[Analysis of TRPV1 gene polymorphisms in Spanish patients with neuropathic pain].

Abstract:

BACKGROUND AND OBJECTIVE:The vanilloid receptor TRPV1 is a molecular integrator of painful stimuli. Several recent studies suggest that TRPV1 may play a role in development and maintenance of chronic pain. In an attempt to determine if genotypic variations in TRPV1 gene could be involved in the susceptibility to suffer neuropathic pain we have studied genetic variants of human TRPV1 gene. PATIENTS AND METHODS:We have studied the distribution of Met315Ile and Ile585Val TRPV1 polymorphisms in a total of 440 Caucasian subjects: 232 patients with neuropathic pain and 208 healthy subjects matched by age and sex. The polymorphisms were analyzed with polymerase chain reaction (PCR) using TaqMan probes specific for each allele. RESULTS:Our results show that the distribution of Met315Ile and Ile585Val genotypes and alleles is similar in patients with neuropathic pain and in healthy subjects. However, the Met315Met genotype is more frequent in females diagnosed as suffering neuropathic pain. No differences were observed when we segregate the patients according to visual analogue scale values. CONCLUSIONS:The observation of differences in the distribution of Met315Ile TRPV1 genotypes only in females diagnosed of neuropathic pain suggests that this polymorphism, together with other physiological factors such as sex, may influence individual susceptibility to neuropathic pain.

journal_name

Med Clin (Barc)

journal_title

Medicina clinica

authors

Armero P,Muriel C,López M,Santos J,González-Sarmiento R

doi

10.1016/j.medcli.2011.10.028

subject

Has Abstract

pub_date

2012-06-02 00:00:00

pages

1-4

issue

1

eissn

0025-7753

issn

1578-8989

pii

S0025-7753(12)00050-4

journal_volume

139

pub_type

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