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Substitution of TAG oil with diacylglycerol oil in food items improves the predicted 10 years cardiovascular risk score in healthy, overweight subjects

Published online by Cambridge University Press:  22 November 2012

Vibeke H. Telle-Hansen
Affiliation:
Department of Health, Nutrition and Management, Faculty of Health Sciences, Oslo and Akershus University College of Applied Sciences, Post Box 4, St. Olavsplass, 0130 Oslo, Norway Department of Nutrition, Institute for Basic Medical Sciences, University of Oslo, Post Box 1046, Blindern, 0317 Oslo, Norway
Ingunn Narverud
Affiliation:
Department of Health, Nutrition and Management, Faculty of Health Sciences, Oslo and Akershus University College of Applied Sciences, Post Box 4, St. Olavsplass, 0130 Oslo, Norway Department of Nutrition, Institute for Basic Medical Sciences, University of Oslo, Post Box 1046, Blindern, 0317 Oslo, Norway
Kjetil Retterstøl
Affiliation:
Department of Nutrition, Institute for Basic Medical Sciences, University of Oslo, Post Box 1046, Blindern, 0317 Oslo, Norway Lipid Clinic, Medical Department, Rikshospitalet, Oslo University Hospital, Post Box 4950, Nydalen, 0424 Oslo, Norway
Nima Wesseltoft-Rao
Affiliation:
Department of Health, Nutrition and Management, Faculty of Health Sciences, Oslo and Akershus University College of Applied Sciences, Post Box 4, St. Olavsplass, 0130 Oslo, Norway Department of Nutrition, Institute for Basic Medical Sciences, University of Oslo, Post Box 1046, Blindern, 0317 Oslo, Norway
Annhild Mosdøl
Affiliation:
Department of Health, Nutrition and Management, Faculty of Health Sciences, Oslo and Akershus University College of Applied Sciences, Post Box 4, St. Olavsplass, 0130 Oslo, Norway
Linda Granlund
Affiliation:
Mills DA, Post Box 4644, Sofienberg, 0506 Oslo, Norway
Kirsti Forstrøm Christiansen
Affiliation:
Mills DA, Post Box 4644, Sofienberg, 0506 Oslo, Norway
Amandine Lamglait
Affiliation:
Mills DA, Post Box 4644, Sofienberg, 0506 Oslo, Norway
Bente Halvorsen
Affiliation:
Research Institute for Internal Medicine, Faculty of Medicine, University of Oslo, Rikshospitalet, Oslo University Hospital, Post Box 4950, Nydalen, 0424 Oslo, Norway
Kirsten B. Holven*
Affiliation:
Department of Nutrition, Institute for Basic Medical Sciences, University of Oslo, Post Box 1046, Blindern, 0317 Oslo, Norway
Stine M. Ulven
Affiliation:
Department of Health, Nutrition and Management, Faculty of Health Sciences, Oslo and Akershus University College of Applied Sciences, Post Box 4, St. Olavsplass, 0130 Oslo, Norway
*
*Corresponding author: Kirsten B. Holven, fax +47 22851341, email [email protected]

Abstract

Dietary fat is normally in TAG form, but diacylglycerol (DAG) is a natural component of edible oils. Studies have shown that consumption of DAG results in metabolic characteristics that are distinct from those of TAG, which may be beneficial in preventing and managing obesity. The objective of the present study was to investigate if food items in which part of the TAG oil is replaced with DAG oil combined with high α-linolenic acid (ALA) content would influence metabolic markers. A 12-week double-blinded randomised controlled parallel-design study was conducted. The participants (n 23) were healthy, overweight men and women, aged 37–67 years, BMI 27–35 kg/m2, with waist circumference >94 cm (men) and >88 cm (women). The two groups received 20 g margarine, 11 g mayonnaise and 12 g oil per d, containing either high ALA and sn-1,3-DAG or high ALA and TAG. Substitution of TAG oil with DAG oil in food items for 12 weeks led to an improvement of the predicted 10 years cardiovascular risk score in overweight subjects by non-significantly improving markers of health such as total body fat percentage, trunk fat mass, alanine aminotransferase, systolic blood pressure, γ-glutamyl transferase, alkaline phosphatase and total fat-free mass. This may suggest that replacing TAG oil with DAG oil in healthy, overweight individuals may have beneficial metabolic effects.

Type
Human and Clinical Nutrition
Creative Commons
Creative Common License - CCCreative Common License - BYCreative Common License - NCCreative Common License - SA
The online version of this article is published within an Open Access environment subject to the conditions of the Creative Commons Attribution-NonCommercial-ShareAlike licence . The written permission of Cambridge University Press must be obtained for commercial re-use.
Copyright
Copyright © The Author(s) 2012.

Prevention and treatment of obesity and obesity-related diseases are major public health challenges(Reference Rao, Thethi and Fareed1Reference Kotsis, Stabouli and Papakatsika3) and both the total amount of fat and the distribution of fat in the body are important determinants of the complications associated with obesity(Reference Wajchenberg4). Surplus energy intake is stored as TAG in adipose tissue either as subcutaneous or visceral fat. Visceral fat depots, located in the trunk surrounding the organs, are recognised to be a more active endocrine organ, and contribute to an increased risk of metabolic complications, than subcutaneous fat depots(Reference Wajchenberg4Reference Galic, Oakhill and Steinberg7). Hence, the endocrine activity of visceral adipose tissue is an important factor in the development of the metabolic syndrome(Reference Despres and Lemieux8), and central obesity is more strongly associated with increased risk of insulin resistance, the metabolic syndrome and CVD than BMI alone(Reference Nedungadi and Clegg9). The endocrine activity of adipose tissue includes secretion of a number of adipokines (cytokines and hormones) leading to a pro-inflammatory state, and it has been shown that the reduction of visceral fat effectively prevents cardiovascular events(Reference Kishida, Funahashi and Shimomura10). Also, hepatic accumulation of fat is common in obese individuals and is associated with hepatic dysfunction(Reference Stefan, Kantartzis and Haring11). Increased adipose tissue, and in particular visceral adipose tissue, is linked to increased levels of circulating liver function markers, such as alanine aminotransferase (ALAT) and γ-glutamyl transferase (γ-GT)(Reference Mochizuki, Miyauchi and Misaki12Reference van Barneveld, Seidell and Traag16).

Dietary fat is normally in TAG form, but diacylglycerol (DAG) is a natural component of various edible oils(Reference Yanai, Tomono and Ito17) and is currently used in small quantities in foods as an emulsifier. Recent studies have shown that high consumption of DAG results in metabolic characteristics that are distinct from those of TAG, and that these characteristics may be beneficial in preventing and managing obesity. Experimental studies in human subjects have shown that DAG (mainly sn-1,3-DAG) decreases postprandial TAG compared with TAG controls(Reference Taguchi, Watanabe and Onizawa18, Reference Tada, Watanabe and Matsuo19). Kamphuis et al. showed that meals rich in DAG increase fat oxidation(Reference Kamphuis, Mela and Westerterp-Plantenga20). Dietary DAG has also been shown to reduce body fat (total, subcutaneous, visceral and hepatic fat mass) compared with TAG(Reference Nagao, Watanabe and Goto21), and consumption of DAG oil as part of a reduced-energy diet enhances loss of body weight and fat compared with TAG control oil(Reference Maki, Davidson and Tsushima22).

Vegetable oils such as flaxseed oil and rapeseed oils are the main dietary sources of the vegetable n-3 fatty acid α-linolenic acid (ALA; 18 : 3). The relation between intake of ALA and CVD has been studied less extensively than the marine n-3 fatty acids and the relation is less clear. Some studies, including clinical trials, epidemiological investigations and experimental studies, have shown that intake of ALA has been beneficially associated with CVD risk(Reference Xie, Zhang and Li23) or markers of risk(Reference Rodriguez-Leyva, Dupasquier and McCullough24). Other studies have found no effect of ALA on CVD risk markers(Reference Dewell, Marvasti and Harris25Reference Barcelo-Coblijn, Murphy and Othman28).

