Association of the estrogen receptor alpha gene polymorphisms with osteoporosis in the Mexican population
Abstract
The estrogen receptor gene (ERα) has been implicated in the development of osteoporosis. In this study, the association of two ERα gene polymorphic markers (a TA dinucleotide repeat and a single nucleotide polymorphism, G2014A) with osteoporosis was tested in 70 osteoporotic women, 70 non-osteoporotic women and 500 subjects from the Mexican population. According to the genetic analysis of the Mexican population using eight unlinked polymorphic markers, we found that our population is structured into three subpopulations; therefore, the allele-phenotype relationship was analyzed with a statistical method that considered population stratification. We found that the G2014A polymorphism is associated with the presence of osteoporosis while the TA dinucleotide repeat is not. The G allele and the GG genotype frequencies of the G2014A marker were significantly higher in osteoporotic than in non-osteoporotic women. Likewise, subjects bearing the G allele in heterozygous or homozygous displayed lower values for lumbar bone mineral density and T score than those who did not present any G allele. The effect of confounders for osteoporosis on the association of G allele-osteoporosis was ruled out. In summary, we conclude that the G2014 polymorphism may become a useful marker for genetic studies of osteoporosis in the Mexican population. © 2007 The Authors Journal compilation © 2007 Blackwell Munksgaard.
Más información
Título según WOS: | Association of the estrogen receptor alpha gene polymorphisms with osteoporosis in the Mexican population |
Título según SCOPUS: | Association of the estrogen receptor a gene polymorphisms with osteoporosis in the Mexican population |
Título de la Revista: | CLINICAL GENETICS |
Volumen: | 72 |
Número: | 6 |
Editorial: | Wiley |
Fecha de publicación: | 2007 |
Página de inicio: | 574 |
Página final: | 581 |
Idioma: | English |
URL: | http://doi.wiley.com/10.1111/j.1399-0004.2007.00898.x |
DOI: |
10.1111/j.1399-0004.2007.00898.x |
Notas: | ISI, SCOPUS |