Cystathionine beta synthase deficiency and brain edema associated with methionine excess under betaine supplementation: Four new cases and a review of the evidence
Bernd C. Schwahn,
Thomas Scheffner,
Hedwig Stepman,
Peter Verloo,
Anibh M Das,
Janice Fletcher,
Henk J Blom,
Jean‐Francois Benoist,
Bruce A. Barshop,
Jaime J. Barea,
Annette Feigenbaum
Affiliations
Bernd C. Schwahn
Willink Metabolic Unit, Manchester Centre for Genomic Medicine Manchester University Hospitals NHS Foundation Trust Manchester UK
Thomas Scheffner
Klinikum am Steinenberg, Klinik für Kinder und Jugendmedizin School of Medicine University of Tübingen Reutlingen Germany
Hedwig Stepman
Laboratory for Metabolic diseases Ghent University Hospital Ghent Belgium
Peter Verloo
Department of Pediatric Neurology and Metabolic Diseases University Hospital Ghent Ghent Belgium
Anibh M Das
Medizinische Hochschule Hannover Klinik für Pädiatrische Nieren‐, Leber‐ und Stoffwechselerkrankungen Hannover Germany
Janice Fletcher
Genetics and Molecular Pathology SA Pathology Adelaide Australia
Henk J Blom
Metabolic Unit, Department of Clinical Genetics Center for Lysosomal and Metabolic Diseases. Erasmus Medical Center Rotterdam The Netherlands
Jean‐Francois Benoist
Service de Biochimie Hormonologie Hôpital Robert Debré, APHP Paris France
Bruce A. Barshop
Department of Pediatrics, Division of Biochemical Genetics, Rady Children's Hospital‐San Diego University of California San Diego California
Jaime J. Barea
Department of Pediatrics, Division of Biochemical Genetics, Rady Children's Hospital‐San Diego University of California San Diego California
Annette Feigenbaum
Department of Pediatrics, Division of Biochemical Genetics, Rady Children's Hospital‐San Diego University of California San Diego California
Abstract CBS deficient individuals undergoing betaine supplementation without sufficient dietary methionine restriction can develop severe hypermethioninemia and brain edema. Brain edema has also been observed in individuals with severe hypermethioninemia without concomitant betaine supplementation. We systematically evaluated reports from 11 published and 4 unpublished patients with CBS deficiency and from additional four cases of encephalopathy in association with elevated methionine. We conclude that, while betaine supplementation does greatly exacerbate methionine accumulation, the primary agent causing brain edema is methionine rather than betaine. Clinical signs of increased intracranial pressure have not been seen in patients with plasma methionine levels below 559 μmol/L but occurred in one patient whose levels did not knowingly exceed 972 μmol/L at the time of manifestation. While levels below 500 μmol/L can be deemed safe it appears that brain edema can develop with plasma methionine levels close to 1000 μmol/L. Patients with CBS deficiency on betaine supplementation need to be regularly monitored for concordance with their dietary plan and for plasma methionine concentrations. Recurrent methionine levels above 500 μmol/L should alert clinicians to check for clinical signs and symptoms of brain edema and review dietary methionine intake. Levels approaching 1000 μmol/L do increase the risk of complications and levels exceeding 1000 μmol/L, despite best dietetic efforts, should be acutely addressed by reducing the prescribed betaine dose.