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Dietary Carbohydrate and Internal Body Fat

Not Applicable
Completed
Conditions
Adiposity
Interventions
Behavioral: Acellular carbohydrate diet
Behavioral: Cellular carbohydrate diet
Behavioral: Low-carbohydrate high-fat diet
Registration Number
NCT03401970
Lead Sponsor
Haukeland University Hospital
Brief Summary

This is a 2-year randomized controlled trial to test the effect of dietary carbohydrates, both quality and quantity, on changes in internal body fat mass. Up to 250 women and men with obesity are recruited in Bergen, Norway, and randomized to one of the following normo- and isocaloric dietary patterns (same amount of protein, polyunsaturated fatty acids and moderate energy, 2,000 - 2,500 kcal per day): 1) a low-fat high-carbohydrate diet primarily with refined (e.g., flour-based) carbohydrate sources, 2) a low-fat high-carbohydrate diet based on minimally refined (e.g., cellular) carbohydrate sources, and 3) a very-high-fat low-carbohydrate diet.

Detailed Description

Obesity, and high internal fat storage in particular, represents a tremendous and increasing health challenge across the world, and is linked to the recent introduction and globalization of an ultra-processed food supply largely based on refined carbohydrates. However, more high-quality studies are needed to directly assess the role of carbohydrate quality in abdominal adiposity. We also need studies with greater long-term adherence to prescribed food profiles, which may be achievied with the help of new electronic tools such as meal planning applications.

The participants select and plan all meals among a list of carefully designed options, using an application/recipe booklet developed for the study. Each recipe/meal/snack is designed to fully comply with the overall macronutrient- and dietary profile for the respective groups. We will further instruct the participants to record their meal choices during three days every 14 days, and to record all deviations throughout the intervention.

Enrolled participants are invited to study visits at baseline and after 3, 6, 9, 12 and 24 months. At all or some of these time points, the participants provide biological samples (blood, urine and feces, and for some, adipose and/or muscle tissue) and undergo phenotyping, e.g., measurement of body weight and fat mass by bioelectrical impedance analysis and low-radiation CT imaging, and a standardized meal test with blood sample collection up to 4 hours postprandially. In addition, participants will be asked to fill out a collection of questionnaires that assess quality of life, motivation, fatigue, gastrointestinal health, appetite and physical activity. We ask the participants to maintain the same level of physical activity throughout the study.

The primary outcome measure is change in internal body fat mass (visceral adipose tissue) measured by CT imaging. Secondary outcome measures include change in 2-hour postprandial serum concentrations of insulin, change in 4-hour postprandial serum concentrations of triacylglycerols, and change in fecal microbiota composition measured by 16S sequencing.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
150
Inclusion Criteria
  • Body-mass index (BMI) equal to or above 30 kg/m2 and/or waist circumference equal to or above 102 cm for men and 88 cm for women
  • Weight stable during the last 2 months before start of the study (less than 5 % change in body weight up or down)
  • No known diabetes or consumption of diabetes medication
  • Desire to follow a specified dietary pattern using specific recipes throughout the time of the study period
  • Ability to periodically record food intake using a specially designed app for the study
Exclusion Criteria
  • Use of statins and/or diabetes medication
  • Recent surgical or antibiotics treatment during the last 2 months before start of the study
  • Chronic inflammatory bowel disease
  • Serious disease
  • Smoking
  • Pregnancy or breast feeding
  • Alcohol consumption during the study of more than 2 alcohol units per day (1 unit = 15 ml (12.8 g) pure alcohol)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Acellular carbohydrate dietAcellular carbohydrate dietPrescribed dietary pattern. Carbohydrates from acellular sources, e.g., refined flour/bakery products, at least 500 grams of fruits/vegetables per day, and a macronutrient composition within typical nutritional recommendations for the general population.
Cellular carbohydrate dietCellular carbohydrate dietPrescribed dietary pattern. Carbohydrates from cellular sources, e.g., root vegetables, fruits, whole-grain rice, non-flour grain products, at least 500 grams of fruits/vegetables per day, and a macronutrient composition within typical nutritional recommendations for the general population similar to the acellular carbohydrate diet.
Low-carbohydrate high-fat dietLow-carbohydrate high-fat dietPrescribed dietary pattern. Energy largely from fat, cellular carbohydrate sources, and otherwise similar food types as in the acellular/cellular carbohydrate diets including at least 500 grams of fruits/vegetables per day.
Primary Outcome Measures
NameTimeMethod
Change in internal body fatBaseline and 6, 12 and 24 months

