Ricci Federico, Zampatti Stefania, D'Abbruzzi Francesca, Missiroli Filippo, Martone Claudia, Lepre Tiziana, Pietrangeli Ilenia, Sinibaldi Cecilia, Peconi Cristina, Novelli Giuseppe, Giardina Emiliano
Unità Operative Semplici Dipartimentali Patologia Retinica Fondazione PTV Policlinico Tor Vergata, Rome, Italy.
Arch Ophthalmol. 2009 Oct;127(10):1368-72. doi: 10.1001/archophthalmol.2009.237.
To determine the effects of the polymorphisms CFH Tyr402His and ARMS2 del443ins54 on susceptibility to age-related macular degeneration (AMD) and to find the frequencies of these single-nucleotide polymorphisms in an Italian population that was not examined clinically.
A total of 286 control subjects (126 men and 160 women) and 159 white patients (73 men and 86 women) harboring exudative AMD in 1 eye were recruited. A third group of 182 DNA samples from blood donors of the same geographical areas were also typed to assess the frequency of CFH Tyr402His and ARMS2 del443ins54 polymorphisms in the general population. The data were analyzed statistically by a standard 2 x 2 table, Fisher exact tests, and odds ratios.
The deletion-insertion at chromosome 10q26 (del443ins54) showed the strongest association with AMD in terms of both P value and odds ratio (P = 2.7 x 10(-15); odds ratio = 3.25), and a highly significant association was also confirmed for Tyr402His at the CFH locus (P = 9.9 x 10(-13); odds ratio = 2.86). We found no differences in allele and genotype association between classic and occult choroidal neovascularization. We also observed that 39% of the samples in the general Italian population were at least 5.4 times more likely than control subjects to develop AMD.
To our knowledge, this is the first confirmation of the association of del443ins54 in Italian patients with AMD, and we also confirmed the association of Tyr402His with CFH. Genetic analysis of the general population suggested that analysis of the ARMS2 and CFH risk alleles alone may be helpful in differentiating high-risk individuals (odds ratio > 5.00) from low-risk individuals (odds ratio < 0.45).
Individuals at high risk for developing AMD could be identified and selected for specific prevention programs. In this context, the development of prevention programs based on dietary antioxidants or on close monitoring of at-risk individuals should be considered or suggested.
确定补体因子H(CFH)基因Tyr402His多态性和含血管生成素样蛋白2(ARMS2)基因del443ins54多态性与年龄相关性黄斑变性(AMD)易感性的关系,并在未经临床检查的意大利人群中找出这些单核苷酸多态性的频率。
共招募了286名对照受试者(126名男性和160名女性)以及159名单眼患有渗出性AMD的白人患者(73名男性和86名女性)。还对来自同一地理区域的182名献血者的DNA样本进行基因分型,以评估CFH基因Tyr402His多态性和ARMS2基因del443ins54多态性在普通人群中的频率。采用标准的2×2列联表、Fisher精确检验和比值比进行统计学分析。
就P值和比值比而言,位于10号染色体q26区域的缺失插入突变(del443ins54)与AMD的关联性最强(P = 2.7×10⁻¹⁵;比值比 = 3.25),并且CFH基因座上的Tyr402His多态性也显示出高度显著的关联性(P = 9.9×10⁻¹³;比值比 = 2.86)。我们发现典型性和隐匿性脉络膜新生血管之间的等位基因和基因型关联性并无差异。我们还观察到,在意大利普通人群中,39%的样本发生AMD的可能性至少是对照受试者的5.4倍。
据我们所知,这是首次证实del443ins54多态性与意大利AMD患者的关联性,并且我们也证实了Tyr402His多态性与CFH基因的关联性。普通人群的基因分析表明,仅对ARMS2和CFH风险等位基因进行分析可能有助于区分高风险个体(比值比 > 5.00)和低风险个体(比值比 < 0.45)。
可以识别出有发生AMD高风险的个体,并将其纳入特定的预防项目。在此背景下,应考虑或建议制定基于膳食抗氧化剂或对高风险个体进行密切监测的预防项目。