Gestational Obesity and Interventions With Probiotics or Fish Oil Trial
GOPROFIT
Impact of Fish Oil or Probiotic Intake on Maternal Obesity and Molecular Biomarkers in the Placenta
1 other identifier
interventional
80
1 country
1
Brief Summary
Obesity is one of the most concerning health issues in the modern world, especially due to its association with greater risk of developing a wide range of chronic diseases. Pre-gestational obesity may increase the chances of maternal and fetal morbimortality, such as gestational diabetes mellitus, preeclampsia, macrosomia and, even, fetal death. It may also lead to long term disorders, enhancing the risk of excessive adiposity and metabolic syndrome in later life and, thus, contributing to the maintenance of the obesity cycle and its health effects through the subsequent generations. Alterations in placental function are thought to be deeply involved in this scenario, however further research on its molecular and biological mechanisms is needed. During pregnancy, there is a physiological enhancement of the inflammatory state, marked by higher circulating cytokines and macrophage placental infiltration, which favors fetal nutrient supply and adequate growth; however, this response is exacerbated in women with pre-pregnancy obesity, leading to adverse outcomes. In this context, interventions aiming to reduce excessive inflammation may prevent or minimize the negative impact of pre-pregnancy obesity on both maternal and offspring's health. There is strong evidence suggesting an important role of n-3 LC-PUFA (EPA and DHA) on the attenuation and resolution of inflammatory states, besides influencing maternal lipid profile, fetal and infant adipogenesis and neurodevelopment. Additionally, the consumption of probiotic supplements during gestation seams to promote adequate maternal weight gain and improve the profile of inflammatory molecules secreted in the milk. Therefore, the nutritional interventions with fish oil, as a source of EPA and DHA, or probiotics, in women with pre-pregnancy obesity, may change the intrauterine environment and reduce the risk of both short and long term metabolic disorders. This study aims to investigate the metabolic and molecular changes promoted by gestational obesity and evaluate the effectiveness of different dietary interventions (fish oil or probiotic) on preventing or minimizing such alterations. We expect to contribute to the understanding of the physiological and molecular mechanisms underlying maternal obesity and its association with adverse pregnancy outcomes, associated with increased risk of chronic diseases in adulthood.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable obesity
Started Mar 2015
Typical duration for not_applicable obesity
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2015
CompletedFirst Submitted
Initial submission to the registry
July 10, 2017
CompletedFirst Posted
Study publicly available on registry
July 12, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2017
CompletedJuly 12, 2017
July 1, 2017
2.5 years
July 10, 2017
July 10, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Association between maternal obesity and systemic Inflammation in the Mother and the Activation of Placental Inflammatory Pathways
28 weeks
Association between fish oil intake in obese mothers and systemic Inflammation in the Mother and the Activation of Placental Inflammatory Pathways
28 weeks
Investigation of the effects of fish oil supplementation on the metabolome of maternal serum, umbilical cord serum and placenta in obese pregnant women.
The metabolome of maternal serum, umbilical cord serum and placenta of obese and healthy pregnant women was analyzed by nuclear magnetic resonance.
28 weeks
Association between probiotic supplementation and bacterial colonization in the maternal intestinal and vaginal microbiota
Evaluation of the maternal intestinal and vaginal microbiota through the quantification of bacteria
36 weeks
Secondary Outcomes (3)
Association between maternal obesity and placental fatty acid transporter expression
28 weeks
Association between fish oil intake in obese mothers and placental fatty acid transporter
28 weeks
Association between maternal inflammatory status and pregnancy outcomes
28 weeks
Study Arms (4)
Eutrophy Control
PLACEBO COMPARATORGelatin capsules a day, from 28ª week to 36ª week gestation.
Eutrophy+ Probiotic
EXPERIMENTALCapsules gastro resistant containing 2.5 billions colony forming unit (UFC) Lactobacillus rhamnosus GG + 2.5 billions colony forming unit (UFC) Bifidobacterium bifidum a day, from 28ª week to 36ª week gestation
Obesity + Fish oil
EXPERIMENTALDHA (100 mg) + EPA (137 mg) a day, from 13ª week gestation to 36ª week gestation
Obesity + Probiotic
EXPERIMENTAL2.5 billions colony forming unit (UFC) Lactobacillus rhamnosus GG + 2.5 billions colony forming unit (UFC) Bifidobacterium bifidum a day, from 28ª week to 36ª week gestation
Interventions
Eligibility Criteria
You may qualify if:
- aged between 19 and 40 years
- gestational age of 13 weeks;
- BMI prepregnancy greater than 29.9 and less than 40 kg / m² \[ degrees obesity 1 and 2, according to the World Health Organization (WHO, 2002) \] or prepregnancy BMI between 18.5 and 24 9 kg / m² \[ eutrophic ( WHO, 2002 ) \]
- be free of chronic diseases (hypertension , cardiovascular disease, type 2 diabetes , thyroid diseases , cirrhosis , chronic hepatitis and chronic renal failure
- be free of infectious and parasitic diseases
- present gestation single fetus
- not being a smoker
- do not consume alcoholic beverages
- do not consume supplement containing AG
You may not qualify if:
- receive confirmation of diagnosis of chronic noncommunicable diseases (except obesity) and / or infectious
- pregnant women who did not complete all the steps provided for in the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Universidade Federal do Rio de Janeirolead
- Maternidade Escola da UFRJcollaborator
Study Sites (1)
Maternidade Escola da Universidade Federal do Rio de Janeiro
Rio de Janeiro, Rio de Janeiro, 22240-000, Brazil
Related Publications (38)
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PMID: 24132975RESULT
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
FĂ¡tima LĂºcia C Sardinha, PhD
Instituto de NutriĂ§Ă£o JosuĂ© de Castro/ UFRJ
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
July 10, 2017
First Posted
July 12, 2017
Study Start
March 1, 2015
Primary Completion
September 1, 2017
Study Completion
December 1, 2017
Last Updated
July 12, 2017
Record last verified: 2017-07