Genetic variants of folate metabolism and the risk of multiple sclerosis

BACKGROUND AND AIMS: Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) of unknown cause. Alterations in one-carbon metabolism have impact in the pathophysiology by genetic susceptibility to MS and increased the risk of MS. The aim of this study was to investigate the contribution of the gene polymorphism on Methylenetetrahydrofolate Reductase (MTHFR), Methionine Synthase Reductase (MTRR), Methionine Synthase (MTR) enzymes and of the essential factors (homocysteine, Hcy; cysteine, Cys; and vitamin B12, VitB12) in folate metabolism.

METHODS: Eligible MS patients (n = 147) and health controls (n = 127) were participated. The gene polymorphisms were analyzed by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) and the levels of plasma Hcy, Cys and VitB12 were measured by Enzyme Linked Immunuabsorbent Assay (ELISA).

RESULTS AND CONCLUSION: Our results showed that the levels of Hcy and VitB12 were lower and the levels of Cys were higher in MS compared to controls. The observation of high Cys values in all 3 gene polymorphisms suggests that the transsulfiration pathway of Hcy is directed towards Cys formation since the methionine synthesis pathway does not work. We could not find any association with all gene polymorphisms with the risk of MS. The T allele of MTHFR C677T and G allele of MTR A2756G are risk factors for serum Cys level on MS. As for MTR A2756G, serum vitB12 was observed in MS patients with G allele.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - year:2024

Enthalten in:

Neurological research - (2024) vom: 02. Apr., Seite 1-9

Sprache:

Englisch

Beteiligte Personen:

Aşcı, Ali Erkan [VerfasserIn]
Orhan, Gürdal [VerfasserIn]
Karahalil, Bensu [VerfasserIn]

Links:

Volltext

Themen:

Cysteine
Folate metabolism
Gene polymorphism
Homocystein
Journal Article
MTHFR
MTR
MTRR
VitB12

Anmerkungen:

Date Revised 02.04.2024

published: Print-Electronic

Citation Status Publisher

doi:

10.1080/01616412.2024.2337519

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM370546415