Investigation of the low-density lipoprotein receptor gene and cholesterol as a risk factor for migraine


Autoria(s): Curtain, R.; Lea, R. A.; Quinlan, S.; Bellis, C.; Tajouri, L.; Hughes, R.; MacMillan, J.; Griffiths, L. R.
Contribuinte(s)

N. Oktar

Data(s)

01/01/2004

Resumo

The Low-Density Lipoprotein Receptor (LDLR) gene is a cell surface receptor that plays an important role in cholesterol homeostasis. We investigated the (TA)n polymorphism in exon 18 of the LDLR gene on chromosome 19p13.2 performing an association analysis in 244 typical migraine-affected patients, 151 suffering from migraine with aura (MA), 96 with migraine without aura (MO) and 244 unaffected controls. The populations consisted of Caucasians only, and controls were age- and sex-matched. The results showed no significant difference between groups for allele frequency distributions of the (TA)n polymorphism even after separation of the migraine-affected individuals into subgroups of MA and MO affected patients. This is in contradiction to Mochi et al. [Mochi M, Cevoli S, Cortelli P, Pierangeli G, Scapoli C, Soriani S, Montagna P. Investigation of an LDLR gene polymorphism (19p13.2) in susceptibility to migrane without aura. J Neurol Sci 2003; 213 (1-2): 7-10.] who found a positive association of this variant with MO. Our study discusses possible differences between the two studies and extends this research by investigating circulating cholesterol levels in a migraine-affected population. (C) 2004 Elsevier B.V. All rights reserved.

Identificador

http://espace.library.uq.edu.au/view/UQ:71791

Idioma(s)

eng

Publicador

Ege University Press

Palavras-Chave #Clinical Neurology #Neurosciences #Migraine #Chromosome 19 #Association #Ldlr #Polymorphism #Cholesterol #Familial Hemiplegic Migraine #Autosomal-dominant Arteriopathy #Typical Migraine #Chromosome 19p13 #Cacna1a Gene #Aura #Cadasil #Susceptibility #Mutations #Alleles #C1 #321011 Medical Genetics #730107 Inherited diseases (incl. gene therapy)
Tipo

Journal Article