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首页> 外文期刊>Investigative ophthalmology & visual science >Variants in the APOE Gene Are Associated with Improved Outcome after Anti-VEGF Treatment for Neovascular AMD
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Variants in the APOE Gene Are Associated with Improved Outcome after Anti-VEGF Treatment for Neovascular AMD

机译:APOE基因的变异与抗VEGF治疗新生血管性AMD后的改善结果相关。

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Purpose.: Anti-vascular endothelial growth factor (anti-VEGF) drugs have dramatically improved the treatment of neovascular AMD. In pivotal studies, almost 90% of patients maintain vision, with approximately 30% showing significant improvement. Despite these successes, 10% to 15% of patients continue to lose vision, even with treatment. It has been reported that variants in some AMD-associated genes influence treatment outcome. This study showed an association of treatment outcome with variants in the apolipoprotein E (APOE) gene. Methods.: One hundred ninety-two patients receiving anti-VEGF treatment for subfoveal choroidal neovascularization secondary to AMD were enrolled. Information on demographics, lesion characteristics, delay until treatment, visual acuity (VA), and number of treatments was collected, and variants of APOE were assessed in all patients at baseline. Best corrected logarithm of the minimum angle of resolution (logMAR) VA was recorded in all patients. Results.: The presence of the APOE ?μ4 allele was associated with improved treatment outcome at 3 (P = 0.02) and 12 (P = 0.06) months, compared with the presence of the ?μ2 allele, after adjustment for baseline acuity, treatment delay after first symptoms, age, and sex. Patients with an APOE ?μ4 allele had an odds ratio (OR) of 4.04 (95% confidence interval [CI], 1.11a??14.70) for a 2-line gain in vision from baseline at 3 months (P = 0.03) and an OR of 2.54 (95% CI, 0.61a??10.52; P = 0.20) at 12 months after treatment, based on multivariate analysis. Conclusions.: In patients with neovascular AMD, the presence of the APOE ?μ4 allele conferred significantly better visual outcomes after anti-VEGF treatment than did the ?μ2 allele. These findings suggest a possible role for a personalized approach to treatment with anti-VEGF.
机译:目的:抗血管内皮生长因子(anti-VEGF)药物极大地改善了新血管AMD的治疗。在关键性研究中,几乎90%的患者保持视力,其中大约30%的患者表现出明显的改善。尽管取得了这些成功,即使经过治疗,仍有10%至15%的患者会失去视力。据报道,某些AMD相关基因的变异会影响治疗效果。这项研究表明治疗结果与载脂蛋白E(APOE)基因的变异有关。方法:入选了192例接受抗VEGF治疗的继发于AMD的小凹下脉络膜新生血管的患者。收集有关人口统计学,病变特征,治疗延迟,视敏度(VA)和治疗次数的信息,并在基线时评估所有患者的APOE变异。记录了所有患者的最小分辨角(VA)的最佳校正对数。结果:与基线水平敏锐度调整后的βμ2等位基因相比,APOEβμ4等位基因的存在与3(P = 0.02)和12(P = 0.06)个月的治疗结果改善相关。延迟出现第一个症状,年龄和性别。患有APOEμ4等位基因的患者在3个月时从基线获得2线视力的优势比(OR)为4.04(95%置信区间[CI],1.11a ?? 14.70),且根据多变量分析,治疗后12个月的OR为2.54(95%CI,0.61a≤10.52; P = 0.20)。结论:在新生血管性AMD患者中,抗VEGF治疗后APOEβ?4等位基因的存在显着优于?μ2等位基因。这些发现暗示了个性化抗VEGF治疗方法的可能作用。

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