Jiang Feng, Xiao Ou, Guo Xinxing, Yin Qiuxia, Luo Lixia, He Mingguang, Li Zhixi
State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-Sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangdong Provincial Clinical Research Center for Ocular Diseases, Guangzhou, Guangdong, China.
Wilmer Eye Institute, Johns Hopkins University, Maryland, Baltimore, USA.
Br J Ophthalmol. 2025 Jan 28;109(2):257-263. doi: 10.1136/bjo-2023-324430.
To investigate the characteristics of myopic maculopathy among highly myopic Chinese children and adolescents and explore its associated risk factors.
Children and adolescents aged 7-17 years with spherical equivalent (SE) ≤ -6.00 dioptres (D) were recruited. Myopic maculopathy was categorised based on the International Meta-Analysis of Pathological Myopia Classification. The extent of diffuse choroidal atrophy (DCA) was classified using Early Treatment Diabetic Retinopathy Study grid (ETDRS). The area of DCA was categorised into three classes relative to optic disk area (DA): A1 (≤1 DA), A2 (1 to ≤5 DA) and A3 (5 to ≤10 DA). Logistic regression was used to identify risk factors associated with myopic maculopathy.
Of the 425 participants aged 13.66±2.67 years, the proportions of tessellated fundus and DCA were 11.76% and 12.24%, and no more severe fundus lesions or 'plus' lesions. The proportion of DCA was 27.03% in children under 11, significantly higher than the 9.12% observed in those aged 11 and older (p<0.001). The percentages of DCA involving the outer, middle and central circles of the ETDRS grid were 42.31%, 55.77% and 1.92%. Myopic maculopathy was significantly associated with younger age (p<0.001), longer axial length (AL; p<0.001) and larger β-zone peripapillary atrophy (β-PPA; p=0.012).
In highly myopic children and adolescents, myopic maculopathy predominantly manifested as DCA (12.24%), with no cases of worse myopic maculopathy or 'plus' lesions. Younger age, longer AL and larger β-PPA were risk factors for myopic maculopathy.
研究高度近视中国儿童和青少年近视性黄斑病变的特征,并探讨其相关危险因素。
招募等效球镜(SE)≤ -6.00 屈光度(D)的7至17岁儿童和青少年。根据病理性近视国际荟萃分析分类对近视性黄斑病变进行分类。使用早期糖尿病视网膜病变研究网格(ETDRS)对弥漫性脉络膜萎缩(DCA)的程度进行分类。DCA面积相对于视盘面积(DA)分为三类:A1(≤1 DA)、A2(1至≤5 DA)和A3(5至≤10 DA)。采用逻辑回归分析确定与近视性黄斑病变相关的危险因素。
425名年龄为13.66±2.67岁的参与者中,眼底呈镶嵌状和DCA的比例分别为11.76%和12.24%,无更严重的眼底病变或“加”性病变。11岁以下儿童DCA比例为27.03%,显著高于11岁及以上儿童的9.12%(p<0.001)。DCA累及ETDRS网格外、中、内圈的百分比分别为42.31%、55.77%和1.92%。近视性黄斑病变与年龄较小(p<0.001)、眼轴长度较长(AL;p<0.001)和较大的视盘周围β区萎缩(β-PPA;p=0.012)显著相关。
在高度近视儿童和青少年中,近视性黄斑病变主要表现为DCA(12.24%),无更严重近视性黄斑病变或“加”性病变的病例。年龄较小、AL较长和β-PPA较大是近视性黄斑病变的危险因素。