The aim of the present study was to investigate whether intake of food items in which part of the TAG-based oil has been replaced with DAG combined with high ALA content would influence metabolic markers such as C-reactive protein (CRP), blood lipids, body composition, liver function markers and overall cardiovascular risk score in healthy, overweight individuals.

Experimental methods

Subjects

Healthy, overweight men and women who were willing to consume margarine, mayonnaise and oil daily for 14 weeks were recruited via advertisements in local newspapers from October 2008 to February 2009. The inclusion criteria were: age 18–70 years, BMI 27–40 kg/m2 and waist circumference >94 cm for men and >88 cm for women. Exclusion criteria were: type 2 diabetes mellitus, kidney-, liver-, gall bladder-, coronary-, endocrine- or chronic rheumatic disease, malign cancer during the last 5 years, hypertension (≥160/100 mmHg), pregnancy and lactation. Regular use of anti-inflammatory, lipid lowering and anti-hypertensive medications was not permitted. The present study was conducted according to the guidelines laid down in the Declaration of Helsinki and all procedures involving human subjects were approved by the Regional Committee of Medical Ethics (approval no. 6.2008.1368) and by the Norwegian Social Science Data Services (approval no. 19667). Written informed consent was obtained from all subjects. The study was registered at http://www.clinicaltrials.gov (no. NCT01034436).

Study design

The present study is part of a larger study involving healthy overweight subjects randomised to three different intervention groups: high ALA-DAG (n 10), high ALA-TAG (n 13) and low ALA-TAG (n 10) where the aim of the study was (Reference Rao, Thethi and Fareed1) to study the effect of replacing TAG-based food items with DAG-based food items and (Reference Kahn, Hull and Utzschneider2) to study the effect of low v. high ALA in TAG-based food items. In the present study, only data relating to the first aim are presented. In total, ninety-six subjects were screened for eligibility (minimum 4 weeks prior to the run-in period). For the present aim, forty-nine subjects were randomised and thirty-nine subjects received allocated interventions. Of the subjects, ten discontinued the intervention (declined to eat products, hospitalisation, lack of time and no explanation) and six had to be excluded from the analyses, leaving twenty-three subjects (n 10 and 13) included in the final statistical analyses. A 12-week double-blinded randomised controlled parallel-design study was conducted at Akershus University College from February to June 2009. Subjects were allocated to high ALA-DAG or high ALA-TAG further described in detail later. During a 2-week run-in period prior to the intervention period, all subjects included the same set of test products. The test products in the run-in period consisted of sunflower oil-based margarine (20 g) and mayonnaise (11 g) and sunflower oil (12 g). Fatty acids were given as TAG and the total amount of ALA in the run-in period was 0·15 g per d.

At baseline, subjects were randomly assigned and stratified by sex into the intervention groups receiving products containing either high ALA (8·29 g/d) and sn-1,3-DAG or high ALA (8·51 g/d) and TAG (from now on referred to as the high-ALA-DAG group and high-ALA-TAG group, respectively) (Table 1). The test products were 20 g margarine, 11 g mayonnaise and 12 g (13 ml) oil per d. Margarine was the only test product where sn-1,3-DAG oil was added. Rapeseed oil was used in mayonnaise as TAG (8·84 g/d), and in the margarine either as sn-1,3-DAG (11·2 g/d) and TAG (2·88 g/d) (high-ALA-TAG group) or as TAG only (14·12 g/d) (high-ALA-TAG group) (Table 1). The 12 g oil per d was the identical flaxseed oil in the two groups in order to obtain a standardised and high level of ALA in the diet. The products constituted in total approximately 35 g fat per d (Table 1), corresponding to about 1255·2 kJ/d (300 kcal/d). The food items were delivered at baseline and after 6 weeks of intervention. At 4 weeks prior to the run-in period and during the intervention period, the subjects were not allowed to use n-3 fatty acid supplements and other dietary supplements. At each visit they were reminded by a nutritionist to keep a stable weight. Fasting body weight and body composition measurements were registered at all visits. The subjects were informed not to change the physical activity and dietary habit during the study. The diet was registered at each visit using the SmartDiet questionnaire which is a validated qualitative dietary questionnaire(Reference Svilaas, Strom and Svilaas29).

Table 1. Fatty acid composition in the test products (g per portion* and g per d)

ALA, α-linolenic acid; DAG, diacylglycerol; LA, linoleic acid.

* One portion of margarine, mayonnaise and oil equals 20, 11 and 12 g, respectively.

† Flaxseed oil.

Blinding and randomisation

The present study was double-blinded by the identical appearance of different food items; their contents were identifiable only by ID numbers on the food items. Randomisation was performed by LINK Medical Research AS using Microsoft Excel and its random generator.

Compliance

Participants were instructed to bring back food containers (lids of margarine, sachets of mayonnaise and bottles of oil) and compliance was estimated by counting the empty food containers and estimating the leftovers. We estimated compliance by dividing the amount of leftovers by the total amount of food scheduled for the intervention period. The mean compliance for each subject was expressed as a percentage. According to the protocol, subjects with low compliance (<70 %) were excluded from the study. Compliance was estimated to be 90–100 % in both groups.

Study products

Margarine and mayonnaise were based on commercial products manufactured by Mills DA. Mayonnaise with 80 % fat was based on refined sunflower oil (Aarhus Karlshamn) for the run-in period and refined rapeseed oil (Aarhus Karlshamn) for the high-ALA groups. Mayonnaise was packed in commercial portion sachets of 11 g.

Margarine with 70 % fat was based on sunflower oil (run-in period), refined rapeseed oil (AarhusKarlshamn AB) (high-ALA-TAG group) or rapeseed oil with DAG (Kao Corporation) (high-ALA-DAG group), produced by Danisco AS. The margarine was packed in commercial lids, 140 g in each.

Refined sunflower oil (AarhusKarlshamn AB) (run-in period) was filled into green, transparent polyethylene ferephthalate bottles of 500 ml. Cold pressed flaxseed oil (Norsk Fropresse AS) (high-ALA groups) was fortified with vitamin E acetate from BASF in order to obtain equal amounts of vitamin E for both groups and filled into identical bottles. The participants were told to cover the bottles with aluminum foil and keep the oil refrigerated.

The fatty acid profile and vitamin E in the products were analysed by the GC method in a routine laboratory (Eurofins). Results are shown in Table 1.

Measurements of body composition

Subjects wore light clothing and no shoes. Two trained persons carried out all measurements. Height was measured by a wall-mounted stadiometer to the nearest 0·1 cm. Weight was measured by the Tanita BC-418 manufactured by Tanita Corporation to the nearest 0·1 kg. To correct for light clothing, 1 kg was subtracted from the measured value. BMI was calculated by the Tanita BC-418. Waist circumference and hip circumference were measured to the nearest mm with a standard, non-stretch tape. Waist circumference was measured at the point midway between the iliac crest and the lower rib margin. Hip circumference was measured at the maximum circumference of the buttocks posterior and the symphysis anterior. All subjects were measured while standing in a relaxed position and with normal respiration. Body composition was estimated by bioelectric impedance analysis (Tanita BC-418), a hand-to-foot system, according to the manufacturer's manual. Information on age, height and body type (all were routinely classified as ‘standard’ body type) was entered before measuring. Bioelectric impedance analysis measurements were carried out at a frequency of 50 kHz.

Blood and urine sampling

The day prior to blood sampling, the subjects were told to refrain from alcohol consumption and vigorous physical activity; venous blood samples were drawn after an overnight fast (≥12 h). Serum was obtained from silica gel tubes (Becton Dickinson vacutainer) and kept at room temperature for at least 30 min, until centrifugation (1500 g, 12 min). Serum was kept at room temperature and immediately prepared for subsequent analysis of routine laboratory analysis or aliquoted and stored at −80°C until further analyses. Plasma was obtained from EDTA tubes (Becton Dickinson vacutainer), immediately placed on ice and centrifuged within 10 min (2000 g, 4°C). Plasma samples were aliquoted and stored at −80°C until further analyses. Morning spot urine samples were refrigerated (4°C) until aliquoted and stored at −80°C until further analysis.

