|
|
||||||||
1 From the Singapore National Eye Centre and Singapore Eye Research Institute, Singapore; 2 Departments of Ophthalmology and 3 Community, Occupational and Family Medicine, National University of Singapore, Singapore; 4 Department of Ophthalmology and Visual Sciences, University of Wisconsin, Madison; 5 Institute of Ophthalmology, University College London, United Kingdom; and 6 Department of International Health, Johns Hopkins University School of Public Health, Baltimore, Maryland.
| Abstract |
|---|
|
|
|---|
METHODS. This study was a population-based, cross-sectional survey of adult Chinese persons aged 40 to 81 years residing in Tanjong Pagar district, Singapore. Axial ocular dimensions, including axial length (AL), anterior chamber depth (ACD), lens thickness (LT), and vitreous chamber depth (VCD) were measured using an A-scan ultrasound device. Corneal curvature (CC) and noncycloplegic refraction were measured with an autorefractor, with refraction further refined subjectively. Lens nuclear opacity (NO) was graded clinically using the modified Lens Opacity Classification System III (LOCS III) score.
RESULTS. A total of 1717 subjects were eligible for the survey, of whom 1232 (71.8%) participated. Biometric and refraction data were available for 1004 (58.5%) phakic subjects. The AL, ACD, LT, VCD, CC, and LOCS III scores were 23.23 ± 1.17 mm, 2.90 ± 0.44 mm, 4.75 ± 0.47 mm, 15.58 ± 1.11 mm, 7.65 ± 0.27 mm, and 3.2 ± 0.9 (mean ± SD), respectively. On average, people aged 40 to 49 years, when compared with those 70 to 81 years, had longer ALs (mean difference, +0.58 mm), deeper ACDs (+0.52 mm), longer VCDs (+0.72 mm), but thinner lenses (-0.70 mm) and less severe NO (-1.7 LOCS III score). CCs did not vary significantly with age. After controlling for age, women had shorter ALs and VCDs, shallower ACDs, but thicker lenses and steeper CCs than men. The variation in noncycloplegic refraction with age was nonlinear. Among people aged 40 to 59 years, a higher prevalence of hyperopia was seen in older compared with younger persons (on average, a difference of +1.3 D for every 10-year difference in age, P < 0.001), explained principally by shorter AL (and VCD) in older persons. Among those 60 to 81 years, this pattern was not obvious (a difference of -0.03 D for every 10-year difference in age, P = 0.12), as NO became an additional determinant of refraction, with greater degrees of NO in older persons driving refraction in the "minus" direction.
CONCLUSIONS. Ocular dimensions vary with age and gender in adult Chinese persons in Singapore. The variation in noncycloplegic refraction in people 40 years and older may be explained by differences in axial lengths (principally vitreous chamber depths) between older and younger persons and, from 60 years onwards, differences in lens nuclear opacification as well.
| Introduction |
|---|
|
|
|---|
Biometric data (e.g., axial length, corneal curvature, lenticular power) may help explain the variation in refraction observed. In children, adolescents and young adults, for example, biometric studies have shown that differences in axial lengths (principally vitreous chamber depths) account for most of the variation in refraction in the young.10 11 12 13 14 15 16 17 18 19 Likewise, differences in axial lengths have been hypothesized to explain the variation in refraction observed in older adults.6 However, biometric data are lacking from current population-based studies to support this hypothesis.1 2 3 4 5
In a recent survey in adult Chinese persons 40 years and older residing in Singapore, we observed a similar cross-sectional pattern of refraction as in other studies.1 2 3 4 5 20 We now describe the variation in ocular dimensions in this population and evaluate the association between individual components and refraction.
| Methods |
|---|
|
|
|---|
The study was part of a population-based survey of ocular disorders among adult Chinese living in Singapore. Detailed population selection and methodology have been previously reported.20 22 In brief, the 1996 Singapore electoral register in the district of Tanjong Pagar was used as the sampling frame in this study. Tanjong Pagar is located in the center of Singapore and was chosen because the population demographics of the Chinese residents are representative of the rest of Singapore. The electoral register listed 15,082 names of Chinese persons between the ages of 40 to 79 years residing in the district. Two thousand (13.3%) names were selected using a disproportionate (with more weights given to the older age groups), stratified, clustered, random sampling method. These persons were invited for a comprehensive eye examination at the study center. After this, an abbreviated domiciliary examination on nonrespondents was conducted. This study was approved by the ethics committee of Singapore National Eye Center and carried out in accordance with the tenets of the World Medical Associations Declaration of Helsinki. Written informed consent was obtained, and the study was conducted between October 1997 and August 1998.
