Markers of Inflammation, Oxidative Stress, and Endothelial Dysfunction and the 20-Year Cumulative Incidence of Early Age-Related Macular Degeneration The Beaver Dam Eye Study

被引:118
作者
Klein, Ronald [1 ,2 ]
Myers, Chelsea E. [1 ]
Cruickshanks, Karen J. [1 ,3 ]
Gangnon, Ronald E. [2 ,3 ]
Danforth, Lorraine G. [1 ]
Sivakumaran, Theru A. [4 ,5 ,6 ,7 ]
Iyengar, Sudha K. [4 ,5 ,6 ]
Tsai, Michael Y. [8 ]
Klein, Barbara E. K. [1 ]
机构
[1] Univ Wisconsin, Sch Med & Publ Hlth, Dept Ophthalmol & Visual Sci, Madison, WI 53726 USA
[2] Univ Wisconsin, Sch Med & Publ Hlth, Dept Biostat & Med Informat, Madison, WI 53726 USA
[3] Univ Wisconsin, Sch Med & Publ Hlth, Dept Populat Hlth Sci, Madison, WI 53726 USA
[4] Case Western Reserve Univ, Dept Epidemiol & Biostat, Cleveland, OH 44106 USA
[5] Case Western Reserve Univ, Dept Genet, Cleveland, OH 44106 USA
[6] Case Western Reserve Univ, Dept Ophthalmol, Cleveland, OH 44106 USA
[7] Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA
[8] Univ Minnesota, Sch Med, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
COMPLEMENT FACTOR-H; C-REACTIVE PROTEIN; RETINAL-PIGMENT EPITHELIUM; VISUAL-ACUITY; CHOROIDAL NEOVASCULARIZATION; CARDIOVASCULAR-DISEASE; ATHEROSCLEROSIS RISK; LIPID-PEROXIDATION; UNITED-STATES; MACULOPATHY;
D O I
10.1001/jamaophthalmol.2013.7671
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
IMPORTANCE Modifying levels of factors associated with age-related macular degeneration (AMD) may decrease the risk for visual impairment in older persons. OBJECTIVE To examine the relationships of markers of inflammation, oxidative stress, and endothelial dysfunction to the 20-year cumulative incidence of early AMD. DESIGN, SETTING, AND PARTICIPANTS This longitudinal population-based cohort study involved a random sample of 975 persons in the Beaver Dam Eye Study without signs of AMD who participated in the baseline examination in 1988-1990 and up to 4 follow-up examinations in 1993-1995,1998-2000, 2003-2005, and 2008-2010. EXPOSURES Serum markers of inflammation (high-sensitivity C-reactive protein, tumor necrosis factor-a receptor 2, interleukin-6, and white blood cell count), oxidative stress (8-isoprostane and total carbonyl content), and endothelial dysfunction (soluble vascular cell adhesion molecule-1 and soluble intercellular adhesion molecule-i) were measured. Interactions with complement factor H (rs1061170), age-related maculopathy susceptibility 2 (rs10490924), complement component 3 (rs2230199), and complement component 2/complement factor B (rs4151667) were examined using multiplicative models. Age-related macular degeneration was assessed from fundus photographs. MAIN OUTCOMES AND MEASURES Early AMD defined by the presence of any size drusen and the presence of pigmentary abnormalities or by the presence of large-sized drusen (> 125-pm diameter) in the absence of late AMD. RESULTS The 20-year cumulative incidence of early AMD was 23.0%. Adjusting for age, sex, and other risk factors, high-sensitivity C-reactive protein (odds ratio comparing fourth with first quartile, 2.18; P =.005), tumor necrosis factor-a receptor 2 (odds ratio, 1.78; P =.04), and interleukin-6 (odds ratio, 1.78; P =.03) were associated with the incidence of early AMD. Increased incidence of early AMD was associated with soluble vascular cell adhesion molecule-1 (odds ratio per SD on the logarithmic scale, 1.21; P =.04). CONCLUSIONS AND RELEVANCE We found modest evidence of relationships of serum high-sensitivity C-reactive protein, tumor necrosis factor-a receptor 2, interleukin-6, and soluble vascular cell adhesion molecule-1 to the 20-year cumulative incidence of early AMD independent of age, smoking status, and other factors. It is not known whether these associations represent a cause and effect relationship or whether other unknown confounders accounted for the findings. Even if inflammatory processes are a cause of early AMD, it is not known whether interventions that reduce systemic inflammatory processes will reduce the incidence of early AMD.
引用
收藏
页码:446 / 455
页数:10
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