Vickers James C, Craig Jamie E, Stankovich Jim, McCormack Graeme H, West Adrian K, Dickinson Joanne L, McCartney Paul J, Coote Michael A, Healey Danielle L, Mackey David A
School of Medicine, University of Tasmania, Hobart, Tasmania, Australia.
Mol Vis. 2002 Oct 14;8:389-93.
Inheritance of a particular apolipoprotein E gene polymorphism, the epsilon4 allele, has been associated with elevated risk for Alzheimer's disease and a poor outcome following head injury. The neuronal injury associated with Alzheimer's disease and brain injury may have a number of similarities with the nerve cell changes associated with glaucoma. Thus, we have investigated the association of inheritance of apolipoprotein E allelic isoforms (epsilon2, [epsilon]3, and epsilon4) with relative risk for different forms of glaucoma.
Apolipoprotein E genotype was examined in a Tasmanian population sample comprised of glaucoma sufferers with elevated or normal intraocular pressure and compared to a control sample of elderly Tasmanians without glaucoma.
Approximately twice as many normal tension (38.0%) and high tension (34.2%) glaucoma cases possessed an epsilon4 allele compared to control cases (18.9%). The odds of epsilon4 carriers having normal tension glaucoma were significantly greater than for epsilon3 homozygotes (odds ratio 2.45, 95% confidence interval [1.02-5.91]) even after adjusting for age and gender (odd ratio 2.87 [1.02-8.05]). The increased odds of high tension glaucoma among [epsilon]4 allele carriers were not significant (adjusted odds ratio 1.53 [0.64-3.68]).
The data indicate that, in the Tasmanian population, inheritance of the [epsilon]4 allele is associated with elevated risk for glaucomatous changes that are not related to increased intraocular pressure.
特定载脂蛋白E基因多态性,即ε4等位基因的遗传,与阿尔茨海默病风险升高以及头部受伤后预后不良有关。与阿尔茨海默病和脑损伤相关的神经元损伤可能与青光眼相关的神经细胞变化有许多相似之处。因此,我们研究了载脂蛋白E等位基因亚型(ε2、ε3和ε4)的遗传与不同类型青光眼相对风险之间的关联。
在一个塔斯马尼亚人群样本中检测了载脂蛋白E基因型,该样本由眼压升高或正常的青光眼患者组成,并与无青光眼的塔斯马尼亚老年对照样本进行比较。
与对照病例(18.9%)相比,正常眼压(38.0%)和高眼压(34.2%)青光眼病例中携带ε4等位基因的人数大约是其两倍。即使在调整年龄和性别后,ε4携带者患正常眼压青光眼的几率也显著高于ε3纯合子(优势比2.45,95%置信区间[1.02 - 5.91])(调整后优势比2.87 [1.02 - 8.05])。ε4等位基因携带者中高眼压青光眼几率的增加并不显著(调整后优势比1.53 [0.64 - 3.68])。
数据表明,在塔斯马尼亚人群中,ε4等位基因的遗传与与眼压升高无关的青光眼性变化风险升高有关。