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分析 CFH Y402H 多态性与新生血管性年龄相关性黄斑变性(nAMD)患者对玻璃体内雷珠单抗治疗反应的关系。

Analysis of the association between CFH Y402H polymorphism and response to intravitreal ranibizumab in patients with neovascular age-related macular degeneration (nAMD).

机构信息

Malaysian Research Institute on Ageing, Universiti Putra Malaysia, Serdang, Selangor DE, Malaysia.

出版信息

Bosn J Basic Med Sci. 2018 Aug 1;18(3):260-267. doi: 10.17305/bjbms.2018.2493.

Abstract

Pharmacogenetic studies indicate that a variable response to anti-vascular endothelial growth factor (VEGF) therapy in patients with neovascular form of AMD (nAMD) may be due to polymorphisms in the complement factor H gene (CFH). This study is the first to investigate the association between CFH Y402H polymorphism and the response to ranibizumab therapy in Malaysian patients with nAMD. We included 134 patients with nAMD, examined between September 2014 and February 2016. The diagnosis of nAMD was confirmed by ophthalmologic examination, before ranibizumab therapy was started. Each patient received an intravitreal injection of 0.5 mg/0.05 ml ranibizumab following a treat-and-extend (TE) regimen. Best-corrected visual acuity (BCVA) and central retinal thickness (CRT) were recorded after 3 and 6 months following the first injection and compared with the baseline values. Genotyping of Y402H (rs1061170) polymorphism was performed using PCR-RFLP and the amplified product was digested with MluCI restriction enzyme. Association between the Y402H genotypes and response to treatment was determined by a logistic regression analysis of responder (n = 49) and non-responder (n = 84) group. Significantly worse mean BCVA was observed for the CC genotype compared to the TT + CT genotype in the total sample after 6-month follow-up (p = 0.018). Comparing the baseline and 6-month point measurements, improved mean BCVA was observed in responder group, while worse mean BCVA was recorded for non-responder group. However, our regression analysis, adjusted for confounding factors, showed no significant association between the Y402H genotypes and response to treatment in nAMD patients under the recessive model (p > 0.05). Overall, our results suggest that factors other than Y402H polymorphism may be involved in the progression of nAMD after treatment with anti-VEGF agents, in Malaysian population.

摘要

药物遗传学研究表明,血管内皮生长因子(VEGF)治疗在新生血管性年龄相关性黄斑变性(nAMD)患者中的反应存在差异,这可能与补体因子 H 基因(CFH)的多态性有关。本研究首次探讨了 CFH Y402H 多态性与马来亚 nAMD 患者对雷珠单抗治疗反应之间的相关性。我们纳入了 134 例 nAMD 患者,这些患者于 2014 年 9 月至 2016 年 2 月间接受检查。在开始雷珠单抗治疗之前,通过眼科检查确认 nAMD 的诊断。每位患者在开始治疗后均接受了玻璃体内注射 0.5mg/0.05ml 的雷珠单抗,采用治疗后随访(TE)方案。在第一次注射后 3 个月和 6 个月时记录最佳矫正视力(BCVA)和中心视网膜厚度(CRT),并与基线值进行比较。使用 PCR-RFLP 对 Y402H(rs1061170)多态性进行基因分型,用 MluCI 限制酶对扩增产物进行消化。通过对应答者(n=49)和非应答者(n=84)组的逻辑回归分析,确定 Y402H 基因型与治疗反应之间的关系。在总样本中,6 个月随访时 CC 基因型的平均 BCVA 明显低于 TT+CT 基因型(p=0.018)。与基线和 6 个月的测量值相比,应答组的平均 BCVA 有所改善,而非应答组的平均 BCVA 则有所下降。然而,我们的回归分析调整混杂因素后,在隐性模型下,nAMD 患者的 Y402H 基因型与治疗反应之间无显著相关性(p>0.05)。总体而言,我们的结果表明,马来亚人群在接受抗 VEGF 药物治疗后,除了 Y402H 多态性外,其他因素可能也与 nAMD 的进展有关。

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