Role of Macronutrient Diet Composition and Infant Metabolic Outcomes in Gestational Diabetes
Status: | Completed |
---|---|
Conditions: | Diabetes |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | 18 - 40 |
Updated: | 7/11/2015 |
Start Date: | August 2007 |
End Date: | June 2013 |
Contact: | Linda A Barbour, MD, MSPH |
Email: | lynn.barbour@ucdenver.edu |
Phone: | 303-724-3954 |
Role of Macronutrient Diet Composition on Maternal and Infant Metabolic Outcomes in Gestational Diabetes
A better understanding of the optimal diet for women with gestational diabetes is
fundamental to the management of this rapidly growing problem in pregnancy. Careful
comparison studies of the current low- carbohydrate, higher-fat diet versus a diet higher in
complex carbohydrate but lower in fat is critical in order to determine which diet results
in a more favorable maternal 24-hour glucose, lipid, and inflammatory profile, all of which
directly effect optimal fetal growth and may influence the future health of the offspring.
fundamental to the management of this rapidly growing problem in pregnancy. Careful
comparison studies of the current low- carbohydrate, higher-fat diet versus a diet higher in
complex carbohydrate but lower in fat is critical in order to determine which diet results
in a more favorable maternal 24-hour glucose, lipid, and inflammatory profile, all of which
directly effect optimal fetal growth and may influence the future health of the offspring.
Despite the doubling in the prevalence of gestational diabetes mellitus (GDM) over the last
10 years, dietary management guidelines remain ambiguous due to the paucity of randomized
controlled trials. New diagnostic criteria recently developed for the diagnosis of GDM are
expected to increase the prevalence to 10-15% of all pregnant women. There is growing
recognition that GDM has long-term implications on maternal risk for diabetes and that the
intrauterine GDM environment is an independent risk factor for childhood obesity and
impaired glucose tolerance. Yet, how diet can be used to modify fetal fuel and attenuate
this risk remains unknown in humans. Fundamental to the management of GDM is dietary
intervention, yet the historic practice of advising a low-carbohydrate (CHO), higher-fat
diet has not been sufficiently tested. Both animal and non-human primate data support a
fetal programming influence that maternal high-fat diets may promote insulin resistance,
glucose intolerance, and hepatic steatosis in the offspring. Recent human data suggest that
high maternal triglycerides (TG) and free fatty acids (FFA), variables sensitive to dietary
manipulation, are independent risk factors for fetal macrosomia and adiposity. As a result,
consensus groups have abandoned any specific diet recommendations for women with GDM.
Despite the pivotal role of diet therapy in the treatment of GDM, no randomized trials have
directly compared glycemic and lipoprotein profiles of the conventional higher-fat diet with
any other diet. To address this critical need, the aims of this randomized cross-over trial
are to study the effects of a high complex carbohydrate/low-fat diet (HC/LF; 60% CHO, 25%
fat, 15% protein) compared to the usual care, low-CHO/higher fat diet (LC/HF; 40% CHO, 45%
fat, and 15% protein) in GDM women on: 1) 72-hour glycemic profiles using a continuous
glucose monitoring system within subjects; 2) postprandial lipemia by measuring serial
plasma TG and FFA over a 5-hour, post-breakfast meal period within subjects; and 3) maternal
lipoproteins, inflammatory profiles, and in-vitro adipose tissue lipolysis after 6-8 weeks
of diet therapy between subjects. We will also measure neonatal adiposity by air
displacement plethysmography and newborn markers of lipid peroxidation, inflammation, and
dietary fat intake in the babies born to mothers with GDM. This pilot study will directly
test which GDM diet is most effective in limiting maternal hyperglycemia and hyperlipidemia
in a randomized controlled fashion, potentially optimizing fetal substrate availability and
fetal growth. Our goal is to determine which diet intervention might favorably impact a
cycle that could otherwise perpetuate future diabetes, obesity, and CVD in both mother and
offspring.
