Dietary Carbohydrate Type and Cardiovascular Disease (CVD) Risk Indicators
NCT ID: NCT01610661
Last Updated: 2018-07-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
10 participants
INTERVENTIONAL
2012-01-31
2017-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
SINGLE
Study Groups
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Unrefined-carbohydrate
unrefined carbohydrate diet
Diet
Unrefined-carbohydrate refers to foods made with 100% whole grains (wheat, rice, corn). Refined-carbohydrate refers to foods made with white flour (e.g., bread, pasta) or white rice. Simple-carbohydrate refers to foods made with sucrose (50% glucose/50% fructose) and high-fructose corn syrup.
Refined-carbohydrate
refined carbohydrate diet
Diet
Unrefined-carbohydrate refers to foods made with 100% whole grains (wheat, rice, corn). Refined-carbohydrate refers to foods made with white flour (e.g., bread, pasta) or white rice. Simple-carbohydrate refers to foods made with sucrose (50% glucose/50% fructose) and high-fructose corn syrup.
Simple-carbohydrate
simple carbohydrate diet
Diet
Unrefined-carbohydrate refers to foods made with 100% whole grains (wheat, rice, corn). Refined-carbohydrate refers to foods made with white flour (e.g., bread, pasta) or white rice. Simple-carbohydrate refers to foods made with sucrose (50% glucose/50% fructose) and high-fructose corn syrup.
Interventions
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Diet
Unrefined-carbohydrate refers to foods made with 100% whole grains (wheat, rice, corn). Refined-carbohydrate refers to foods made with white flour (e.g., bread, pasta) or white rice. Simple-carbohydrate refers to foods made with sucrose (50% glucose/50% fructose) and high-fructose corn syrup.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* \> 50 years (all females postmenopausal, as defined by complete natural cessation of menses for \> 12 months or a bilateral oophorectomy)
* BMI \> 25 and \< 35 kg/m2
* Normal kidney function as assessed by serum creatinine and blood urea nitrogen
* Normal liver function as assessed by serum glutamic oxaloacetic transaminase and alkaline phosphatase
* Normal thyroid function as assessed by serum thyroid stimulating hormone concentrations
* Normal gastrointestinal function
* Fasting plasma glucose concentrations \< 120 mg/dL
* Normotensive with or without medication
* Non-smoker for at least 12 months
* Alcohol intake of less than 7 drinks per week
* Consistent physical activity pattern
Exclusion Criteria
* BMI \< 25 and \> 35 kg/m2
* LDL cholesterol \<100 mg/dL
* Abnormal fasting plasma glucose levels \>120 mg/dL
* Use of medications known to affect lipid metabolism:
* Bile Acid Sequestrants (Cholestyramine, Colestipol, Colesevelam, etc.)
* Cholesterol Absorption Inhibitors (Ezetimibe \[Zetia\])
* Nicotinic Acid Agents (Niacin, Niacor, Slo-Niacin, etc)
* Fibrates (Gemfibrozil \[Lopid\], Ciprofibrate, Fenofibrate \[Tricor\], etc)
* Probucol
* Use of anticoagulants (Coumadin, Heparin, Plavix, etc), anabolic steroids, and hydrocortisone
* Use of hormone therapy medications containing estrogen
* Use of fish oil / omega-3 supplements, and Metamucil (or fiber containing dietary supplements)
* Any Aspirin, non-steroidal anti-inflammatory drugs (NSAID) or antihistamine use or therapies that cannot be discontinued by subject for 72 hours prior to blood draws and adipose tissue collection and any NSAIDS for 72 hours after the procedure for obtaining adipose tissue sample
* Established cardiovascular disease as defined by history of myocardial infarction, stroke, heart failure, coronary artery bypass graft, stenosis \>50%, angina and peripheral arterial disease
* Uncontrolled hypertension or high blood pressure reading at the discretion of the study physician or nurse
* Renal or kidney disease, as defined by a history of chronic kidney disease or by glomerular filtration rate of \< 60 ml.min/1.73 m2 calculated from screening blood tests
* Liver disease, as defined by a history of chronic hepatitis B or C, cholestatic or cirrhotic liver disease, nonalcoholic fatty liver disease, elevations of serum glutamic-pyruvic transaminase (SGPT) or serum glutamic oxaloacetic transaminase (SGOT) greater than 1.5 times the upper limit of normal at screening, bilirubin greater than 2 mg/dL (in the absence of benign causes of elevated bilirubin such as Gilbert's syndrome) at screening, or albumin below the lower limit of normal
* Hypothyroidism or hyperthyroidism, defined as screening TSH outside of normal ranges (\<0.4 or \>4.5), unless controlled with medication for at least 6 months
* Type I and II diabetes
* Gastrointestinal disease
* Lidocaine Allergy
* Smoking within the past 12 months.
* Alcohol intake \> 7 drinks per week or unwillingness to not consume alcohol while participating in the study
* Unwillingness to maintain body weight during participation in the study
* Unwillingness to adhere to diet and study protocol
* Weight gain or loss of more than 15 lb within 6 months prior to enrollment
* Non-English speaking subjects
* No Social Security number
* Food allergies or aversions
* Blood donation within the past 8 weeks
50 Years
ALL
Yes
Sponsors
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Tufts University
OTHER
Responsible Party
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Principal Investigators
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Alice H. Lichtenstein, D.Sc.
Role: PRINCIPAL_INVESTIGATOR
Tufts University
Locations
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Jean Mayer Human Nutrition Research Center on Aging
Boston, Massachusetts, United States
Countries
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References
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Faits T, Walker ME, Rodriguez-Morato J, Meng H, Gervis JE, Galluccio JM, Lichtenstein AH, Johnson WE, Matthan NR. Exploring changes in the human gut microbiota and microbial-derived metabolites in response to diets enriched in simple, refined, or unrefined carbohydrate-containing foods: a post hoc analysis of a randomized clinical trial. Am J Clin Nutr. 2020 Dec 10;112(6):1631-1641. doi: 10.1093/ajcn/nqaa254.
Meng H, Matthan NR, Fried SK, Berciano S, Walker ME, Galluccio JM, Lichtenstein AH. Effect of Dietary Carbohydrate Type on Serum Cardiometabolic Risk Indicators and Adipose Tissue Inflammatory Markers. J Clin Endocrinol Metab. 2018 Sep 1;103(9):3430-3438. doi: 10.1210/jc.2018-00667.
Other Identifiers
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2735
Identifier Type: -
Identifier Source: org_study_id
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