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BMC Research Notes 2010
A microsatellite polymorphism in IGF1 gene promoter and longevity in a Han Chinese populationAbstract: We recruited 493 elderly Han Chinese individuals (females ≥ 94; males ≥ 90) and 425 young individuals (controls) from Dujiangyan (Sichuan province, China). The genotype distributions and allele frequencies of the microsatellite site in the elderly and control groups were compared by chi square test.Our results suggested that there was no association between the microsatellite polymorphism and longevity in our Han Chinese population. However, there were more male persons with 18/21 genotype in elderly group than that in control group (11.11 vs. 5.45%, p = 0.011). As the difference was not significant when corrected by Bonferroni method, we speculate that the 18/21 genotype can not be functional in longevity; however, it may link with the real functional loci as there is a long haplotype block embracing the microsatellite locus.There was no association between polymorphism of the microsatellite in promoter of IGF1 gene and longevity in our study. Future association studies containing the long haplotype block are deserved and can test our speculation of the potential linkage of 18/21 genotype and functional loci.IGF1 (Insulin-like growth factor 1) plays a number of important roles in the human body. It is involved in physiological processes such as growth, development, and metabolism [1], and has been implicated as a factor in the development of common diseases [2]. Meanwhile, a conserved insulin/IGF1 signal pathway which may affect ageing and longevity is known in E.coli, yeast, drosophila, mice and humans [3-7]. Elucidating the functions of insulin/IGF1 pathway in ageing and longevity is a current hot spot in longevity research [8].Serum IGF1 levels appear to influence susceptibility to disease, and therefore longevity. For example, people with a high level of circulating IGF1 are more susceptible to cancers, while a low level of circulating IGF1 is a risk factor for cardiovascular diseases, premature atherogenesis, and diabetes [5]. Furthermore, Yang et al. suggeste
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