Routine laboratory analysis

Fasting serum high-sensitivity CRP (hsCRP), total cholesterol, LDL-cholesterol, HDL-cholesterol, TAG, glucose, C-peptide, insulin, HbA1c, thyroid-stimulating hormone, γ-GT, alkaline phosphatase (ALP), ALAT and aspartame aminotransferase (ASAT) were measured by standard methods at a routine laboratory (Fürst Medical Laboratory). Fasting plasma NEFA were measured by standard methods (Department of Medical Biochemistry, Rikshospitalet University Hospital, Norway).

8-iso-PGF and creatinine in morning spot urine samples were determined by Vitas AS. Urinary 8-iso-PGF was analysed by liquid chromatography with negative electrospray ionisation coupled to tandem mass spectrometric detection according to Bastani et al. (Reference Bastani, Gundersen and Blomhoff30). Urinary levels of 8-iso-PGF are presented as the ratio of 8-iso-PGF to creatinine. Urine creatinine was determined by ELISA using the Cayman Chemical Creatinine Assay kit. The ninety-six-well plate format ELISA kit, validated for urine samples, uses colorimetric detection at 495 nm. Assay range: 0–150 mg/l (normal range 250–4000 mg/l).

Plasma α-tocopherol analysis(Reference Panfili, Fratianni and Irano31) and quantification of fatty acids in plasma lipids(Reference Haug, Sagmo and Zeiss32) were performed by Vitas AS.

Enzyme immunoassay

Serum was stored at −80°C in multiple aliquots until analysis. Serum leptin, adiponectin, resistin and fetuin-A were measured by enzyme immunoassay by R&D Systems according to the manufacturer's instructions.

Statistics

Sample size was calculated based on the existing literature primarily on the effects of ALA on hsCRP in dietary intervention studies since this outcome measurement would require the highest number of subjects. The calculations used an expected change in hsCRP from baseline to the end of the study of 20 (sd 0·5) %. The level of significance was set to 5 % (two-sided) and the power to 80 %. A total of seventy-five subjects were required in the main study (twenty-five per arm; three arms). Seventy-five subjects in total were randomised, with forty-nine subjects being randomised to the present two groups. Due to a high withdrawal rate, a total of twenty-three subjects completed the study. Due to sample size, data were analysed with non-parametric tests and are presented as median (25–75 percentiles). Differences between the randomisation groups were analysed at baseline and after 12 weeks of intervention (baseline adjusted values). The changes between the two groups or within groups after 12 weeks of intervention were analysed by the Mann–Whitney U test or the Wilcoxon matched-pair signed-rank test, respectively. Bonferroni correction to adjust for multiple testing was performed (adjusted P ≤ 0·001). Correlation analysis was performed using Spearman's rank-order correlation. All analyses were performed using SPSS for Windows (version 19.0).

Results

In the present study, twenty-three healthy, overweight subjects (six women and seventeen men) participated, randomised in two intervention groups. The subjects were 52 (Reference Murase, Nagasawa and Suzuki45Reference Rallidis, Paschos and Liakos62) years, with a median BMI of 30 (Reference Barcelo-Coblijn, Murphy and Othman28Reference Haug, Sagmo and Zeiss32) kg/m2. At baseline there were no differences in age between the intervention groups.

Body composition

At baseline there were no significant differences in blood pressure and body composition (total body fat percentage, total body fat mass, trunk fat mass and fat-free mass (FFM)) between the intervention groups. Prior to Bonferroni adjustment, there was a significant difference between the two groups in weight, BMI and waist circumference at baseline (P = 0·03, 0·05 and 0·01, respectively); however, these differences disappeared after Bonferroni adjustment (Table 2).

Table 2. Clinical characteristics and body composition at baseline and after 12 weeks of intervention (Medians and 25th–75th percentiles)

ALA, α-linolenic acid; DAG, diacylglycerol; BP, blood pressure; FFM, fat-free mass.

* Within the high-ALA-DAG group (prior to Bonferroni correction).

† Within the high-ALA-TAG group (prior to Bonferroni correction).

‡ Comparing change from baseline to the end of the study between the high-ALA-DAG and high-ALA-TAG groups (prior to Bonferroni correction).

Since intake of DAG oil has been associated with weight loss, we investigated the effect on weight change. After 12 weeks of intervention, body weight did not change between or within the two groups. However, there was a non-significant trend towards an increase in weight in the high-ALA-DAG group (P = 0·07). We also investigated the effect on body composition. Prior to Bonferroni adjustment, there was a significant decrease in both total body fat percentage and trunk fat mass within the high-ALA-DAG group from baseline to 12 weeks of intervention (P = 0·04 and 0·05, respectively) and this decrease was significantly different from the effect observed in the high-ALA-TAG group (P = 0·03 and 0·04, respectively). There was no significant change within or between the groups in total body fat mass. Concomitantly, there was a significant increase in the amount of FFM within the high-ALA-DAG group (P = 0·016) from baseline to the end of the study and this change in FFM was borderline significant (P = 0·06) between the two groups (Table 2). All differences disappeared after Bonferroni adjustment.

Blood pressure

Systolic and diastolic blood pressure was measured at baseline and after 12 weeks of intervention (Table 2). Prior to Bonferroni adjustment, there was a significant decrease in systolic blood pressure within the high-ALA-DAG group (P = 0·05) after intervention, and the change in systolic blood pressure was significantly different between the two groups (P = 0·05); however, this was non-significant after Bonferroni adjustment. There was no significant difference in diastolic blood pressure after 12 weeks of intervention between or within any of the groups (Table 2).

Serum lipids, C-reactive protein and insulin sensitivity markers

At baseline, no differences in serum levels of hsCRP, glucose, insulin, C-peptide, HbA1c, total cholesterol, LDL-cholesterol, HDL-cholesterol and TAG between the intervention groups were observed (Table 3). Baseline values of homeostatic model assessment for insulin resistance (HOMA-IR) were significantly different between the two groups (P = 0·05). After 12 weeks of intervention, there was no significant difference in the serum hsCRP, glucose, insulin, HOMA-IR, C-peptide, HbA1c, total cholesterol, HDL-cholesterol and TAG between or within the two groups (Table 3). However, after 12 weeks of intervention, there was a non-significant (P = 0·06) difference in LDL-cholesterol between the high-ALA groups, with a non-significant decrease in the high-ALA-DAG group (4·0–3·7 mmol/l) and a non-significant increase in the high-ALA-TAG group (3·3–3·6 mmol/l) (Table 3). All significant differences disappeared after Bonferroni adjustment.

Table 3. Plasma lipids and biochemical measurements at baseline and after 12 weeks of intervention (Medians and 25th–75th percentiles)

ALA, α-linolenic acid; DAG, diacylglycerol; HOMAir, homeostasis model assessment for insulin resistance; hsCRP, high-sensitivity C-reactive protein; TSH, thyroid-stimulating hormone.

* Within the high-ALA-DAG group (prior to Bonferroni correction).

† Within the high-ALA-TAG group (prior to Bonferroni correction).

‡ Comparing change from baseline to the end of the study between the high-ALA-DAG and high-ALA-TAG groups (prior to Bonferroni correction).

§ HOMAir = (fasting plasma insulin (mU/l) × fasting plasma glucose (mmol/l))/22·5, where 1 mU/l = 6·945 pmol/l.

