Document Detail


Infantile hypermethioninemia and hyperhomocysteinemia due to high methionine intake: a diagnostic trap.
MedLine Citation:
PMID:  12765841     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Studies were carried out to identify the cause of combined severe hypermethioninemia and moderate hyperhomocysteinemia in a cluster of 10 infants ascertained between 1999 and early 2001. Although several were thought initially to have cystathionine beta-synthase (CBS) deficiency and treated accordingly, CBS deficiency and other known genetic causes of hypermethioninemia were ruled out by assay of CBS activity in fibroblasts of four patients and by assays of plasma cystathionine and S-adenosylmethionine. Retrospective data on dietary methionine intakes and plasma concentrations of methionine and related metabolites established that the hypermethioninemia in nine of the 10 babies was related to ingestion of an infant protein hydrolysate formula, the methionine content of which had been increased from May 1998 to February 2001. The formula in question has now been reformulated and is no longer available. The 10th infant manifested similar metabolic abnormalities while receiving TPN containing excessive methionine. Brain MRI abnormalities indicative of cerebral edema, most marked in the cerebral cortex and posterior brainstem, occurred in two patients near times of extreme hypermethioninemia. Metabolic and MRI abnormalities resolved when the methionine intake decreased. A third infant had a normal MRI 1 day after the formula was changed. The possible relationship between extreme hypermethioninemia and cerebral edema is discussed and a working hypothesis offered to explain the relative sensitivity of the inferior colliculi, based upon the facts that this is the region most active in glucose utilization and that Na(+),K(+)-ATPase is inhibited by methionine and related metabolites.
Authors:
S Harvey Mudd; Nancy Braverman; Martin Pomper; Kamer Tezcan; Jonathan Kronick; Parul Jayakar; Cheryl Garganta; Mary G Ampola; Harvey L Levy; Shawn E McCandless; Hobart Wiltse; Sally P Stabler; Robert H Allen; Conrad Wagner; Marlene W Borschel
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Molecular genetics and metabolism     Volume:  79     ISSN:  1096-7192     ISO Abbreviation:  Mol. Genet. Metab.     Publication Date:  2003 May 
Date Detail:
Created Date:  2003-05-26     Completed Date:  2004-02-10     Revised Date:  2008-11-21    
Medline Journal Info:
Nlm Unique ID:  9805456     Medline TA:  Mol Genet Metab     Country:  United States    
Other Details:
Languages:  eng     Pagination:  6-16     Citation Subset:  IM    
Affiliation:
NIMH/DIRP/LMB, Laboratory of Molecular Biology, National Institute of Mental Health, Building 36, Room 1B-08, 36 Convent Drive, MSC 4034, Bethesda, MD 20892-4034, USA. shm@codon.nih.gov
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MeSH Terms
Descriptor/Qualifier:
Brain Edema / diagnosis,  etiology
Female
Food, Fortified / adverse effects*
Humans
Hyperhomocysteinemia / etiology*
Infant
Infant Food / adverse effects*
Infant Nutritional Physiological Phenomena
Infant, Newborn
Magnetic Resonance Imaging
Male
Methionine / blood*
Chemical
Reg. No./Substance:
63-68-3/Methionine

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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