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眼轴长度与近视性黄斑变性和房水中分子因子水平的相关性。

Correlation of axial length and myopic macular degeneration to levels of molecular factors in the aqueous.

机构信息

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.

出版信息

Sci Rep. 2019 Oct 31;9(1):15708. doi: 10.1038/s41598-019-52156-y.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f66a/6823508/058a42a12b6a/41598_2019_52156_Fig1_HTML.jpg

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