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Invest Ophthalmol Vis Sci. 2020 May 11;61(5):48. doi: 10.1167/iovs.61.5.48.
Ultraviolet radiation from sunlight contributes to age-related cataract and skin cancer. The EPHA2 gene is implicated in both these diseases. The purpose of this study was to determine whether age-related cataract and skin cancer are associated in a cohort of older Australians.
A cross-sectional study was performed using the Historical Cohort of the Registry of Senior Australians. Individuals aged ≥65 years or aged ≥50 years and of Aboriginal or Torres Strait Islander descent, who had an aged care eligibility assessment between July 2005 and June 2015, and had a history of cataract surgery and/or skin cancer according to the Australian Government Medicare Benefits Schedule dataset, during the 3-year period prior, were evaluated (N = 599,316). A multivariable logistic regression model was used to determine association and multiple hypothesis correction was employed.
Of the evaluated individuals, 87,097 (14.5%) had a history of cataract and 170,251 (28.4%) a history of skin cancer. Among those with a history of cataract, 20,497 (23.5%), 1127 (1.3%), and 14,730 (16.9%) individuals had a concurrent history of keratinocyte, melanoma, and premalignant/solar keratosis, respectively. Those with a history of cataract were 19% more likely to have a history of skin cancer (odds ratio [OR], 1.19; 95% confidence interval [CI], (1.17-1.21). Co-occurrence of keratinocyte skin cancer was 16% (OR, 1.16; 95% CI, 1.14-1.18), melanoma 21% (OR, 1.21; 95% CI, 1.13-1.29), and premalignant/solar keratosis 19% (OR, 1.19; 95% CI, 1.17-1.22) more in the presence than absence of history of cataract.
Age-related cataract is positively associated with skin cancer and its subtypes, including premalignant lesions in an older Australian population.
阳光中的紫外线辐射导致与年龄相关的白内障和皮肤癌。EPHA2 基因与这两种疾病都有关。本研究的目的是确定在澳大利亚老年人群体中,与年龄相关的白内障和皮肤癌是否相关。
本研究采用澳大利亚老年人登记处的历史队列进行了一项横断面研究。在 2005 年 7 月至 2015 年 6 月期间,年龄≥65 岁或年龄≥50 岁且为原住民或托雷斯海峡岛民的个体,有资格进行老年护理评估,并且在过去 3 年期间根据澳大利亚政府医疗保险福利计划数据集接受了白内障手术和/或皮肤癌治疗(N=599316)。采用多变量逻辑回归模型确定关联,同时进行了多重假设校正。
在所评估的个体中,87097 人(14.5%)有白内障病史,170251 人(28.4%)有皮肤癌病史。在有白内障病史的人群中,分别有 20497 人(23.5%)、1127 人(1.3%)和 14730 人(16.9%)有同时存在的角化细胞癌、黑色素瘤和癌前/日光性角化病病史。有白内障病史的个体发生皮肤癌的可能性增加 19%(优势比[OR],1.19;95%置信区间[CI],(1.17-1.21)。同时存在角化细胞皮肤癌的可能性增加 16%(OR,1.16;95% CI,1.14-1.18)、黑色素瘤增加 21%(OR,1.21;95% CI,1.13-1.29)和癌前/日光性角化病增加 19%(OR,1.19;95% CI,1.17-1.22)。
在澳大利亚老年人群体中,与年龄相关的白内障与皮肤癌及其亚型呈正相关,包括癌前病变。