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This study will evaluate the effects of whole vs. nonfat milk consumption on body composition, cardiometabolic disease risk factors, and dietary quality.
Background The optimal type of milk is a topic of much debate. Several recent observational studies indicate that consuming whole (full-fat), compared to reduced-fat milk, is associated with less weight gain and decreased cardiometabolic disease risk. The observed beneficial effect of consuming whole milk on body weight may be due to its greater satiety value, leading to consumption of fewer calories from other lower quality (e.g., sugary) foods. Mechanistic studies indicate that substitution of carbohydrate with certain saturated fatty acids in milk increases low-density lipoprotein cholesterol (LDL-C). However, this increase has been attributed to large, buoyant particles that are less atherogenic than small, dense particles; is accompanied by an increase in high-density lipoprotein cholesterol (HDL-C); and may not elevate overall risk compared to carbohydrate.
Specific Aims and Hypotheses
Design Randomized Controlled Trial. Participants (N=200, aged 9 to 12 years, BMI≥75th percentile) will be randomly assigned for 1 year to receive: 1) Whole milk, 3 cups/d or 2) Nonfat milk, 3 cups/d. To promote adherence to the interventions, the investigators will rely on home delivery of milk using methods consistent with previous successful studies.
Study Outcomes The primary outcome is change in fat mass measured by air displacement plethysmography (BodPod) at 3 time points (baseline and 6 and 12 months). To evaluate cardiometabolic disease risk factors, the investigators will obtain a plasma MetaboProfile®(LabCorp) that includes lipoprotein particle sizes and subfraction concentrations, novel measures of insulin-resistant dyslipoproteinemia and inflammation, and a conventional lipid profile. The investigators will also measure blood pressure.
For the Ancillary Study, outcomes include salivary cariogenicity (pH, flow, and buffering capacity); caries prevalence; dietary quality (cariogenic potential); and serum 25-hydroxyvitamin D.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Whole milk | Experimental | 3 cups a day of whole milk for 1 year |
|
| Nonfat milk | Experimental | 3 cups a day of nonfat milk for 1 year |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Whole milk | Behavioral | Weekly home delivery of whole milk, daily text messages, monthly virtual visits |
|
| Measure | Description | Time Frame |
|---|---|---|
| Fat mass | Primary outcome for the overall study, main outcome for Specific Aim #1, measured by air displacement plethysmography (BodPod) | Change from start of trial (time of randomization) through end of trial (12 months) |
| Measure | Description | Time Frame |
|---|---|---|
| Lean body mass | Measured by air displacement plethysmography (BodPod) | Change from start of trial (time of randomization) through end of trial (12 months) |
| Percent body fat | Measured by air displacement plethysmography (BodPod) |
| Measure | Description | Time Frame |
|---|---|---|
| Pentadecanoic acid (C15:0) | Process measure, biomarker of milk fast consumption, fatty acid in red blood cell membranes which comes primarily from milk fat | Change from start of trial (time of randomization) through end of trial (12 months) |
| Heptadecanoic acid (C17:0) |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Donna L Lesperance, MA, MPH | Contact | 617-919-7305 | Donna.Lesperance@childrens.harvard.edu |
| Name | Affiliation | Role |
|---|---|---|
| Cara B Ebbeling, PhD | Boston Children's Hospital | Principal Investigator |
| David S Ludwig, MD, PhD | Boston Children's Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| New Balance Foundation Obesity Prevention Center | Recruiting | Boston | Massachusetts | 02115 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 18779274 | Background | Albala C, Ebbeling CB, Cifuentes M, Lera L, Bustos N, Ludwig DS. Effects of replacing the habitual consumption of sugar-sweetened beverages with milk in Chilean children. Am J Clin Nutr. 2008 Sep;88(3):605-11. doi: 10.1093/ajcn/88.3.605. | |
| 31901161 | Background | Ebbeling CB. Confusion at the milk cooler: opportunity to bolster the evidence base for preventive nutrition. Am J Clin Nutr. 2020 Feb 1;111(2):240-241. doi: 10.1093/ajcn/nqz319. No abstract available. |
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We will share de-identified IPD on Open Science Framework.
