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Study of Phosphatidylcholine in a Patient With Methionine Adenosyltransferase Deficiency - Article


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S-adenosyl methionine (SAM-e)

Ademetionine; S-adenosyl-L-methionine; S-Adenosylmethionine; SAM; SAMe; Sammy 




Clinical Trial: Study of Phosphatidylcholine in a Patient With Methionine Adenosyltransferase Deficiency

This study has been completed.

Sponsors and Collaborators: National Center for Research Resources (NCRR)
UNC Lineberger Comprehensive Cancer Center
Information provided by: Office of Rare Diseases (ORD)

Purpose

OBJECTIVES: I. Determine whether plasma choline and breast milk choline levels are low at fasting in a patient with methionine adenosyltransferase deficiency, and if the choline levels are low, determine whether choline levels respond to dietary supplementation with phosphatidylcholine. II. Determine whether this patient has a fatty liver by magnetic resonance spectroscopy.

Condition Treatment or Intervention
Methionine Adenosyltransferase Deficiency
Metabolism, Inborn Errors
 Drug: phosphatidylcholine

MedlinePlus related topics:  Birth Defects;   Genetic Disorders;   Metabolic Disorders

Study Type: Interventional
Study Design: Treatment

Further Study Details: 

Expected Total Enrollment:  1

Study start: January 2000;  Study completion: January 2000

PROTOCOL OUTLINE: Blood is drawn for liver function tests and measurement of plasma choline levels and breast milk samples are taken for measurement of breast milk choline levels at fasting and at 1 hour after breakfast on day 1. The patient then undergoes magnetic resonance spectroscopy of the liver to assess liver density and choline compound mass. The patient then receives oral phosphatidylcholine supplement, and plasma and breast milk samples are taken at 3 and 6 hours after the dose. Oral phosphatidylcholine supplements continue for 30 days. The above studies are repeated on day 31.

Eligibility

Ages Eligible for Study:  20 Years   -   20 Years,  Genders Eligible for Study:  Female

Criteria

  • Patient with methionine adenosyltransferase deficiency who is nursing

Location Information

Study chairs or principal investigators

Steven H. Zeisel,  Study Chair,  UNC Lineberger Comprehensive Cancer Center   

More Information

Study ID Numbers:  199/15077; UNCCH-GCRC-1405
Record last reviewed:  July 2000
Last Updated:  October 13, 2004
Record first received:  July 5, 2000
ClinicalTrials.gov Identifier:  NCT00006061
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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November 27, 2009



Page Updated: May 11, 2006
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