Visceral fat mass (cm3) measured by computed tomography (CT) imaging

Secondary Outcome Measures
NameTimeMethod
Change in postprandial non-esterified fatty acidsBaseline and 3, 6, 9, 12 and 24 months

Circulating non-esterified fatty acid concentrations before and after 60, 120 and 240 minutes after intake of a standardized mixed meal

Change in abdominal subcutaneous fat massBaseline and 6, 12 and 24 months

Abdominal subcutaneous fat mass (cm3) measured by computed tomography (CT) imaging

Change in body-mass indexBaseline and 3, 6, 9, 12 and 24 months

Body-mass index measured as body weight (kg) divided by height (m) squared

Change in postprandial insulinBaseline and 3, 6, 9, 12 and 24 months

Circulating insulin concentrations measured before and 2 hours after intake of a standardized mixed meal

Change in liver densityBaseline and 6, 12 and 24 months

Calculated as liver/spleen attenuation index (Hounsfield units) based on quantification by computed tomography (CT) imaging

Change in pericardial fat massBaseline and 6, 12 and 24 months

Pericardial fat mass (cm3) measured by computed tomography (CT) imaging

Change in fasting insulinBaseline and 3, 6, 9, 12 and 24 months

Circulating fasting insulin concentrations

Change in fasting C-peptideBaseline and 3, 6, 9, 12 and 24 months

Circulating fasting C-peptide concentrations

Change in waist circumferenceBaseline and 3, 6, 9, 12 and 24 months

Waist circumference (cm) measured by a measuring tape

Change in postprandial C-peptideBaseline and 3, 6, 9, 12 and 24 months

Circulating C-peptide concentrations measured before and 2 hours after intake of a standardized mixed meal

Change in fasting LDL cholesterolBaseline and 3, 6, 9, 12 and 24 months

Circulating fasting low-density lipoprotein cholesterol (LDL-C)

Change in postprandial triacylglycerolBaseline and 3, 6, 9, 12 and 24 months

Triacylglycerol concentrations measured before and 4 hours after intake of a mixed meal

Change in postprandial area under the curve (AUC) glucoseBaseline and 3, 6, 9, 12 and 24 months

Circulating glucose measured before and after 30, 60, 90, 120 and 240 minutes after intake of a standardized mixed meal

Change in fecal microbiome compositionBaseline and 3, 6, 9, 12 and 24 months

Microbiome composition measured by 16S sequencing

Change in coronary artery calcification (CAC)Baseline and 6, 12 and 24 months

CAC score calculated based on computed tomography (CT) imaging

Change in circulating and urine metabolites associated with one-carbon metabolismBaseline and 3, 6, 9, 12 and 24 months

Circulating metabolites in the serine, glycine and histidine pathways measured in the fasted state by GC-MS/MS

Change in gastrointestinal symptoms by the Roma III questionnaireBaseline and 3, 6, 9, 12 and 24 months

Gastrointestinal health will be surveyed and quantified by a questionnaire (Rome III Diagnostic Criteria for Irritable Bowel Syndrome (IBS)). The questionnaire surveys criteria for diagnosis of IBS within a 12-week period. The criteria for IBS are based on recurrent abdominal pain or discomfort, 3 days per month in the last 3 months (12 weeks), associated with ≥2 of the following criteria: 1.Improvement with defecation; 2. Onset associated with a change in stool frequency; 3. Onset associated with a change in stool form (appearance). The criteria are fulfilled with symptoms onset 6 months prior to diagnosis.

