Inflammation, Pregnancy Related
Conditions
Keywords
Inflammation, DHA, Pregnancy, preterm, overweight
Brief summary
Purpose: Determine the effects of maternal docosahexaenoic acid (DHA) supplementation during pregnancy on levels of DHA, synaptamide (novel anti-inflammatory metabolite), and inflammatory biomarkers during pregnancy and at delivery Research Design: Double blind randomized placebo-controlled study of maternal DHA supplementation during pregnancy. Methodology /Technical Approach: Investigators plan to enroll 100 pregnant women with a high risk pregnancy related to (1) a pre-pregnancy Body Mass Index (BMI) of ≥30.0 kg/m2 and/or (2) a history of prior preterm delivery at ≤35+6 weeks gestation. Women will be enrolled between the 8th and 14th week of pregnancy and randomized to receive a once daily DHA supplement (DSM Nutritional Products, Columbia Maryland, DHA capsule 441mg/cap) or a placebo (DSM Nutritional Products, Columbia Maryland, Corn Oil/Soybean oil 50/50 mix) for the duration of the pregnancy. DHA is an omega-3 long chain polyunsaturated fatty acid (LCPUFA) and placebo composed of omega-6 LCPUFA's. Investigators will measure maternal levels of plasma DHA, Synaptamide and inflammatory biomarkers at enrollment, at 26-30 weeks of pregnancy, and from cord blood at delivery. Sociodemographic and clinical characteristics will be collected for each mother from pregnancy onset until discharge following delivery. The infant health record and parental report will be reviewed to record clinical data from birth to 12 months corrected age for short term health outcomes potentially related to inflammation-related morbidities, including growth and development, acute infection requiring hospital admission, and any allergic disorder. All plasma samples will be processed at Dr. Kim's NIAAA/NIH laboratories using high-performance liquid chromatography with tandem mass spectrometry
Detailed description
All pregnant women meeting the inclusion/exclusion criteria will be identified at the time of their regular OB appointments between the 8th and the 14th week of pregnancy (+/- 3 days) Research team members will approach potential subjects to explain the study and obtain consent for their participation Patients who give their consent for enrollment will be asked to complete a dietary survey at the time of enrollment Patients will be given a paper script for study drug to be taken to the Walter Reed Military Medical Center pharmacy to obtain study drug The Investigational Pharmacy will randomize the patients in double blinded fashion to the intervention group or placebo group. Patients in the intervention group will recieve a \ 1000mg capsule containing \ 400mg of DHA. This is not standard of care and is being done for research purposes only Patients in the Placebo group will recieve a \ 1000mg capusle containing no DHA and filled with 50:50 mix of corn and soybean oils. This oil is ubiquitous in the american diet and only a very small amount of additional oil will be ingested for study purposes. Giving pregnant women this oil is not standard of care and is being done for research purposes only The placebo and intervention drugs will be packaged in the same capsule membrane and will be indistinguishable by color, shape, or taste. Patients will be instructed to take 1 capule PO daily until their child is delivered Patients will be issued a 3 month supply of study drug at enrollment and will get refills from the investigational pharmacy ≤5ml of whole blood will be obtained from each subject at enrollment and at 26-30 weeks gestation (+/- 3 days), as part of a routine blood sampling. It is standard of care to collect blood at this point in pregnancy for lab evaluation. The additional tube of blood collected for this study is for research purposes only and not part of the standard of care. This sample will be centrifuged, and the separated plasma will be labeled and frozen at -80° C pending transport to Dr. Kim's lab at the National Institute on Alcohol Abuse and Alcoholism (NIAAA) for bulk analyses. At delivery, ≤5ml of umbilical cord blood will be obtained from an umbilical artery and from the umbilical vein. These samples will be processed and stored in a similar fashion as the earlier samples. Cord blood is a medical waste product, and collection will therefore have no adverse effect for either mother or newborn. It is standard of care to collect cord blood by OB request for lab evaluation. Collecting additional cord blood for this study anaylsis is for research purposes only All enrollees will complete a dietary survey upon enrollment at 8-14 weeks (+/- 3 days), at 26-30th week of pregnancy (+/- 3 days), and during the delivery admission. This survey will also include the subject's self-report on compliance with taking the study supplement All plasma samples collected will be processed at Dr. Kim's National Institute on Alcohol Abuse and Alcoholism/ National Insititute of Health (NIAAA/NIH) laboratories The Cytokine Assays for IL-6, Il-10, TNF- alpha will be run in Dr Kim's lab using Ensyme Linked Immunosorbent Assay (ELISA) testing The DHA and Synaptamide levels will be analyzed in Dr. Kim's lab using High performance liquid chromatrography with tandem mass spectrometry All babies from multiple birth pregnancies will be enrolled in this study The offspring of enrolled women will be followed through 12 months corrected age to assess the longer term outcomes of study intervention Information will be collected from the maternal medical record at time of enrollment, infant delivery and postpartum discharge. Information will be collected from the infant medical record at time of birth discharge, and 12 months corrected age.
