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Clinical and Epidemiologic Research  |   October 2014
Prevalence of Age-Related Macular Degeneration in an Elderly Urban Chinese Population in China: The Jiangning Eye Study
Author Notes
  • Department of Ophthalmology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China 
  • Correspondence: Peiquan Zhao, Department of Ophthalmology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, 1665 Kongjiang Road, Shanghai 200092, People's Republic of China; [email protected]
Investigative Ophthalmology & Visual Science October 2014, Vol.55, 6374-6380. doi:https://doi.org/10.1167/iovs.14-14899
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      Hehua Ye, Qi Zhang, Xiaohong Liu, Xuan Cai, Wenjing Yu, Siyi Yu, Tianyu Wang, Wuyi Lu, Xiang Li, Haiying Jin, Yiqian Hu, Xiaoli Kang, Peiquan Zhao; Prevalence of Age-Related Macular Degeneration in an Elderly Urban Chinese Population in China: The Jiangning Eye Study. Invest. Ophthalmol. Vis. Sci. 2014;55(10):6374-6380. https://doi.org/10.1167/iovs.14-14899.

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Abstract

Purpose.: To describe the prevalence of AMD in an elderly urban Chinese population in China.

Methods.: A population-based, cross-sectional study was conducted using a cluster random sample of residents aged 50 years or older living in the Jiangning Road Subdistrict, Jing'an District, Shanghai, China. All participants underwent a standardized interview and comprehensive eye examinations, including digital retinal photography and spectral-domain optical coherence tomography (OCT) examinations of both eyes between November 2012 and February 2013. Trained graders assessed the presence and severity of AMD lesions based on a modified version of the Wisconsin Age-Related Maculopathy Grading System.

Results.: Of the 2044 subjects who participated (82.5% response rate), 2005 had fundus photographs and OCT results of sufficient quality for grading of AMD signs. Early and late AMD were present in 206 (10.3%) and 23 (1.1%) participants, respectively. After age standardization, the prevalence of early AMD in Chinese persons aged 50 years or older was 9.5% (95% confidence interval [CI], 8.2–10.8) and that of late AMD was 1.0% (95% CI, 0.5–1.5).

Conclusions.: The prevalence of early and late AMD in this urban Chinese sample was higher than that reported in the Beijing and Handan studies. Age-related macular degeneration is highly prevalent among the elderly urban Chinese population in mainland China.