Circulating NEFA

Circulating NEFA have been shown to be elevated in obese subjects; we therefore measured fasting plasma NEFA concentrations. At baseline, there was no difference in the NEFA concentration between the intervention groups (Table 3). The changes in circulating fasting NEFA concentration were non-significantly (after Bonferroni adjustment) different (P = 0·02) between the two groups after 12 weeks of intervention, with a non-significant decrease within the high-ALA-DAG group and a non-significant increase within the high-ALA-TAG group (Table 3).

Liver function parameters

Obesity leads to accumulation of fatty acids in the liver and therefore we measured markers of liver function such as ASAT, ALAT, γ-GT and ALP. At baseline no differences in these markers between the intervention groups were observed (Table 4). However, prior to Bonferroni adjustment, the concentration of ALAT, γ-GT and ALP was significantly reduced within the high-ALA-DAG group (P = 0·02, 0·02 and 0·01, respectively) and the change in ALAT was significantly different from the high-ALA-TAG group (P = 0·02), whereas the change in γ-GT and ALP was not significantly different from the high-ALA-TAG group (Table 4). These differences disappeared after Bonferroni adjustment. No significant differences within or between the groups in the ASAT:ALAT ratio after 12 weeks of intervention were observed (data not shown). The change in ALAT was positively correlated with the change in trunk fat mass (r 0·5; P = 0·007) and total body fat mass (r 0·5; P = 0·03) in the groups calculated together. The change in γ-GT and ALP did not correlate with the change in total body fat mass or trunk fat mass in any of the groups. In addition, we measured the serum concentration of fetuin-A, a suggested marker for hepatic steatosis(Reference Stefan, Hennige and Staiger33). However, no changes in serum concentration of fetuin-A were found within or between the groups (Table 4).

Table 4. Plasma liver function markers at baseline and after 12 weeks of intervention (Medians and 25th–75th percentiles)

ALA, α-linolenic acid; DAG, diacylglycerol; ASAT, aspartate aminotransferase; ALAT, alanine aminotransferase; γGT, γ-glutamyl transpeptidase; ALP, alkaline phosphatase.

* Within the high-ALA-DAG group (prior to Bonferroni correction).

† Within the high-ALA-TAG group (prior to Bonferroni correction).

‡ Comparing change from baseline to the end of the study between the high-ALA-DAG and high-ALA-TAG groups (prior to Bonferroni correction).

Adipokines in serum and plasma

Adipokines are secreted from adipose tissue and since intake of DAG oil has been shown to influence body composition, we measured the circulating hormones leptin, resistin and adiponectin. Despite a non-significant decrease in total body fat percentage and trunk fat mass, no changes between or within any of the groups were observed in any of these hormones after 12 weeks of intervention (Table 5). Also, there were no correlations between the change in hormones and total body fat mass or trunk fat mass.

Table 5. Adipokines and oxidative stress markers in serum and plasma at baseline and after 12 weeks of intervention (Medians and 25th–75th percentiles)

ALA, α-linolenic acid; DAG, diacylglycerol.

* Within the high-ALA-DAG group (prior to Bonferroni correction).

† Within the high-ALA-TAG group (prior to Bonferroni correction).

‡ Comparing change from baseline to the end of the study between the high-ALA-DAG and high-ALA-TAG groups (prior to Bonferroni correction).

§ The plasma concentration of α-tocopherol is normalised to the α-tocopherol to total lipid concentration (α-tocopherol/total cholesterol + TAG), expressed as the plasma α-tocopherol:plasma total lipid ratio.

Oxidative stress markers

Since ALA has been shown to be rapidly oxidised(Reference Arterburn, Hall and Oken34), we measured the oxidative stress markers urinary 8-iso-PGF and the antioxidant vitamin E. No significant changes between or within the groups were observed for urinary 8-iso-PGF after 12 weeks of intervention (Table 5). Prior to Bonferroni adjustment, the ratio of α-tocopherol:total lipids was significantly reduced within the high-ALA-DAG group (P = 0·02) and the high-ALA-TAG group (P = 0·05), with no significant difference between the groups after 12 weeks of intervention (Table 5). These differences disappeared after Bonferroni adjustment.

Fatty acid composition in plasma

The fatty acid composition in plasma was measured and is shown in Table 6. Prior to Bonferroni adjustment, a significant increase in ALA was observed both within the high-ALA-DAG (P = 0·005) and the high-ALA-TAG groups (P = 0·002) (Table 6). The change in plasma ALA between the groups was significantly different (P = 0·04) after 12 weeks of intervention, with the largest increase observed in the high-ALA-TAG group. Plasma EPA (20 : 5n-3) was significantly increased within both groups (P = 0·04 and 0·02, respectively), but the change was not significantly different between the groups. No increase was observed in plasma DHA (22 : 6n-3) either within or between the two groups. Linoleic acid (18 : 2n-6) was significantly reduced within both groups (P = 0·03 in both groups) after 12 weeks of intervention, but there was no significant difference between them. Arachidonic acid (20 : 4n-6) was not changed within any of the groups, but a significant change between the two groups (P = 0·05) was found. Minor changes were observed among the other fatty acids (Table 6). All these differences disappeared after Bonferroni adjustment.

Table 6. Fatty acid composition (µg/ml) in plasma at baseline and after 12 weeks of intervention (Medians and 25th–75th percentiles)

ALA, α-linolenic acid; DAG, diacylglycerol.

* Within the high-ALA-DAG group (prior to Bonferroni correction).

† Within the high-ALA-TAG group (prior to Bonferroni correction).

‡ Comparing change from baseline to the end of the study between the high-ALA-DAG and high-ALA-TAG groups (prior to Bonferroni correction).

Risk of CVD (10-year risk)

A cardiovascular risk profile has been developed based on the results of the Framingham heart study(Reference Ridker, Buring and Rifai35, Reference Ridker, Paynter and Rifai36) for use in primary care (http://www.reynoldsriskscore.org/). In addition to sex, age, systolic blood pressure, total cholesterol, HDL-cholesterol and hsCRP, the Reynold risk score uses information about smoking and genetic disposure (whether or not a parent had a heart attack before the age of 60 years) to predict CVD risk. In the present study, even though the cardiovascular risk score was relatively low, there was a mean predicted relative risk reduction of 18·5 % (from 6·5 5 % to 5·3 5 %, P = 0·04) in the high-ALA-DAG group, while the high-ALA-TAG group had a relative risk increase of 13·3 % (from 7·5 3 % to 8·5 3 %, P = 0·4) after intervention. There was a significant difference in relative risk reduction between the two groups (P = 0·001). This significant difference remained valid even after full Bonferroni adjustment.

Discussion

In the present study, we found that replacing part of the TAG-containing margarine with DAG-containing margarine (20 g) for 12 weeks led to an improved predicted 10 years cardiovascular risk score in healthy, overweight subjects. This reduction in cardiovascular risk may possibly be due to an improved metabolic phenotype appearing as reduced total body fat percentage and reduced trunk fat mass, and increased total FFM, in addition to reduced blood pressure. Additionally, the liver function markers ALAT, γ-GT and ALP were also non-significantly decreased after DAG intake.

The results are in line with other studies that showed a change in body composition after intake of DAG with a reduction of visceral fat mass(Reference Nagao, Watanabe and Goto21, Reference Yanagisawa, Kawabata and Tanaka37, Reference Teramoto, Watanabe and Ito38) and total fat mass(Reference Nagao, Watanabe and Goto21, Reference Maki, Davidson and Tsushima22, Reference Teramoto, Watanabe and Ito38) or total fat percentage(Reference Yanagisawa, Kawabata and Tanaka37). The different metabolic effects after intake of DAG compared with those after intake of TAG may be due to their structural differences and not only their fatty acid composition since the energy value, absorptive and digestive properties are similar(Reference Taguchi, Nagao and Watanabe39). The main end products of lipase action on sn-1,3-DAG are free glycerol and NEFA(Reference Hara, Onizawa and Honda40). These end-products of DAG are less readily re-synthesised into chylomicron TAG because such a synthesis requires a glycerol-3-phosphate intermediate. Therefore, fatty acids from DAG are likely to bypass the lymphatic system and enter the blood via the portal vein(Reference Tada41, Reference Rudkowska, Roynette and Demonty42) and may hence lead to increased hepatic β-oxidation, which have been reported both in animal(Reference Murata, Ide and Hara43Reference Murase, Aoki and Tokimitsu47) and human studies(Reference Kamphuis, Mela and Westerterp-Plantenga20, Reference Hibi, Takase and Yasunaga48Reference Kimura, Tsuchiya and Inage51).