Procedures
Measurements of axial length (AL), anterior chamber depth (ACD),
lens thickness (LT) and vitreous chamber depth (VCD) were obtained
using a 10-MHz A-mode ultrasound device (Storz Compuscan; Storz, St.
Louis, MO). The hard-tipped, corneal contact ultrasound probe was
mounted on a tonometer (Haag-Streit, Bern, Switzerland) set to
the individuals intraocular pressure. The mean of 16 separate
readings was recorded, together with the SD of each parameter. An SD
for axial length measurement of less than or equal to 0.13 mm was
required. If the SD was greater, the reading was repeated up to another
two times. If it was not possible to achieve an SD within these limits,
the data were still accepted but were not analyzed in this report.
Corneal curvature was assessed using a handheld autorefractor/keratometer (Retinomax K-plus; Nikon, Tokyo, Japan). The device recorded up to eight separate estimates of corneal curvature along two meridia, each 90° apart. A mean value along each meridian was recorded, and the mean corneal curvature (CC) was calculated as the average of the greater and lesser curvature. Lens nuclear opacity (NO) was graded at a slitlamp using the modified Lens Opacity Classification System III (LOCS III) score.23 Under this system, nuclear opacity was classified in increasing severity as grades 1 to 6.
Noncycloplegic refraction was performed as follows. First, objective refraction was assessed with the same handheld autorefractor used to measure corneal curvature (Retinomax K-plus; Nikon). A single optometrist then performed a subjective refinement of the refractive correction with a phoropter, using the results of the objective refraction as the starting point.
Definitions and Analysis
Biometric data for right and left eyes were analyzed separately.
Because the results between the two eyes were similar, only data on the
right eye are presented in this study. Noncycloplegic refraction data
were converted to spherical equivalents (SE) and were based on
subjective refraction when participants had both subjective and
objective refraction and on objective refraction when only this
information was available. Preliminary analysis indicated high overall
agreement between objective and subjective refraction in
SE.20
The data analysis was conducted as follows. First, the variation in individual biometric components was analyzed across the entire age spectrum (4081 years). Next, the participants were divided into two age groups (4059 and 6081 years), and the variation in biometric components within each group was analyzed separately. This was done because our previous study showed refraction was nonlinearly associated with age.20 Before 60 years, there was a trend toward "plus" SE in older compared with younger persons, but after 60 years, this pattern was less distinct (see Results and Fig. 7 ). Within each group, linear regressions were performed to assess the effect of age and gender (independent variables) on the variations in individual biometric components and refraction (dependent variables). Linear regression models were then constructed to evaluate the independent effects of different biometric components (independent variables) on refraction (dependent variable). Standardized regression coefficients in these models were used to determine the relative role/importance of each biometric component on refraction.24 Statistical analyses of the data were carried out using SPSS (SPSS Inc., Chicago, IL).
|
| Results |
|---|
|
|
|---|
|
|
|
|
|
|
|
|
|
|
The relationship between different ocular dimensions and noncycloplegic refraction is shown in Table 5 . As expected, persons with a more "minus" SE were younger, had longer ALs, deeper ACDs, and longer VCD than subjects with "plus" SE. However, subjects with "plus" SE had thicker lens and greater severity of nuclear opacity. There was no significant variation in CCs between different refractive states.
|
|
| Discussion |
|---|
|
|
|---|
Existing biometric data are based mostly on studies in children, adolescents, and young adults11 12 13 14 16 17 18 or on selected populations (such as medical students15 or clinical microscopists19 ). In adults after 40 years, comparable population-based data are less readily available.1 2 3 4 5 Among Eskimos in Alaska, shorter ALs in older compared with younger persons were observed by van Rens and colleagues.25 In a nonrandom survey of 220 adult Chinese older than 40 years living in Hong Kong, older persons and women were found to have shorter ALs and VCDs, compared with younger persons and men, respectively.26 Other nonpopulation-based studies have noted shorter ALs in older people,27 28 relative stability of CCs with age,29 30 and shorter ALs and CCs in women.31 32 33 The explanation for the variation in ocular dimensions with gender is not clear but is likely to reflect differences in both genetic and environmental factors between men and women.6 7 8 32
More interesting, and difficult to explain, is the variation in axial ocular dimensions with age. Inferences on age-related (longitudinal) trends can be problematic, based on cross-sectional data. This is illustrated by comparing alternative explanations for the variation in AL versus LT in our study. Shorter ALs in older compared with younger persons could be related to either a cohort effect (i.e., with older generations have shorter ALs because of poorer nutrition, general health, or other unknown factors than younger generations6 ) or to an actual reduction in AL with increasing age. Data on which of the two hypotheses is more likely are inconsistent. Although some studies indicate that an age-related reduction in a persons AL is possible,27 28 other studies have also shown that this parameter remains fairly constant in adolescents.11 12 13 29 34 Our data do not provide sufficient information to distinguish whether an age-related change or a cohort effect is more likely. On the other hand, a cohort effect is an unlikely explanation for variation in LT between older compared with younger persons. The crystalline lens has been shown to continue growing throughout life.35 Previous research has demonstrated that the LT increases at a rate of approximately 0.02 mm/y.36 Our cross-sectional data were consistent with this observation. We found a difference in lens thickness of 0.035 mm/y in subjects aged 40 to 59 years and 0.019 mm/y in subjects aged 60 to 81 years. Therefore, the variation in lens thickness appears to be an age-related longitudinal change rather than a cohort effect.