Chinese Abstract

Introduction
Age-related macular degeneration (AMD) is the leading cause of visual impairment among the elderly in developed countries, and as of 2010, it has been responsible for approximately 5% of all blindness globally. 13 To date, the introduction of novel therapeutic options (e.g., use of anti-VEGF agents) has offered remarkable clinical benefits for patients with neovascular AMD. 4 However, because these benefits are associated with an increased financial burden of providing care for these patients, accurately determining the epidemiology of AMD is important in order to develop preventive measures for this disease. 5,6  
Mainland China comprises one-fifth of the world's population with 1.34 billion people, including 178 million persons aged 60 years and above, and a substantial increase in the number of older persons is expected in the next few decades. 7 Although the epidemiology of AMD has been well described in many Western populations, 810 few studies have reported the epidemiology of AMD in mainland China. 1114 The results of two previous studies, the Beijing Eye Study and the Handan Eye Study, indicated that the prevalence of early and late AMD in mainland Chinese persons was relatively lower than in white populations. 1214 However, an increasing number of recent studies have reported a prevalence similar to or higher than that of white populations in Chinese persons in Taiwan 15,16 and Singapore 17 and in nearby Asian populations, 6,18 as well as in American Chinese individuals. 19 In addition, both of the previous studies were conducted in rural or suburban areas of Northern China; no studies were conducted in the urban populations or in other regions of mainland China. 
Therefore, we performed a population-based study to describe the age- and sex-specific prevalence of early and late AMD in the city of Shanghai, which is the largest city by population in China. The findings gained will provide new insights into the epidemiology of AMD in urban Chinese populations and may be helpful in planning public health strategies for patients with AMD in the future. 
Methods
Study Population
The Jiangning Eye Study, a population-based, cross-sectional study of Chinese urban elders aged 50 years and older living in the Jiangning Road Subdistrict, Jing'an District, Shanghai, China was conducted to investigate prevalence and risk factors of eye diseases. Shanghai sits on the Yangtze River Delta on China's eastern coast, and is the largest Chinese city by population in the world. In 2012, the gross domestic product per capita in Shanghai exceeded US $13,000, which approaches the level of developed countries. 20 The Jiangning Road Subdistrict is situated in the center of downtown Shanghai. According to the official household registration of local Health & Family Planning Commission in 2011, the total number of eligible residents aged 50 years and older in Jiangning was 30,341. After excluding vacant households, 2478 residents were randomly selected using a stratified, clustered, and multistage sampling technique, with probabilities proportionate to the size of the population of each cluster. The sample size calculations were based on an estimated prevalence of AMD of 5.5% with 95% confidence interval and a precision of ±0.011 and a design effect of 1.2, and allowing for a response rate of 80%. 1114,21 Of the 2478 randomly selected individuals, 2044 (82.5%) participated in the ophthalmic examination between November 2012 and February 2013. Informed written consent was obtained from all participants before enrollment. The study complied with the guidelines in the Declaration of Helsinki, and ethics approval was received from the Medical Ethics Committee of the Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine (Shanghai, People's Republic of China). 
Study Procedures
All examinations were carried out in temporary clinics among the community houses. A detailed interviewer-administrated questionnaire was conducted to collect information about medical history (e.g., hypertension, diabetes, hyperlipemia, and stroke), cigarette smoking (defined as current, past, and never), alcohol consumption (defined as yes or no), current medication use (e.g., aspirin, vitamin), socioeconomic status factors (e.g., marital status, final education level and income level), ocular status or history (e.g., history of eye surgery, glasses or contact lens prescriptions). Pulse rate, systolic and diastolic blood pressure (BP) were measured in a standard manner after 5 minutes of rest with a digital automatic BP monitor. Body mass index was calculated as body weight (kilograms) divided by body height (meters) squared. 
The eye examinations were conducted according to a standardized protocol that included visual acuity measurement with Early Treatment Diabetic Retinopathy Study (ETDRS) charts and recorded in each eye separately with best corrected acuity, autorefraction (KR-8900; Topcon, Tokyo, Japan), noncontact tonometry (CT-80A; Topcon), slit-lamp biomicroscopy (SL-1E; Topcon), indirect ophthalmoscopy (YE6F; 66 Vision, Suzhou, China), optical measurement of axial length, keratometry, anterior chamber depth, and white-to-white (IOL Master; Carl Zeiss, Jena, Germany), corneal thickness measurement (A-Scan model SW-1000, Suoer, Tianjin, China), and spectral-domain optical coherence tomography (SD-OCT; Topcon 3D OCT-2000; Topcon). Lens opacities were graded by slit-lamp biomicroscopy according to the Lens Opacities Classification System III (LOCS III). Fundus photography was undertaken with a 45° 16.2-megapixel digital nonmydriatic fundus camera (integrated high resolution fundus camera of Topcon 3D OCT-2000; Topcon) in a darkened room. At least two photography fields were obtained from each eye: one centered at the fovea and the other at the optic disc. Digital images of fundus photographs were communicated and analyzed with IMAGEnet digital imaging system and integrated software package of 3D OCT-2000 (Topcon). 
Grading of Images
Grading of AMD was based on a modified version of Wisconsin Age-Related Maculopathy Grading System (WARMGS). 2224 Features of AMD were classified into five mutually exclusive grades: grade 0 (no early or late AMD); grade 1, soft distinct drusen (≥63 μm) only or pigmentary irregularities only; grade 2, soft indistinct (≥125 μm) or reticular drusen only or soft distinct drusen (≥63 μm) with pigmentary irregularities; grade 3, soft indistinct (≥125 μm) or reticular drusen with pigmentary irregularities; grade 4, either choroidal neovascularization (CNV; presence of any of the following: serous or hemorrhagic retinal or RPE detachment, subretinal neovascular membrane, and periretinal fibrous scar) or geographic atrophy (GA; well-demarcated area of retinal pigment atrophy with visible choroidal vessels). Early AMD was defined as grades 1 to 3 and late AMD as grade 4. 
Two experienced graders initially assessed photographs for AMD signs independently in a masked fashion. Before grading was initiated for all subjects, intergrader and intragrader agreements were assessed using the κ statistic on a random subset of 50 eyes. For intergrader agreement, the κ of presence of soft distinct drusen, number of large drusen, and presence of retinal pigment abnormalities were 0.88, 0.76, and 0.64, respectively. For intragrader agreement, the κ for two graders were high for all these three features (all κ ≥ 0.61). All cases with positive findings were further adjudicated by a retinal specialist. All questionable lesions and all eyes classified as late AMD were discussed and adjudicated by the results of OCT. Any lesions considered to be due to other causes such as myopia and inflammatory disease were excluded. When CNV and GA were both present in the same eye, we classified the eye as CNV. When both eyes of a participant had lesions of different severity, AMD was defined according to the worse eye. 
Statistical Analysis
The overall age- and sex-specific prevalence (%) of AMD and its individual signs were calculated. Age-standardized prevalence was estimated using direct standardization of the study samples to the Chinese population at the 2010 Chinese census ([in the public domain] http://www.stats.gov.cn/english/Statisticaldata/CensusData/rkpc2010/indexch.htm). The Student's t-test and χ2 test were used to compare demographic characteristics between participants with and without AMD. Logistic regression analysis was performed to determine risk factors for early and late AMD using odds ratio (OR) estimates with 95% confidence intervals (CI). For multivariate analysis, we included risk factors with P less than 0.05 in the age-adjusted model (sex, alcohol consumption, hyperlipemia, and axial myopia) and also well-established risk factors (age and smoking habit). Statistical analysis was performed using a commercially available statistical software package (SAS; SAS Institute, Inc., Cary, NC, USA). All P values were two-sided and were considered statistically significant when the values were less than 0.05. 
Results
Of 2478 eligible subjects identified for this study, 2044 (82.5% response rate) underwent an eye examination in a temporary clinic established within the community. Of those individuals, 2005 had fundus photographs and OCT results of sufficient quality for grading of AMD signs; the age (±SD) was 64.8 (±9.9) years, and 56.3% were women. The age distribution of this study population was 50 to 59, 757 (37.8%); 60 to 69, 672 (33.5%); 70 to 79, 355 (17.7%), and 80 years or older, 221 (11.0%). 
The demographic characteristics of the study population by the presence or absence of early and late AMD are shown in Table 1. Persons with AMD were significantly older than those without AMD (P < 0.001). Men outnumbered women among AMD cases (P = 0.025). Systolic BP and the proportions of cataract surgery history and stroke were significantly higher in AMD group compared with those without AMD (P < 0.001, P = 0.010 and 0.008, respectively), whereas the proportion of axial myopia and hyperlipemia were significantly lower in AMD group (P < 0.001 and P = 0.019, respectively). 
Table 1
 
Demographic Characteristics by Presence or Absence of Early and Late AMD in the Jiangning Eye Study
Table 1
 
