Institute of Human Genetics, University of Regensburg, 93053 Regensburg, Germany.
Department of Ophthalmology, Regensburg University Medical Center, 93053 Regensburg, Germany.
Int J Mol Sci. 2022 May 29;23(11):6094. doi: 10.3390/ijms23116094.
Anti-VEGF treatment for neovascular age-related macular degeneration (nAMD) has been FDA-approved in 2004, and since then has helped tens of thousands of patients worldwide to preserve vision. Still, treatment responses vary widely, emphasizing the need for genetic biomarkers to robustly separate responders from non-responders. Here, we report the findings of an observational study compromising 179 treatment-naïve nAMD patients and their reaction to treatment after three monthly doses of anti-VEGF antibodies. We show that established criteria of treatment response such as visual acuity and central retinal thickness successfully divides our cohort into 128 responders and 51 non-responders. Nevertheless, retinal thickness around the fovea revealed significant reaction to treatment even in the formally categorized non-responders. To elucidate genetic effects underlying our criteria, we conducted an undirected genome-wide association study followed by a directed replication study of 30 previously reported genetic variants. Remarkably, both approaches failed to result in significant findings, suggesting study-specific effects were confounding the present and previous discovery studies. Of note, all studies so far are greatly underpowered, hampering interpretation of genetic findings. In consequence, we highlight the need for an extensive phenotyping study with sample sizes exceeding at least 15,000 to reliably assess anti-VEGF treatment responses in nAMD.
抗血管内皮生长因子(VEGF)治疗新生血管性年龄相关性黄斑变性(nAMD)于 2004 年获得美国食品和药物管理局(FDA)批准,此后为数以万计的全球患者保留了视力。尽管如此,治疗反应差异很大,这强调了需要遗传生物标志物来稳健地区分应答者和非应答者。在这里,我们报告了一项观察性研究的结果,该研究包括 179 名未经治疗的 nAMD 患者及其在接受三剂抗 VEGF 抗体治疗后的反应。我们发现,视力和中心视网膜厚度等既定的治疗反应标准成功地将我们的队列分为 128 名应答者和 51 名无应答者。然而,即使在正式归类为无应答者中,黄斑周围的视网膜厚度也显示出对治疗有明显反应。为了阐明我们标准背后的遗传效应,我们进行了一项无向全基因组关联研究,随后对 30 个先前报道的遗传变异进行了定向复制研究。值得注意的是,这两种方法都没有产生显著的发现,这表明研究特定的影响混淆了目前和以前的发现研究。值得注意的是,到目前为止,所有的研究都大大缺乏效力,阻碍了对 nAMD 中抗 VEGF 治疗反应的遗传发现的解释。因此,我们强调需要进行广泛的表型研究,样本量至少超过 15000 例,以可靠地评估 nAMD 中的抗 VEGF 治疗反应。