Change in TAG/HDL-C ratioBaseline and 3, 6, 9, 12 and 24 months

The ratio of circulating fasting triacylglycerol (TAG) and high-density lipoprotein cholesterol (HDL-C)

Change in apolipoprotein profileBaseline and 3, 6, 9, 12 and 24 months

Circulating fasting apolipoprotein profile measured by multiplex ELISA

Change in lean massBaseline and 3, 6, 9, 12 and 24 months

Lean mass will be measured by bioimpedance analysis (BIA)

Change in fasting TAGBaseline and 3, 6, 9, 12 and 24 months

Circulating fasting triacylglycerol concentrations

Change in fasting HDL cholesterolBaseline and 3, 6, 9, 12 and 24 months

Circulating fasting high-density lipoprotein cholesterol (HDL-C)

Change in total fat massBaseline and 3, 6, 9, 12 and 24 months

Total fat mass measured by bioimpedance analysis (BIA)

Change in appetite/fullnessBaseline and 3, 6, 9, 12 and 24 months

Subjective appetite and fullness assessed and quantified by the VAS questionnaire

Change in gastrointestinal symptoms by the IBS-SSS questionnaireBaseline and 3, 6, 9, 12 and 24 months

Gastrointestinal health will be surveyed by the IBS-SSS questionnaire. Scores on the IBS-SSS range from 0 to 500 with higher scores indicating more severe symptoms. Subjects can be categorized as having mild (75-175), moderate (175-300), or severe (\>300) IBS. A decrease of 50 points is associated with a clinically meaningful improvement. Each question on the VAS ranges from 0-100mm, where higher score indicates more severe symptoms.

The categorization based on scores (total possible score = 500) are as follows:

0-75 = not IBS 75-175= mild IBS 175-300 = moderate IBS 300-500 = severe IBS

Change in perception of health / quality of lifeBaseline and 3, 6, 9, 12 and 24 months

Obesity-specific quality of life is measured with "Patient-Reported Outcomes in Obesity" (PROS), which consists of 8 items tapping how different life domains are affected by obesity. PROS have one overall score, ranging from 0 (optimal) to 3 (poorest).

Generic health-related quality of life is measured with RAND-36, which consists of dimensions ranging from 0 (poorest) to 100 (optimal). There are 8 subscales; physical functioning, physical role functioning, bodily pain, general health, vitality, social functioning, emotional role functioning and mental health. In addition, RAND-36 also have 2 summary scores: the physical component summary (PCS) (tapping from physical functioning, physical role functioning, bodily pain and general health) and mental component summary (MCS) (tapping from vitality, social functioning, emotional role functioning and mental health).

Change in quality of life related to gastrointestinal symptomsBaseline and 3, 6, 9, 12 and 24 months

The SF-NDI (Short-Form Nepean Dyspepsia Index (SF-NDI)) questionnaire will be used to assess quality of life / psychological wellbeing related to gastrointestinal symptoms. The 10-item SF-NDI was constructed and validated in patients with functional gastrointestinal disorders for measuring health-related quality of life. The 10-item short form includes five subscales: tension, interference with daily activities, eating/drinking, knowledge/control, and work/study, and each subscale contains two items. The items were measured by a 5-point graded Likert scale from 1 to 5. A total sum score for quality of life and a sum score for each of the five subscales were calculated by adding up scores for each item (range of total quality of life, 10-50; range of each subscale, 2-10). Higher scores indicate worse functioning or symptoms.

Change in fatigueBaseline and 3, 6, 9, 12 and 24 months

The Fatigue Impact Scale will be used to compute a total score for fatigue by summing up the scores for subclasses as follows: cognitive functioning (10 items, subscale range: 0-40), physical functioning (10 items, subscale range: 0-40), and psychosocial functioning (20 items, subscale range: 0-80). The statements are ranged on a five-level scale (0 = no problem to 4 = extreme problems), giving a maximum total FIS score of 160 (total scale range: 0-160) where low scores indicate less fatigue-related issues.

Trial Locations

Locations (1)

Forskningsenhet for helseundersøkelser (research unit for clinical trials), Department of Clinical Science, University of Bergen

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Bergen, Norway

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