TY - JOUR
T1 - Association of Choroidal Thickness with Intermediate Age-Related Macular Degeneration in a Japanese Population
AU - Sasaki, Mariko
AU - Ito, Yoshikazu
AU - Yamasaki, Tomoyo
AU - Yanagi, Yasuo
AU - Gemmy Cheung, Chui Ming
AU - Motomura, Kaoru
AU - Kawakami, Setsuko
AU - Kinoshita, Takamasa
AU - Yuki, Kenya
AU - Hanyuda, Akiko
AU - Mimura, Masaru
AU - Sawada, Norie
AU - Tsugane, Shoichiro
AU - Tsubota, Kazuo
N1 - Funding Information:
Supported in part by the Japan Society for the Promotion of Science , Tokyo, Japan (a Grant-in-Aid for Scientific Research no.: JSPS KAKENHI 26460778 [M.S.]). The cohort study originally was supported by the National Cancer Center Research and Development Fund.
Funding Information:
Supported in part by the Japan Society for the Promotion of Science, Tokyo, Japan (a Grant-in-Aid for Scientific Research no.: JSPS KAKENHI 26460778 [M.S.]). The cohort study originally was supported by the National Cancer Center Research and Development Fund.
Publisher Copyright:
© 2020 American Academy of Ophthalmology
PY - 2021/6
Y1 - 2021/6
N2 - Purpose: To determine the relationship of choroidal thickness with the early stages of age-related macular degeneration (AMD) and their disease features in a Japanese population. Design: Cross-sectional survey. Participants: A total of 1293 Japanese persons 65 to 86 years of age residing in the Saku area who underwent eye screening as part of the Japan Public Health Center-based Prospective Study. Methods: Comprehensive ophthalmic assessment included fundus photography, measurement of intraocular pressure, and determination of refractive status. OCT with enhanced depth imaging mode was performed and subfoveal choroidal thickness was assessed. Multinomial logistic regression models were used to assess the relationships of choroidal thickness with the early stages of AMD, namely early AMD and intermediate AMD, and their disease features, after adjustment for potential confounders. Main Outcome Measures: Relationship of choroidal thickness with early AMD, intermediate AMD, and their disease features. Results: Of 1293 potential participants, 901 (mean age, 73.2 years) had choroidal thickness data, fundus photographs of sufficient quality, and no concomitant retinal disease (including 5 with late AMD). Mean choroidal thickness was 246.1 μm, 15.1% had early AMD, and 9.0% had intermediate AMD. After adjustment for age, gender, and refractive status, choroidal thickness was associated positively with presence of intermediate AMD (for each 1- standard deviation [SD] μm increase: odds ratio [OR], 1.43; 95% confidence interval [CI], 1.13–1.81), whereas no significant association was found with presence of early AMD. Among intermediate AMD features, choroidal thickness was associated positively with presence of AMD pigmentary abnormalities (associated with at least medium drusen; for each 1-SD μm increase: OR, 2.21; 95% CI, 1.42–3.42), whereas no significant association was found with presence of large drusen alone. In addition, among large drusen subtypes, choroidal thickness was associated positively with presence of pachydrusen (for each 1-SD μm increase: OR, 1.53; 95% CI, 1.10–2.13). Furthermore, exploratory analysis revealed that choroidal thickness was associated positively with presence of non-AMD pigmentary abnormalities (for each 1-SD μm increase: OR, 1.92; 95% CI, 1.31–2.18). Conclusions: Choroidal thickness seems to be associated with the pathology of intermediate AMD and its features in Asians.
AB - Purpose: To determine the relationship of choroidal thickness with the early stages of age-related macular degeneration (AMD) and their disease features in a Japanese population. Design: Cross-sectional survey. Participants: A total of 1293 Japanese persons 65 to 86 years of age residing in the Saku area who underwent eye screening as part of the Japan Public Health Center-based Prospective Study. Methods: Comprehensive ophthalmic assessment included fundus photography, measurement of intraocular pressure, and determination of refractive status. OCT with enhanced depth imaging mode was performed and subfoveal choroidal thickness was assessed. Multinomial logistic regression models were used to assess the relationships of choroidal thickness with the early stages of AMD, namely early AMD and intermediate AMD, and their disease features, after adjustment for potential confounders. Main Outcome Measures: Relationship of choroidal thickness with early AMD, intermediate AMD, and their disease features. Results: Of 1293 potential participants, 901 (mean age, 73.2 years) had choroidal thickness data, fundus photographs of sufficient quality, and no concomitant retinal disease (including 5 with late AMD). Mean choroidal thickness was 246.1 μm, 15.1% had early AMD, and 9.0% had intermediate AMD. After adjustment for age, gender, and refractive status, choroidal thickness was associated positively with presence of intermediate AMD (for each 1- standard deviation [SD] μm increase: odds ratio [OR], 1.43; 95% confidence interval [CI], 1.13–1.81), whereas no significant association was found with presence of early AMD. Among intermediate AMD features, choroidal thickness was associated positively with presence of AMD pigmentary abnormalities (associated with at least medium drusen; for each 1-SD μm increase: OR, 2.21; 95% CI, 1.42–3.42), whereas no significant association was found with presence of large drusen alone. In addition, among large drusen subtypes, choroidal thickness was associated positively with presence of pachydrusen (for each 1-SD μm increase: OR, 1.53; 95% CI, 1.10–2.13). Furthermore, exploratory analysis revealed that choroidal thickness was associated positively with presence of non-AMD pigmentary abnormalities (for each 1-SD μm increase: OR, 1.92; 95% CI, 1.31–2.18). Conclusions: Choroidal thickness seems to be associated with the pathology of intermediate AMD and its features in Asians.
KW - Age-related macular degeneration
KW - Chroidal thickness
KW - Intermediate age-related macular degeneration
KW - Pachydrusen
KW - Pigmentary abnormalities
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U2 - 10.1016/j.oret.2020.09.001
DO - 10.1016/j.oret.2020.09.001
M3 - Article
C2 - 32896678
AN - SCOPUS:85100672630
SN - 2468-7219
VL - 5
SP - 528
EP - 535
JO - Ophthalmology Retina
JF - Ophthalmology Retina
IS - 6
ER -