Seitsonen S P, Jarvela I E, Meri S, Tommila P V, Ranta P H, Immonen I J
Department of Ophthalmology, Helsinki University Central Hospital, Helsinki, Finland.
Eur J Ophthalmol. 2007 Nov-Dec;17(6):943-9. doi: 10.1177/112067210701700612.
Photodynamic therapy (PDT) has been widely used in the treatment of age-related macular degeneration (AMD). The complement cascade has an important role in the tissue reactions occurring after PDT. The Y402H polymorphism of the complement factor H (CFH) gene has been identified as a risk factor for AMD. Since CFH is central in the regulation of the complement system the authors wanted to analyze whether the CFH Y402H polymorphism modifies the PDT outcome in AMD.
A total of 88 patients having been treated with PDT and without further scheduled PDT sessions were analyzed. Depending on the situation at their final PDT session the patients were classified retrospectively as PDT-responders or PDT-nonresponders. All patients were genotyped for the CFH Y402H polymorphism.
The proportion of PDT-responders was 18/26 (69.2%) in patients homozygous for the CFH Y402H risk allele, 34/50 (68.0%) in heterozygous, and 7/12 (58.3%) in patients with the normal genotype (p=0.520). The median number of PDT treatments of the PDT-responders was three for all the genotypes.
The dysfunction of the CFH related to the risk of AMD and caused by the Y402H polymorphism does not modify the outcome of PDT. Genotyping for CFH Y402H cannot be used to select patients for this treatment.
光动力疗法(PDT)已广泛应用于年龄相关性黄斑变性(AMD)的治疗。补体级联反应在PDT后的组织反应中起重要作用。补体因子H(CFH)基因的Y402H多态性已被确定为AMD的一个危险因素。由于CFH在补体系统调节中起核心作用,作者想要分析CFH Y402H多态性是否会改变AMD患者的PDT治疗结果。
共分析了88例接受过PDT治疗且没有进一步计划进行PDT治疗的患者。根据他们最后一次PDT治疗时的情况,将患者回顾性地分为PDT反应者或PDT无反应者。所有患者均进行CFH Y402H多态性基因分型。
CFH Y402H风险等位基因纯合患者中PDT反应者的比例为18/26(69.2%),杂合子患者中为34/50(68.0%),正常基因型患者中为7/12(58.3%)(p = 0.520)。所有基因型的PDT反应者的PDT治疗中位数均为3次。
与AMD风险相关且由Y402H多态性引起的CFH功能障碍不会改变PDT的治疗结果。CFH Y402H基因分型不能用于选择接受该治疗的患者。