GD-BRAIN: Early Biomarkers of Neurodevelopment in Offspring of Diabetic Mothers

Sponsor
Universidad de Murcia (Other)
Overall Status
Unknown status
CT.gov ID
NCT03032991
Collaborator
Universidad de Granada (Other)
174
1
59
2.9

Study Details

Study Description

Brief Summary

The prospective multicenter study GD-Brain provides a better knowledge on the basis of neurological impairment in children born to mothers with gestational diabetes (GDM). GDM modifies placental structure and affect materno-fetal nutrient transfer. Docosahexaenoic acid (DHA) play an important role on neurodevelopment, and it is reduced in venous cord blood of newborns born to GDM. In previous studies, we have already demonstrated impaired DHA fetal levels not only using label fatty acids with stable isotopes administrated to pregnant women, but also in observational studies in GDM as the prevention of obesity study (PREOBE study) in Granada and other similar study in Murcia. The impaired cord DHA levels were associated to disturbed neurodevelopment in these children during the first year of life. However, it is uncertain the mechanisms underlying this impaired materno-fetal DHA transfer and implications for later life.

The recent publication in Nature Journal of a selective transmembrane carrier for DHA in brain named "major facilitator superfamily domain 2a" (MFSD2a) open new expectations. We detected disturbed MFSD2a levels in placentas from GDM which could be due to structural problems in this organ; inflammation, oxidation and metabolic changes related to diabetes might affect MFSD2a activity. Moreover, it is difficult to know whether disturbed MFSD2a levels in placenta may also indicate altered levels of this carrier in the brain from children born to GDM mothers, which could contribute to neurodevelopment impairment in these subjects. Recent studies also indicate that obesity alters the biosynthesis of eicosanoids derived from DHA, with a decrease of protectins and resolvin of D-series, which have powerful anti-inflammatory properties.

The main aim of this study is to analyse potential differences on neurodevelopment, and brain structure and functioning, in children 8 years old born to GDM respect to those born to healthy normoweight mothers, as well as to identify early biomarkers consistently related to neurodevelopment from early stages of life.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    We will contact to participants from the PREOBE study and Murcia's cohorts study to get involved a total of 174 children at 8 years of age. The results from neurodevelopment evaluation by neuropsychological testing, neurological functions rhythms and neuroimaging (fMRI and DTI) at 8 years old will be associated to clinical and metabolic data recorded during pregnancy.

    As secondary aim, we would discern whether the decrease on DHA levels in offspring of GDM at birth is associated to disturbed neurodevelopment at 8 years old.

    The impact of maternal diabetes on placental MFSD2a and children's resolvin and protectins derived from DHA will be measured in urine samples at 8 years old.

    Gut microbiota composition and function will be also studied to detect its role in the potential disturbances regarding the production of anti-inflammatory mediators.

    A part from the clinical study, we will perform an intervention trial using animal models. Gestational rats with diabetes and control rats will be treated with antioxidants and adipoRon in order to delay neuro-degeneration in these animals because of the diabetes, as well as their influence on MFSD2a levels in placenta and brain. All these studies may provide to the industry of valuable information to improve nutritional supplements during gestation or infancy to avoid potential delay of cognitive functions in offspring of diabetic mothers.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    174 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Early Biomarkers of Neurodevelopment in Offspring of Diabetic Mothers (GD-BRAIN)
    Study Start Date :
    Jan 1, 2016
    Anticipated Primary Completion Date :
    Dec 1, 2020
    Anticipated Study Completion Date :
    Dec 1, 2020

    Arms and Interventions

    Arm Intervention/Treatment
    Control

    Children at 8 years old born from healthy pregnancies

    GDM

    Children at 8 years old born from mothers with gestational diabetes during pregnancy

    Outcome Measures

    Primary Outcome Measures

    1. Neuropsychological battery [8 years old]

      Neuropsychological battery to cover different neuropsychological domains: processing speed, memory, attention, language, executive functions, and behaviour (parent-completed measure).

    2. Neuroimaging ( functional MRI) [8 years]

      Anatomical magnetic resonance imaging (fMRI)

    3. Electroencephalography (EEG) [8 years]

      Stereotyped electrophysiological response to several external stimulus

    Secondary Outcome Measures

    1. Fatty acids [8 years old]

      Fatty acid profile in oral mucose

    2. Metabolomic [8 years old]

      Prostaglandins, thromboxans, isoprostanes, resolvin in urine samples

    Other Outcome Measures

    1. Microbiome [8 years old]

      Metagenome

    2. Maturation of circadian rhythm [8 years old]

      Analysis of the circadian rhythm of temperature, activity and sleep

    3. Nutritional evaluation [8 years old]

      Dietary assessment by food frequency questionnaire and by 3 day of dietary record

    4. Physical activity [8 years old]

      questionnaires

    5. Physical Activity [8 years old]

      Accelerometers will be used also to record activity of the subjects

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    8 Years to 9 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Children from healthy pregnancies and GDM pregnancies from the ^PREOBE study and GDM Murcia study.
    Exclusion Criteria:

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Elvira Larqué Murcia Spain 30100

    Sponsors and Collaborators

    • Universidad de Murcia
    • Universidad de Granada

    Investigators

    • Principal Investigator: Elvira Larqué, Dr., Universidad de Murcia
    • Principal Investigator: Cristina Campoy, MD, Universidad de Granada

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Elvira Larqué, Professor, Universidad de Murcia
    ClinicalTrials.gov Identifier:
    NCT03032991
    Other Study ID Numbers:
    • SAF2015-69265
    First Posted:
    Jan 26, 2017
    Last Update Posted:
    Jan 26, 2017
    Last Verified:
    Jan 1, 2017
    Keywords provided by Elvira Larqué, Professor, Universidad de Murcia
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 26, 2017