The Study Protocol will be posted prior to enrollment of the first study participant. The IPD and Analytic Code for each peer reviewed manuscript from the study will be posted at the time of publication.
The data will be available to any interested party through Open Science Framework.
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| ID | Term |
|---|---|
| D009765 | Obesity |
| D003920 | Diabetes Mellitus |
| D002318 | Cardiovascular Diseases |
| ID | Term |
|---|---|
| D050177 | Overweight |
| D044343 | Overnutrition |
| D009748 | Nutrition Disorders |
| D009750 | Nutritional and Metabolic Diseases |
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Participants will be randomly assigned for 1 year to receive home delivery of: 1) Whole milk, 3 cups a day or 2) Nonfat milk, 3 cups a day.
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| Nonfat milk | Behavioral | Weekly home delivery of nonfat milk, daily text messages, monthly virtual visits |
|
| Change from start of trial (time of randomization) through end of trial (12 months) |
| Height | Linear growth | Change from start of trial (time of randomization) through end of trial (12 months) |
| Body mass index (BMI) | Weight in kg divided by height in meters squared | Change from start of trial (time of randomization) through end of trial (12 months) |
| Leptin | "Satiety" hormone, released by fat cells, measured by ELISA assay | Change from start of trial (time of randomization) through end of trial (12 months) |
| Ghrelin | "Hunger" hormone, released primarily in the stomach, measured by ELISA assay | Change from start of trial (time of randomization) through end of trial (12 months) |
| Insulin-like growth factor-1 (IGF-1) | Indicator of growth hormone action, measured by ELISA assay | Change from start of trial (time of randomization) through end of trial (12 months) |
| Insulin-like growth factor-binding protein 3 (IGF-BP3) | Measured by ELISA assay | Change from start of trial (time of randomization) through end of trial (12 months) |
| Lipoprotein insulin resistance (LPIR) | Main outcome for Specific Aim #2; a 6-component weighted score of triglyceride-rich, high-density, and low-density lipoprotein particle (TRL-P, HDL-P, LDL-P) sizes and subfraction concentrations (sum of large and very large TRL-P, large HDL-P, small LDL-P), measured by nuclear magnetic resonance spectroscopy | Change from start of trial (time of randomization) through end of trial (12 months) |
| Triglyceride-rich lipoprotein particle (TRL-P) size | Measured by nuclear magnetic resonance spectroscopy | Change from start of trial (time of randomization) through end of trial (12 months) |
| High-density lipoprotein particle (HDL-P) size | Measured by nuclear magnetic resonance spectroscopy | Change from start of trial (time of randomization) through end of trial (12 months) |
| Low-density lipoprotein particle (LDL-P) size | Measured by nuclear magnetic resonance spectroscopy | Change from start of trial (time of randomization) through end of trial (12 months) |
| Sum of large and very large TRL-P concentration | Measured by nuclear magnetic resonance spectroscopy | Change from start of trial (time of randomization) through end of trial (12 months) |
| Large HDL-P concentration | Measured by nuclear magnetic resonance spectroscopy | Change from start of trial (time of randomization) through end of trial (12 months) |
| Small LDL-P concentration | Measured by nuclear magnetic resonance spectroscopy | Change from start of trial (time of randomization) through end of trial (12 months) |
| Large LDL-P concentration | Measured by nuclear magnetic resonance spectroscopy | Change from start of trial (time of randomization) through end of trial (12 months) |
| Triglycerides (TG) | Part of conventional lipid profile | Change from start of trial (time of randomization) through end of trial (12 months) |
| High-density lipoprotein cholesterol (HDL-C) | Part of conventional lipid profile | Change from start of trial (time of randomization) through end of trial (12 months) |
| Low-density lipoprotein cholesterol (LDL-C) | Part of conventional lipid profile | Change from start of trial (time of randomization) through end of trial (12 months) |
| Glucose | Measured enzymatically using hexokinase method | Change from start of trial (time of randomization) through end of trial (12 months) |