Our biometric data are useful in explaining the variation in refraction observed in previous studies1 2 3 4 5 and in ours.20 Specifically, these studies have shown that in adults after age 40 years, older persons tend to have higher rates of hyperopia (and lower rates of myopia), compared with younger persons (which will be referred to as the "hyperopic shift" in this discussion).1 2 3 4 5 After 60 years, the hyperopic shift appears to be less prominent,1 2 3 4 5 and some studies have shown a pattern in the opposite "minus" direction with age, with increasing prevalence of myopia seen in elderly persons.1 2 The variation in our study is depicted in Figure 7 . Refractive status in children, adolescents, and younger adults are explained mainly by variation in ALs and VCDs.10 11 12 13 14 15 16 17 18 19 Likewise, we found AL and VCD to be the most "important" relative predictors of refraction in our adult population (Table 6 , models 14). Shorter ALs and VCDs in older compared with younger persons appeared to explain the hyperopic shift in our population. After 60 years of age, we showed that NO became an additional significant predictor of refraction (Table 6 , models 3 and 4). Greater nuclear opacification in older persons appeared to drive the refraction in the "minus" direction, explaining why the hyperopic shift was less prominent in the group aged 60 to 81 years. This was consistent with data from the Visual Impairment Project in Melbourne3 and in the Beaver Dam Eye Study,9 which showed that increased nuclear opacity of the lens in older persons was associated with a more "minus" refraction status.
However, we should point out that as cycloplegia was not used in our study, the effect of accommodation on refraction in our population was not known. In younger adults, this could be significant, and the hyperopic shift in Figure 7 could also be explained by the loss of accommodation in older compared with younger persons. Manual subjective refraction techniques in our study would theoretically reduce the effects of accommodation (compared with objective autorefraction), and in participants more than 50 years old, accommodative ability was expected to be minimal.
The principal strength of our study was the population-based random sampling strategy, avoiding the bias seen in studies of biometry in specific, highly selected patient groups.14 15 16 17 19 In addition, as the prevalence of refractive errors in our population was high, any variation in the biometric components was potentially accentuated. The problems with inferences based on cross-sectional data and noncycloplegic refraction have already been noted. Another potential problem was selection bias. For example, shorter axial dimensions in older persons and women could be explained by selective exclusion of older persons and women with longer axial dimension, due either to higher cataract extraction rates in these people (biometric data on pseudophakic and aphakic participants were not analyzed), higher mortality, or other unknown reasons for nonparticipation.
In conclusion, we observed age and gender variation in ocular biometry in adult Chinese persons more than 40 years old in Singapore, with older people and women generally having shorter axial ocular dimensions. Vitreous chamber depth was the most "important" determinant of refraction in adults more than 40 years old. Shorter vitreous chamber depths in older compared with younger persons appear to explain the hyperopic shift seen cross-sectionally in previous population-based studies. After 60 years of age, lens nuclear opacity was a significant additional determinant of refraction, with greater lens opacities in older persons driving the refraction in the "minus" direction, possibly explaining why the hyperopic shift in older persons was less prominent.
| Footnotes |
|---|
Submitted for publication June 20, 2000; revised August 9, 2000; accepted September 12, 2000.
Commercial relationships policy: N.
