Literature DB >> 26092490

Clinical, etiological and therapeutic aspects of cerebral folate deficiency.

Marta Molero-Luis1, Mercedes Serrano, Maria M O'Callaghan, Cristina Sierra, Belén Pérez-Dueñas, Angels García-Cazorla, Rafael Artuch.   

Abstract

Cerebral folate deficiency is defined as any neurological condition associated with low cerebrospinal fluid folate concentrations. It is becoming increasingly associated with several neurological diseases, either genetic or environmental. Treatment of cerebral folate deficiency by folate supplementation is generally effective, improving the neurological outcome of some patients. However, to treat cerebral folate deficiency, the proper choice of one of the available folate forms is essential. The distinct brain folate metabolism features compared with peripheral folate metabolic pathways strongly suggest the investigation of different folate forms, such as the biologically active folinic acid and 5-methyltetrahydrofolate, since they are efficiently transported to the brain. Regarding the oral doses of the different folate forms, despite the fact that there are some recommendations, there is no general consensus. Further investigation and designing clinical trials are advisable to elucidate these aspects.

Entities:  

Keywords:  5-methyltetrahydrofolate; cerebral folate deficiency; choroid plexus; folate transport and metabolism; folic acid; folinic acid; neurological diseases

Mesh:

Substances:

Year:  2015        PMID: 26092490     DOI: 10.1586/14737175.2015.1055322

Source DB:  PubMed          Journal:  Expert Rev Neurother        ISSN: 1473-7175            Impact factor:   4.618


  7 in total

Review 1.  Folate nutrition and blood-brain barrier dysfunction.

Authors:  Patrick J Stover; Jane Durga; Martha S Field
Journal:  Curr Opin Biotechnol       Date:  2017-02-10       Impact factor: 9.740

Review 2.  Emerging Concepts in Nutrient Needs.

Authors:  Patrick J Stover; Cutberto Garza; Jane Durga; Martha S Field
Journal:  J Nutr       Date:  2020-10-01       Impact factor: 4.798

Review 3.  Treatable inherited rare movement disorders.

Authors:  H A Jinnah; Alberto Albanese; Kailash P Bhatia; Francisco Cardoso; Gustavo Da Prat; Tom J de Koning; Alberto J Espay; Victor Fung; Pedro J Garcia-Ruiz; Oscar Gershanik; Joseph Jankovic; Ryuji Kaji; Katya Kotschet; Connie Marras; Janis M Miyasaki; Francesca Morgante; Alexander Munchau; Pramod Kumar Pal; Maria C Rodriguez Oroz; Mayela Rodríguez-Violante; Ludger Schöls; Maria Stamelou; Marina Tijssen; Claudia Uribe Roca; Andres de la Cerda; Emilia M Gatto
Journal:  Mov Disord       Date:  2017-09-01       Impact factor: 10.338

Review 4.  A Review of Targeted Therapies for Monogenic Epilepsy Syndromes.

Authors:  Vincent Zimmern; Berge Minassian; Christian Korff
Journal:  Front Neurol       Date:  2022-02-17       Impact factor: 4.003

5.  Luteolin Enhances Choroid Plexus 5-MTHF Brain Transport to Promote Hippocampal Neurogenesis in LOD Rats.

Authors:  Hui-Zhen Li; Kai-Ge Liu; Ning-Xi Zeng; Xiao-Feng Wu; Wen-Jun Lu; Han-Fang Xu; Can Yan; Li-Li Wu
Journal:  Front Pharmacol       Date:  2022-03-25       Impact factor: 5.810

6.  Dihydropyridine Reductase Deficiency: Acute Encephalopathy Related to Folinic Acid Treatment Interruption in a Girl.

Authors:  Maria Grazia Pappalardo; Alessandra Di Nora; Andrea Giugno; Concetta Meli; Annamaria Sapuppo; Piero Pavone; Agata Fiumara
Journal:  Glob Med Genet       Date:  2022-09-19

7.  Cerebral folate deficiency in two siblings caused by biallelic variants including a novel mutation of FOLR1 gene: Intrafamilial heterogeneity following early treatment and the role of ketogenic diet.

Authors:  Maria T Papadopoulou; Efterpi Dalpa; Michalis Portokalas; Irene Katsanika; Katerina Tirothoulaki; Martha Spilioti; Spyros Gerou; Barbara Plecko; Athanasios E Evangeliou
Journal:  JIMD Rep       Date:  2021-06-04
  7 in total

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