- Research
- Open access
- Published:
The inclusion of a partial meal replacement with or without inulin to a calorie restricted diet contributes to reach recommended intakes of micronutrients and decrease plasma triglycerides: A randomized clinical trial in obese Mexican women.
Nutrition Journal volume 11, Article number: 44 (2012)
Abstract
Background
Obesity is a major public health problem in many poor countries where micronutrient deficiencies are prevalent. A partial meal replacement may be an effective strategy to decrease obesity and increase micronutrient intake in such populations. The objective was to evaluate the efficacy of a partial meal replacement with and without inulin on weight reduction, blood lipids and micronutrients intake in obese Mexican women.
Methods
In a randomized controlled clinical trial 144 women (18–50 y) with BMI ≥ 25 kg/m2, were allocated into one of the following treatments during 3 months: 1) Two doses/d of a partial meal replacement (PMR), 2) Two doses/d of PMR with inulin (PMR + I) , 3) Two doses/d of 5 g of inulin (INU) and 4) Control group (CON). All groups received a low calorie diet (LCD). Weight, height, hip and waist circumference were measured every 2 weeks and body composition, lipids and glucose concentration and nutrient intake were assessed at baseline and after 3 months.
Results
All groups significantly reduced weight, BMI, waist and hip circumference. Differences between groups were only observed in BMI and weight adjusted changes: At 45 days PMR group lost more weight than INU and CON groups by 0.9 and 1.2Kg, respectively. At 60 days, PMR + I and PMR groups lost more weight than in INU by 0.7 and 1Kg, respectively. Subjects in PMR, PMR + I and INU significantly decreased triglycerides. Energy intake was reduced in all groups. Fiber intake increased in PMR + I and INU groups. Some minerals and vitamins intakes were higher in PMR and PMR + I compared with INU and CON groups.
Conclusion
Inclusion of PMR with and without inulin to a LCD had no additional effect on weight reduction than a LCD alone but reduced triglycerides and improved intake of micronutrients during caloric restriction. PMR could be a good alternative for obese populations with micronutrient deficiencies.
ClinicalTrials.Gov ID
NCT01505023
Introduction
The prevalence of obesity is increasing in many countries and has become a public health challenge in populations worldwide. It is estimated that at least one billion of individuals worldwide are overweight (body mass index, BMI ≥ 25 kg/m2) and at least 300 million are obese (BMI ≥ 30 kg/m2) [1, 2]. The prevalence of obesity has specially increased in populations in developing countries; for example, a recent survey carried out in Mexico found that the prevalence of obesity in adults in 2006 was 24.2% in men and 34.5% in women, increasing 4% in only 6 years [3, 4].
Recent studies have suggested that micronutrient deficiencies might be associated with a higher susceptibility for obesity which might partially explain why obesity in poor countries has increased more rapidly [5]. The possible association of some micronutrient deficiencies with a higher susceptibility for fat deposition and obesity has recently been revised [6]. Since calorie restricted diets might worsen micronutrient deficiencies, a strategy to reduce calories in obese population with a high probability of having some micronutrient deficiencies, should contemplate increasing the intake of vitamins and minerals.
Low calorie diets (LCD) and an increase in physical activity are effective strategies to reduce body fat and to control body weight [7]; however a high proportion of individuals trying to lose weight find it very difficult to reduce energy intake [8]. Partial meal replacements (PMR) are single food or selection of foods intended as replacement of one or two daily meals to reduce energy intake. PMR are made with variety of food preparations, they can be liquid or powder formulas, frozen foods or bars fortified, all fortified with vitamins and minerals [9]. In addition to energy intake reduction, PMR have been used to increase the intake of vitamins, minerals and proteins and thus decrease the risk of deficiencies that are common during energy restriction diets [10, 11]. Several studies have evaluated the effectiveness of PMR to reduce weight among obese individuals with different results [10, 12]. Most of these studies however, have been carried out in developed populations with a low risk of having micronutrients deficiencies.
