Lactation Clinical Trial
Official title:
Maternal Transmission of Dietary Sugars in Breast Milk
Verified date | January 2017 |
Source | University of Oklahoma |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The majority of pregnant women in the United States are either overweight or obese at
conception with their offspring having greater adiposity at birth, a 2-fold greater risk of
later obesity and neonatal insulin resistance.
Conventional wisdom holds that breast-milk composition is uniform; recently our group has
questioned this. An increase in consumption of dietary sugars including fructose over the
past 30 years has risen, and this has been associated with chronic metabolic and endocrine
disorders and phenotypic alterations that promote obesity and diabetes. However, no prior
studies have examined how maternal increases of sugars/fructose during lactation affects
breast-milk composition with potential transmission to the infant. The objective of this
proposal is to comprehensively assess the presence and pharmacokinetics of sugars, including
fructose in human breast-milk in response to maternal consumption. The central hypothesis is
that a graded, dose-response relationship be-tween maternal adiposity and sugar
concentrations in breast-milk exist and that milk fructose concentrations are associated
with altered body composition in the first months of life. This proposal, guided by
compelling preliminary data will examine the evidence linking high intakes of milk fructose
with altered metabolism and early obesity by pursuing two Specific Aims: 1) Test novel
relationships between breast-milk sugars and changes in infant fat mass and 2) Characterize
the pharmacokinetics of milk sugars after consuming a 20 oz. cola. These aims are
significant given the intractability of obesity/diabetes and a potentially identifiable
novel target, making for a clear but powerful public message to reduce sugary beverage
consumption during lactation.
Status | Completed |
Enrollment | 41 |
Est. completion date | December 2016 |
Est. primary completion date | June 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 45 Years |
Eligibility |
Inclusion Criteria: - Exclusively lactating mothers - Mothers must be 3 weeks to 6 weeks postpartum Exclusion Criteria: - Smoked during pregnancy or are currently smoking - Unable to provide breast milk samples using a breast pump |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University of Oklahoma |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Fructose in breast milk will be measured in human breast milk at one month. | Breast milk fructose at one month will be analyzed. | One month | |
Primary | The change in fructose in breast milk from one to six months. | The potential change in breast milk fructose from one to six months will be investigated. | Six months | |
Secondary | Breast milk fructose will be measured after the ingestion of a regular 20 ounce bottle of coke and a 12 ounce can of diet rite. | After the ingestion of either a regular 20 ounce bottle of coke or a 12 ounce can of diet rite at ~ 6:00 am a milk sample will be obtained every hour until 12:00 pm. | 6 hours. |
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