Risk Factors for Progression of Age-Related Macular Degeneration: Population-Based Amish Eye Study.
Risk Factors for Progression of Age-Related Macular Degeneration: Population-Based Amish Eye Study.
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DOI:
10.3390/jcm11175110
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发表时间:
2022-08-30
影响因子:
3.9
通讯作者:
中科院分区:
文献类型:
--
作者:
Objective: To evaluate the optical coherence tomography (OCT)-based risk factors for progression to late age-related macular degeneration (AMD) in a population-based study of elderly Amish. Methods: A total of 1332 eyes of 666 consecutive subjects who completed a 2-year follow-up visit were included in this multicenter, prospective, longitudinal, observational study. Imaging features were correlated with 2-year incidence of late AMD development. Odds ratios for imaging features were estimated from logistic regression. Baseline OCT images were reviewed for the presence of drusen volume ≥0.03 mm3 in the central 3 mm ring, intraretinal hyperreflective foci (IHRF), hyporeflective drusen cores (hDC), subretinal drusenoid deposits (SDD), and drusenoid pigment epithelium detachment (PED). Subfoveal choroidal thickness, drusen area, and drusen volume within 3 and 5 mm circles centered on the fovea were also assessed. Results: Twenty-one (1.5%) of 1332 eyes progressed to late AMD by 2 years. The mean age of the study subjects was 65 ± 10.17 (±SD) years and 410 subjects were female. Univariate logistic regression showed that drusen area and volume in both 3 mm and 5 mm circles, subfoveal choroidal thickness, drusen volume ≥ 0.03 mm3 in the 3 mm ring, SDD, IHRF, and hDC were all associated with an increased risk for development of late AMD. The multivariate regression model identified that drusen volume in the 3 mm ring (OR: 2.59, p = 0.049) and presence of IHRF (OR: 57.06, p < 0.001) remained as independent and significant risk factors for progression to late AMD. Conclusions: This population-based study confirms previous findings from clinic-based studies that high central drusen volume and IHRF are associated with an increased risk of progression to late AMD. These findings may be of value in risk-stratifying patients in clinical practice or identifying subjects for early intervention clinical trials.
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影响因子:
13.7
作者:
Finger, Robert P.;Chong, Elaine;Guymer, Robyn H.
通讯作者:
Guymer, Robyn H.
影响因子:
4.4
作者:
Lee, Sun Young;Stetson, Paul F.;Sadda, SriniVas R.
通讯作者:
Sadda, SriniVas R.
影响因子:
4.4
作者:
Lindner, Moritz;Bezatis, Athanasios;Fleckenstein, Monika
通讯作者:
Fleckenstein, Monika
DOI:
10.1097/iae.0000000000002990
发表时间:
2021-04-01
影响因子:
3.3
作者:
Corvi, Federico;Tiosano, Liran;Sadda, Srinivas R.
通讯作者:
Sadda, Srinivas R.
影响因子:
4.4
作者:
Nittala, Muneeswar Gupta;Ruiz-Garcia, Humberto;Sadda, SriniVas R.
通讯作者:
Sadda, SriniVas R.