Besides the addition of vitamins and minerals, the effectiveness of PMR may be improved by being used as a vehicle for substances with a potential benefit for the obese. Inulin is a non-digestible and non-flavored polisaccharide with low energy content that has been shown to have a positive effect on lipids metabolism [13–20]. A recent meta-analysis by Brighenti [21] reviewed 15 studies and concluded that supplementing individuals with 7 to 10 g/d of inulin reduces their serum triglycerides by 7.5%. A reduction of triglycerides in obese patients would be beneficial since about 36% of individuals with obesity have high serum triglycerides [22]. It has also been suggested that inulin may increase the absorption of minerals such as zinc, iron, magnesium and calcium [23].
The objective of this study was to test the efficacy of a PMR added with vitamins, minerals and inulin on weight reduction, blood lipids and micronutrients intake in obese Mexican women.
Methods
Subjects and treatments
A total of 144 non-pregnant, non-lactating, overweight or obese women (BMI ≥ 25 kg/m 2) were included in the study. The sample size considered an alpha error of 0.05, statistical power of 0.80 and a lost to follow up rate of 20% to detect a difference in body weight reduction of 4% between treatments and control with an estimated standard deviation of 6%. Women were excluded if they had been previously diagnosed with diabetes, hypertension or if they had fasting glucose ≥126 mg/dL and blood triglycerides ≥400 mg/dL. All subjects received oral and written information of the study protocol, including benefits and potential risks, and voluntarily accepted to participate in the study. The study protocol was reviewed and approved by the Bioethics Committee of the University of Queretaro.
The study was a randomized, controlled, longitudinal, clinical trial. Women who accepted to participate were randomized into one of 4 groups of 36 women each, with a computer generated randomization list. Women in each group received during 3 months one of the following treatments: 1) PMR alone; 2) PMR + 10 g of inulin (PMR + I); 3) 10 g of inulin alone (INU) or 4) Control group with no additional treatment (CON). In addition, a LCD was provided to subjects in all 4 groups. The LCD consisted of educating subjects in detail with a printed guideline developed according with the official food guide for Mexican population (NOM-043-SSA2-2005) and with the National Institutes of Health guide to treat overweight and obese adults [24]. The guide showed the appropriate proportions of the different food groups in a meal and included a list of foods with high content of fat and/or sugar that should be avoided and replaced by equivalent low calorie foods (i.e. whole milk for skimmed milk). The guide also provided suggestions to include high fiber products and water and the size of food portions to include in the diet.
The PMR was developed before the initiation of the clinical trial by a pharmaceutical laboratory located in the city of Queretaro where the study was carried out ( EsbeliaTM). The PMR was designed to contain sufficient amounts of all vitamins and minerals, especially those that have been reported to be deficient in Mexicans [25]. The nutrient composition of the PMR used in this study is shown in Table 1. An additional version of the PMR was also developed which contained 5 g of inulin per dose; inulin was obtained from BeneoTM Orafti. Treatments PMR and PMR + I were delivered to women in can containers with 400 grams of products every other week and were available in chocolate and vanilla flavors. Women were instructed to consume 2 servings per day of the respective treatment at breakfast and dinner, each consisting of 33 g of powder dissolved in 250 ml of skim milk. Subjects were instructed not to consume any additional foods for breakfast or dinner. Women in the INU group received two can containers with 100 g of inulin every two weeks; they were asked to consume one 5 g serving of inulin mixed with any drink at breakfast and same amount at dinner (10 g of inulin/d).
The participants were followed by visits to the clinic every two weeks and by a phone interview once every week. During the first visit, women in the PMR, PMR + I and INU groups received oral and written information explaining how to prepare the treatments and how to follow the LCD. Women in the control group only received the LCD. At every visit, women were asked to bring empty cans or cans with remaining product to exchange for new ones. During the visits at the clinics and during telephone calls, nutritionists reviewed the LCD guide again with the subjects and answered any questions they might have.
Women in PMR, PMR + I and INU treatment groups filled an adherence log dairy to record the consumption of treatments; they were asked to register if they consumed or did not consume the treatment at breakfast and dinner. Adherence to treatments was defined as the number of days that each treatment was consumed divided by the total number of days that each subject was followed.
