Singapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore.
Ophthalmology and Visual Sciences Academic Clinical Program, Duke-NUS Medical School, National University of Singapore, Singapore, Singapore.
Sci Rep. 2019 Oct 31;9(1):15708. doi: 10.1038/s41598-019-52156-y.
To elucidate the molecular processes associated with the development of myopic macular degeneration (MMD), we measured the intraocular concentrations of molecular factors in emmetropic and myopic eyes. This is a retrospective clinic-based case-control study that included eyes undergoing routine cataract surgery whereby aqueous humour samples were obtained. We measured the concentrations of pigment epithelium derived factor(PEDF), matrix metalloproteinase 2(MMP-2), tissue inhibitor of metalloproteinase(TIMP-2), vascular endothelial growth factor isoform A(VEGF-A), interleukin 8(IL-8), interleukin 6(IL-6), C-reactive protein(CRP), angiopoietin 2(Ang2), and amphiregulin. 38 eyes (axial length (AL): 22.4-32.4 mm), including 12 highly myopic (HM) eyes (AL ≥ 26.5 mm) without MMD and 12 HM eyes with MMD but without neovascularization were included. Eyes with MMD were found to have significantly lower VEGF-A levels (p = 0.007) and higher MMP-2 levels (p = 0.02) than control eyes after adjusting for age and gender. MMP-2 levels correlated positively (r = 0.58, p = 0.002), while VEGF-A levels correlated negatively with longer axial length (r = -0.75, p < 0.001). Both the concentrations of VEGF-A (P = 0.25) and MMP-2 (P = 0.69) were not significantly associated with MMD after adjusting for AL. These findings suggest that the predominant mechanism underlying the development of non-neovascular MMD may be axial elongation, driven in part by MMP-2 related mechanisms.
为了阐明与近视性黄斑变性(MMD)发展相关的分子过程,我们测量了正视眼和近视眼的眼内分子因子浓度。这是一项回顾性基于临床的病例对照研究,包括接受常规白内障手术的眼睛,在此过程中获得房水样本。我们测量了色素上皮衍生因子(PEDF)、基质金属蛋白酶 2(MMP-2)、金属蛋白酶组织抑制剂 2(TIMP-2)、血管内皮生长因子 A 同工型(VEGF-A)、白细胞介素 8(IL-8)、白细胞介素 6(IL-6)、C 反应蛋白(CRP)、血管生成素 2(Ang2)和 Amphiregulin 的浓度。纳入了 38 只眼(眼轴(AL):22.4-32.4 毫米),包括 12 只高度近视(HM)眼(AL≥26.5 毫米),无 MMD 和 12 只 HM 眼伴 MMD 但无新生血管形成。调整年龄和性别后,发现 MMD 眼的 VEGF-A 水平显著降低(p=0.007),MMP-2 水平显著升高(p=0.02)。MMP-2 水平与眼轴长度呈正相关(r=0.58,p=0.002),而 VEGF-A 水平与眼轴长度呈负相关(r=-0.75,p<0.001)。调整 AL 后,VEGF-A(P=0.25)和 MMP-2(P=0.69)的浓度与 MMD 均无显著相关性。这些发现表明,非新生血管性 MMD 发展的主要机制可能是轴向伸长,部分由 MMP-2 相关机制驱动。