TY - JOUR
T1 - Folic acid inhibits 5-methyltetrahydrofolate transport across the blood–cerebrospinal fluid barrier
T2 - Clinical biochemical data from two cases
AU - Akiyama, Tomoyuki
AU - Kuki, Ichiro
AU - Kim, Kiyohiro
AU - Yamamoto, Naohiro
AU - Yamada, Yumi
AU - Igarashi, Kazuya
AU - Ishihara, Tomohiko
AU - Hatano, Yuya
AU - Kobayashi, Katsuhiro
N1 - Funding Information:
We would like to thank Dr. Ichizo Nishino and Dr. Yuichi Goto of the National Center of Neurology and Psychiatry, Tokyo, Japan, for muscle pathological diagnosis and mitochondrial DNA analysis. We are grateful for the physicians who provided their patients' serum and CSF samples. T.A. received grant support from the Japan Society for the Promotion of Science (Grant Number JP 21K07798) and the Ministry of Health, Labour and Welfare (Grant Number 21FC1015). These funding sources had no involvement in the study design, the collection, analysis, and interpretation of data, the writing of the report, or the decision to submit this article. We thank Eibunkosei.net (https://www. eibunkousei.net/) for English language editing.
Publisher Copyright:
© 2022 The Authors. JIMD Reports published by John Wiley & Sons Ltd on behalf of SSIEM.
PY - 2022/11
Y1 - 2022/11
N2 - Objective: The use of folic acid (FA) has been discouraged in cerebral folate deficiency (CFD) because, theoretically, it could inhibit the transport of 5-methyltetrahydrofolic acid (5MTHF) across the blood–cerebrospinal fluid (CSF) barrier. We present the clinical biochemical data of two cases with CFD to support this hypothesis. Methods: We measured CSF and serum 5MTHF concentrations in a patient with Kearns-Sayre syndrome (KSS) and a patient homozygous for MTHFR C677T polymorphism before and during folate supplementation therapy. To evaluate these 5MTHF concentrations, we also analyzed CSF and serum samples in pediatric patients without folate supplementation. Results: Both patients had low CSF 5MTHF before treatment and high-dose FA therapy did not normalize CSF 5MTHF. There was a dissociation between serum total folate and 5MTHF concentrations during FA therapy, which was considered to be due to the appearance of unmetabolized FA. The addition of folinic acid did not improve low CSF 5MTHF in the KSS patient and the cessation of FA resulted in the normalization of CSF 5MTHF. In the patient homozygous for MTHFR C677T, minimization of the FA dosage resulted in the normalization of CSF 5MTHF and an increased CSF-to-serum 5MTHF ratio. Conclusions: Our data suggest that excess supplementation of FA impaired 5MTHF transport across the blood–CSF barrier. In the treatment of CFD, supplementation of folinic acid or 5MTHF (in cases of impaired 5MTHF synthesis) is preferred over the use of FA. The reference values of CSF 5MTHF concentration based on 600 pediatric cases were also provided.
AB - Objective: The use of folic acid (FA) has been discouraged in cerebral folate deficiency (CFD) because, theoretically, it could inhibit the transport of 5-methyltetrahydrofolic acid (5MTHF) across the blood–cerebrospinal fluid (CSF) barrier. We present the clinical biochemical data of two cases with CFD to support this hypothesis. Methods: We measured CSF and serum 5MTHF concentrations in a patient with Kearns-Sayre syndrome (KSS) and a patient homozygous for MTHFR C677T polymorphism before and during folate supplementation therapy. To evaluate these 5MTHF concentrations, we also analyzed CSF and serum samples in pediatric patients without folate supplementation. Results: Both patients had low CSF 5MTHF before treatment and high-dose FA therapy did not normalize CSF 5MTHF. There was a dissociation between serum total folate and 5MTHF concentrations during FA therapy, which was considered to be due to the appearance of unmetabolized FA. The addition of folinic acid did not improve low CSF 5MTHF in the KSS patient and the cessation of FA resulted in the normalization of CSF 5MTHF. In the patient homozygous for MTHFR C677T, minimization of the FA dosage resulted in the normalization of CSF 5MTHF and an increased CSF-to-serum 5MTHF ratio. Conclusions: Our data suggest that excess supplementation of FA impaired 5MTHF transport across the blood–CSF barrier. In the treatment of CFD, supplementation of folinic acid or 5MTHF (in cases of impaired 5MTHF synthesis) is preferred over the use of FA. The reference values of CSF 5MTHF concentration based on 600 pediatric cases were also provided.
KW - 5-formyltetrahydrofolic acid
KW - cerebral folate deficiency
KW - folate receptor 1
KW - folinic acid
KW - Kearns-Sayre syndrome
KW - methylenetetrahydrofolate reductase deficiency
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U2 - 10.1002/jmd2.12321
DO - 10.1002/jmd2.12321
M3 - Article
AN - SCOPUS:85141671923
SN - 2192-8304
VL - 63
SP - 529
EP - 535
JO - JIMD Reports
JF - JIMD Reports
IS - 6
ER -