103.Google Scholar
Cummings, NK, Soares, MJ, Chan She Ping-Delfos, W, James, AP, Sivakumar, P, Mamo, J, Piers, LS, Gastric emptying of high calcium breakfast meals: potential effect of paracetamol (acetaminophen) on substrate oxidation rates. Aust Soc Study Obes (2004) 79 P 25.Google Scholar
Davies, MK, Heaney, RP, Recker, RP, Calcium intake and body weight. J Clin Endocrinol Metab (2000) 85 46354638.Google ScholarPubMed
Ferranini, E, The theoretical bases of indirect calorimetry: a review. Metabolism (1988) 37 287301.CrossRefGoogle Scholar
Flatt, JP, Body composition, respiratory quotient and weight maintenance. Am J Clin Nutr (1995) 62 1107S1117S.CrossRefGoogle ScholarPubMed
Frayn, KN, Non-esterified fatty acid metabolism and postprandial lipaemia. Atherosclerosis (1998) 141 S41S46.CrossRefGoogle ScholarPubMed
Gunther, CW, Lyle, RM, Legowski, PA, James, JM, McCabe, LD, McCabe, GP, Peacock, M, Teegarden, D, Fat oxidation and its relation to serum parathyroid hormone in young women enrolled in a 1-y dairy calcium intervention. Am J Clin Nutr (2005) 82 12281234.CrossRefGoogle Scholar
Harvey-Berino, J, Gold, BC, Lauber, R, Starinski, A, The impact of calcium and dairy product consumption on weight loss. Obes Res (2005) 13 17201726.CrossRefGoogle ScholarPubMed
Heaney, RP, Rafferty, K, Dowell, MS, Bierman, J, Calcium fortification systems differ in bioavailability. J Am Diet Assoc (2005) 105 807809.CrossRefGoogle ScholarPubMed
Holick, MF, Vitamin D: importance in the prevention of cancers, type 1 diabetes, heart disease, and osteoporosis. Am J Clin Nutr (2004) 79 362371.CrossRefGoogle ScholarPubMed
Institute of Medicine Food and Nutrition Board Dietary Reference Intakes: calcium, phosphorus, magnesium, vitamin D and fluoride Washington DC: National Academy Press. 1999.Google Scholar
Jacobsen, R, Lorenzen, JK, Toubro, S, Krog-Mikkelsen, I, Astrup, A, Effect of short-term high dietary calcium intake on 24-h energy expenditure, fat oxidation, and fecal fat excretion. Int J Obes (Lond) (2005) 29 292301.CrossRefGoogle ScholarPubMed
Mathews, JN, Altman, DG, Campbell, MJ, Royston, P, Analysis of serial measurements in medical research. BMJ (1990) 300 230235.CrossRefGoogle Scholar
Mehansho, H, Kanerva, RL, Hudepohl, GR, Smith, KT, Calcium bioavailability and iron-calcium interaction in orange juice. J Am Coll Nutr (1989) 8 6168.CrossRefGoogle ScholarPubMed
Melanson, EL, Donahoo, WT, Dong, F, Ida, T, Zemel, MB, Effect of low- and high-calcium dairy-based diets on macronutrient oxidation in humans. Obes Res (2005) 13 21022112.CrossRefGoogle ScholarPubMed
Melanson, EL, Sharp, TA, Schneider, J, Donahoo, WT, Grunwald, GK, Hill, JO, Relation between calcium intake and fat oxidation in adult humans. Int J Obes Relat Metab Disord (2003) 27 196203.CrossRefGoogle ScholarPubMed
National Health and Medical Research Council Acting on Australia's Weight: A Strategic Plan for the Prevention of Overweight and Obesity CanberraAustralian Government Publishing Service 1997Google Scholar
Newmark, HL, Heaney, RP, Lachance, PA, Should calcium and vitamin D be added to the current enrichment program for cereal-grain products?. Am J Clin Nutr (2004) 80 264270.CrossRefGoogle Scholar
Norton, K, Olds, TAnthropometrica SydneyUniversity of New South Wales Press 2000Google Scholar
