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成纤维细胞生长因子1基因启动子多态性与晚发型阿尔茨海默病的相关性研究

Correlation between the Promoter Polymorphism of Fibroblast Growth Factor 1 gene and Late-onset Alzheimer's Disease
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摘要 目的探讨成纤维细胞生长因子1(FGF-1)基因启动子多态性是否与晚发型阿尔茨海默病(LOAD)相关。方法收集206例尸体检查的样本,包括100例LOAD和年龄匹配的对照组106例。PCRRFLP(Restrictionfragmentlengthpolymorphism)法分析FGF1基因启动子(-1385A/G)的基因型。结果FGF1基因启动子(-1385A/G)的基因型频率分布是:AA型20例(10%),GA型89例(43%),GG型97例(47%),在LOAD组和对照组之间,不同基因型频率分布有显著性差异(P=0.027);GG基因型与LOAD呈正相关(oddsratio=2.02,95%CI:1.16~3.52)。结论FGF1基因启动子(-1385A/G)多态性与LOAD显著相关。 Objective To evaluate the correlation between the promoter polymorphism of Fibroblast Growth Factor 1 (FGF-1) and late-onset Alzheimer's disease (LOAD). Methods Clinic pathological data from 206 autopsies were analyzed, including 100 autopsy-confirmed LOAD patients and 106 age-matched non-demented controls. PCR-RFLP (Restriction fragment length polymorphism) approach was used to determine the genotype of the promoter polymorphism of FGF-1 gene. Results The genotyping frequencies of the promoter polymorphism (-1385 A/G) were AA 20 (10%), GA 89 (43%), GG 97 (47%), respectively. There was significant (P = 0.027) difference of genotyping frequencies between the cases and controls; GG genotype was positively associated with LOAD (odds ratio = 2.02, 95% CI: 1.16~3.52). Conclusion The promoter polymorphism (-1385 A/G) of FGF-1 gene was associated with LOAD.
出处 《中国康复理论与实践》 CSCD 2006年第5期394-395,共2页 Chinese Journal of Rehabilitation Theory and Practice
关键词 晚发型阿尔茨海默病(LOAD) 成纤维细胞生长因子1(FGF-1)基因 启动子多态性 相关性 late-onset Alzheimer's disease fibroblast growth factor 1 (FGF 1) gene promoter polymorphism correlation
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  • 1Selkoe DJ.Alzheimer's disease:genes,proteins,and therapy[J].Physiol Rev,2001,81:741-766.
  • 2Eckenstein FP.Fibroblast growth factors in the nervous system[J].J Neurobiol,1994,25:1467-1480.
  • 3Guo Z,Mattson M.Neurotrophic factors protect cortical synaptic terminals against amyloid-and oxidative stress-induced impairment of glucose transport,glutamate transport and mitochondrial function[J].Cereb Cortex,2000,10:50-57.
  • 4Thorns V,Masliah E.Evidence for neuroprotective effects of acidic fibroblast growth factor in Alzheimer disease[J].J Neuropathol Exp Neurol,1999,58:296-306.
  • 5Everall IP,Trillo-Pazos G,Bell C,et al.Amelioration of neurotoxic effects of HIV envelopo protein gp120 by fibroblast growth factor:a strategy for neuroprotection[J].J Neuropathol Exp Neurol,2001,60:293-301.
  • 6Tooyama I,Akiyama H,McGeer PL,et al.Acidic fibroblast growth factor-like immunoreactivity in brain of Alzheimer patients[J].Neurosci Lett,1991,121:155-158.
  • 7Kimura H,Tooyama I,McGeer PL,et al.Acidic FGF expression in the surroundings of senile plaques[J].Tohoku J Exp Med,1994,174:279-293.
  • 8Ueno S,Ito J,Nagayasu Y,et al.An acidic fibroblast growth factor-like factor secreted into the brain cell culture medium upregulates APOE synthesis,HDL secretion and cholesterol metabolism in rat astrocytes[J].Biochim Biophys Acta,2002,1589:261-272.
  • 9Tada T,Ito J,Asai M,et al.Fibroblast growth factor 1 is produced prior to apolipoprotein E in the astrocytes after cryo-injury of mouse brain[J].Neurochem Int,2004,45:23-30.
  • 10Thorns V,Licastro F,Masliah E,et al.Locally reduced levels of acidic FGF lead to decreased expression of 28-kDa calbindin and contribute to the selective vulnerability of the neurons in the entorhinal cortex in Alzheimer's disease[J].Neuropathology,2001,21:203-211.

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