年龄相关性黄斑病变易感性 2 基因变异与光动力疗法联合玻璃体内阿柏西普治疗息肉状脉络膜血管病变 12 个月结局的相关性。
Association of an age-related maculopathy susceptibility 2 gene variant with the 12-month outcomes of intravitreal aflibercept combined with photodynamic therapy for polypoidal choroidal vasculopathy.
机构信息
Department of Surgery, Division of Ophthalmology, Kobe University Graduate School of Medicine, 7-5-2 Kusunoki-cho, Chuo-ku, Kobe, 650-0017, Japan.
Department of Ophthalmology and Visual Sciences, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka, 545-8585, Japan.
出版信息
Jpn J Ophthalmol. 2019 Sep;63(5):389-395. doi: 10.1007/s10384-019-00683-6. Epub 2019 Aug 2.
PURPOSE
To determine the association of age-related maculopathy susceptibility 2 (ARMS2) gene polymorphisms with the 12-month outcomes of intravitreal aflibercept combined with photodynamic therapy (IVA+PDT) in polypoidal choroidal vasculopathy (PCV).
STUDY DESIGN
Interventional cohort study.
METHODS
This was a retrospective study of 48 consecutive treatment-naïve PCV patients. The patients underwent IVA+PDT as the initial therapy and were followed up for more than 12 months under a pro re nata regimen. The single nucleotide polymorphism (SNP) at rs10490924 in the ARMS2 gene was genotyped using the TaqMan assay. The clinical characteristics and outcomes of IVA+PDT were compared among the 3 genotypes at rs10490924. Multivariate regression analysis was performed to evaluate the influence of the clinical cofactors on the association of rs10490924 with the visual outcome at 12 months after the first IVA+PDT.
RESULTS
No significant difference was found in the baseline characteristics among the 3 genotypes (n = 9, 23, and 16 for the GG, GT, and TT genotypes, respectively). All the patients, regardless of genotype, showed a significant improvement in vision, central retinal thickness, and subfoveal choroidal thickness at all time points measured after the initial IVA+PDT. The number of treatments was significantly smaller in the patients with the GG genotype than in those with the GT or the TT genotype. On multivariate logistic regression analysis, the number of the T allele at rs10490924 was significantly associated with the chance of retreatment after the initial IVA+PDT.
CONCLUSION
The presence of the G allele at rs10490924 in the ARMS2 gene is likely associated with a lower chance of retreatment after IVA+PDT in patients with PCV.
目的
确定年龄相关性黄斑病变易感性 2(ARMS2)基因多态性与息肉状脉络膜血管病变(PCV)中玻璃体内阿柏西普联合光动力疗法(IVA+PDT)治疗 12 个月的结果之间的关联。
研究设计
干预性队列研究。
方法
这是一项回顾性研究,共纳入 48 例未经治疗的 PCV 患者。患者接受IVA+PDT 作为初始治疗,并在 12 个月以上的时间内根据需要进行治疗。使用 TaqMan 检测法对 ARMS2 基因 rs10490924 处的单核苷酸多态性(SNP)进行基因分型。比较 rs10490924 处 3 种基因型的 IVA+PDT 临床特征和结局。采用多变量回归分析评估临床合并因素对 rs10490924 与首次 IVA+PDT 后 12 个月视力结果之间关联的影响。
结果
3 种基因型(GG、GT 和 TT 基因型的患者分别为 9、23 和 16 例)之间的基线特征无显著差异。所有患者,无论基因型如何,在初始 IVA+PDT 后所有测量时间点的视力、中心视网膜厚度和中心凹下脉络膜厚度均有显著改善。与 GT 或 TT 基因型的患者相比,GG 基因型患者的治疗次数明显减少。多变量逻辑回归分析显示,rs10490924 处 T 等位基因的数量与初始 IVA+PDT 后再次治疗的机会显著相关。
结论
ARMS2 基因 rs10490924 处 G 等位基因的存在可能与 PCV 患者 IVA+PDT 后再次治疗的机会较低有关。