| Insulin | Measured by electrochemiluminescence immunoassay | Change from start of trial (time of randomization) through end of trial (12 months) |
| Insulin resistance | Measured by homeostasis model assessment (HOMA), using fasting glucose and insulin concentrations | Change from start of trial (time of randomization) through end of trial (12 months) |
| Adiponectin - total and high molecular weight | Hormone released from fat cells, promotes insulin sensitivity and helps regulate blood glucose, measured by ELISA assay | Change from start of trial (time of randomization) through end of trial (12 months) |
| Hemoglobin A1c (HgA1c) | Marker of blood glucose control, measured using a system based turbidimetric immunoinhibition | Change from start of trial (time of randomization) through end of trial (12 months) |
| High-sensitivity C-reactive protein (hsCRP) | Indicator of chronic inflammation, measured by immunoturbidimetric assay | Change from start of trial (time of randomization) through end of trial (12 months) |
| Interleukin-6 (IL-6) | Protein which stimulates synthesis of hsCRP, measured by ELISA assay | Change from start of trial (time of randomization) through end of trial (12 months) |
| Fibrinogen | Protein involved in blood clotting, measured by immunoturbidimetric assay | Change from start of trial (time of randomization) through end of trial (12 months) |
| Plasminogen activator inhibitor-1 (PAI-1) | Protein involved in blood clotting, measured by ELISA assay | Change from start of trial (time of randomization) through end of trial (12 months) |
| Systolic blood pressure | Measured by auscultation | Change from start of trial (time of randomization) through end of trial (12 months) |
| Diastolic blood pressure | Measured by auscultation | Change from start of trial (time of randomization) through end of trial (12 months) |
| Salivary cariogenicity | (Ancillary Study) Risk for dental caries (cavities), measured using the GC Dental America Saliva-Check Buffer Kit (pH, flow, and buffering capacity) | Change from start of trial (time of randomization) through end of trial (12 months) |
| Caries prevalence | (Ancillary Study) Assessed by clinical examination and digital radiograph (x-rays) | Difference between start of trial (time of randomization) and end of trial (12 months) |
| Serum 25-hydroxyvitamin D [25(OH)D] | (Ancillary Study) Measured by a competitive electrochemiluminescence immunoassay | Change from start of trial (time of randomization) through end of trial (12 months) |
Process measure, biomarker of milk fast consumption, fatty acid in red blood cell membranes which comes primarily from milk fat |
| Change from start of trial (time of randomization) through end of trial (12 months) |
| trans Palmitoleic acid (tC16:1ω-7) | Process measure, biomarker of milk fast consumption, fatty acid in red blood cell membranes which comes primarily from milk fat | Change from start of trial (time of randomization) through end of trial (12 months) |
| Alternative Healthy Eating Index (AHEI) | Main outcome for Specific Aim #3, calculated using data from 24-hour dietary recalls | Change from start of trial (time of randomization) through end of trial (12 months) |
| Milk intake | Process outcome, measured by 24-hour dietary recalls | Change from start of trial (time of randomization) through end of trial (12 months) |
| Nutrient profile | Added sugars, saturated fat, fiber, calcium; measured by 24-hour dietary recalls | Change from start of trial (time of randomization) through end of trial (12 months) |
| Food and beverage intake pattern | Vegetables, fruits, legumes, and sugar-sweetened beverages; measured by 24-hour dietary recalls (Ancillary Study) Frequency of consuming between-meal-sugar-containing foods or beverages and consumption of foods (grams) with a high cariogenic potential, measured by 24-hour dietary recalls | Change from start of trial (time of randomization) through end of trial (12 months) |
| 32053300 | Background | Willett WC, Ludwig DS. Milk and Health. N Engl J Med. 2020 Feb 13;382(7):644-654. doi: 10.1056/NEJMra1903547. No abstract available. |
| D001835 |
| Body Weight |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D004700 | Endocrine System Diseases |