Title

Dairy Modulation of Oxidative and Inflammatory Stress in Overweight and Obese Subjects
  • Phase

    N/A
  • Study Type

    Interventional
  • Status

    Completed No Results Posted
  • Study Participants

    20
The objective of this study is to determine the acute effects of a dairy supplement compared to a soy supplement on oxidative and inflammatory stress in overweight and obese subjects in the absence of any changes in adiposity.
Obesity is associated with sub-clinical chronic oxidative and inflammatory stress, both of which are major contributors to obesity-associated co-morbidities. Calcitriol (1, 25-(OH)2-D3) regulates adipocyte lipid metabolism, while dietary calcium inhibits obesity by suppression of calcitriol. We have recently shown calcitriol to increase oxidative stress and to stimulate the expression and release of inflammatory cytokines, while inhibiting the expression and release of anti-inflammatory cytokines. We have also shown that inhibition of calcitriol with high calcium diets decreases both adipose tissue and systemic oxidative and inflammatory stress in a mouse model of obesity. Moreover, dairy exerted a greater effect on both oxidative and inflammatory stress. These mice also exhibited significant reductions in adiposity, which could lead to confounding, as this reduction will independently reduce oxidative and inflammatory stress. However, the supporting cellular/mechanistic data indicate an effect which is independent of adiposity reduction. Consequently, we propose that low calcium diets exacerbate oxidative and inflammatory stress and that high dairy diets can attenuate both independently of changes in adiposity, thereby significantly reducing the risk of obesity-associated co-morbidities. Accordingly, the objective of this study is to determine the acute effects of a dairy-rich diet on oxidative and inflammatory stress in overweight and obese subjects in the absence of any changes in adiposity.

Twenty subjects (10 obese and 10 overweight) will undergo a randomized crossover study of low dairy and high dairy eucaloric diets. Each dietary period will be four weeks, and the two dietary periods will be separated by a four-week washout period. Primary outcomes will be circulating indices of oxidative stress and of inflammation. Secondary outcomes include blood pressure, circulating glucose, insulin, lipids, calcium-regulatory hormones and body composition.
Study Started
Jan 31
2007
Primary Completion
Dec 31
2008
Study Completion
May 31
2009
Last Update
Jul 29
2009
Estimate

Dietary Supplement Milk

Milk-based smoothie containing 170 kcal, 10 g protein, 1 g fat, 30 g carbohydrate adn 350 mg Ca. Three consumed each day.

Dietary Supplement Soy

Soy-based smoothie containing 170 kcal, 10 g protein, 1 g fat, 30 g carbohydrate and 30 mg Ca. Three consumed each day for 28 days,

Soy Active Comparator

Soy-based supplement to normal diet

  • Dietary Supplement Soy

Milk Experimental

Milk-based supplement to normal diet

  • Dietary Supplement Milk

Criteria

Inclusion Criteria:

Body mass index (BMI) 25-29.9 (n=10); 30-34.9 kg/m2 (n=10)
Age 18-50 years
Weight stable: no more than 3 kg weight loss during past three months

Exclusion Criteria:

BMI < 25 or >35
Type II diabetes requiring the use of any oral antidiabetic agent and/or insulin (because of confounding effects on ROS)
Adverse response to study foods (lactose intolerance, dairy intolerance, dairy allergy); this will be determined by self-report.
history or presence of significant metabolic disease which could impact on the results of the study (i.e. endocrine, hepatic, renal disease)
history of eating disorder
presence of active gastrointestinal disorders such as malabsorption syndromes
pregnancy or lactation
use of obesity pharmacotherapeutic agents within the last 6 months
use of over-the-counter anti-obesity agents (e.g. those containing phenylpropanalamine, ephedrine and/or caffeine) within the last 6 months
Recent (current or past 12 weeks) use of any psychotropic medication
Recent (past four weeks) initiation of an exercise program
Recent (past twelve weeks) initiation of hormone replacement therapy or change in HRT regimen
Recent (past twelve weeks) initiation of hormonal birth control or change in hormonal birth control regimen
Recent (current or past 12 weeks) history of smoking
No Results Posted