Nowson, CA, Margerison, C, Vitamin D intake and vitamin D status of Australians. Med J Aust (2002) 177 149152.CrossRefGoogle ScholarPubMed
Parikh, SJ, Yanovski, JA, Calcium intake and adiposity. Am J Clin Nutr (2003) 77 17.CrossRefGoogle ScholarPubMed
Piers, LS, Soares, MJ, Makan, T, Shetty, PS, Thermic effect of a meal 1. Methodology and variation in normal young adults. Br J Nutr (1992) 67 165175.CrossRefGoogle ScholarPubMed
Piers, LS, Walker, KZ, Stoney, RM, Soares, MJ, O'Dea, K, The influence of the type of dietary fat on postprandial fat oxidation rates: monounsaturated (olive oil) vs. saturated fat (cream). Int J Obes Relat Metab Disord (2002) 26 814821.CrossRefGoogle ScholarPubMed
Ravussin, E, Bogardus, CRelationship of genetics, age, and physical fitness to daily energy expenditure and fuel utilization. Am J Clin Nutr (1989) 49 968975.CrossRefGoogle ScholarPubMed
Sakhaee, K, Bhuket, T, Adams-Huet, B, Rao, DS, Meta-analysis of calcium bioavailability: a comparison of calcium citrate with calcium carbonate. Am J Ther (1999) 6 313321.CrossRefGoogle ScholarPubMed
Sawaya, AL, Fuss, PL, Dallal, GE, Tsay, R, McCrory, MA, Young, V, Roberts, SB, Meal palatability, substrate oxidation and blood glucose in young and older men. Physiol Behav (2001) 72 512.CrossRefGoogle Scholar
Soares, MJ, Binns, C, Lester, L, Higher intakes of calcium are associated with lower BMI and waist circumference in Australian adults: an examination of the 1995 National Nutrition Survey. Asia Pac J Clin Nutr (2004a) 13 S85.Google Scholar
Soares, MJ, Piers, LS, Kraai, L, Shetty, PS, Day-to-day variations in basal metabolic rates and energy intakes of human subjects. Eur J Clin Nutr (1989) 43 465472.Google ScholarPubMed
Soares, MJ, Ping-Delfos, WC, James, AP, Cummings, NK, Dairy calcium and vitamin D stimulate postprandial thermogenesis:effect of sequential meals. Asia Pac J Clin Nutr (2004b) 13 S56.Google Scholar
Thompson, WG, Rostad Holdman, N, Janzow, DJ, Slezak, JM, Morris, KL, Zemel, MB, Effect of energy-reduced diets high in dairy products and fiber on weight loss in obese adults. Obes Res (2005) 13 13441353.CrossRefGoogle ScholarPubMed
Thorburn, AW, Prevalence of obesity in Australia. Obes Rev (2005) 6 187189.CrossRefGoogle ScholarPubMed
Zemel, MB, Regulation of adiposity and obesity risk by dietary calcium: mechanisms and implications. J Am Coll Nutr (2002) 21 146S151S.CrossRefGoogle ScholarPubMed
Zemel, MB, Mechanisms of dairy modulation of adiposity. J Nutr (2003) 133 252S256S.CrossRefGoogle ScholarPubMed
Zemel, MB, Role of calcium and dairy products in energy partitioning and weight management. Am J Clin Nutr (2004) 79 Suppl. 907S912S.CrossRefGoogle ScholarPubMed
Zemel, MB, Richards, J, Mathis, S, Milstead, A, Gebhardt, L, Silva, E, Dairy augmentation of total and central fat loss in obese subjects. Int J Obes (Lond) (2005a) 29 391397.CrossRefGoogle ScholarPubMed
Zemel, MB, Richards, J, Milstead, A, Campbell, P, Effects of calcium and dairy on body composition and weight loss in African-American adults. Obes Res (2005b) 13 12181225.CrossRefGoogle ScholarPubMed
Zemel, MB, Shi, H, Greer, B, Dirienzo, D, Zemel, P, Regulation of adiposity by dietary calcium. FASEB J (2000) 14 11321138.CrossRefGoogle ScholarPubMed