Histamine-N-methyl transferase polymorphism and risk for multiple sclerosis.

Abstract:

BACKGROUND:Histamine N-methyltransferase (HNMT) is the main metabolizing enzyme of histamine (a mediator of inflammation implicated in the pathogenesis of multiple sclerosis-MS) in the CNS. We have investigated the possible association between a single nucleotide polymorphism of the HNMT (chromosome 2q22.1), that causes the amino acid substitution Thr105Ile (decreasing enzyme activity) and the risk for MS. METHODS:We studied the frequency of the HNMT genotypes and allelic variants in 228 MS patients and 295 healthy controls using a PCR-RLFP method. RESULTS:The frequencies of the HNMT genotypes and allelic variants did not differ significantly between MS patients and controls, and were unrelated with the age of onset of MS, gender, and course of MS. CONCLUSION:The HNMT polymorphism is not related with the risk for MS.

journal_name

Eur J Neurol

authors

García-Martín E,Martínez C,Benito-León J,Calleja P,Díaz-Sánchez M,Pisa D,Alonso-Navarro H,Ayuso-Peralta L,Torrecilla D,Agúndez JA,Jiménez-Jiménez FJ

doi

10.1111/j.1468-1331.2009.02720.x

subject

Has Abstract

pub_date

2010-02-01 00:00:00

pages

335-8

issue

2

eissn

1351-5101

issn

1468-1331

pii

ENE2720

journal_volume

17

pub_type

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