Plasma levels of NEFA have been shown to be elevated in obese subjects(Reference Jensen, Haymond and Rizza52) as a consequence of increased release from the enlarged adipose tissue and reduced clearance(Reference Bjorntorp, Bergman and Varnauskas53). NEFA have been shown to inhibit the anti-lipolytic action of insulin, which again will further increase the level of NEFA and subsequently induce insulin resistance(Reference Boden54, Reference Boden, Chen and Ruiz55). However, the mechanisms by which obesity and NEFA cause insulin resistance are not clearly understood; nevertheless the reduced release of NEFA into the circulation improves insulin sensitivity(Reference Santomauro, Boden and Silva56). In the present study, we found no significant difference in the change in NEFA between the two groups, and no correlation was found between the change in NEFA concentration and the change in insulin resistance markers (insulin, glucose, C-peptide, HbA1c and HOMA-IR) (data not shown).

Despite a non-significant reduction in total body fat percentage and trunk fat mass, total body weight in the high-ALA-DAG group was not reduced; rather a non-significant increase was observed. Inconsistent results have been described regarding the effect on body weight after intervention with dietary DAG, with some finding a reduced body weight(Reference Nagao, Watanabe and Goto21, Reference Maki, Davidson and Tsushima22) while others find no change in weigh(Reference Yamamoto, Asakawa and Tokunaga57, Reference Yasunaga, Glinsmann and Seo58). The lack in weight reduction in the present study may be partly explained by the finding that the amount of FFM was non-significantly increased in the high-ALA-DAG group. The change in FFM in the high-ALA-DAG group corresponds to a 1·3 kg or 2 % increase in FFM, thus balancing the potential positive effect of the reduced trunk fat mass. However, taken together, these small non-significant changes in body composition may suggest an improvement of the metabolic phenotype in healthy, overweight individuals after dietary DAG intervention.

Even though the total trunk fat mass was slightly reduced in the high-ALA-DAG group, hip circumference was not changed after DAG intervention, indicating the potential effect of DAG intake on visceral fat mass in preference to subcutaneous fat mass. Visceral fat and subcutaneous fat are recognised to have distinct metabolic activities(Reference Kershaw and Flier6Reference Nedungadi and Clegg9, Reference Vohl, Sladek and Robitaille59), in which adipokines (cytokines and hormones) are secreted in different proportions. While cytokines are mainly secreted from visceral fat, the proportion of secreted hormones is higher from subcutaneous fat(Reference Wajchenberg4, Reference Havel60). In the present study, we did not observe any change in the adipocyte hormone concentration (leptin, resistin and adiponectin) which may be partly explained by the lack of reduction in subcutaneous fat depots. In addition, we did not observe any changes in levels of hsCRP in any of the groups after intervention. This is in accordance with Nelson et al., who did not find any change in inflammatory markers, including CRP, after intervention with ALA in overweight, healthy individuals(Reference Kaul, Kreml and Austria27, Reference Barcelo-Coblijn, Murphy and Othman28, Reference Nelson, Stevens and Hickey61). However, this is in contrast to what others have previously shown regarding the anti-inflammatory effects of ALA(Reference Rallidis, Paschos and Liakos62Reference Bemelmans, Lefrandt and Feskens64). These studies were also different in duration, population and samples size and thus may be explaining some of the observed discrepancy regarding CRP.

Hypertension is common in obesity(Reference Kotsis, Stabouli and Bouldin65, Reference Stabouli, Kotsis and Papamichael66) and a feature of the metabolic syndrome, and is also an established risk factor for CVD(Reference Stamler, Stamler and Neaton67). Systolic blood pressure was slightly reduced both within the high-ALA-DAG group and compared with the high-ALA-TAG group. The underlying molecular mechanisms controlling blood pressure are multi-factorial. Weight loss, and in particular reduced visceral fat, is associated with reduced blood pressure(Reference MacMahon, Cutler and Brittain68). The high-ALA-DAG group non-significantly reduced the body trunk fat mass after intervention and this small change in body fat may contribute to partly explain the observed improvement in blood pressure in this group, although there was no association between change in body fat and change in systolic blood pressure (data not shown).

In the present study, we did not find any significant changes in serum lipids after DAG intake; only a non-significant reduction in total cholesterol and LDL-cholesterol was found after 12 weeks of intervention with DAG. Others have found effects on plasma lipids after DAG intake; however, these studies have mainly focused on postprandial measurements and/or in groups of patients(Reference Taguchi, Watanabe and Onizawa18, Reference Yanagisawa, Kawabata and Tanaka37, Reference Yamamoto, Asakawa and Tokunaga57, Reference Meguro, Higashi and Hase69).

Elevated levels of circulating ALAT and γ-GT, without fatty liver or hepatic dysfunction, in healthy and asymptomatic subjects may predict the future development of metabolic diseases(Reference Vozarova, Stefan and Lindsay14, Reference Kim, Park and Lee70Reference Wannamethee, Shaper and Lennon73). Furthermore, elevated levels of ALAT and γ-GT activities have recently been shown to be positively associated with accumulation of visceral fat(Reference Mochizuki, Miyauchi and Misaki12). In the present study, we found that the high-ALA-DAG group non-significantly reduced their circulating concentrations of ALAT, γ-GT and ALP after intervention. Also, there was a positive association between the reduction in ALAT concentration and the reduction in body trunk fat mass and total body fat mass. This is in accordance with the findings of Mochizuki et al. and supports the notion that reduction in visceral fat is favourable for improved liver function(Reference Mochizuki, Miyauchi and Misaki12). The present study indicates that fatty acids taken as TAG or DAG will affect liver function in different ways, since there was no association between ALAT and body or trunk fat mass in the TAG group. This differential action on lipid metabolism, explained by specific structural differences of DAG isomers, and not only the fatty acid composition of DAG or TAG, has previously been reported(Reference Murase, Mizuno and Omachi74). Murase et al. have previously shown that increased hepatic β-oxidation may be the reason for reduced fatty liver formation after DAG intake(Reference Murase, Aoki and Tokimitsu47). Fetuin-A, a marker of hepatic steatosis(Reference Stefan, Hennige and Staiger33), was not changed within or between the groups after intervention. However, fetuin-A is a marker of a more established disease (hepatic steatosis) while the other liver function markers we measured (ASAT, ALAT, ALP and γ-GT) reflect a more general hepatic dysfunction. This may partly explain why fetuin-A is not changed during intervention in the present group of healthy, overweight subjects.

The Reynold risk score is a score based on several risk factors of CVD (sex, age, blood pressure, CRP, total cholesterol, HDL-cholesterol, smoking habits and familiar disposal). The risk score gives a CVD prediction for the following 10 years and is intended for use in primary care. In the present study, even though the cardiovascular risk score was relatively low at intervention start, intervention with DAG led to a relative risk reduction of 18·5 % and this reduction was significantly different from the TAG group, supporting the notion of improved health after DAG intake.