Demographic Characteristics by Presence or Absence of Early and Late AMD in the Jiangning Eye Study
Characteristic No AMD, n = 1776 AMD
Total, n = 229 Early AMD, n = 206 Late AMD, n = 23
Mean (SD)
Age, y* 64.0 (9.5) 70.4 (11.0) 69.9 (10.9) 75.5 (11.1)
Body mass index, kg/m2 24.0 (3.2) 23.9 (3.3) 23.9 (3.2) 24.4 (4.0)
Systolic BP, mm Hg* 137.7 (19.4) 142.6 (19.8) 142.4 (19.9) 144.7 (19.8)
Diastolic BP, mm Hg 74.4 (11.1) 74.6 (11.1) 74.8 (11.1) 73.0 (11.4)
Pulse rate, BPM 81.7 (11.7) 81.3 (11.3) 81.2 (11.5) 82.4 (10.2)
Number (%)
Male* 761 (42.8) 116 (50.7) 100 (48.5) 16 (69.6)
Married 1757 (98.9) 223 (97.4) 200 (97.1) 23 (100)
High school or higher education 981 (55.2) 117 (51.1) 110 (53.4) 7 (30.4)
Current cigarette smoker, ≥20 pack-years 374 (21.1) 49 (21.4) 43 (20.9) 6 (26.1)
Alcohol consumption, ≥20 g/d 309 (17.4) 48 (21.0) 44 (21.4) 4 (17.4)
Aspirin 48 (2.7) 5 (2.2) 3 (1.5) 2 (8.7)
Vitamin 166 (9.3) 19 (8.3) 18 (8.7) 1 (4.3)
Axial myopia, axial length ≥ 25.0 mm* 423 (23.8) 26 (11.4) 25 (12.1) 1 (4.3)
Glass wear 894 (50.3) 108 (47.2) 98 (47.6) 10 (43.5)
Cataract surgery, at least 1 eye* 84 (4.7) 20 (8.7) 17 (8.3) 3 (13.0)
Self-reported medical history
Hypertension 690 (38.9) 97 (42.4) 85 (41.3) 12 (52.2)
Hyperlipemia* 138 (7.8) 8 (3.5) 8 (3.9) 0
Diabetes mellitus 201 (11.3) 31 (13.5) 26 (12.6) 5 (21.7)
Stroke* 222 (12.5) 43 (18.8) 38 (18.4) 5 (21.7)
The crude prevalence rates of early AMD in men, women, and the entire study sample were 11.4%, 9.4%, and 10.3%, respectively (Table 2). The crude prevalence rates of late AMD in men, women, and the entire study sample were 1.8%, 0.6%, and 1.1%, respectively. Both early and late AMD increased with age (P < 0.001). After age standardization to the Chinese population (2010 census), the prevalence rates of early AMD in Chinese men and women and in all Chinese populations in mainland China were estimated to be 10.2%, 8.8%, and 9.5%, respectively; the corresponding prevalence rates of late AMD were 1.4%, 0.6%, and 1.0% (Table 2). 
Table 2
 
Prevalence of Early and Late AMD and its Specific Lesions by Sex and Age in the Jiangning Eye Study
Table 2
 
Prevalence of Early and Late AMD and its Specific Lesions by Sex and Age in the Jiangning Eye Study
Age Group, y N at Risk Soft Indistinct Drusen/ Reticular Drusen Soft Distinct Drusen Pigment Abnormalities Early AMD Late AMD
n % n % n % n % n %
Men
 50–59 297 7 2.4 24 8.1 17 5.7 22 7.4 1 0.3
 60–69 321 13 4.0 43 13.4 35 10.9 38 11.8 3 0.9
 70–79 159 11 6.9 20 12.6 18 11.3 20 12.6 6 3.8
 80–95 100 10 10.0 23 23.0 14 14.0 20 20.0 6 6.0
 Total population 877 41 4.7 110 12.5 84 9.6 100 11.4 16 1.8
 P value for trend* P = 0.001 P < 0.001 P = 0.007 P = 0.001 P < 0.001
 Age-standardized prevalence, %† 10.2 (8.2, 12.2) 1.4 (0.6, 2.2)
Women
 50–59 460 8 1.7 32 7.0 27 5.9 24 5.2 1 0.2
 60–69 351 10 2.8 23 6.6 21 6.0 23 6.6 2 0.6
 70–79 196 13 6.6 30 15.3 22 11.2 34 17.3 2 1.0
 80–95 121 7 5.8 22 18.2 17 14.0 25 20.7 2 1.7
 Total population 1128 38 3.4 107 9.5 87 7.7 106 9.4 7 0.6
 P value for trend* P = 0.001 P < 0.001 P = 0.001 P < 0.001 P = 0.058
 Age-standardized prevalence, %† 8.8 (7.1, 10.5) 0.6 (0.1, 1.1)
Both sexes
 50–59 757 15 2.0 56 7.4 44 5.8 46 6.1 2 0.3
 60–69 672 23 3.4 66 9.8 56 8.3 61 9.1 5 0.7
 70–79 355 24 6.8 50 14.1 40 11.3 54 15.2 8 2.3
 80–95 221 17 7.7 45 20.4 31 14.0 45 20.4 8 3.6
 Total population 2005 79 3.9 217 10.8 171 8.5 206 10.3 23 1.1
 P value for trend* P < 0.001 P < 0.001 P < 0.001 P < 0.001 P < 0.001
 Age-standardized prevalence, %† 9.5 (8.2, 10.8) 1.0 (0.5, 1.5)
Table 2 also lists the prevalence of specific early and late AMD signs. There were significant age-related trends in the prevalence of soft drusen and pigmentary abnormalities (P value for trend, all P < 0.001). Geographic atrophy and neovascular AMD were found in 14 (0.70%) and 9 (0.45%) of the 2005 subjects, respectively. Bilateral AMD signs were seen in 71 (34.5%) of the 206 early AMD cases and in 3 (13.0%) of the 23 late AMD cases. 
The results of age- and multivariate-adjusted logistic regression analyses of risk factors for the development of early and late AMD are shown in Table 3. After adjusting for age, alcohol consumption was a significant risk factor for the development of early AMD (OR, 1.52, 95% CI, 1.05–2.19), and in males was a significant risk factor for late AMD (OR, 2.83, 95% CI, 1.15–6.97). However, hyperlipemia (OR, 0.45, 95% CI, 0.22–0.94) and axial myopia (OR, 0.46, 95% CI, 0.30–0.72) were significant protective factors for early AMD. In multivariate analysis, older age was significantly associated with both early and late AMD (per 1-year increase, OR, 1.06, 95% CI, 1.04–1.07, and OR, 1.11, 95% CI, 1.06–1.16, respectively), whereas axial myopia was still associated negatively with early AMD (OR, 0.47, 95% CI, 0.30–0.73). 
Table 3
 