10 years, dietary management guidelines remain ambiguous due to the paucity of randomized
controlled trials. New diagnostic criteria recently developed for the diagnosis of GDM are
expected to increase the prevalence to 10-15% of all pregnant women. There is growing
recognition that GDM has long-term implications on maternal risk for diabetes and that the
intrauterine GDM environment is an independent risk factor for childhood obesity and
impaired glucose tolerance. Yet, how diet can be used to modify fetal fuel and attenuate
this risk remains unknown in humans. Fundamental to the management of GDM is dietary
intervention, yet the historic practice of advising a low-carbohydrate (CHO), higher-fat
diet has not been sufficiently tested. Both animal and non-human primate data support a
fetal programming influence that maternal high-fat diets may promote insulin resistance,
glucose intolerance, and hepatic steatosis in the offspring. Recent human data suggest that
high maternal triglycerides (TG) and free fatty acids (FFA), variables sensitive to dietary
manipulation, are independent risk factors for fetal macrosomia and adiposity. As a result,
consensus groups have abandoned any specific diet recommendations for women with GDM.
Despite the pivotal role of diet therapy in the treatment of GDM, no randomized trials have
directly compared glycemic and lipoprotein profiles of the conventional higher-fat diet with
any other diet. To address this critical need, the aims of this randomized cross-over trial
are to study the effects of a high complex carbohydrate/low-fat diet (HC/LF; 60% CHO, 25%
fat, 15% protein) compared to the usual care, low-CHO/higher fat diet (LC/HF; 40% CHO, 45%
fat, and 15% protein) in GDM women on: 1) 72-hour glycemic profiles using a continuous
glucose monitoring system within subjects; 2) postprandial lipemia by measuring serial
plasma TG and FFA over a 5-hour, post-breakfast meal period within subjects; and 3) maternal
lipoproteins, inflammatory profiles, and in-vitro adipose tissue lipolysis after 6-8 weeks
of diet therapy between subjects. We will also measure neonatal adiposity by air
displacement plethysmography and newborn markers of lipid peroxidation, inflammation, and
dietary fat intake in the babies born to mothers with GDM. This pilot study will directly
test which GDM diet is most effective in limiting maternal hyperglycemia and hyperlipidemia
in a randomized controlled fashion, potentially optimizing fetal substrate availability and
fetal growth. Our goal is to determine which diet intervention might favorably impact a
cycle that could otherwise perpetuate future diabetes, obesity, and CVD in both mother and
offspring.
Inclusion Criteria:Inclusion Criteria. Potential participants will be ≥ 0-36 years old,
which includes the offspring of the pregnant mothers with GDM. Pregnant women will be
between the ages of 18-40 years and will have a BMI of 26 - 35 kg/m2 at the time of
diagnosis, a singleton pregnancy, and will not be taking medication for their GDM on
entrance to the study. Subjects will have been diagnosed with GDM according to the
criteria established by the ADA and the ACOG (19;35;53), specifically, they will meet the
following criteria:
- A 50-gram Glucola in which the one hour reading is >200 mg/dL and the FBG is >95
mg/dL
- Two abnormal values on a 100-gram 3 hour glucose tolerance test based on the Coustan
and Carpenter criteria as adopted by the ADA and Fourth International Workshop on
Gestational Diabetes (76;77):
- Fasting > or = to 95 mg/dL but <126 mg/dL
- 1 hr >/= 180 mg/dL
- 2 hr >/= 155 mg/dL
- 3 hr >/=140 mg/dL
Exclusion Criteria:Those women with overt diabetes and those suspected of having
preexisting diabetes by any of the following criteria will be excluded, including:
- Fasting glucose >110 mg/dL, due to the high likelihood of rapidly failing diet and
requiring medical treatment (35).
- Random glucose > 200 mg/dL
- Glycosylated hemoglobin A1C > 6.5
- Non-English speaking patient
- Fasting TG > 400 mg/dL
Women who smoke will be excluded since this is the leading cause of low birth weight. In
addition, women with other risk factors for placental insufficiency, including
hypertension requiring beta-blocker treatment, renal disease, thrombophilias,
preeclampsia, steroid use, history of pancreatitis or infectious disease such as
hepatitis, or intrauterine growth restriction will be excluded.
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We found this trial at
1
site
13001 E 17th Pl
Aurora, Colorado 80045
Aurora, Colorado 80045
(303) 724-5000
University of Colorado Anschutz Medical Campus Located in the Denver metro area near the Rocky...
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