Vitamin D Status and Metabolism in Human Pregnancy
- Conditions
- Pregnancy
- Registration Number
- NCT03051867
- Lead Sponsor
- Cornell University
- Brief Summary
The purpose of the present study is to understand the effect of pregnancy on vitamin D metabolism and requirements as well as the modulatory role of the placenta in vitamin D metabolism during pregnancy. In addition, a human placental cell culture model will be employed to examine vitamin D metabolic flux in human trophoblast cells. The impact of maternal vitamin D status on maternal and fetal bone health during gestation will also be examined.
- Detailed Description
Rationale
Despite mounting evidence that maternal vitamin D status is linked to pregnancy outcomes \[1,2\], the impact of pregnancy on vitamin D metabolism and requirement has yet to be clearly defined. In addition, although the placenta is known to express all components of the vitamin D metabolic pathway \[3,4\], very little is known about placental vitamin D metabolism. Moreover, although vitamin D is known to affect bone health in the nonpregnant state, the effect of maternal vitamin D status on maternal and fetal bone health in human pregnancy is unclear \[5-7\]. Therefore, the present study seeks to advance current understanding of vitamin D metabolism and requirements during pregnancy.
Objective and Research Questions
This study aims to examine: 1) the effect of pregnancy on a comprehensive panel of blood biomarkers of vitamin D status and metabolism; 2) the role of the placenta in modulating circulating vitamin D metabolites; and 3) the impact of maternal vitamin D status on maternal and fetal markers of bone metabolism.
Study Population, Design, and Exposure
As a secondary analysis, this study uses biological samples obtained from pregnant and nonpregnant control women who participated in a 12-wk randomized controlled trial in 2009-2010 which featured two doses of choline (i.e., 480 or 930 mg choline/d) (NCT01127022) \[8\]. Throughout the controlled feeding period, 26 third-trimester pregnant women and 21 nonpregnant women (both reproductive groups aged \> 21 y) in a good health status consumed equivalent intakes of vitamin D (511 IU/d), calcium (1.6 g/d) and phosphorus (1.9 g/d) from the study diet and prenatal multivitamin supplement (Pregnancy Plus; Fairhaven Health LLC) for ≥ 10 weeks.
Dependent variables:
1. Blood biomarkers of vitamin D metabolism at week 0 (study-baseline) and week 10 (representing study-end)
2. Placental biomarkers of vitamin D metabolism at delivery
3. Markers of bone metabolism in maternal and fetal cord blood as well as maternal urine
Ethical considerations
The study protocol of the original RCT was approved by the Institutional Review Board for Human Study Participant Use at Cornell University and the Cayuga Medical Center where pregnant women delivered their babies. Informed consent was obtained from all participants before study entry, and the original study was registered at clinicaltrials.gov as NCT01127022. For this secondary analysis, deidentified data will be used.
Dissemination Findings
Findings from the present study will be reported in manuscripts that will be submitted for publication to a leading medical/nutrition journal in an appropriate field (i.e. nutrition, bone, placenta, and reproductive physiology). In addition, findings will be presented as abstracts, posters, and presentations at research conferences.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 47
- Age of 21-40 y
- Healthiness as assessed by health-related questionnaire, a blood chemistry profile, and a complete blood count
- Normal liver and kidney function
- Willingness to comply with the study protocol
- Singleton pregnancy (pregnant women only)
- Use of tobacco, drug, or alcohol
- Use of prescription medications known to affect liver function
- Pregnancy associated complications
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Maternal circulating concentrations of 25-hydroxyvitamin D Baseline (week 0; 26-29 wk gestation) and study-end (week 10; 36-39 wk gestation) Serum 25-hydroxyvitamin D \[25(OH)D\] will be measured using an isotope dilution LC-MS/MS methodology, and the effect of reproductive state on serum 25(OH)D will be examined using a linear mixed model which considers confounding factors.
Maternal circulating concentrations of 1,25-dihydroxyvitamin D Baseline (week 0; 26-29 wk gestation) and study-end (week 10; 36-39 wk gestation) Plasma 1,25-dihydroxyvitamin D \[1,25(OH)2D\] will be measured using an EIA kit, and the effect of reproductive state on circulating 1,25(OH)2D will be examined using a linear mixed model which considers confounding factors.
Maternal circulating concentrations 24,25-dihydroxyvitamin D Baseline (week 0; 26-29 wk gestation) and study-end (week 10; 36-39 wk gestation) Plasma 24,25-dihydroxyvitamin D \[24,25(OH)2D\] will be measured using an isotope dilution LC-MS/MS methodology, and the effect of reproductive state on circulating 24,25(OH)2D will be examined using a linear mixed model which considers potential confounders.
Placental mRNA abundance of 25-hydroxylase Delivery Placental mRNA abundance of 25-hydroxylase \[CYP2R1\] will be measured using a qPCR, and the associations of placental CYP2R1 mRNA abundance with serum 25(OH)D will be examined using a linear mixed model which considers potential confounders.
Placental mRNA abundance of 24-hydroxylase Delivery Placental mRNA abundance of 24-hydroxylase \[CYP24A1\] will be measured using a qPCR, and the associations of placental CYP24A1 mRNA abundance with circulating 24,25(OH)2D will be examined using a linear mixed model which considers potential confounders.
Placental 25-hydroxyvitamin D Delivery 25(OH)D will be measured from placental tissue using an isotope dilution LC-MS/MS methodology, and the associations of placental 25(OH)D with serum 25(OH)D as well as placental CYP2R1 mRNA abundance will be examined using a Pearson correlation test and a linear mixed model which considers potential confounders.
Placental 24,25-dihydroxyvitamin D Delivery 24,25(OH)2D will be measured from placental tissue using an isotope dilution LC-MS/MS methodology, and the associations of placental 24,25(OH)2D with circulating 25(OH)D and 24,25(OH)2D as well as placental CYP24A1 mRNA abundance will be examined using a Pearson correlation test and a linear mixed model which adjusts for potential confounders.
- Secondary Outcome Measures
Name Time Method Maternal circulating carboxy-terminal cross-linking telopeptide of type 1 collagen Baseline (week 0; 26-29 wk gestation), study-end (week 10; 36-39 wk gestation), and delivery Plasma carboxy-terminal cross-linking telopeptide of type 1 collagen \[CTx\] will be measured using an ELISA kit, and the relationships of maternal serum 25(OH)D with maternal CTx will be assessed using a linear mixed model which considers potential confounders.
Maternal circulating intact parathyroid hormone Baseline (week 0; 26-29 wk gestation) and study-end (week 10; 36-39 wk gestation) Plasma intact parathyroid hormone \[iPTH\] will be measured using an automated immunoassay, and the relationship of maternal serum 25(OH)D with maternal iPTH will be assessed using a linear mixed model which considers potential confounders.
Maternal urinary deoxypyridinoline/creatinine Baseline (week 0; 26-29 wk gestation), study-end (week 10; 36-39 wk gestation) Urinary deoxypyridinoline/creatinine \[DPD/Cr\] will be measured using an ELISA kit, and the relationships of maternal serum 25(OH)D with maternal DPD/Cr will be assessed using a linear mixed model which considers potential confounders.
Maternal circulating osteocalcin Baseline (week 0; 26-29 wk gestation), study-end (week 10; 36-39 wk gestation), and delivery Plasma osteocalcin \[OC\] will be measured using an ELISA kit, and the relationships of maternal serum 25(OH)D with maternal OC will be assessed using a linear mixed model which considers potential confounders.
Trial Locations
- Locations (1)
Human Metabolic Research Unit, Cornell University
🇺🇸Ithaca, New York, United States