Gestational Diabetes Clinical Trial
Official title:
Breast Milk Hormones and Early Infant Growth of Women With Gestational Diabetes Mellitus
Background: Breastfeeding has been associated with attenuated risk of obesity and type 2
diabetes in children born to women with diabetes. However, breast milk (BM) components
responsible for the protective effects remain to be unveiled.
Objective: To evaluate the hormone concentrations in BM of women with gestational diabetes
mellitus (GDM) and their influence on early infant growth.
Design: The investigators followed nulliparous women with and without GDM and their
breastfed term singletons. Women diagnosed with GDM received dietary therapy or insulin
injection to maintain euglycemia during pregnancy. Hormone concentrations in BM (i.e.,
adiponectin, leptin, insulin, and ghrelin) were tested and infant growth was evaluated on
days 3, 42 and 90. The investigators compared the hormone concentrations between the GDM and
healthy groups, and tested the associations of hormone concentrations with maternal factors
(i.e., BMI, plasma glucose concentration, gestational age, and delivery mode) and early
infant growth.
Hypothesis: Hormone concentrations in BM could be determined by multiple maternal factors,
including metabolic and obstetrical factors. GDM should be a significant influencing factor
for hormone concentrations in BM.
Subjects Nulliparous women with GDM and healthy women, who intended to exclusively
breastfeed their singletons, were recruited consecutively from the obstetric wards at the
Peking Union Medical College Hospital and the Beijing Obstetrics and Gynecology Hospital
during the 37th gestational week. The exclusion criteria were: pre-pregnancy diabetes, fetal
anomaly, gestational hypertension, preeclampsia, fetal growth restriction, ruptured
membranes, postpartum glucose abnormalities (see below), and introduction of formula feeding
during the follow-ups. Women with plasma glucose>7.8mmol/L in the 1-hour 50g glucose load
test (GLT) during the 24th-28th gestational weeks underwent a 3-hour 100g diagnostic oral
glucose tolerance test (OGTT) following a 12-hour overnight fast. GDM was diagnosed if two
or more plasma glucose reads in the OGTT equaled or exceeded the threshold according to
Carpenter and Coustan. All subjects diagnosed with GDM initially received dietary therapy to
attain glycemic targets: 3.3-5.6 mmol/L at fasting, 3.3-5.8 mmol/L pre-prandially, 4.4-6.7
mmol/L 2-hours post-prandially, and 4.4-6.7 mmol/L at night. The participants were followed
by dietitians to ensure euglycemia, appropriate weight gain, and adequate nutritional
intake. The participants who did not attain glycemic targets in 2 weeks after starting the
dietary therapy were given insulin via injection. As macronutrients in BM were mainly
determined by the maternal glucose metabolic status, the investigators excluded women with
postpartum glucose abnormalities, i.e., impaired glucose tolerance (IGT) with the 2-hour
plasma glucose between 7.8 and 11.0 mmol/l and type 2 diabetes with the 2-hour plasma
glucose ≥11.1 mmol/l in the 75g OGTT on postpartum day 42.
Anthropometric measurements Data was recorded using customized case report forms. Obstetric
data, such as glycemic tests, gestational age, and mode of delivery, were retrieved from the
medical records. Pre-pregnancy weight was self-reported. Mothers' height was measured twice
to the nearest 0.1 cm with a wall-mounted stadiometer. Mothers' weight was measured twice to
the nearest 0.1 kg with a medical balance scale before delivery, on postpartum days 42 and
90. The weight, length, and head circumference of the infants were measured at birth, on
days 42 and 90. The infants were weighed twice in nude using a precision scale (Seca, CA,
USA). Body length and head circumference were measured twice to the nearest 0.1 cm with a
length board and non-stretchable measuring tapes (Seca, CA, USA). The mean values of the two
readings were used for data analysis.
Milk sample collection, processing, and laboratory tests Colostrum samples were collected
between 8 a.m. and 9 a.m. before infant feeding on the third day after delivery. Mature
milk, including both foremilk and hindmilk, was delivered and collected from one breast
before infant feeding using an electric pump (Medela, Baar, Switzerland) between 2 p.m. and
4 p.m. on days 42 and 90 in the clinics. The milk samples were frozen immediately in
sterilized plastic tubes at -80°C. Before quantifying the hormones in BM, the samples were
thawed at 4°C, sonicated, and centrifuged. The samples were sonicated using a sonicator
(Braun-sonic sonicator, B. Braun, Melsungen, Germany) at 50 watts for 3 bursts with
10-second intervals, and centrifuged at 100,000g for 1 hour at 4°C. The supernatant fat was
discarded and the skim milk was used for quantifying adiponectin, leptin, insulin, and
ghrelin by ELISA at the Key Laboratory of Endocrinology in the Peking Union Medical College
Hospital. The assay had an intra- and inter-assay CV of <5.4 and <8.5% for adiponectin, and
<7.4% and <9.3% for leptin, respectively. The insulin assay had no cross-reactivity to
proinsulin (<0.05%), and had sensitivity of 0.5 mU/L and an inter-assay CV of <9.0%. Total
ghrelin was tested using the total human ghrelin ELISA kit (Millipore, USA). The intra- and
inter-assay CVs for the ghrelin assay were <1.9% and <7.7%.
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