Anthropometry and body composition
Weight, height, hip and waist circumference were measured at baseline and every 2 weeks during three months. Measurements were carried out by trained nutritionists following standard procedures [26]. Weight was measured to the nearest 100 g using electronic scales (SECA ONDA 843, Hamburg, Germany). Height was measured with a stadiometer (SECA 206, Hanover, MD) to the nearest 0.1 cm. Waist and hip circumference was measured to the nearest 0.1 cm with a flexible band (SECA 200; Seca Deutschland) following procedures recommended by WHO [27]. Measurements on each subject on different occasions were done by the same examiner to reduce variability.
Body composition was determined with bioelectrical impedance (Quantum X BIA, RJL Systems Inc. Clinton Township, MI) at baseline and every month during the three months of follow-up. Women were asked to lay down in a quiet room and remain calmed for the duration of the measurement. Fat percent was calculated from resistance and reactance using Kotler equations [28].
Glucose and lipid profile
A fasting blood sample was taken at baseline and after 3 months to measure plasma lipids and glucose concentrations. Plasma glucose was determined using the glucose oxidase method. Total serum cholesterol, HDL-cholesterol, and triglycerides were measured using a colorimetric method with an auto analyzer RA 50 (Johnson&Johnson Vitros DT60 II Chemistry System Rochester, NY USA). LDL was estimated with the Friedewald equations [29].
Food and nutrient intake evaluation
Food intake was assessed at baseline and after three months using three 24-recalls, one was applied on a weekend day and two on days of the week, Nutrient intake was determined using food composition tables from the US department of agriculture [30] and from the National Institute of Medical Sciences and Nutrition [31]. Percents of adequacy were calculated from the recommended nutrients intake for Mexican population [32, 33].
Statistical analysis
Descriptive analysis was carried out for all variables. Within treatment change in anthropometry, body fat and lipids concentration, by treatment group, were compared with paired T-test; this test was used because the independent variable has two levels (pre-treatment and post-treatment). To evaluate the effect of treatment on anthropometry and lipids concentration an analysis of variance (ANOVA) adjusted for initial values was carried out considering the change (final-initial value) as the dependent variable. Unadjusted ANOVA to evaluate nutrients intake was used to compare between treatments. All reported p-values are based on two-sided tests and compared to a significance level of 0.05. SPSS version 10 (SPSS Inc, Chicago, IL, U.S.A.) software was used for all statistical calculations.
Results
Flow diagram of participants is shown in Figure 1. The subjects that did not finish the intervention, abandoned the study for personal reasons not related to the treatment. Characteristics of subjects by treatment group at the beginning of the study are described in Table 2. No differences were observed between groups in any of the study variables at baseline or between subjects that were lost to follow up and subjects that remained to the end of the study.
Effect of treatments on anthropometry and body composition
All groups significantly reduced their weight, BMI, and waist and hip circumferences. Weight was significantly lower from baseline value in all treatment groups since the first post-treatment evaluation after 2wk, and weight loss was maintained along the trial. After 90 days, weight reduction of women in the PMR + I, PMR, INU and CON groups was [Mean (95%CI)]: –3.88 (−4.92, -2.84), -4.09 (−4.97, -3.20), -2.81 (−3.68, -1.93) and −2.89 (−3.85, -1.94) Kg, respectively. There were no significant differences in unadjusted changes between groups. The differences of adjusted changes found were as follows: After 45 days a greater reduction of BMI was observed in PMR group (mean; 95% CI) (−1.16; -1.40, -0.91 kg/m2) compared with INU (−0.68; -0.94, -0.42) and CON (−0.80; -1.06, -0.54) groups. At 60 days, BMI decreased more in PMR + I (−1.24; -1.56, -0.93) and PMR (−1.37; -1.66, -1.08) than in INU (−0.75; -1.05, -0.44). After 75 and 90 days no differences were observed between groups. Similarly, weight loss was greater at 45 days in PMR group (−2.85; -3.45, -2.25Kg) compared with INU (−1.64; -2.26, -1.01) and CON (−1.97; -2.59, -1.35) groups. And at 60 days, weight decreased more in PMR + I (−3.07; -3.84, -2.29) and PMR (−3.36; -4.07, -2.66) than in INU (−1.84; -2.59, -1.10) (Figure 2). Adjusted waist circumference reduction after 60 days was 1.8 cm greater, in PMR group (−4.87; -5.77, -3.96) compared with INU group (−3.06; -4.02, -2.11) (Figure 3). Body fat after the intervention was statistically similar than baseline.