Age- and Multivariate-adjusted ORs of Risk Factors for the Development of Early and Late AMD in the Jiangning Eye Study
Table 3
 
Age- and Multivariate-adjusted ORs of Risk Factors for the Development of Early and Late AMD in the Jiangning Eye Study
Risk Factor Early AMD Late AMD
Age Adjusted Multivariate Adjusted Age Adjusted Multivariate Adjusted
OR (95% CI) P OR (95% CI) P OR (95% CI) P OR (95% CI) P
Age, per 1 y 1.06 (1.04–1.07) 0.000† 1.11 (1.06–1.16) 0.000†
Male 1.24 (0.93–1.67) 0.147 1.12 (0.79–1.59) 0.533 2.83 (1.15–6.97) 0.024* 2.62 (0.98–7.04) 0.055
Body mass index 0.99 (0.95–1.04) 0.721 1.06 (0.94–1.19) 0.381
Smoking 1.34 (0.93–1.95) 0.118 1.08 (0.69–1.67) 0.746 2.58 (0.95–7.00) 0.062 1.69 (0.56–5.11) 0.350
Alcohol 1.52 (1.05–2.19) 0.025* 1.36 (0.90–2.07) 0.144 1.33 (0.44–4.01) 0.616 0.72 (0.22–2.31) 0.577
Hypertension 0.90 (0.66–1.21) 0.483 1.20 (0.52–2.77) 0.675
Diabetes mellitus 0.98 (0.63–1.54) 0.945 1.78 (0.64–4.92) 0.268
Hyperlipemia 0.45 (0.22–0.94) 0.034* 0.48 (0.23–1.01) 0.054 Omitted‡ Omitted‡
Stroke 1.03 (0.69–1.53) 0.903 0.90 (0.32–2.55) 0.849
Glass wear 0.99 (0.74–1.33) 0.936 0.92 (0.40–2.14) 0.850
Axial myopia 0.46 (0.30–0.72) 0.001† 0.47 (0.30–0.73) 0.001† 0.17 (0.02–1.30) 0.089 0.17 (0.02–1.30) 0.089
Cataract surgery 1.00 (0.57–1.77) 0.999 1.16 (0.32–4.19) 0.816
Discussion
This population-based study reports on the prevalence of AMD in an elderly Chinese population in an urban setting in mainland China and shows that early AMD was present in 10.3% and late AMD in 1.1% of the study sample. After age standardization to the China 2010 population, the prevalence rates of early and late AMD in mainland Chinese individuals 50 years of age or older were estimated to be 9.5% and 1.0%, respectively. 
We have summarized the prevalence rates of AMD among Chinese populations using data from previous studies in Table 4. The age-standardized prevalence of early and late AMD in the present study was similar to that reported in the Singapore Chinese Eye Study (9.1% vs. 8.2% and 0.8% vs. 1.0%, respectively). 17 For participants aged greater than 65 years, the age-standardized prevalence of early AMD (14.4%) more closely reflected the results of the Puzih Eye Study (14.8%), 16 while the prevalence of late AMD (1.9%) was a little lower than that reported in the Shihpai Eye Study (2.7%). 15  
Table 4
 
Crude and Age-Standardized Prevalence of Early and Late AMD Among Chinese From the Jiangning and Other Eye Studies
Table 4
 
