Age-related macular degeneration and mortality in older women: the study of osteoporotic fractures.
Age-related macular degeneration and mortality in older women: the study of osteoporotic fractures.
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DOI:
10.1111/jgs.13405
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发表时间:
2015-05
影响因子:
6.3
通讯作者:
Study of Osteoporotic Fractures Research Group
中科院分区:
文献类型:
--
作者:
Pedula KL;Coleman AL;Yu F;Cauley JA;Ensrud KE;Hochberg MC;Fink HA;Hillier TA;Study of Osteoporotic Fractures Research Group
To examine the association of age-related macular degeneration (AMD) with all-cause and cause-specific mortality in a population of older women. Prospective cohort study. Four U.S. clinical centers A random sample of 1202 women with graded fundus photographs at year 10 visit of the Study of Osteoporotic Fractures (Mean age =79.5 years). Forty-five degree stereoscopic fundus photographs were graded for presence and severity (early vs. late) of AMD. Vital status was adjudicated from death certificates. Cox proportional hazards models, adjusted for appropriate confounders, were used to estimate mortality hazards ratios. Prevalence of any AMD was 40.5% at baseline, with 441 (36.7%) having early AMD and 46 (3.8%) having late AMD. Cumulative mortality was 51.6% in over 15 years of follow-up. Overall, there was no significant association between AMD presence or severity with all-cause or cause-specific mortality. Because there was a significant interaction between AMD and age in predicting mortality (p<0.05 for each mortality type) analyses were stratified by age group. Among women younger than 80 years, after adjusting for covariates, late AMD was associated with CVD mortality (Hazard ratio[HR], 2.61; 95% confidence interval [CI], 1.05–6.46). Among women 80 years and older, early AMD was associated with all-cause (HR, 1.39; 95% CI, 1.11–1.75)and non-CVD/non-cancer (HR, 1.45; 95% CI, 1.05–2.00) mortality. Additionally, any AMD was associated with all-cause (HR, 1.42; 95% CI, 1.13–1.78) and CVD (HR, 1.45; 95% CI, 1.01–2.09) mortality in women ≥ 80 years. AMD is a predictor of poorer survival among women, especially if 80 or older. Determination of shared risk factors may identify novel pathways for intervention that may reduce the risk of both conditions.
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影响因子:
13.7
作者:
Buch, H;Vinding, T;Nielsen, NV
通讯作者:
Nielsen, NV
DOI:
10.1111/j.1532-5415.2006.00983.x
发表时间:
2006-12-01
影响因子:
6.3
作者:
Pedula, Kathryn L.;Coleman, Anne L.;Mangione, Carol M.
通讯作者:
Mangione, Carol M.
影响因子:
120.7
作者:
NEVITT, MC;CUMMINGS, SR;BLACK, D
通讯作者:
BLACK, D
影响因子:
13.7
作者:
Milton, RC;Clemons, TE;Sperduto, RD
通讯作者:
Sperduto, RD
影响因子:
--
作者:
Ösby, U;Brandt, L;Sparén, P
通讯作者:
Sparén, P