Effect of treatments on lipids and glucose concentration
Groups PMR + I, PMR, INU, significantly reduced by 21.5%, 19.3% and 20% respectively, their triglycerides concentration after 3 months of intervention (Table 3). No other significant changes were found in lipids or glucose concentrations.
Food and nutrient intake
The energy, carbohydrates, protein, fat and cholesterol intake was significantly reduced in all groups (Table 4). Fat intake reduction was greater in PMR and PMR + I groups than in INU and CON groups, and fiber intake increased more in PMR + I and INU groups than in PMR and CON groups. Cholesterol intake was lower in PMR and PMR + I groups than CON group. Protein intake was higher in PMR + I and INU groups than the CON group.
Macronutrient and micronutrient intakes as percent of adequacy from the recommended intake by treatment group at baseline and during the intervention are shown in Table 5. Following the intervention PMR and PMR + I groups had a higher percent of adequacy of calcium, iron, zinc, vitamins C, B1, B2, B6, B12 niacin and folic acid than the CON group. Intakes of sodium, potassium, vitamin A and B12 were similar among treatment groups.
Discussion
Results of PMR effect on body weight have been controversial. Recent revisions and meta-analysis suggest that their use have a moderate effect resulting in weight loss of around 9%–10% of total body weight in the short term (3–6 months), and 6%–8% in the long term (> 1 years), when used as part of an overall low-energy diet plan [11, 12, 17, 34]. Our results showed that the inclusion of PMR alone or in combination with inulin to a LCD was equally effective to reduce weight compared to LCD alone. After 90 days, both groups with PMR lost an average of 4 Kg or about 5.4% of initial weight. This reduction was about 28% higher than the reduction with the LCD alone but the difference was not statistically significant. Similarly to our results Noakes [35] compared a group of obese men with PMR and LCD with a group with LCD alone and found after 3 months, a loss of body weight of 6.6 Kg (6.9%) and 6.0 Kg (6.3%), respectively. Another study in obese women found after one year of treatment a weight reduction of 5.0 Kg (6.2%) with PMR plus LCD and 6.1 Kg (8%) with LCD alone; the difference was not statistically significant [10]. Two previous studies [11] found reductions in average weight of 7.1 kilograms after 3 months or 7.7 kilograms after one year with the inclusion of PMR to a LCD ; but in these studies the effect was significantly higher than LCD mainly because the effect of LCD was very low (1.3 and 3.4 kilograms, respectively). One recent study found a significant positive effect on weight reduction by the inclusion of PMR to a LCD [36]. Obese subjects lost in average 13.5 kilograms (12.3%) with LCD plus PMR compared with 6.5 kilograms (6.7%) with LCD alone after 16 weeks. In this study, subjects had an average BMI at the beginning of the study of 38 Kg/cm2, which was much higher than the baseline average BMI in our study of 31 Kg/cm2. This suggests that the inclusion of PMR to an LCD is more effective when subjects are “more obese”.
Treatments with PMR, PMR + I and INU significantly reduced triglycerides after 3 months of treatment. Both groups with inulin and PMR alone had an effect, so this could be attributed to inulin or its combination with a loss of body fat. Of 11 studies reviewed by Delzenne [13] on the effect of inulin on blood lipids, 4 studies did not find an effect of inulin on total cholesterol and triglycerides, 3 studies showed significant reduction in triglycerides, and 5 studies showed a modest reduction in total cholesterol and LDL cholesterol. Brighenti [21] conducted a meta-analysis that included studies and concluded that the intake of inulin was associated with significant decreases in serum triglycerides of 0.17 mmol/L (15 mg/dL) or 7.5%. Brighenti [16] found a marked reduction on plasma triglycerides and moderate decrease in plasma cholesterol in twelve healthy men consuming 9 g inulin/d. Letexier et al. [18] observed a 16% decrease in plasma triglycerides in eight subjects consuming 10 g inulin/d. In the present study, a significant reduction of 21.3%, 21.9% and 20.3% of plasma triglycerides was found with PMR + I, PMR and INU groups. In average, our subjects did not show elevated concentration of cholesterol or triglycerides at the beginning of the study; thus the effect that we found in reducing triglycerides could be more important in obese subjects that have high lipids concentrations as has been reported in other studies [19, 20, 37][38].
