Lin Jonathan B, Serghiou Stylianos, Miller Joan W, Vavvas Demetrios G
Department of Ophthalmology, Mass Eye and Ear and Harvard Medical School, Boston, MA 02114, USA.
Google LLC, Mountain View, CA 94043, USA.
J Clin Med. 2022 Apr 23;11(9):2371. doi: 10.3390/jcm11092371.
Although complement inhibition has emerged as a possible therapeutic strategy for age-related macular degeneration (AMD), there is not a clear consensus regarding what aspects of the complement pathway are dysregulated in AMD and when this occurs relative to disease stage. We recently published a systematic review describing systemic complement activation profiles in patients with early/intermediate AMD or geographic atrophy (GA) compared to non-AMD controls. Here, we sought to meta-analyze these results to estimate the magnitude of complement dysregulation in AMD using restricted maximum likelihood estimation. The seven meta-analyzed studies included 710 independent participants with 23 effect sizes. Compared with non-AMD controls, patients with early/intermediate nonexudative AMD (N = 246) had significantly higher systemic complement activation, as quantified by the levels of complement proteins generated by common final pathway activation, and significantly lower systemic complement inhibition. In contrast, there were no statistically significant differences in the systemic levels of complement common final pathway activation products or complement inhibition in patients with GA (N = 178) versus non-AMD controls. We provide evidence that systemic complement over-activation is a feature of early/intermediate nonexudative AMD; no such evidence was identified for patients with GA. These findings provide mechanistic insights and inform future clinical trials.
尽管补体抑制已成为年龄相关性黄斑变性(AMD)一种可能的治疗策略,但对于补体途径的哪些方面在AMD中失调以及相对于疾病阶段何时发生失调,目前尚无明确共识。我们最近发表了一项系统评价,描述了与非AMD对照相比,早期/中期AMD或地图样萎缩(GA)患者的全身补体激活情况。在此,我们试图对这些结果进行荟萃分析,以使用限制最大似然估计来估计AMD中补体失调的程度。纳入荟萃分析的七项研究包括710名独立参与者,有23个效应量。与非AMD对照相比,早期/中期非渗出性AMD患者(N = 246)的全身补体激活显著更高,这通过共同终末途径激活产生的补体蛋白水平来量化,且全身补体抑制显著更低。相比之下,GA患者(N = 178)与非AMD对照相比,全身补体共同终末途径激活产物水平或补体抑制在统计学上无显著差异。我们提供的证据表明,全身补体过度激活是早期/中期非渗出性AMD的一个特征;未在GA患者中发现此类证据。这些发现提供了机制性见解,并为未来的临床试验提供了参考。