Article (Scientific journals)
Psychomotor retardation, spastic paraplegia, cerebellar ataxia and dyskinesia associated with low 5-methyltetrahydrofolate in cerebrospinal fluid: A novel neurometabolic condition responding to folinic acid substitution
Ramaekers, Vincent; Häusler, M.; Opladen, T. et al.
2002In Neuropediatrics, 33 (6), p. 301-308
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Keywords :
Blood-Brain Barrier; Folate; Folate Receptor; Brain Diseases, Metabolic, Inborn; Carrier Proteins; Child; Child, Preschool; DNA-Binding Proteins; Erythrocytes; Female; Humans; Infant; Leucovorin; Male; Membrane Proteins; Membrane Transport Proteins; Mental Retardation; Movement Disorders; Neurologic Examination; Paraplegia; Psychomotor Disorders; Receptors, Cell Surface; Replication Protein C; Spinocerebellar Degenerations; Tetrahydrofolates; Transcription Factors
Abstract :
[en] Introduction: Normal brain development and function depend on the active transport of folates across the blood-brain barrier. The folate receptor-1 (FR1) protein is localized at the basolateral surface of the choroid plexus, which is characterized by a high binding affinity for circulating 5-methyltetrahydrofolate (5- MTHF). Patients and Methods: We report on the clinical and metabolic findings among five children with normal neurodevelopmental progress during the first four to six months followed by the acquisition of a neurological condition which includes marked irritability, decelerating head growth, psychomotor retardation, cerebellar ataxia, dyskinesias (choreoathetosis, ballism), pyramidal signs in the lower limbs and occasional seizures. After the age of six years the two oldest patients also manifested a central visual disorder. Known disorders have been ruled out by extensive investigations. Cerebrospinal fluid (CSF) analysis included determination of biogenic monoamines, pterins and 5-MTHF. Results: Despite normal folate levels in serum and red blood cells with normal homocysteine, analysis of CSF revealed a decline towards very low values for 5-methyltetrahydrofolate (5-MTHF), which suggested disturbed transport of folates across the blood-brain barrier. Genetic analysis of the FR1 gene revealed normal coding sequences. Oral treatment with doses of the stable compound folinic acid (0.5-1 mg/kg/day Leucovorin®) resulted in clinical amelioration and normalization of 5-MTHF values in CSF. Conclusion: Our findings identified a new condition manifesting after the age of 6 months which was accompanied by low 5-MTHF in cerebrospinal fluid and responded to oral supplements with folinic acid. However, the cause of disturbed folate transfer across the blood-brain barrier remains unknown.
Disciplines :
Pediatrics
Neurology
Author, co-author :
Ramaekers, Vincent ;  Division of Paediatric Neurology, Department of Paediatrics, University Hospital Aachen, Pauwelsstraße 30, 52074 Aachen, Germany
Häusler, M.;  Division of Paediatric Neurology, Department of Paediatrics, University Hospital Aachen, Pauwelsstraße 30, 52074 Aachen, Germany
Opladen, T.;  Division of Paediatric Neurology, Department of Paediatrics, University Hospital Aachen, Pauwelsstraße 30, 52074 Aachen, Germany
Heimann, G.;  Division of Paediatric Neurology, Department of Paediatrics, University Hospital Aachen, Pauwelsstraße 30, 52074 Aachen, Germany
Blau, N.;  Division of Biochemistry, University Children's Hospital, Zurich, Switzerland
Language :
English
Title :
Psychomotor retardation, spastic paraplegia, cerebellar ataxia and dyskinesia associated with low 5-methyltetrahydrofolate in cerebrospinal fluid: A novel neurometabolic condition responding to folinic acid substitution
Publication date :
December 2002
Journal title :
Neuropediatrics
ISSN :
0174-304X
eISSN :
1439-1899
Publisher :
Georg Thieme Verlag, Germany
Volume :
33
Issue :
6
Pages :
301-308
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 07 June 2014

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