Crude and Age-Standardized Prevalence of Early and Late AMD Among Chinese From the Jiangning and Other Eye Studies
Shihpai Study 1999–2000, N = 1058 Beijing Study 2001, N = 4376 Handan Study 2006–2007, N = 6581 Singapore Chinese Study 2009–2011, N = 3312 Puzih Study 2010–2012, N = 673 Jiangning Study 2012–2013, N = 2005
Region Taiwan Beijing Handan Singapore Taiwan Shanghai
Setting Urban 43.8% Rural Rural Urban Urban Urban
Age, range, y 65–85+ 40–75+ 30–70+ 40–85 65–80+ 50–80+
Age, mean (SD) 71.8 (4.8) 56.1 (10.5) 51.8 (11.7) 59.7 (9.9) 74.1 64.8 (9.9)
Crude prevalence, %
Early AMD 9.2 5.1 3.0 7.3  15.0 10.3
Late AMD 1.9 0.3 0.1 0.8  7.3  1.1
Adjusted prevalence, %*
Early AMD (age ≥ 50) 11.1† N/A 4.6 8.2‡ 14.8†  9.5
Late AMD (age ≥ 50)  2.7† 0.3 0.1 1.0‡ 6.7†  1.0
Although mainland China has the largest population in the world and a substantial increase in the number of older persons is expected, reports regarding the epidemiology of AMD in mainland Chinese populations are relatively rare. A previous study carried out in another block in Shanghai in 2002 reported a higher prevalence rate of AMD (15.5% of 1023 subjects older than 50 years old had AMD and 1.9% had exudative AMD) than our results indicated. 11 However, this study applied ophthalmoscopy diagnosis and was based on the Chinese Ophthalmologic Society definition of AMD. The differences in photographic and grading techniques and the definition of AMD make it difficult to compare the two studies. To our knowledge, there are only two other population-based studies in mainland China that have reported results regarding the prevalence of AMD based on a commonly used classification and grading system (Table 4). In the Beijing Eye Study, the crude prevalence rates of early and late AMD were 5.1% and 0.3%, respectively. 12,13 The Handan Eye Study reported a lower, crude prevalence rate of early and late AMD (3.0% for early and 0.1% for late AMD prevalence). 14 The authors suggested that Chinese populations had a relatively lower prevalence rate for AMD compared with white populations. However, the prevalence rate in our study was significantly higher than the rates in both the Beijing and Handan eye studies. Several possible reasons might explain the differences in findings between the previous two studies and our present study. First, the present study were conducted in urban populations with a higher prevalence rate of AMD, whereas the Beijing Eye Study was conducted in a partially rural population (rural part, 43.8%), and the Handan Eye Study was conducted in a rural population with the lowest prevalence rate of AMD among the four studies (Table 4). With economic/political reforms primarily targeting large metropolitan cities, there exists a great divide between urban and rural areas in mainland China after more than 3 decades of development. Possible differences between the rural and urban populations of the same race include environmental (e.g., UV exposure), lifestyle (e.g., diet, physical activity, and education), or broader healthcare factors. 25 It has been hypothesized that people growing up in a rural and self-sustained economy are less affected by AMD compared with urban residents. 26 The present sample represents a population living in a metropolitan environment exposed to Western cultures, lifestyles, and influences; it is possible that the consequent lifestyle change and westernization of the diet may have had a marked impact on the prevalence of AMD in this urban Chinese population. 25 Second, different inclusion criteria in the studies also accounted for the discrepancy. The present study recruited participants 50 years of age and older (mean age, 64.8 years), older than those of the Beijing (mean age, 56.1 years) and Handan (mean age, 51.8 years) eye studies (Table 4). The higher prevalence of AMD in the present study could have been anticipated, given that our study sample had a larger proportion of the old age group. Third, both the Beijing and Handan eye studies were conducted in populations living in Northern China, whereas the present study was conducted in Southeastern China. The discrepancy in AMD rate might be caused partly by regional differences in climate, environmental parameters, and lifestyle. Finally, all participants of the present study received SD-OCT examination. SD-OCT has the advantage of detecting and evaluating small changes in the morphology of the retinal layers and subretinal space, which is valuable in detecting AMD lesions. 2729 The information offered by SD-OCT was used to assist in the identification and grading of AMD in the questioned cases (11 cases in the present study), which may also have increased the AMD rate in our study. 
Regarding specific AMD signs, our results showed a higher prevalence of GA (0.75%) than the Beijing study (0.1%), 12 the Handan study (0%), 14 and the Shihpai study (0.09%) did. 15 It has been reported that polypoidal choroidal vasculopathy (PCV) is frequently observed in Asian patients with exudative AMD. 21 However, among nine subjects with neovascular AMD in our study, there was no highly suspected case of typical PCV lesions based on the fundus photography and OCT results. One of limitations of the present study was that fluorescein angiography or indocyanine green angiography was not performed in all subjects with late AMD, which may have led to missing atypical cases of PCV. 
In the risk factors analysis, increasing age has consistently been shown to be strongly associated with increasing risk of AMD. In the present study, the prevalence of early AMD increased with age from 6.1% in the 50 to 59 range to 20.4% in participants older than 80 years. Subjects older than 80 had a nearly 12-fold higher risk of acquiring late AMD than did those aged 50 to 59. On the other hand, our finding that axial myopia was negatively associated with the prevalence of early AMD confirmed previous prevalence studies in which myopia had a protective role in AMD. 30,31 Although the precise mechanisms remain unclear, recent studies suggest that the reasons may include the decrease of scleral rigidity and intraocular concentration of VEGF in longer myopic eyes. 3234 Many studies of white populations have reported that smoking was an important, independent, and avoidable risk factor for AMD. 35,36 However, a current habit of smoking was not associated with AMD in our study, which was in agreement with most previous Asian population studies. 15,16,26,3739 It was possibly because there were relatively few subjects with late AMD and only current smoking status had been assessed in the present study. Further investigation is needed to identify the relationships between incidence and risk factors. 
In summary, the current study suggests that AMD is highly prevalent among the elderly urban Chinese population in mainland China. The prevalence rate is higher than the rates of the Beijing and Handan eye studies. These data represent a unique insight into the planning of public health strategies for patients with AMD in the world's most populous nation, with the aging of the population and rapid industrialization of cities in China. Further investigation is needed to identify the causes of variations in the prevalence rates and the relationships between incidence and risk factors. 
Supplementary Materials
Acknowledgments
The authors thank Jian Zhang (Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China) for providing suggestions on study sampling and statistical analysis. 
Disclosure: H. Ye, None; Q. Zhang, None; X. Liu, None; X. Cai, None; W. Yu, None; S. Yu, None; T. Wang, None; W. Lu, None; X. Li, None; H. Jin, None; Y. Hu, None; X. Kang, None; P. Zhao, None 