The strength of the present study is the randomised controlled design and the high compliance regarding intake of the study products. However, a major weakness in the present study is that the number of participants was considerably reduced due to a high withdrawal rate during the study. In a previous study investigating bioavailability of flaxseed oil, a relatively high withdrawal rate was also observed(Reference Austria, Richard and Chahine75). In the present study, the subjects were randomised and stratified according to sex and age. Due to the high withdrawal rate, however, the final groups had a skewed sex distribution. We therefore recalculated the results based on the male population alone (n 6 and n 11 in the high-ALA-TAG and high-ALA-DAG group, respectively), and the majority of the results still showed the same pattern. Within the high-ALA-DAG group (Wilcoxon matched-pair signed-rank test) a reduction after intervention was found for the following parameters: systolic blood pressure, ASAT, γ-GT, ALP, Reynold risk score and α-tocopherol/total lipids even though not all the recalculated results (only the males) now reached statistical significance. Differences (non-significant) between the two groups (MannWhitney U test) were still observed for ALAT, fat percentage and Reynold risk score similarly to the whole group. In the present study, power analysis was based on the existing literature on the effect of ALA on hsCRP, based on the assumption that changes in hsCRP would require the largest sample size. However, in addition to hsCRP, the present study aimed to investigate several other metabolic markers after intake of DAG oil in a Norwegian population, and may therefore be considered exploratory. Due to the limited numbers of subjects and the multiple testing, we performed Bonferroni correction. We cannot rule out the possibility that the results regarding some of the other markers would have been different in a larger population. However, body composition, another outcome in the present study, is shown by others to significantly change with approximately ten subjects in each group(Reference Teramoto, Watanabe and Ito38, Reference Yamamoto, Tomonobu and Asakawa76, Reference Matsuyama, Shoji and Watanabe77), which is comparable to our sample size. In order to further study beneficial health effects of DAG, future studies should include larger sample size and individuals with features of the metabolic syndrome which are more at risk of developing chronic diseases such as fatty liver, CVD and type 2 diabetes mellitus.

In conclusion, the results from the present study show that replacing TAG-based food items with DAG-based food items led to improved predicted 10 years cardiovascular risk score together with a possible beneficial effect on body composition and blood pressure. Even though weight was not reduced, intake of DAG-containing food items seemed to improve the metabolic phenotype in healthy, overweight subjects with small beneficial non-significant changes in total body fat percentage and trunk fat mass, FFM, ALAT, γ-GT and ALP. Altogether, this may potentially suggest beneficial health effects of DAG in healthy overweight subjects.

Acknowledgements

The present work was performed at Oslo and Akershus University College of Applied Sciences, Post Box 4, St. Olavsplass, 0130 Oslo, Norway. We thank our research participants for their dedication to the project. We are also grateful to Professor Jan I. Pedersen and Professor Lene Frost Andersen at Department of Nutrition, The Medical Faculty at the University of Oslo for valuable discussions and critical reading of the manuscript, and Ellen Raael at Oslo and Akershus University College of Applied Sciences for valuable assistance with this project. We also thank Danisco AS (Brabrand, Denmark), Norsk fropresse AS (Lysaker, Norway) and Kao Corporation (Tokyo, Japan). This study was supported by Oslo and Akershus University College of Applied Sciences, Norway, The Throne Holst Foundation, The Nordic Center of Excellence on Systems Biology in controlled dietary interventions and cohort studies, SYSDIET (no. 070014), Mills DA, Oslo, Norway, and The Research Council of Norway (P.O. Box 2700, St. Hanshaugen, N-0131 Oslo, Norway). V. H. T.-H., I. N., N. W.-R., K. R., A. M., B. H., K. B. H. and S. M. U. have no conflicts of interest, or any financial or personal interest. L. G. is a researcher and nutrition manager, K. F. C. and A. L. are researchers in Mills DA, Oslo, Norway. They have no financial or personal interest. V. H. T.-H., I. N., K. R., N. W.-R., A. M., L. G., K. F. C., A. L., B. H., K. B. H. and S. M. U. designed the research (project conception, development of overall research plan and study oversight). V. H. T.-H., I. N., N. W.-R., K. F. C., A. L., K. B. H. and S. M. U. conducted research (hands-on conduct of the experiments and data collection). V. H. T.-H., K. B. H. and S. M. U. analysed the data or performed statistical analysis. V. H. T.-H., I. N., K. R., N. W.-R., A. M., L. G., K. F. C., A. L., B. H., K. B. H. and S. M. U. wrote the paper (the only authors who made a major contribution). V. H. T.-H., K. B. H. and S. M. U. had primary responsibility for the final content.

