Gestational Diabetes Clinical Trial
Official title:
Association Between Trimethylamine-N-oxide Levels and Risk of Gestational Diabetes Mellitus
Verified date | January 2018 |
Source | Huazhong University of Science and Technology |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Background: The microbiota-dependent metabolite trimethylamine-N-oxide (TMAO) has been
reported as a novel and independent risk factor for the development of cardiovascular and
metabolic diseases, but the association with gestational diabetes mellitus (GDM) remains
unclear.
Objective: To investigate the association between plasma TMAO concentration and GDM in a
two-phase study.
Design: The initial discovery phase included 866 pregnant women (433 GDM cases and 433
matched controls) in Wuhan China. Study participants were recruited from pregnant women who
attended the outpatient clinics of the Department of Endocrinology, Tongji Hospital, to
screen for GDM between August 2012 and April 2015, or pregnant women who visited the Hubei
Maternal and Child Health Hospital or the Central Hospital of Wuhan for a routine antenatal
checkup from May 2014 to November 2016. The inclusion criteria of participants were: age ≥ 20
years, gestational age between 24 and 32 weeks, no history of a diagnosis of diabetes or
gestational diabetes, and no history of receiving pharmacological treatment known to affect
glucose metabolism. An independent replication phase study was nested within an ongoing
prospective cohort study, namely the Tongji Maternal and Child Health Cohort (TMCHC).
Beginning in January 2013, women receiving prenatal care prior to 16 weeks of gestation were
invited to join the TMCHC. Exclusion criteria included pre-pregnancy diabetes, clinically
significant neurological, endocrinological or other systemic diseases and multiple
pregnancies. All enrolled pregnant women received a regular prenatal checkup in hospital and
underwent an oral glucose tolerance test (OGTT) during 24-32 weeks of gestation to screen for
GDM. 276 members who developed GDM before May 2016 and had fasting blood collected before 20
weeks'gestation were included as cases in this analysis. Two controls were individually
matched to each case from among women without GDM. These two studies were approved by the
ethics committee of Tongji Medical College. All the participants gave informed written
consent before they were included in the study. Plasma TMAO concentrations were determined by
stable isotope dilution liquid chromatography with online electrospray ionization tandem mass
spectrometry.
Status | Completed |
Enrollment | 1694 |
Est. completion date | June 30, 2017 |
Est. primary completion date | November 30, 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 20 Years to 45 Years |
Eligibility |
Inclusion Criteria: - Age = 20 years; - Screened for GDM during 24-32 weeks of gestation; - With fasting blood samples collected before 20 weeks of gestation (only for nested case-control subjects). Exclusion Criteria: - History of a diagnosis of diabetes or gestational diabetes; - History of receiving pharmacological treatment known to affect glucose metabolism; - Clinically significant neurological, endocrinological or other systemic diseases and multiple pregnancies. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Huazhong University of Science and Technology |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Gestational diabetes mellitus | Glucose intolerance with onset or first diagnosis during pregnancy | During 24-32 weeks of gestation |
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