S‐adenosylmethionine and S‐adenosylhomocysteine in plasma and cerebrospinal fluid in Rett syndrome and the effect of folinic acid supplementation. Issue 6 (8th February 2013)

• Record Type: Journal Article
• Authors: Hagebeuk, Eveline E. O.; Duran, Marinus; Abeling, Nico G. G. M.; Vyth, Arno; Poll‐The, Bwee Tien
• Is Part Of: Journal of inherited metabolic disease. Volume 36:Issue 6(2013)
• Page Start: 967
• Page End: 972
• Publication Date: 2013-02-08
• Subjects: Metabolism, Inborn errors of -- Periodicals; Metabolism -- Disorders -- Periodicals; 616.39042
• DOI: 10.1007/s10545-013-9590-6
• Languages: English
• ISSNs: 0141-8955

Abstract

Abstract: Rett syndrome is a neurodevelopmental disorder characterized by cognitive and locomotor regression and stereotypic hand movements. The disorder is caused by mutations in the X chromosomal MECP2 a gene encoding methyl CpG‐binding protein. It has been associated with disturbances of cerebral folate homeostasis, as well as with speculations on a compromised DNA‐methylation. Folinic acid is the stable form of folate. Its derived intermediate 5‐MTHF supports the conversion of homocysteine to methionine, the precursor of S‐adenosylmethionine (SAM). This in turn donates its methyl group to various acceptors, including DNA, thereby being converted to S‐adenosylhomocysteine (SAH). The SAM/SAH ratio reflects the methylation potential. The goal of our study was to influence DNA methylation processes and ameliorate the clinical symptoms in Rett syndrome. Therefore we examined the hypothesis that folinic acid supplementation, besides increasing cerebrospinal fluid (CSF) 5‐MTHF ( p = 0.003), influences SAM and SAH and their ratio. In our randomized, double‐blind crossover study on folinic acid supplementation, ten female Rett patients received both folinic acid and placebo for 1 year each. It was shown that both SAM and SAH levels in the CSF remained unchanged following folinic acid administration ( p = 0.202 and p = 0.097, respectively) in spite of a rise of plasma SAM and SAH ( p = 0.007; p = 0.009). There was no significant change in the SAM/SAH ratio either in plasma or CSF. The apparent inability of Rett patients to upregulate SAM and SAH levels in the CSF may contribute to the biochemical anomalies of the Rett syndrome. Our studies warrant further attempts to promote DNA methylation in the true region of interest, i.e. the brain.