Total energy and carbohydrates intakes decreased similarly in all groups and fat intake, including cholesterol, was reduced significantly more in both groups with PMR compared with INU and CON groups. Ditschuneit [11] found similar results; PMR reduced cholesterol intake 17% more than a group with LCD alone and fat intake decreased significantly 48% in the PMR group and the control group decreased 19%. Also, Ashley [10] found a decrease in the intake of saturated fat and cholesterol by the inclusion of PMR. As expected, PMR + I and INU groups significantly increased total fiber intake from 13.9 to 17.5, and 13.6 to 20.8 g/d per day, respectively. An increase in dietary fiber intake is highly recommended in obese subjects [39]. These results suggest that PMR added with inulin can contribute with a reduction in fat intake and an increase in dietary fiber intake which could be beneficial in obese individuals with a higher risk of developing hyperlipidemia, or insulin resistance.
An important finding of this study is that PMR could contribute to increase the intake of essential nutrients, which is especially important during caloric restriction and in populations that need to reduce calories but that are at risk of having micronutrient deficiencies. In Mexico for example, there is a high prevalence of obesity, about 30% of adults and 16% of children less than 12 years are obese[4]; and in many individuals, obesity occurs simultaneously with some micronutrient deficiencies [6]; prevalence of some micronutrient deficiencies documented in Mexican adults are: 27% in zinc, 34% in vitamin E, 34% in vitamin C, 20% in vitamin B2 and 20% have iron deficiency [40–42]. Treatments with PMR increased intake of vitamins and minerals compared with LCD alone, especially calcium, iron, magnesium, zinc, vitamin B1, B2, B6, B12, niacin, folic acid and vitamin C and contribute to meet recommendations of such nutrients during LCD´s . Because PMR is prepared with skimmed milk, the groups that included PMR increased milk and calcium intake. Calcium intake increased 20 and 30% in the PMR + I and PMR groups, respectively. Long term use of LCD´s have been associated with bone resorption in obese adults due to low intake of calcium which can lead to bone demineralization [43]. Treatments with PMR increased intake of vitamins and minerals compared with LCD alone, especially calcium, iron, magnesium, zinc, vitamin B1, B2, B6, B12, niacin, folic acid and vitamin C and contribute to meet recommendations of such nutrients during LCD´s . Because PMR is prepared with skimmed milk, the groups that included PMR increased milk and calcium intake. Calcium intake increased 20 and 30% in the PMR + I and PMR groups, respectively. Long term use of LCD´s have been associated with bone resorption in obese adults due to low intake of calcium which can lead to bone demineralization [43]. This is one of the reasons why intake of calcium supplements and/or milk has been found to have beneficial effects on mineralization during prolonged LCD´s [44, 45]. Our study suggests that the use of PMR´s could contribute to meet recommended intakes of nutrients specially when there is need to reduce calorie intake and in individuals with micronutrient deficiencies.
As it is common in dietary intake data, there was a considerable variability in the nutrient intake data, even when some statistical differences were found, some micronutrient comparisons were low powdered because the sample size was calculated upon body weight. In addition, the study did not find body fat change statistically different between treatments, it has been documented that other methods such as DEXA could have provided more accurate results [46]. Since this study was not intended to confirm the improvement of nutrient status, more studies are needed to evaluate if increased nutrient intake also increases micronutrient absorption and improves micronutrient status.
