Intermittent fasting combined with calorie restriction is effective for weight loss and cardio-protection in obese women

Monica C Klempel, Cynthia M Kroeger, Surabhi Bhutani, John F Trepanowski, Krista A Varady, Monica C Klempel, Cynthia M Kroeger, Surabhi Bhutani, John F Trepanowski, Krista A Varady

Abstract

Background: Intermittent fasting (IF; severe restriction 1 d/week) facilitates weight loss and improves coronary heart disease (CHD) risk indicators. The degree to which weight loss can be enhanced if IF is combined with calorie restriction (CR) and liquid meals, remains unknown.

Objective: This study examined the effects of IF plus CR (with or without a liquid diet) on body weight, body composition, and CHD risk.

Methods: Obese women (n = 54) were randomized to either the IFCR-liquid (IFCR-L) or IFCR-food based (IFCR-F) diet. The trial had two phases: 1) 2-week weight maintenance period, and 2) 8-week weight loss period.

Results: Body weight decreased more (P = 0.04) in the IFCR-L group (3.9 ± 1.4 kg) versus the IFCR-F group (2.5 ± 0.6 kg). Fat mass decreased similarly (P < 0.0001) in the IFCR-L and IFCR-F groups (2.8 ± 1.2 kg and 1.9 ± 0.7 kg, respectively). Visceral fat was reduced (P < 0.001) by IFCR-L (0.7 ± 0.5 kg) and IFCR-F (0.3 ± 0.5 kg) diets. Reductions in total and LDL cholesterol levels were greater (P = 0.04) in the IFCR-L (19 ± 10%; 20 ± 9%, respectively) versus the IFCR-F group (8 ± 3%; 7 ± 4%, respectively). LDL peak particle size increased (P < 0.01), while heart rate, glucose, insulin, and homocysteine decreased (P < 0.05), in the IFCR-L group only.

Conclusion: These findings suggest that IF combined with CR and liquid meals is an effective strategy to help obese women lose weight and lower CHD risk.

Figures

Figure 1
Figure 1
Study flow chart. IFCR-L: Intermittent fasting calorie restriction-liquid diet; IFCR-F: Intermittent fasting calorie restriction-food based diet.
Figure 2
Figure 2
Body weight and body composition changes during the weight loss period. IFCR-L: Intermittent fasting calorie restriction-liquid diet (n = 28); IFCR-F: Intermittent fasting calorie restriction-food based diet (n = 26); BW: Body weight; FM: Fat mass; FFM: Fat free mass, VAT: Visceral adipose tissue; SAT: Abdominal subcutaneous adipose tissue. A. Changes in body weight, fat mass, and fat free mass in the IFCR-L and IFCR-F groups. IFCR-L group lost more body weight (P = 0.04) compared to the IFCR-F group (Repeated-measures ANOVA). *Week 10 absolute values significantly different from baseline (week 3) absolute values, P < 0.0001 (Repeated-measures ANOVA). B. Changes in visceral adipose tissue and abdominal subcutaneous adipose tissue in the IFCR-L and IFCR-F groups. *Week 10 absolute values significantly different from baseline (week 3) absolute values, P < 0.001 (Repeated-measures ANOVA).
Figure 3
Figure 3
Change in visceral and subcutaneous adipose tissue area after the IFCR-L intervention. A. Abdominal visceral fat (58 cm2) and subcutaneous fat (245 cm2) before the intermittent fasting calorie restriction-liquid diet (IFCR-L) at the L3-L4 vertebrae (week 3). B. Abdominal visceral fat (17 cm2) and subcutaneous fat (173 cm2) after the IFCR-L regimen at the L3-L4 vertebrae (week 10).
Figure 4
Figure 4
Plasma lipid changes during the weight loss period. IFCR-L: Intermittent fasting calorie restriction-liquid diet (n = 28); IFCR-F: Intermittent fasting calorie restriction-food based diet (n = 26); TC: Total cholesterol; LDL: Low density lipoprotein cholesterol; HDL: High density lipoprotein cholesterol; TG: Triglycerides. *Week 10 values significantly different from baseline (week 3) values, P < 0.01 (Repeated-measures ANOVA). IFCR-L group experienced significantly greater reductions in total cholesterol and LDL cholesterol concentrations when compared to the IFCR-F group (P < 0.05) (Repeated-measures ANOVA).

