Myers Chelsea E, Klein Barbara E K, Gangnon Ronald, Sivakumaran Theru A, Iyengar Sudha K, Klein Ronald
Department of Ophthalmology and Visual Sciences, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
Department of Ophthalmology and Visual Sciences, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
Ophthalmology. 2014 Oct;121(10):1949-55. doi: 10.1016/j.ophtha.2014.04.040. Epub 2014 Jun 20.
To examine the association of current cigarette smoking and pack-years smoked with the incidence and progression of age-related macular degeneration (AMD) and to examine the interactions of current smoking and pack-years smoked with complement factor H (CFH, rs1061170) and age-related maculopathy susceptibility 2 (ARMS2, rs10490924) genotype.
A longitudinal population-based study of AMD in a representative American community. Examinations were performed every 5 years over a 20-year period.
A total of 4439 participants in the population-based Beaver Dam Eye Study (BDES).
Age-related macular degeneration status was determined from grading retinal photographs. Multi-state models were used to model the relationship of current smoking and pack-years smoked and interactions with CFH and ARMS2 with the incidence and progression of AMD over the entire age range.
Incidence and progression of AMD over a 20-year period and interactions between current smoking and pack-years smoked with CFH and ARMS2 genotype.
The incidence of early AMD over the 20-year period was 24.4%, and the incidence of late AMD was 4.5%. Current smoking was associated with an increased risk of transitioning from minimal to moderate early AMD. A greater number of pack-years smoked was associated with an increased risk of transitioning from no AMD to minimal early AMD and from severe early AMD to late AMD. Current smoking and a greater number of pack-years smoked were associated with an increased risk of death. There were no statistically significant multiplicative interactions between current smoking or pack-years smoked and CFH or ARMS2 genotype.
Current smoking and a greater number of pack-years smoked increase the risk of the progression of AMD. This has important health care implications because smoking is a modifiable behavior.
研究当前吸烟情况及吸烟包年数与年龄相关性黄斑变性(AMD)的发病率和病情进展之间的关联,并研究当前吸烟及吸烟包年数与补体因子H(CFH,rs1061170)和年龄相关性黄斑病变易感性2(ARMS2,rs10490924)基因分型之间的相互作用。
一项基于美国代表性社区人群的AMD纵向研究。在20年期间每5年进行一次检查。
基于人群的比弗迪尔姆眼研究(BDES)中的4439名参与者。
根据视网膜照片分级确定年龄相关性黄斑变性状态。使用多状态模型来模拟当前吸烟情况、吸烟包年数以及与CFH和ARMS2的相互作用与整个年龄范围内AMD发病率和病情进展之间的关系。
20年期间AMD的发病率和病情进展,以及当前吸烟和吸烟包年数与CFH和ARMS2基因分型之间的相互作用。
20年期间早期AMD的发病率为24.4%,晚期AMD的发病率为4.5%。当前吸烟与从轻度早期AMD转变为中度早期AMD的风险增加相关。吸烟包年数越多,与从无AMD转变为轻度早期AMD以及从重度早期AMD转变为晚期AMD的风险增加相关。当前吸烟和吸烟包年数越多与死亡风险增加相关。当前吸烟或吸烟包年数与CFH或ARMS2基因分型之间没有统计学上显著的相乘相互作用。
当前吸烟以及吸烟包年数越多会增加AMD病情进展的风险。这具有重要的医疗保健意义,因为吸烟是一种可改变的行为。