In conclusion, we found no additional effect of including PMR or a PMR added with inulin to a calorie restricted diet on changes in body weight, BMI or fat loss, than a LCD alone; however, intake of PMR, PMR added with inulin or inulin alone contribute to reduce plasma triglycerides during calorie restriction. In addition, treatment of obesity with LCD that includes a PMR significantly increased intake of essential amino acids, vitamins and minerals and contributed to meet daily recommendations. Results of the present study are particular relevant for populations that have increased prevalence of obesity and that at the same time have high prevalence of micronutrient deficiencies. This study points out the importance of using adequately fortified meal replacement products to ensure nutrient adequacy during energy intake restriction for weight loss.
Abbreviations
- PMR:
-
Partial meal replacement
- PMR + I:
-
Partial meal replacement with inulin
- INU:
-
Inulin
- CON:
-
Control group
- LCD:
-
Low calorie diet
- ANOVA:
-
Analysis of Variance.
References
De-Onis M, Blössner M: Prevalence and trends of overweight among pre-shoolchildren in developing countries. Am J Clin Nutr. 2000, 72: 1032-1039.
Global Strategy on Diet, Physical Activity and Health. Obesity and Overweight. http://www.who.int/dietphysicalactivity/publications/facts/obesity/en/,
Ford ES, Mokdad AH: Epidemiology of obesity in the Western Hemisphere. J Clin Endocrinol Metab. 2008, 93: S1-S8. 10.1210/jc.2008-1356.
Olaiz-Fernandez G, Rivera-Domarco J, Shama-Levy T, Rojas R, Villalpando-Hernández S, Hernández-Ávila M, Sepúlveda-Amor J: Encuesta Nacional de Salud y Nutricion 2006. 2006, Cuernavaca, Mexico: Instituto Nacional de Salud Pública
Gonzalez T, Rivera J, Shaman T, Ramírez I, Barquera S, Morales MC, Safdie M: Capítulo 4. Encuesta Nacional de Nutrición 1999: Estado nutricio de niños y mujeres en México. 2000, Cuernavaca, Mexico: Instituto Nacional de Salud Pública
Garcia OP, Long KZ, Rosado JL: Impact of micronutrient deficiencies on obesity. Nutr Rev. 2009, 67: 559-572. 10.1111/j.1753-4887.2009.00228.x.
Vidal-Guevara ML, Samper M, Martínez-Silla G, Canteras M, Ros G, Gil A, Abellán P: 2004. Nutr Hosp. 2004, 19: 202-208.
Dubnov-Raz G, Berry EM: The dietary treatment of obesity. Endocrinol Metab Clin North Am. 2008, 37: 873-886. 10.1016/j.ecl.2008.08.002.
Cabanillas M, Moya Chimenti E, Gonzalez Candela C, Loria Kohen V, Dassen C, Lajo T: [Usefulness of meal replacement: analysis of the principal meal replacement products commercialised in Spain]. Nutr Hosp Organo Oficial Soc Esp Nutr Parenteral y Enteral. 2009, 24: 535-542.
Ashley JM, Herzog H, Clodfelter S, Bovee V, Schrage J, Pritsos C: Nutrient adequacy during weight loss interventions: a randomized study in women comparing the dietary intake in a meal replacement group with a traditional food group. Nutr J. 2007, 6: 12-10.1186/1475-2891-6-12.
Ditschuneit HH, Flechtner-Mors M: Value of structured meals for weight management: risk factors and long-term weight maintenance. Obes Res. 2001, 9 (Suppl 4): 284S-289S.
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: 537-549. 10.1038/sj.ijo.0802258.
Delzenne NM, Williams CM: Prebiotics and lipid metabolism. Curr Opin Lipidol. 2002, 13: 61-67. 10.1097/00041433-200202000-00009.
Williams CM: Effects of inulin on lipid parameters in humans. J Nutr. 1999, 129: 1471S-1473S.
Williams CM, Jackson KG: Inulin and oligofructose: effects on lipid metabolism from human studies. Br J Nutr. 2002, 87 (Suppl 2): S261-S264.