References

1.Rao, GH, Thethi, I & Fareed, J (2011) Vascular disease: obesity and excess weight as modulators of risk. Expert Rev Cardiovasc Ther 9, 525534.CrossRefGoogle ScholarPubMed
2.Kahn, SE, Hull, RL & Utzschneider, KM (2006) Mechanisms linking obesity to insulin resistance and type 2 diabetes. Nature 444, 840846.Google Scholar
3.Kotsis, V, Stabouli, S, Papakatsika, S, et al. (2010) Mechanisms of obesity-induced hypertension. Hypertens Res 33, 386393.CrossRefGoogle ScholarPubMed
4.Wajchenberg, BL (2000) Subcutaneous and visceral adipose tissue: their relation to the metabolic syndrome. Endocr Rev 21, 697738.CrossRefGoogle ScholarPubMed
5.Perrini, S, Leonardini, A, Laviola, L, et al. (2008) Biological specificity of visceral adipose tissue and therapeutic intervention. Arch Physiol Biochem 114, 277286.Google Scholar
6.Kershaw, EE & Flier, JS (2004) Adipose tissue as an endocrine organ. J Clin Endocrinol Metab 89, 25482556.CrossRefGoogle ScholarPubMed
7.Galic, S, Oakhill, JS & Steinberg, GR (2010) Adipose tissue as an endocrine organ. Mol Cell Endocrinol 316, 129139.CrossRefGoogle ScholarPubMed
8.Despres, JP & Lemieux, I (2006) Abdominal obesity and metabolic syndrome. Nature 444, 881887.CrossRefGoogle ScholarPubMed
9.Nedungadi, TP & Clegg, DJ (2009) Sexual dimorphism in body fat distribution and risk for cardiovascular diseases. J Cardiovasc Transl Res 2, 321327.CrossRefGoogle ScholarPubMed
10.Kishida, K, Funahashi, T & Shimomura, I (2011) Clinical significance of visceral fat reduction through health education in preventing atherosclerotic cardiovascular disease – lesson from the Amagasaki Visceral Fat Study: a Japanese perspective. Nutr Metab (Lond) 8, 57.CrossRefGoogle ScholarPubMed
11.Stefan, N, Kantartzis, K & Haring, HU (2008) Causes and metabolic consequences of fatty liver. Endocr Rev 29, 939960.CrossRefGoogle ScholarPubMed
12.Mochizuki, K, Miyauchi, R, Misaki, Y, et al. (2011) Accumulation of visceral fat is positively associated with serum ALT and gamma-GTP activities in healthy and preclinical middle-aged Japanese men. J Nutr Sci Vitaminol (Tokyo) 57, 6573.Google Scholar
13.Bo, S, Gambino, R, Durazzo, M, et al. (2005) Associations between gamma-glutamyl transferase, metabolic abnormalities and inflammation in healthy subjects from a population based cohort: a possible implication for oxidative stress. World J Gastroenterol 11, 71097117.Google Scholar
14.Vozarova, B, Stefan, N, Lindsay, RS, et al. (2002) High alanine aminotransferase is associated with decreased hepatic insulin sensitivity and predicts the development of type 2 diabetes. Diabetes 51, 18891895.Google Scholar
15.Marchesini, G, Brizi, M, Bianchi, G, et al. (2001) Nonalcoholic fatty liver disease: a feature of the metabolic syndrome. Diabetes 50, 18441850.Google Scholar
16.van Barneveld, T, Seidell, JC, Traag, N, et al. (1989) Fat distribution and gamma-glutamyl transferase in relation to serum lipids and blood pressure in 38-year old Dutch males. Eur J Clin Nutr 43, 809818.Google ScholarPubMed
17.Yanai, H, Tomono, Y, Ito, K, et al. (2007) Diacylglycerol oil for the metabolic syndrome. Nutr J 6, 43.Google Scholar
18.Taguchi, H, Watanabe, H, Onizawa, K, et al. (2000) Double-blind controlled study on the effects of dietary diacylglycerol on postprandial serum and chylomicron triacylglycerol responses in healthy humans. J Am Coll Nutr 19, 789796.Google Scholar
19.Tada, N, Watanabe, H, Matsuo, N, et al. (2001) Dynamics of postprandial remnant-like lipoprotein particles in serum after loading of diacylglycerols. Clin Chim Acta 311, 109117.Google Scholar
20.Kamphuis, MM, Mela, DJ & Westerterp-Plantenga, MS (2003) Diacylglycerols affect substrate oxidation and appetite in humans. Am J Clin Nutr 77, 11331139.Google Scholar
21.Nagao, T, Watanabe, H, Goto, N, et al. (2000) Dietary diacylglycerol suppresses accumulation of body fat compared to triacylglycerol in men in a double-blind controlled trial. J Nutr 130, 792797.Google Scholar
22.Maki, KC, Davidson, MH, Tsushima, R, et al. (2002) Consumption of diacylglycerol oil as part of a reduced-energy diet enhances loss of body weight and fat in comparison with consumption of a triacylglycerol control oil. Am J Clin Nutr 76, 12301236.CrossRefGoogle ScholarPubMed
23.Xie, N, Zhang, W, Li, J, et al. (2011) α-Linolenic acid intake attenuates myocardial ischemia/reperfusion injury through anti-inflammatory and anti-oxidative stress effects in diabetic but not normal rats. Arch Med Res 42, 171181.Google Scholar
24.Rodriguez-Leyva, D, Dupasquier, CM, McCullough, R, et al. (2010) The cardiovascular effects of flaxseed and its omega-3 fatty acid, alpha-linolenic acid. Can J Cardiol 26, 489496.CrossRefGoogle ScholarPubMed
25.Dewell, A, Marvasti, FF, Harris, WS, et al. (2011) Low- and high-dose plant and marine (n-3) fatty acids do not affect plasma inflammatory markers in adults with metabolic syndrome. J Nutr 141, 21662171.CrossRefGoogle Scholar
26.de Goede, J, Verschuren, WM, Boer, JM, et al. (2011) Alpha-linolenic acid intake and 10 year incidence of coronary heart disease and stroke in 20,000 middle-aged men and women in the Netherlands. PLoS One 6, e17967.Google Scholar
27.Kaul, N, Kreml, R, Austria, JA, et al. (2008) A comparison of fish oil, flaxseed oil and hempseed oil supplementation on selected parameters of cardiovascular health in healthy volunteers. J Am Coll Nutr 27, 5158.CrossRefGoogle ScholarPubMed
28.Barcelo-Coblijn, G, Murphy, EJ, Othman, R, et al. (2008) Flaxseed oil and fish-oil capsule consumption alters human red blood cell n-3 fatty acid composition: a multiple-dosing trial comparing 2 sources of n-3 fatty acid. Am J Clin Nutr 88, 801809.CrossRefGoogle ScholarPubMed
29.Svilaas, A, Strom, EC, Svilaas, T, et al. (2002) Reproducibility and validity of a short food questionnaire for the assessment of dietary habits. Nutr Metab Cardiovasc Dis 12, 6070.Google Scholar
30.Bastani, NE, Gundersen, TE & Blomhoff, R (2009) Determination of 8-epi PGF(2alpha) concentrations as a biomarker of oxidative stress using triple-stage liquid chromatography/tandem mass spectrometry. Rapid Commun Mass Spectrom 23, 28852890.Google Scholar
31.Panfili, G, Fratianni, A & Irano, M (2003) Normal phase high-performance liquid chromatography method for the determination of tocopherols and tocotrienols in cereals. J Agric Food Chem 51, 39403944.Google Scholar
32.Haug, IJ, Sagmo, LB, Zeiss, D, et al. (2011) Bioavailability of EPA and DHA delivered by gelled emulsions and soft gel capsules. Eur J Lipid Sci Technol 113, 137145.Google Scholar
33.Stefan, N, Hennige, AM, Staiger, H, et al. (2006) Alpha2-Heremans-Schmid glycoprotein/fetuin-A is associated with insulin resistance and fat accumulation in the liver in humans. Diabetes Care 29, 853857.Google Scholar
34.Arterburn, LM, Hall, EB & Oken, H (2006) Distribution, interconversion, and dose response of n-3 fatty acids in humans. Am J Clin Nutr 83, 1467S1476S.Google Scholar
35.Ridker, PM, Buring, JE, Rifai, N, et al. (2007) Development and validation of improved algorithms for the assessment of global cardiovascular risk in women: the Reynolds Risk Score. JAMA 297, 611619.Google Scholar
36.Ridker, PM, Paynter, NP, Rifai, N, et al. (2008) C-reactive protein and parental history improve global cardiovascular risk prediction: the Reynolds Risk Score for men. Circulation 118, 22432251.Google Scholar
37.Yanagisawa, Y, Kawabata, T, Tanaka, O, et al. (2003) Improvement in blood lipid levels by dietary sn-1,3-diacylglycerol in young women with variants of lipid transporters 54T-FABP2 and -493g-MTP. Biochem Biophys Res Commun 302, 743750.CrossRefGoogle ScholarPubMed
38.Teramoto, T, Watanabe, H, Ito, K, et al. (2004) Significant effects of diacylglycerol on body fat and lipid metabolism in patients on hemodialysis. Clin Nutr 23, 11221126.Google Scholar
39.Taguchi, H, Nagao, T, Watanabe, H, et al. (2001) Energy value and digestibility of dietary oil containing mainly 1,3-diacylglycerol are similar to those of triacylglycerol. Lipids 36, 379382.Google Scholar
40.Hara, K, Onizawa, K, Honda, H, et al. (1993) Dietary diacylglycerol-dependent reduction in serum triacylglycerol concentration in rats. Ann Nutr Metab 37, 185191.CrossRefGoogle ScholarPubMed
41.Tada, N (2004) Physiological actions of diacylglycerol outcome. Curr Opin Clin Nutr Metab Care 7, 145149.CrossRefGoogle ScholarPubMed