References

    1. Mercuro G, Deidda M, Bina A, Manconi E, Rosano GM. Gender-specific aspects in primary and secondary prevention of cardiovascular disease. Curr Pharm Des. 2011;17(11):1082–1089. doi: 10.2174/138161211795656954.
    1. Lindstrom J, Uusitupa M. Lifestyle intervention, diabetes, and cardiovascular disease. Lancet. 2008;371(9626):1731–1733. doi: 10.1016/S0140-6736(08)60740-0.
    1. Mattson MP, Wan R. Beneficial effects of intermittent fasting and caloric restriction on the cardiovascular and cerebrovascular systems. J Nutr Biochem. 2005;16(3):129–137. doi: 10.1016/j.jnutbio.2004.12.007.
    1. Harvie MN, Pegington M, Mattson MP, Frystyk J, Dillon B, Evans G. et al.The effects of intermittent or continuous energy restriction on weight loss and metabolic disease risk markers: a randomized trial in young overweight women. Int J Obes (Lond) 2011;35(5):714–727. doi: 10.1038/ijo.2010.171.
    1. Buschemeyer WC 3rd, Klink JC, Mavropoulos JC, Poulton SH, Demark-Wahnefried W, Hursting SD. et al.Effect of intermittent fasting with or without caloric restriction on prostate cancer growth and survival in SCID mice. Prostate. 2010;70(10):1037–1043. doi: 10.1002/pros.21136.
    1. Davis C, Curtis C, Tweed S, Patte K. Psychological factors associated with ratings of portion size: relevance to the risk profile for obesity. Eat Behav. 2007;8(2):170–176. doi: 10.1016/j.eatbeh.2006.04.002.
    1. Heymsfield SB, van Mierlo CA, van der Knaap HC, Heo M, Frier HI. Weight management using a meal replacement strategy: meta and pooling analysis from six studies. Int J Obes Relat Metab Disord. 2003;27(5):537–549. doi: 10.1038/sj.ijo.0802258.
    1. Tsai AG, Wadden TA. The evolution of very-low-calorie diets: an update and meta-analysis. Obesity (Silver Spring) 2006;14(8):1283–1293. doi: 10.1038/oby.2006.146.
    1. Mifflin MD, St-Jeor ST, Hill LA, Scott BJ, Daugherty SA, Koh YO. A new predictive equation for resting energy expenditure in healthy individuals. Am J Clin Nutr. 1990;51(2):241–247.
    1. Demerath EW, Reed D, Rogers N, Sun SS, Lee M, Choh AC. et al.Visceral adiposity and its anatomical distribution as predictors of the metabolic syndrome and cardiometabolic risk factor levels. Am J Clin Nutr. 2008;88(5):1263–1271.
    1. Demerath EW, Ritter KJ, Couch WA, Rogers NL, Moreno GM, Choh A. et al.Validity of a new automated software program for visceral adipose tissue estimation. Int J Obes (Lond) 2007;31(2):285–291. doi: 10.1038/sj.ijo.0803409.
    1. Hoefner DM, Hodel SD, O'Brien JF, Branum EL, Sun D, Meissner I. et al.Development of a rapid, quantitative method for LDL subfractionation with use of the Quantimetrix Lipoprint LDL System. Clin Chem. 2001;47(2):266–274.
    1. Williams KV, Mullen ML, Kelley DE, Wing RR. The effect of short periods of caloric restriction on weight loss and glycemic control in type 2 diabetes. Diabetes Care. 1998;21(1):2–8. doi: 10.2337/diacare.21.1.2.
    1. Lefevre M, Redman LM, Heilbronn LK, Smith JV, Martin CK, Rood JC. et al.Caloric restriction alone and with exercise improves CVD risk in healthy non-obese individuals. Atherosclerosis. 2009;203(1):206–213. doi: 10.1016/j.atherosclerosis.2008.05.036.
    1. Avenell A, Brown TJ, McGee MA, Campbell MK, Grant AM, Broom J. et al.What are the long-term benefits of weight reducing diets in adults? A systematic review of randomized controlled trials. J Hum Nutr Diet. 2004;17(4):317–335. doi: 10.1111/j.1365-277X.2004.00531.x.
    1. Dattilo AM, Kris-Etherton PM. Effects of weight reduction on blood lipids and lipoproteins: a meta-analysis. Am J Clin Nutr. 1992;56(2):320–328.
    1. Wronska A, Kmiec Z. Structural and biochemical characteristics of various white adipose tissue depots. Acta Physiol (Oxf) 2012;205(2):194–208. doi: 10.1111/j.1748-1716.2012.02409.x.
    1. Kosztaczky B, Foris G, Paragh G Jr, Seres I, Zsiros E, Koncsos P. et al.Leptin stimulates endogenous cholesterol synthesis in human monocytes: New role of an old player in atherosclerotic plaque formation. Leptin-induced increase in cholesterol synthesis. Int J Biochem Cell Biol. 2007;39(9):1637–1645. doi: 10.1016/j.biocel.2007.04.012.
    1. Mantzoros CS, Magkos F, Brinkoetter M, Sienkiewicz E, Dardeno TA, Kim SY. et al.Leptin in human physiology and pathophysiology. Am J Physiol Endocrinol Metab. 2011;301(4):E567–E584. doi: 10.1152/ajpendo.00315.2011.
    1. Klempel MC, Varady KA. Reliability of leptin, but not adiponectin, as a biomarker for diet-induced weight loss in humans. Nutr Rev. 2011;69(3):145–154. doi: 10.1111/j.1753-4887.2011.00373.x.
    1. Juhaeri, Stevens J, Chambless LE, Nieto FJ, Jones D, Schreiner P. et al.Associations of weight loss and changes in fat distribution with the remission of hypertension in a bi-ethnic cohort: the Atherosclerosis Risk in Communities Study. Prev Med. 2003;36(3):330–339. doi: 10.1016/S0091-7435(02)00063-4.
    1. Tzotzas T, Evangelou P, Kiortsis DN. Obesity, weight loss and conditional cardiovascular risk factors. Obes Rev. 2011;12(5):e282–e289. doi: 10.1111/j.1467-789X.2010.00807.x.
    1. Vansant G, Hulens M. The assessment of dietary habits in obese women: influence of eating behavior patterns. Eat Disord. 2006;14(2):121–129. doi: 10.1080/10640260500536284.
    1. Racette SB, Das SK, Bhapkar M, Hadley EC, Roberts SB, Ravussin E. et al.Approaches for quantifying energy intake and%calorie restriction during calorie restriction interventions in humans: the multicenter CALERIE study. Am J Physiol Endocrinol Metab. 2012;302(4):E441–E448. doi: 10.1152/ajpendo.00290.2011.

Source: PubMed

3
S'abonner