Brighenti F, Casiraghi MC, Canzi E, Ferrari A: Effect of consumption of a ready-to-eat breakfast cereal containing inulin on the intestinal milieu and blood lipids in healthy male volunteers. Eur J Clin Nutr. 1999, 53: 726-733. 10.1038/sj.ejcn.1600841.
Keogh JB, Clifton PM: The role of meal replacements in obesity treatment. Obes Rev. 2005, 6: 229-234. 10.1111/j.1467-789X.2005.00171.x.
Letexier D, Diraison F, Beylot M: Addition of inulin to a moderately high-carbohydrate diet reduces hepatic lipogenesis and plasma triacylglycerol concentrations in humans. Am J Clin Nutr. 2003, 77: 559-564.
Jackson KG, Taylor GR, Clohessy AM, Williams CM: The effect of the daily intake of inulin on fasting lipid, insulin and glucose concentrations in middle-aged men and women. Br J Nutr. 1999, 82: 23-30.
Balcazar-Munoz BR, Martinez-Abundis E, Gonzalez-Ortiz M: Effect of oral inulin administration on lipid profile and insulin sensitivity in subjects with obesity and dyslipidemia. Rev Med Chile. 2003, 131: 597-604.
Brighenti F: Dietary fructans and serum triacylglycerols: a meta-analysis of randomized controlled trials. J Nutr. 2007, 137: 2552S-2556S.
Termizy HM, Mafauzy M: Metabolic syndrome and its characteristics among obese patients attending an obesity clinic. Singapore Med J. 2009, 50: 390-394.
Yap KW SM, Yazid AM, Maznah I, Meyer DM: Dose response effects of inulin on fecal short-chain fatty acids content and mineral absorption of formula fed infants. Nutr Food Sci. 2005, 35: 208-219. 10.1108/00346650510605603.
The practical guide. Identification, evaluation, and treatment of overweight and obesity in adults. 2000, NIH Publication
Book Encuesta Nacional de Salud (ENSA) (Editor ed.^eds.). 2000, City: Instituto Nacional de Salud Pública
Lohman TG, Roche AF, Martorell R: Anthropometric standardization reference manual. 1988, Champaign. IL: Human Kinetics
Report of the WHO Expert Commettee: Physical status: the use and interpretation of anthropometry. Book Report of the WHO Expert Commettee. Physical status: the use and interpretation of anthropometry (Editor ed.^eds.). 1995, City: WHO
Kotler DP, Burastero S, Wang J: RNP: Prediction of Body Cell Mass, Fat-Free Mass, and Total Body Water with Bioelectrical Impedance Analysis: Effects of Race, Sex, and Disease. Am J Clin Nutr. 1996, 64: 489S-497S.
Friedewald WT, Levy RI, Fredrickson DS: Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem. 1972, 18: 499-502.
USDA National Nutrient Database for Standard Reference, Release 22. http://www.ars.usda.gov/ba/bhnrc/ndl,
Chávez M, Chávez A, Roldán J, Pérez-Gil S, Hernández S: Tablas de valor nutritivo de los alimentos de mayor consumo en México. 1996, Mexico DF: Pax
Bourges H, Casanueva E, Rosado JL: Recomendaciones de ingestión de nutrimentos para la población mexicana, Tomo I. 2005, Mexico DF: Ed Panamericana
Bourges H, Casanueva E, Rosado JL: Recomendaciones de ingestión de nutrimentos para la población mexicana, Tomo II. 2008, Mexico DF: Ed Panamericana
Anderson JW, Luan J, Hoie LH: Structured weight-loss programs: meta-analysis of weight loss at 24 weeks and assessment of effects of intervention intensity. Adv Ther. 2004, 21: 61-75. 10.1007/BF02850334.
Noakes M, Foster PR, Keogh JB, Clifton PM: Meal replacements are as effective as structured weight-loss diets for treating obesity in adults with features of metabolic syndrome. J Nutr. 2004, 134: 1894-1899.
Davis LM, Coleman C, Kiel J, Rampolla J, Hutchisen T, Ford L, Andersen WS, Hanlon-Mitola A: Efficacy of a meal replacement diet plan compared to a food-based diet plan after a period of weight loss and weight maintenance: a randomized controlled trial. Nutr J. 2010, 9: 11-10.1186/1475-2891-9-11.