Interventions
DIETARY_SUPPLEMENTDHA supplement
Patient's will be randomized to recieve either DHA or 50:50 corn oil/soybean oil supplement as a once daily supplement to be taken from enrollment through delivery of their infant
DIETARY_SUPPLEMENTCorn Oil: Soybean Oil
Patient's will be randomized to recieve either DHA or 50:50 corn oil/soybean oil supplement as a once daily supplement to be taken from enrollment through
Sponsors
National Institutes of Health (NIH)
DSM Nutritional Products, Inc.
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Walter Reed National Military Medical Center
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Masking description
Double blinded, randomized, placebo controlled
Intervention model description
Double Blinded, Randomized, Placebo controlled
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* regnant female military health care beneficiaries ≥18 years of age * Between the 8th and 14th week of pregnancy at enrollment * BMI of ≥30.0 kg/m2 and/or history of previous preterm delivery at \<36 weeks gestation * Planning to deliver at WRNMMC * DEERS-eligible * All infants born to mothers enrolled in this study who do not meet any
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Measure DHA | Sample obtained between 8-14 weeks of pregnancy | Measurement of maternal plasma DHA using tandem mass spec |
| Measure synaptamide | Sample obtained between 8-14 weeks of pregnancy | Measurement of maternal plasma synaptamide using tandem mass spec |
| Measure inflammatory biomarkers | Sample obtained between 8-14 weeks of pregnancy | Measurement of plasma cytokine levels using ELISA human cytokine panel |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Maternal death | From enrollment in study at 8-14 weeks of pregnancy until 6 months after infant delivery | Number of maternal deaths in intervention group vs placebo group |
| Pre-eclampsia | From enrollment in study at 8-14 weeks of pregnancy until 42 weeks of pregnancy or day of infant delivery, whichever happens first | Presence or absence of pre-eclampsia in intervention vs placebo groups |
| chorioamionitis | From enrollment in study at 8-14 weeks of pregnancy until 42 weeks of pregnancy or day of infant delivery, whichever happens first | Presence or absence of chorioamionitis in intervention vs placebo groups |
| Gestational Diabetes Melitus | From enrollment in study at 8-14 weeks of pregnancy until 42 weeks of pregnancy or day of infant delivery, whichever happens first | Presence or absence of Gestational Diabetes Mellitus in intervention vs placebo groups |
| non-gestational Diabetes mellitus | From enrollment in study at 8-14 weeks of pregnancy until 42 weeks of pregnancy or day of infant delivery, whichever happens first | Presence or absence of non-Gestational Diabetes Mellitus in intervention vs placebo groups |
| Preterm Premature Rupture of Membranes | From enrollment in study at 8-14 weeks of pregnancy until 42 weeks of pregnancy or day of infant delivery, whichever happens first | Presence or absence of Preterm Premature Rupture of Membranes in intervention vs placebo groups |
| going past due dates | during last month of pregnancy | Presence or absence of going past due dates in intervention vs placebo groups |
| Placental pathology | at time of delivery | Any placental pathology documented on maternal delivery summary in intervention vs. placebo groups |
| Head circumference at birth | At time of infant birth | Measurement of head circumference at birth in placebo vs. Intervention |
| Length at birth | At time of infant birth | Measurement of length at birth in placebo vs. Intervention |
| weight at birth | At time of infant birth | Measurement of weight at birth in placebo vs. Intervention |
| Gestational age at birth | At time of infant birth | Gestational age at infant birth in both placebo and intervention groups |
| APGAR score at 1 min | At time of infant birth | APGAR score assessed for infants in both placebo and intervention groups |
| APGAR score at 5 min | At time of infant birth | APGAR score assessed for infants in both placebo and intervention groups |
| Resuscitation beyond warm/dry stimulate at birth | At time of infant birth | Presence or absence of any resuscitation beyond warm, dry and stimulate at infant birth |
| Presence or absence or requirement for respiratory assistance within the first 24 hours after birth | From NICU admission to 24 hours after birth | Presence or absence of any respiratory support outside of the delivery room in first 24 hours of birth placebo vs intervention groups |
| Days of antibiotic exposure during birth hospitalization | During birth admission up to 8 months of chronologic age or discharge from hospital whichever happens sooner | Number of 24hr periods in which infant was exposed to antibiotics during birth hospitalization |
| NICU admission | Within the first 5 days of infant's life | Presence or absence of NICU admission in placebo vs intervention groups |
