International Centre for Eye Health, Department of Clinical Research, Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine (LSHTM), Keppel Street, London WC1E 7HT, UK.
Mech Ageing Dev. 2013 Jul-Aug;134(7-8):338-45. doi: 10.1016/j.mad.2013.05.002. Epub 2013 May 20.
Certain anatomic and functional parameters of the eye change with increasing chronological age. They may, therefore, serve as potential biomarkers of ageing. We investigated associations between four such ocular parameters (lens density, retinal vessel calibre, corneal endothelial cells and retinal nerve fibre layer thickness) and two 'cellular' biomarkers of ageing (leukocyte telomere length and CDKN2A expression), with frailty (a clinical correlate of biological ageing) in a population of South African adults. All ocular parameters revealed an association with either telomere length or CDKN2A expression. However, lens density was most strongly correlated with age, increased CDKN2A expression, and with frailty (p=0.05 and 0.03, respectively). Narrow retinal arteriolar diameter, associated with increased chronological age, was also associated with increased CDK2NA expression (0.42 vs. 0.31, p=0.02) but not with frailty. Ocular parameters may aid in determining biological age, warranting investigation in longitudinal studies.
随着年龄的增长,眼睛的某些解剖和功能参数会发生变化。因此,它们可以作为衰老的潜在生物标志物。我们研究了四个这样的眼部参数(晶状体密度、视网膜血管直径、角膜内皮细胞和视网膜神经纤维层厚度)与两种衰老的“细胞”生物标志物(白细胞端粒长度和 CDKN2A 表达)与南非成年人中衰弱(生物学衰老的临床相关物)之间的关系。所有眼部参数均与端粒长度或 CDKN2A 表达呈关联。然而,晶状体密度与年龄、CDKN2A 表达的增加以及衰弱(分别为 p=0.05 和 0.03)的相关性最强。与年龄增加相关的视网膜小动脉直径也与增加的 CDKN2A 表达相关(0.42 与 0.31,p=0.02),但与衰弱无关。眼部参数可能有助于确定生物年龄,值得在纵向研究中进一步研究。