This study was supported by the National Natural Science Foundation Project of China (81200682, 81271045, 81100655; Beijing, China), the Shanghai Outstanding Young Scientist Foundation from the Shanghai Municipal Health Bureau (XBR2011060, Shanghai, China). 
References
Pascolini D Mariotti SP. Global estimates of visual impairment: 2010. Br J Ophthalmol . 2012; 96: 614–618. [CrossRef] [PubMed]
Pascolini D Mariotti SP Pokharel GP 2002 global update of available data on visual impairment: a compilation of population-based prevalence studies. Ophthalmic Epidemiol . 2004; 11: 67–115. [CrossRef] [PubMed]
Congdon N O'Colmain B Klaver CC Causes and prevalence of visual impairment among adults in the United States. Arch Ophthalmol . 2004; 122: 477–485. [CrossRef] [PubMed]
CATT Research Group, Martin DF Maguire MG Ranibizumab and bevacizumab for neovascular age-related macular degeneration. N Engl J Med . 2011; 364: 1897–1908. [CrossRef] [PubMed]
Day S Acquah K Lee PP Mruthyunjaya P Sloan FA. Medicare costs for neovascular age-related macular degeneration, 1994–2007. Am J Ophthalmol . 2011; 152: 1014–1020. [CrossRef] [PubMed]
Nakata I Yamashiro K Nakanishi H Prevalence and characteristics of age-related macular degeneration in the Japanese population: the Nagahama Study. Am J Ophthalmol . 2013; 156: 1002–1009, e1002. [CrossRef] [PubMed]
Tabulation on the 2010 Population Census of the People's Republic of China. Available at: http://www.stats.gov.cn/english/Statisticaldata/CensusData/rkpc2010/indexch.htm. Accessed May 18, 2014.
Klein R Klein BE Cruickshanks KJ. The prevalence of age-related maculopathy by geographic region and ethnicity. Prog Retin Eye Res . 1999; 18: 371–389. [CrossRef] [PubMed]
Friedman DS O'Colmain BJ Munoz B Prevalence of age-related macular degeneration in the United States. Arch Ophthalmol . 2004; 122: 564–572. [CrossRef] [PubMed]
Klein R Chou CF Klein BE Zhang X Meuer SM Saaddine JB. Prevalence of age-related macular degeneration in the US population. Arch Ophthalmol . 2011; 129: 75–80. [CrossRef] [PubMed]
Zou HD Zhang X Xu X Wang FH Zhang SJ. Prevalence study of age-related macular degeneration in Caojiadu blocks, Shanghai [in Chinese]. Zhonghua Yan Ke Za Zhi . 2005; 41: 15–19. [PubMed]
Li Y Xu L Jonas JB Yang H Ma Y Li J. Prevalence of age-related maculopathy in the adult population in China: the Beijing eye study. Am J Ophthalmol . 2006; 142: 788–793. [CrossRef] [PubMed]
Li Y Xu L Wang YX You QS Yang H Jonas JB. Prevalence of age-related maculopathy in the adult population in China: the Beijing eye study. Am J Ophthalmol . 2008; 146: 329. [CrossRef] [PubMed]
Yang K Liang YB Gao LQ Prevalence of age-related macular degeneration in a rural Chinese population: the Handan Eye Study. Ophthalmology . 2011; 118: 1395–1401. [PubMed]
Chen SJ Cheng CY Peng KL Prevalence and associated risk factors of age-related macular degeneration in an elderly Chinese population in Taiwan: the Shihpai Eye Study. Invest Ophthalmol Vis Sci . 2008; 49: 3126–3133. [CrossRef] [PubMed]
Huang EJ Wu SH Lai CH Prevalence and risk factors for age-related macular degeneration in the elderly Chinese population in south-western Taiwan: the Puzih Eye Study. Eye . 2014; 28: 705–714. [CrossRef] [PubMed]
Cheung CM Li X Cheng CY Prevalence, racial variations, and risk factors of age-related macular degeneration in Singaporean Chinese, Indians, and Malays. Ophthalmology . 2014; 121: 1598–1603. [CrossRef] [PubMed]
Oshima Y Ishibashi T Murata T Tahara Y Kiyohara Y Kubota T. Prevalence of age related maculopathy in a representative Japanese population: the Hisayama study. Br J Ophthalmol . 2001; 85: 1153–1157. [CrossRef] [PubMed]
Klein R Klein BE Knudtson MD Prevalence of age-related macular degeneration in 4 racial/ethnic groups in the multi-ethnic study of atherosclerosis. Ophthalmology . 2006; 113: 373–380. [CrossRef] [PubMed]
Shanghai Statistical Yearbook 2013. Available at: http://www.stats-sh.gov.cn/data/toTjnj.xhtml?y=2013e. Accessed May 18, 2014.
Kawasaki R Yasuda M Song SJ The prevalence of age-related macular degeneration in Asians: a systematic review and meta-analysis. Ophthalmology . 2010; 117: 921–927. [CrossRef] [PubMed]
Klein R Davis MD Magli YL Segal P Klein BE Hubbard L. The Wisconsin age-related maculopathy grading system. Ophthalmology . 1991; 98: 1128–1134. [CrossRef] [PubMed]
van Leeuwen R Klaver CC Vingerling JR Hofman A de Jong PT. The risk and natural course of age-related maculopathy: follow-up at 6 1/2 years in the Rotterdam study. Arch Ophthalmol . 2003; 121: 519–526. [CrossRef] [PubMed]
Krishnan T Ravindran RD Murthy GV Prevalence of early and late age-related macular degeneration in India: the INDEYE study. Invest Ophthalmol Vis Sci . 2010; 51: 701–707. [CrossRef] [PubMed]
Gemmy Cheung CM Li X Cheng CY Prevalence and risk factors for age-related macular degeneration in Indians: a comparative study in Singapore and India. Am J Ophthalmol . 2013; 155: 764–773, 773 e761–763. [CrossRef] [PubMed]
Xu L Li Y Zheng Y Jonas JB. Associated factors for age related maculopathy in the adult population in China: the Beijing Eye Study. Br J Ophthalmol . 2006; 90: 1087–1090. [CrossRef] [PubMed]
Fleckenstein M Charbel Issa P Helb HM High-resolution spectral domain-OCT imaging in geographic atrophy associated with age-related macular degeneration. Invest Ophthalmol Vis Sci . 2008; 49: 4137–4144. [CrossRef] [PubMed]
Regatieri CV Branchini L Duker JS. The role of spectral-domain OCT in the diagnosis and management of neovascular age-related macular degeneration. Ophthalmic Surg Lasers Imaging . 2011; 42 (suppl): S56–S66. [CrossRef] [PubMed]
Ouyang Y Heussen FM Hariri A Keane PA Sadda SR. Optical coherence tomography-based observation of the natural history of drusenoid lesion in eyes with dry age-related macular degeneration. Ophthalmology . 2013; 120: 2656–2665. [CrossRef] [PubMed]
Pan CW Ikram MK Cheung CY Refractive errors and age-related macular degeneration: a systematic review and meta-analysis. Ophthalmology . 2013; 120: 2058–2065. [CrossRef] [PubMed]
Li Y Wang J Zhong X Refractive error and risk of early or late age-related macular degeneration: a systematic review and meta-analysis. PLoS One . 2014; 9: e90897. [CrossRef] [PubMed]
Friedman E Ivry M Ebert E Glynn R Gragoudas E Seddon J. Increased scleral rigidity and age-related macular degeneration. Ophthalmology . 1989; 96: 104–108. [CrossRef] [PubMed]
Pallikaris IG Kymionis GD Ginis HS Kounis GA Christodoulakis E Tsilimbaris MK. Ocular rigidity in patients with age-related macular degeneration. Am J Ophthalmol . 2006; 141: 611–615. [CrossRef] [PubMed]
Jonas JB Tao Y Neumaier M Findeisen P. VEGF and refractive error. Ophthalmology . 2010; 117:2234, e2231.
Varma R Fraser-Bell S Tan S Klein R Azen SP; Los Angeles Latino Eye Study Group. Prevalence of age-related macular degeneration in Latinos: the Los Angeles Latino Eye Study. Ophthalmology . 2004; 111: 1288–1297. [CrossRef] [PubMed]
Klein R Knudtson MD Cruickshanks KJ Klein BE. Further observations on the association between smoking and the long-term incidence and progression of age-related macular degeneration: the Beaver Dam Eye Study. Arch Ophthalmol . 2008; 126: 115–121. [CrossRef] [PubMed]
Miyazaki M Nakamura H Kubo M Risk factors for age related maculopathy in a Japanese population: the Hisayama Study. Br J Ophthalmol . 2003; 87: 469–472. [CrossRef] [PubMed]
Song SJ Youm DJ Chang Y Yu HG. Age-related macular degeneration in a screened South Korean population: prevalence, risk factors, and subtypes. Ophthalmic Epidemiol . 2009; 16: 304–310. [CrossRef] [PubMed]
You QS Xu L Yang H Five-year incidence of age-related macular degeneration: the Beijing Eye Study. Ophthalmology . 2012; 119: 2519–2525. [CrossRef] [PubMed]
Footnotes
 HY and QZ contributed equally to the work presented here and should therefore be regarded as equivalent authors.
Table 1
 