| Duration of birth admission | Birth through 12 months of age or infant discharge, whichever occurs sooner | Number of 24hr periods patient was present in hospital during birth admission |
| Requirement for phototherapy during birth admission | Birth through 14 days of infant life | Presence or absence of phototherapy during birth admission in placebo vs intervention groups |
| Culture proven sepsis | From birth through 12 months or until infant discharge whichever occurs sooner | Presence or absence of culture proven sepsis during birth admission in placebo vs intervention groups |
| Infant Death | From birth through 12 months or until infant discharge whichever occurs sooner | Number of infants that died during birth hospitalization in both the placebo and intervention groups |
| Weight at infant hospital discharge | At time of infant's first discharge from hospital or at 12 months corrected, whichever comes first | Weight at infant hospital discharge in placebo vs intervention group |
| head circumference at infant hospital discharge | At time of infant's first discharge from hospital or at 12 months corrected, whichever comes first | head circumference at infant hospital discharge in placebo vs intervention group |
| Length at infant hospital discharge | At time of infant's first discharge from hospital or at 12 months corrected, whichever comes first | Length at infant hospital discharge in placebo vs intervention group |
| Feeding plan at infant discharge | At 12 months chronological if still admitted or at infant discharge, whichever occurs sooner | Feeding plan documented as exclusive breastfeeding, formula and breastfeeding or exclusive formula feeding |
| Infant diagnosis in medical record | at 12 months corrected | Compare infant diagnosis recorded in medical record in placebo vs intervention group |
| infant weight at 6 months corrected age | at 6 months corrected | Weight at 6 months corrected age documented in medical record in placebo vs intervention group |
| infant weight at 12 months corrected age | at 12 months corrected | Weight at 12 months corrected age documented in medical record in placebo vs intervention group |
| head circumferene weight at 6 months corrected age | at 6 months corrected | head circumferene at 6 months corrected age documented in medical record in placebo vs intervention group |
| head circumference weight at 12 months corrected age | at 12 months corrected | head circumference at 12 months corrected age documented in medical record in placebo vs intervention group |
| Length weight at 6 months corrected age | at 6 months corrected | Length at 6 months corrected age documented in medical record in placebo vs intervention group |
| Length weight at 12 months corrected age | at 12 months corrected | Length at 12 months corrected age documented in medical record in placebo vs intervention group |
| Number of outpatient visits for infant during first 12 months corrected | birth through12 months corrected | Number of outpatient visits recorded during first 12 months corrected in placebo vs. intervention groups |
| Failure to thrive in for infant | birth through 12 months corrected | Presence or absence of diagnosis failure to thrive in medical record through first 12 months corrected in placebo vs intervention |
| number of inpatient days for infant through 12 months corrected | birth through 12 months corrected | number of inpatient days for infant through 12 months corrected in intervention vs placebo |
| Maternal Gestational weight gain at end of pregnancy in placebo vs. DHA supplement groups | At time of infant delivery | Compare maternal gestational weight gain at the end of pregnancy between intervention and placebo groups |
| Number of antibiotic prescriptions for infant through first 12 months corrected | birth through 12 months corrected | Number of antibiotic prescriptions for infant through first 12 months corrected in intervention vs placebo |
| Documented infant feeding plan through first year | birth through 12 months corrected | Documented infant feeding plan through first year. Exclusive breastfeeding, formula and breastfeeding or exclusive formula |
| Indication of infant developmental delay in medical record from birth through 12 months corrected | birth through 12 months corrected | Presence or absence of any indication of developmental delay recorded by physician in the medical record through 12 months corrected in intervention vs placebo groups |
| Infant delivery method | At time of infant delivery | Compare delivery method used to delivery infant between intervention and placebo groups |
| Delivery complications | at time of infant delivery | Compare any documented delivery complications between intervention and placebo groups |
Countries
United States
Contacts
Primary ContactPeter F Knickerbocker, DO
Backup ContactCarl Hunt, MD
Outcome results
None listed