Bermejo Pareja, Félix Carro Díaz, Eva
IGF-I gene variability is associated with an increased risk for AD [artículo] - Neurobiology of Aging, 2011 - 32(3):556.e3-e11.
Formato Vancouver:
Vargas T, Martínez García A, Antequera D, Vilella E, Clarimon J, Mateo I, et al. IGF-I gene variability is associated with an increased risk for AD. Neurobiol Aging. 2011;32(3):556.e3-11.
PMID: 21176999
Contiene 60 referencias
Insulin-like growth factor I (IGF-I), a neuroprotective factor with a wide spectrum of actions in the adult brain, is involved in the pathogenesis of Alzheimer's disease (AD). Circulating levels of IGF-I change in AD patients and are implicated in the clearance of brain amyloid beta (Aβ) complexes. To investigate this hypothesis, we screened the IGF-I gene for various well known single nucleotide polymorphisms (SNPs) covering % of the gene variability in a population of 2352 individuals. Genetic analysis indicated different distribution of genotypes of 1 single nucleotide polymorphism, and 1 extended haplotype in the AD population compared with healthy control subjects. In particular, the frequency of rs972936 GG genotype was significantly greater in AD patients than in control subjects (63% vs. 55%). The rs972936 GG genotype was associated with an increased risk for disease, independently of apolipoprotein E genotype, and with enhanced circulating levels of IGF-I. These findings suggest that polymorphisms within the IGF-I gene could infer greater risk for AD through their effect on IGF-I levels, and confirm the physiological role IGF-I in the pathogenesis of AD.
IGF-I gene variability is associated with an increased risk for AD [artículo] - Neurobiology of Aging, 2011 - 32(3):556.e3-e11.
Formato Vancouver:
Vargas T, Martínez García A, Antequera D, Vilella E, Clarimon J, Mateo I, et al. IGF-I gene variability is associated with an increased risk for AD. Neurobiol Aging. 2011;32(3):556.e3-11.
PMID: 21176999
Contiene 60 referencias
Insulin-like growth factor I (IGF-I), a neuroprotective factor with a wide spectrum of actions in the adult brain, is involved in the pathogenesis of Alzheimer's disease (AD). Circulating levels of IGF-I change in AD patients and are implicated in the clearance of brain amyloid beta (Aβ) complexes. To investigate this hypothesis, we screened the IGF-I gene for various well known single nucleotide polymorphisms (SNPs) covering % of the gene variability in a population of 2352 individuals. Genetic analysis indicated different distribution of genotypes of 1 single nucleotide polymorphism, and 1 extended haplotype in the AD population compared with healthy control subjects. In particular, the frequency of rs972936 GG genotype was significantly greater in AD patients than in control subjects (63% vs. 55%). The rs972936 GG genotype was associated with an increased risk for disease, independently of apolipoprotein E genotype, and with enhanced circulating levels of IGF-I. These findings suggest that polymorphisms within the IGF-I gene could infer greater risk for AD through their effect on IGF-I levels, and confirm the physiological role IGF-I in the pathogenesis of AD.
