Oral L-Citrulline and ADMA in Pregnancy

Sponsor
University of Pittsburgh (Other)
Overall Status
Completed
CT.gov ID
NCT00743210
Collaborator
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) (NIH)
41
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2
41
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Study Details

Study Description

Brief Summary

The purpose of this study is to determine if oral of L-citrulline (3 grams/day) for 3 weeks provided in mid-pregnancy to obese subjects will decrease the plasma ADMA/L-arginine ratio, lower maternal blood pressure, improve endothelial-dependent vascular function and peripheral vascular stiffness, and improve uterine artery Doppler resistance and flow.

Condition or Disease Intervention/Treatment Phase
Phase 1

Detailed Description

The pregnancy-specific syndrome preeclampsia is a leading cause of maternal and fetal morbidity and mortality. The underlying cause of preeclampsia is unknown, however several pre-existing maternal conditions are associated with an increased risk of preeclampsia including: diabetes, hypertension, renal dysfunction, and obesity. Among these conditions, obesity has been increasing in the population, such that 30% of the adult population in the US is now considered obese, and because of this obesity has the largest attributable risk for preeclampsia, accounting for 15 to 32% of the population attributable risk for preeclampsia. There is abundant evidence that pre-pregnancy obesity increases the risk of preeclampsia. However, it is unknown how pre-pregnancy obesity increases the risk of preeclampsia, how obesity-mediated metabolic aberrations interact with current hypotheses of the pathogenesis of preeclampsia, and why only a subset of obese women (~6-8%) develops preeclampsia. Several lines of evidence indicate that endothelial dysfunction is a central feature of the pathophysiology of preeclampsia, and endothelial dysfunction is a common endpoint of obesity. Asymmetric dimethylarginine (ADMA) is a methylated metabolite of the amino acid L-arginine and an endogenous inhibitor of nitric oxide synthase (NOS). High concentrations of ADMA contribute to endothelial dysfunction and ADMA inhibits angiogenesis and arteriogenesis, activities important in pregnancy and deficient in preeclampsia. ADMA is higher in obesity and ADMA concentrations are higher early in pregnancy among women who later develop preeclampsia. This protocol describes a randomized placebo-controlled trial of L-citrulline vs. placebo in 80 obese pregnant women from twelve to twenty weeks gestation, to determine whether L-citrulline supplementation decreases the plasma ADMA/L-arginine ratio, lowers maternal blood pressure, improves endothelial-dependent vascular function and peripheral vascular stiffness, and improvement in uterine artery Doppler resistance and flow. We will compare the data obtained from these obese pregnant women to the same measures obtained from 40 untreated lean pregnant women.

Study Design

Study Type:
Interventional
Actual Enrollment :
41 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Basic Science
Official Title:
Phase 1 Study of Oral L-citrulline on ADMA/L-arginine and Endothelial-dependent Vascular Function in Pregnancy.
Study Start Date :
Jan 1, 2010
Actual Primary Completion Date :
Jun 1, 2013
Actual Study Completion Date :
Jun 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Experimental: 1

Oral L-citrulline, 3 grams once per day for 3 weeks.

Drug: L-citrulline
Oral L-citrulline, 3 grams once per day for 3 weeks.

Placebo Comparator: 2

Placebo, 3 grams once per day for 3 weeks.

Drug: Placebo
Placebo, 3 grams once per day for 3 weeks.

Outcome Measures

Primary Outcome Measures

  1. To evaluate blood pressure changes in response to oral L-citrulline or placebo treatment in uncomplicated obese pregnant women during the second trimester of pregnancy. [3 weeks]

Secondary Outcome Measures

  1. To evaluate the changes in plasma ADMA/L-arginine ratio, endothelial-dependent vascular function and peripheral vascular stiffness, and uterine artery Doppler resistance and flow. [3 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
14 Years to 40 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Pre-pregnancy body mass index greater than or equal to 30kg/m2

  • Primiparity

  • Singleton pregnancy

  • Gestational age at randomization between 10 and 14 weeks based on clinical information and evaluation of earliest ultrasound

  • Maternal age between 14 and 40 years

Exclusion Criteria:
  • chronic hypertension

  • pregestational diabetes on medication (insulin, glyburide)

  • major fetal anomaly or demise

  • planned termination of the pregnancy

  • collagen vascular disease (autoimmune disease) on medication

  • renal disease

  • epilepsy or other seizure disorder

  • active or chronic liver disease

  • heart disease

  • cigarette smoker

  • known illicit drug or alcohol abuse during current pregnancy

  • already taking L-citrulline as a supplement (1gram/day or more)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Magee-Womens Hospital of UPMC Pittsburgh Pennsylvania United States 15213

Sponsors and Collaborators

  • University of Pittsburgh
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Investigators

  • Principal Investigator: Carl A Hubel, PhD, Department of Obstetrics & Gynecology and Reproductive Sciences, University of Pittsburgh

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Robert Powers, Associate Professor, University of Pittsburgh
ClinicalTrials.gov Identifier:
NCT00743210
Other Study ID Numbers:
  • 2P01HD030367-ARG
  • P01HD030367-09
First Posted:
Aug 28, 2008
Last Update Posted:
Jul 16, 2014
Last Verified:
Jul 1, 2014
Keywords provided by Robert Powers, Associate Professor, University of Pittsburgh

Study Results

No Results Posted as of Jul 16, 2014