Beylot M: Effects of inulin-type fructans on lipid metabolism in man and in animal models. Br J Nutr. 2005, 93 (Suppl 1): S163-S168.
Causey JL, Feirtag JM, Gallaher DD CTB, Slavin JL: Effects of dietary inulin on serum lipids, blood glucose and the gastrointestinal environment in hypercholesterolemic men. Nutr Res. 2000, 20: 191-201. 10.1016/S0271-5317(99)00152-9.
Liu S, Willett WC AMJ, Hu FB, Rosner B, Colditz G: Relation between changes in intakes of dietary fiber and grain products and changes in weight and development of obesity among middle-aged women. Am J Clin Nutr. 2003, 78: 920-927.
Rivera-Domarco J, Shama-Levy T, Villalpando-Hernández S, González-de-Cossío T, Hernández-Prado B: Encuesta Nacional de Nutrición 1999 (National Nutrition Survey 1999). Book Encuesta Nacional de Nutrición 1999 (National Nutrition Survey 1999) (Editor ed.^eds.). 2001, City: Instituto Nacional de Salud Pública
Rosado JL: Deficiencia de zinc y sus implicaciones funcionales. Salud Publica de Mex. 1998, 40: 181-188. 10.1590/S0036-36341998000200010.
Redman LM, Rood J, Anton SD, Champagne C, Smith SR, Ravussin E: Calorie restriction and bone health in young, overweight individuals. Arch Intern Med. 2008, 168: 1859-1866. 10.1001/archinte.168.17.1859.
Bowen J, Noakes M, Clifton PM: Effect of calcium and dairy foods in high protein, energy-restricted diets on weight loss and metabolic parameters in overweight adults. Int J Obes Lond. 2005, 29: 957-965. 10.1038/sj.ijo.0802895.
Jensen LB, Kollerup G, Quaade F, Sørensen OH: Bone minerals changes in obese women during a moderate weight loss with and without calcium supplementation. J Bone Miner Res. 2001, 16: 141-147. 10.1359/jbmr.2001.16.1.141.
Radak TL: Caloric restriction and calcium's effect on bone metabolism and body composition in overweight and obese premenopausal women. Nutr Rev. 2004, 62: 468-481. 10.1111/j.1753-4887.2004.tb00019.x.
Pateyjohns IR, Brinkworth GD, Buckley JD, Noakes M, Clifton PM: Comparison of Three Bioelectrical Impedance Methods with DXA in Overweight and Obese Men. Obesity. 2006, 14: 2064-2070. 10.1038/oby.2006.241.
Acknowledgments
We are grateful to Paola García and Cynthia de Lira for their valuable help during the fieldwork, and also to personnel at the Health Clinic of Santa Barbara, Querétaro for their support during the study. Finally, we are thankful to Nucitec S.A. de C.V. for its financial assistance that allowed this study to be successfully performed.
Author information
Authors and Affiliations
Corresponding author
Additional information
Competing interests
This study was partially financed by Nucitec SA de CV. MAD was an employee at this company and did not receive any compensation for this study. JLR owns shares of this company. Both participated in the concept and design of the study and providing intellectual interpretation of the results.
Authors’ contributions
ART conducted the fieldwork and wrote the initial draft of the paper; MCC contributed with the data analysis and its interpretation as well as with the writing of the manuscript; SG participated in the design of the study and quality assurance; MAD participated in the concept and design of the project; JLR participated in the concept and design and revised critically and intellectually the manuscript. All authors read and approved the final manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
Rights and permissions
Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/2.0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
About this article
Cite this article
Tovar, A.R., Caamaño, M.d., Garcia-Padilla, S. et al. The inclusion of a partial meal replacement with or without inulin to a calorie restricted diet contributes to reach recommended intakes of micronutrients and decrease plasma triglycerides: A randomized clinical trial in obese Mexican women.. Nutr J 11, 44 (2012). https://doi.org/10.1186/1475-2891-11-44
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/1475-2891-11-44