Demographic Characteristics by Presence or Absence of Early and Late AMD in the Jiangning Eye Study
Table 1
 
Demographic Characteristics by Presence or Absence of Early and Late AMD in the Jiangning Eye Study
Characteristic No AMD, n = 1776 AMD
Total, n = 229 Early AMD, n = 206 Late AMD, n = 23
Mean (SD)
Age, y* 64.0 (9.5) 70.4 (11.0) 69.9 (10.9) 75.5 (11.1)
Body mass index, kg/m2 24.0 (3.2) 23.9 (3.3) 23.9 (3.2) 24.4 (4.0)
Systolic BP, mm Hg* 137.7 (19.4) 142.6 (19.8) 142.4 (19.9) 144.7 (19.8)
Diastolic BP, mm Hg 74.4 (11.1) 74.6 (11.1) 74.8 (11.1) 73.0 (11.4)
Pulse rate, BPM 81.7 (11.7) 81.3 (11.3) 81.2 (11.5) 82.4 (10.2)
Number (%)
Male* 761 (42.8) 116 (50.7) 100 (48.5) 16 (69.6)
Married 1757 (98.9) 223 (97.4) 200 (97.1) 23 (100)
High school or higher education 981 (55.2) 117 (51.1) 110 (53.4) 7 (30.4)
Current cigarette smoker, ≥20 pack-years 374 (21.1) 49 (21.4) 43 (20.9) 6 (26.1)
Alcohol consumption, ≥20 g/d 309 (17.4) 48 (21.0) 44 (21.4) 4 (17.4)
Aspirin 48 (2.7) 5 (2.2) 3 (1.5) 2 (8.7)
Vitamin 166 (9.3) 19 (8.3) 18 (8.7) 1 (4.3)
Axial myopia, axial length ≥ 25.0 mm* 423 (23.8) 26 (11.4) 25 (12.1) 1 (4.3)
Glass wear 894 (50.3) 108 (47.2) 98 (47.6) 10 (43.5)
Cataract surgery, at least 1 eye* 84 (4.7) 20 (8.7) 17 (8.3) 3 (13.0)
Self-reported medical history
Hypertension 690 (38.9) 97 (42.4) 85 (41.3) 12 (52.2)
Hyperlipemia* 138 (7.8) 8 (3.5) 8 (3.9) 0
Diabetes mellitus 201 (11.3) 31 (13.5) 26 (12.6) 5 (21.7)
Stroke* 222 (12.5) 43 (18.8) 38 (18.4) 5 (21.7)
Table 2
 
Prevalence of Early and Late AMD and its Specific Lesions by Sex and Age in the Jiangning Eye Study
Table 2
 