42.Rudkowska, I, Roynette, CE, Demonty, I, et al. (2005) Diacylglycerol: efficacy and mechanism of action of an anti-obesity agent. Obes Res 13, 18641876.Google Scholar
43.Murata, M, Ide, T & Hara, K (1997) Reciprocal responses to dietary diacylglycerol of hepatic enzymes of fatty acid synthesis and oxidation in the rat. Br J Nutr 77, 107121.Google Scholar
44.Murase, T, Aoki, M, Wakisaka, T, et al. (2002) Anti-obesity effect of dietary diacylglycerol in C57BL/6J mice: dietary diacylglycerol stimulates intestinal lipid metabolism. J Lipid Res 43, 13121319.Google Scholar
45.Murase, T, Nagasawa, A, Suzuki, J, et al. (2002) Dietary alpha-linolenic acid-rich diacylglycerols reduce body weight gain accompanying the stimulation of intestinal beta oxidation and related gene expressions in C57BL/KsJ-db/db mice. J Nutr 132, 30183022.Google Scholar
46.Meng, X, Zou, D, Shi, Z, et al. (2004) Dietary diacylglycerol prevents high-fat diet-induced lipid accumulation in rat liver and abdominal adipose tissue. Lipids 39, 3741.Google Scholar
47.Murase, T, Aoki, M & Tokimitsu, I (2005) Supplementation with alpha-linolenic acid-rich diacylglycerol suppresses fatty liver formation accompanied by an up-regulation of beta oxidation in Zucker fatty rats. Biochim Biophys Acta 1733, 224231.CrossRefGoogle ScholarPubMed
48.Hibi, M, Takase, H, Yasunaga, K, et al. (2008) Greater fat oxidation with diacylglycerol oil consumption for 14 days compared with triacylglycerol oil consumption in overweight men and women. Int J Obes (Lond) 32, 18411847.Google Scholar
49.Saito, S, Tomonobu, K, Hase, T, et al. (2006) Effects of diacylglycerol on postprandial energy expenditure and respiratory quotient in healthy subjects. Nutrition 22, 3035.Google Scholar
50.Hibi, M, Takase, H, Yasunaga, K, et al. (2008) Fat utilization in healthy subjects consuming diacylglycerol oil diet: dietary and whole body fat oxidation. Lipids 43, 517524.Google Scholar
51.Kimura, S, Tsuchiya, H, Inage, H, et al. (2006) Effects of dietary diacylglycerol on the energy metabolism. Int J Vitam Nutr Res 76, 7579.Google Scholar
52.Jensen, MD, Haymond, MW, Rizza, RA, et al. (1989) Influence of body fat distribution on free fatty acid metabolism in obesity. J Clin Invest 83, 11681173.Google Scholar
53.Bjorntorp, P, Bergman, H & Varnauskas, E (1969) Plasma free fatty acid turnover rate in obesity. Acta Med Scand 185, 351356.Google Scholar
54.Boden, G (2011) Obesity, insulin resistance and free fatty acids. Curr Opin Endocrinol Diabetes Obes 18, 139143.CrossRefGoogle ScholarPubMed
55.Boden, G, Chen, X, Ruiz, J, et al. (1994) Mechanisms of fatty acid-induced inhibition of glucose uptake. J Clin Invest 93, 24382446.CrossRefGoogle ScholarPubMed
56.Santomauro, AT, Boden, G, Silva, ME, et al. (1999) Overnight lowering of free fatty acids with Acipimox improves insulin resistance and glucose tolerance in obese diabetic and nondiabetic subjects. Diabetes 48, 18361841.Google Scholar
57.Yamamoto, K, Asakawa, H, Tokunaga, K, et al. (2001) Long-term ingestion of dietary diacylglycerol lowers serum triacylglycerol in type II diabetic patients with hypertriglyceridemia. J Nutr 131, 32043207.Google Scholar
58.Yasunaga, K, Glinsmann, WH, Seo, Y, et al. (2004) Safety aspects regarding the consumption of high-dose dietary diacylglycerol oil in men and women in a double-blind controlled trial in comparison with consumption of a triacylglycerol control oil. Food Chem Toxicol 42, 14191429.CrossRefGoogle Scholar
59.Vohl, MC, Sladek, R, Robitaille, J, et al. (2004) A survey of genes differentially expressed in subcutaneous and visceral adipose tissue in men. Obes Res 12, 12171222.CrossRefGoogle ScholarPubMed
60.Havel, PJ (2004) Update on adipocyte hormones: regulation of energy balance and carbohydrate/lipid metabolism. Diabetes 53, Suppl. 1, S143S151.CrossRefGoogle ScholarPubMed
61.Nelson, TL, Stevens, JR & Hickey, MS (2007) Inflammatory markers are not altered by an eight week dietary alpha-linolenic acid intervention in healthy abdominally obese adult males and females. Cytokine 38, 101106.Google Scholar
62.Rallidis, LS, Paschos, G, Liakos, GK, et al. (2003) Dietary alpha-linolenic acid decreases C reactive protein, serum amyloid A and interleukin-6 in dyslipidaemic patients. Atherosclerosis 167, 237242.Google Scholar
63.Zhao, G, Etherton, TD, Martin, KR, et al. (2004) Dietary alpha-linolenic acid reduces inflammatory and lipid cardiovascular risk factors in hypercholesterolemic men and women. J Nutr 134, 29912997.CrossRefGoogle ScholarPubMed
64.Bemelmans, WJ, Lefrandt, JD, Feskens, EJ, et al. (2004) Increased alpha-linolenic acid intake lowers C-reactive protein, but has no effect on markers of atherosclerosis. Eur J Clin Nutr 58, 10831089.CrossRefGoogle ScholarPubMed
65.Kotsis, V, Stabouli, S, Bouldin, M, et al. (2005) Impact of obesity on 24-hour ambulatory blood pressure and hypertension. Hypertension 45, 602607.Google Scholar
66.Stabouli, S, Kotsis, V, Papamichael, C, et al. (2005) Adolescent obesity is associated with high ambulatory blood pressure and increased carotid intimal-medial thickness. J Pediatr 147, 651656.Google Scholar
67.Stamler, J, Stamler, R & Neaton, JD (1993) Blood pressure, systolic and diastolic, and cardiovascular risks. US population data. Arch Intern Med 153, 598615.Google Scholar
68.MacMahon, S, Cutler, J, Brittain, E, et al. (1987) Obesity and hypertension: epidemiological and clinical issues. Eur Heart J 8, Suppl. B, 5770.Google Scholar
69.Meguro, S, Higashi, K, Hase, T, et al. (2001) Solubilization of phytosterols in diacylglycerol versus triacylglycerol improves the serum cholesterol-lowering effect. Eur J Clin Nutr 55, 513517.CrossRefGoogle ScholarPubMed
70.Kim, CH, Park, JY, Lee, KU, et al. (2009) Association of serum gamma-glutamyltransferase and alanine aminotransferase activities with risk of type 2 diabetes mellitus independent of fatty liver. Diabetes Metab Res Rev 25, 6469.Google Scholar
71.Ford, ES, Schulze, MB, Bergmann, MM, et al. (2008) Liver enzymes and incident diabetes: findings from the European Prospective Investigation into Cancer and Nutrition (EPIC) Potsdam Study. Diabetes Care 31, 11381143.Google Scholar
72.Doi, Y, Kubo, M, Yonemoto, K, et al. (2007) Liver enzymes as a predictor for incident diabetes in a Japanese population: the Hisayama study. Obesity (Silver Spring) 15, 18411850.Google Scholar
73.Wannamethee, SG, Shaper, AG, Lennon, L, et al. (2005) Hepatic enzymes, the metabolic syndrome, and the risk of type 2 diabetes in older men. Diabetes Care 28, 29132918.Google Scholar
74.Murase, T, Mizuno, T, Omachi, T, et al. (2001) Dietary diacylglycerol suppresses high fat and high sucrose diet-induced body fat accumulation in C57BL/6J mice. J Lipid Res 42, 372378.Google Scholar
75.Austria, JA, Richard, MN, Chahine, MN, et al. (2008) Bioavailability of alpha-linolenic acid in subjects after ingestion of three different forms of flaxseed. J Am Coll Nutr 27, 214221.Google Scholar
76.Yamamoto, K, Tomonobu, K, Asakawa, H, et al. (2006) Diet therapy with diacylglycerol oil delays the progression of renal failure in type 2 diabetic patients with nephropathy. Diabetes Care 29, 417419.CrossRefGoogle ScholarPubMed
77.Matsuyama, T, Shoji, K, Watanabe, H, et al. (2006) Effects of diacylglycerol oil on adiposity in obese children: initial communication. J Pediatr Endocrinol Metab 19, 795804.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. Fatty acid composition in the test products (g per portion* and g per d)

Figure 1

Table 2. Clinical characteristics and body composition at baseline and after 12 weeks of intervention (Medians and 25th–75th percentiles)

Figure 2

Table 3. Plasma lipids and biochemical measurements at baseline and after 12 weeks of intervention (Medians and 25th–75th percentiles)

Figure 3

Table 4. Plasma liver function markers at baseline and after 12 weeks of intervention (Medians and 25th–75th percentiles)

Figure 4

Table 5. Adipokines and oxidative stress markers in serum and plasma at baseline and after 12 weeks of intervention (Medians and 25th–75th percentiles)

Figure 5

Table 6. Fatty acid composition (µg/ml) in plasma at baseline and after 12 weeks of intervention (Medians and 25th–75th percentiles)