Prevalence of Early and Late AMD and its Specific Lesions by Sex and Age in the Jiangning Eye Study
Age Group, y N at Risk Soft Indistinct Drusen/ Reticular Drusen Soft Distinct Drusen Pigment Abnormalities Early AMD Late AMD
n % n % n % n % n %
Men
 50–59 297 7 2.4 24 8.1 17 5.7 22 7.4 1 0.3
 60–69 321 13 4.0 43 13.4 35 10.9 38 11.8 3 0.9
 70–79 159 11 6.9 20 12.6 18 11.3 20 12.6 6 3.8
 80–95 100 10 10.0 23 23.0 14 14.0 20 20.0 6 6.0
 Total population 877 41 4.7 110 12.5 84 9.6 100 11.4 16 1.8
 P value for trend* P = 0.001 P < 0.001 P = 0.007 P = 0.001 P < 0.001
 Age-standardized prevalence, %† 10.2 (8.2, 12.2) 1.4 (0.6, 2.2)
Women
 50–59 460 8 1.7 32 7.0 27 5.9 24 5.2 1 0.2
 60–69 351 10 2.8 23 6.6 21 6.0 23 6.6 2 0.6
 70–79 196 13 6.6 30 15.3 22 11.2 34 17.3 2 1.0
 80–95 121 7 5.8 22 18.2 17 14.0 25 20.7 2 1.7
 Total population 1128 38 3.4 107 9.5 87 7.7 106 9.4 7 0.6
 P value for trend* P = 0.001 P < 0.001 P = 0.001 P < 0.001 P = 0.058
 Age-standardized prevalence, %† 8.8 (7.1, 10.5) 0.6 (0.1, 1.1)
Both sexes
 50–59 757 15 2.0 56 7.4 44 5.8 46 6.1 2 0.3
 60–69 672 23 3.4 66 9.8 56 8.3 61 9.1 5 0.7
 70–79 355 24 6.8 50 14.1 40 11.3 54 15.2 8 2.3
 80–95 221 17 7.7 45 20.4 31 14.0 45 20.4 8 3.6
 Total population 2005 79 3.9 217 10.8 171 8.5 206 10.3 23 1.1
 P value for trend* P < 0.001 P < 0.001 P < 0.001 P < 0.001 P < 0.001
 Age-standardized prevalence, %† 9.5 (8.2, 10.8) 1.0 (0.5, 1.5)
Table 3
 
Age- and Multivariate-adjusted ORs of Risk Factors for the Development of Early and Late AMD in the Jiangning Eye Study
Table 3
 
Age- and Multivariate-adjusted ORs of Risk Factors for the Development of Early and Late AMD in the Jiangning Eye Study
Risk Factor Early AMD Late AMD
Age Adjusted Multivariate Adjusted Age Adjusted Multivariate Adjusted
OR (95% CI) P OR (95% CI) P OR (95% CI) P OR (95% CI) P
Age, per 1 y 1.06 (1.04–1.07) 0.000† 1.11 (1.06–1.16) 0.000†
Male 1.24 (0.93–1.67) 0.147 1.12 (0.79–1.59) 0.533 2.83 (1.15–6.97) 0.024* 2.62 (0.98–7.04) 0.055
Body mass index 0.99 (0.95–1.04) 0.721 1.06 (0.94–1.19) 0.381
Smoking 1.34 (0.93–1.95) 0.118 1.08 (0.69–1.67) 0.746 2.58 (0.95–7.00) 0.062 1.69 (0.56–5.11) 0.350
Alcohol 1.52 (1.05–2.19) 0.025* 1.36 (0.90–2.07) 0.144 1.33 (0.44–4.01) 0.616 0.72 (0.22–2.31) 0.577
Hypertension 0.90 (0.66–1.21) 0.483 1.20 (0.52–2.77) 0.675
Diabetes mellitus 0.98 (0.63–1.54) 0.945 1.78 (0.64–4.92) 0.268
Hyperlipemia 0.45 (0.22–0.94) 0.034* 0.48 (0.23–1.01) 0.054 Omitted‡ Omitted‡
Stroke 1.03 (0.69–1.53) 0.903 0.90 (0.32–2.55) 0.849
Glass wear 0.99 (0.74–1.33) 0.936 0.92 (0.40–2.14) 0.850
Axial myopia 0.46 (0.30–0.72) 0.001† 0.47 (0.30–0.73) 0.001† 0.17 (0.02–1.30) 0.089 0.17 (0.02–1.30) 0.089
Cataract surgery 1.00 (0.57–1.77) 0.999 1.16 (0.32–4.19) 0.816
Table 4
 
Crude and Age-Standardized Prevalence of Early and Late AMD Among Chinese From the Jiangning and Other Eye Studies
Table 4
 
Crude and Age-Standardized Prevalence of Early and Late AMD Among Chinese From the Jiangning and Other Eye Studies
Shihpai Study 1999–2000, N = 1058 Beijing Study 2001, N = 4376 Handan Study 2006–2007, N = 6581 Singapore Chinese Study 2009–2011, N = 3312 Puzih Study 2010–2012, N = 673 Jiangning Study 2012–2013, N = 2005
Region Taiwan Beijing Handan Singapore Taiwan Shanghai
Setting Urban 43.8% Rural Rural Urban Urban Urban
Age, range, y 65–85+ 40–75+ 30–70+ 40–85 65–80+ 50–80+
Age, mean (SD) 71.8 (4.8) 56.1 (10.5) 51.8 (11.7) 59.7 (9.9) 74.1 64.8 (9.9)
Crude prevalence, %
Early AMD 9.2 5.1 3.0 7.3  15.0 10.3
Late AMD 1.9 0.3 0.1 0.8  7.3  1.1
Adjusted prevalence, %*
Early AMD (age ≥ 50) 11.1† N/A 4.6 8.2‡ 14.8†  9.5
Late AMD (age ≥ 50)  2.7† 0.3 0.1 1.0‡ 6.7†  1.0
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