Corresponding author: Steve K. L. Seah, Singapore National Eye Centre, 11 Third Hospital Avenue, Singapore 168751. snecss{at}pacific.net.sg
| References |
|---|
|
|
|---|
This article has been cited by other articles:
![]() |
T. Sugita, M. Kondo, C.-H. Piao, Y. Ito, and H. Terasaki Correlation between Macular Volume and Focal Macular Electroretinogram in Patients with Retinitis Pigmentosa Invest. Ophthalmol. Vis. Sci., August 1, 2008; 49(8): 3551 - 3558. [Abstract] [Full Text] [PDF] |
||||
![]() |
A Nagai-Kusuhara, M Nakamura, M Fujioka, Y Tatsumi, and A Negi Association of retinal nerve fibre layer thickness measured by confocal scanning laser ophthalmoscopy and optical coherence tomography with disc size and axial length Br. J. Ophthalmol., February 1, 2008; 92(2): 186 - 190. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. Ip, S. C. Huynh, A. Kifley, K. A. Rose, I. G. Morgan, R. Varma, and P. Mitchell Variation of the Contribution from Axial Length and Other Oculometric Parameters to Refraction by Age and Ethnicity Invest. Ophthalmol. Vis. Sci., October 1, 2007; 48(10): 4846 - 4853. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. L. Young, R. Metlapally, and A. E. Shay Complex Trait Genetics of Refractive Error Arch Ophthalmol, January 1, 2007; 125(1): 38 - 48. [Abstract] [Full Text] [PDF] |
||||
![]() |
T Y Wong, S-C Loon, and S-M Saw The epidemiology of age related eye diseases in Asia. Br. J. Ophthalmol., April 1, 2006; 90(4): 506 - 511. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Ojaimi, I. G. Morgan, D. Robaei, K. A. Rose, W. Smith, E. Rochtchina, and P. Mitchell Effect of Stature and Other Anthropometric Parameters on Eye Size and Refraction in a Population-Based Study of Australian Children Invest. Ophthalmol. Vis. Sci., December 1, 2005; 46(12): 4424 - 4429. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Shufelt, S. Fraser-Bell, M. Ying-Lai, M. Torres, R. Varma, and the Los Angeles Latino Eye Study Group Refractive Error, Ocular Biometry, and Lens Opalescence in an Adult Population: The Los Angeles Latino Eye Study Invest. Ophthalmol. Vis. Sci., December 1, 2005; 46(12): 4450 - 4460. [Abstract] [Full Text] [PDF] |
||||
![]() |
S.-Y. Wu, Y. J. Yoo, B. Nemesure, A. Hennis, M. C. Leske, and the Barbados Eye Studies Group Nine-Year Refractive Changes in the Barbados Eye Studies Invest. Ophthalmol. Vis. Sci., November 1, 2005; 46(11): 4032 - 4039. [Abstract] [Full Text] [PDF] |
||||
![]() |
S M Saw, W H Chua, G Gazzard, D Koh, D T H Tan, and R A Stone Eye growth changes in myopic children in Singapore Br. J. Ophthalmol., November 1, 2005; 89(11): 1489 - 1494. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Aung, W. P. Nolan, D. Machin, S. K. L. Seah, J. Baasanhu, P. T. Khaw, G. J. Johnson, and P. J. Foster Anterior Chamber Depth and the Risk of Primary Angle Closure in 2 East Asian Populations Arch Ophthalmol, April 1, 2005; 123(4): 527 - 532. [Abstract] [Full Text] [PDF] |
||||
![]() |
P J Foster Myopia in Asia Br. J. Ophthalmol., April 1, 2004; 88(4): 443 - 444. [Full Text] [PDF] |
||||
![]() |
S. Wickremasinghe, P. J. Foster, D. Uranchimeg, P. S. Lee, J. G. Devereux, P. H. Alsbirk, D. Machin, G. J. Johnson, and J. Baasanhu Ocular Biometry and Refraction in Mongolian Adults Invest. Ophthalmol. Vis. Sci., March 1, 2004; 45(3): 776 - 783. [Abstract] [Full Text] [PDF] |
||||
![]() |
C.-Y. Cheng, W.-M. Hsu, J.-H. Liu, S.-Y. Tsai, and P. Chou Refractive Errors in an Elderly Chinese Population in Taiwan: The Shihpai Eye Study Invest. Ophthalmol. Vis. Sci., November 1, 2003; 44(11): 4630 - 4638. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Fernandes, D. V. Bradley, M. Tigges, J. Tigges, and J. G. Herndon Ocular Measurements throughout the Adult Life Span of Rhesus Monkeys Invest. Ophthalmol. Vis. Sci., June 1, 2003; 44(6): 2373 - 2380. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Y. Wong, P. J. Foster, G. J. Johnson, and S. K. L. Seah Refractive Errors, Axial Ocular Dimensions, and Age-Related Cataracts: The Tanjong Pagar Survey Invest. Ophthalmol. Vis. Sci., April 1, 2003; 44(4): 1479 - 1485. [Abstract] [Full Text] [PDF] |
||||
![]() |
T Y Wong, P J Foster, G J Johnson, and S K L Seah Education, socioeconomic status, and ocular dimensions in Chinese adults: the Tanjong Pagar Survey Br. J. Ophthalmol., September 1, 2002; 86(9): 963 - 968. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. E. Lee, B. E. K. Klein, R. Klein, and T. Y. Wong Changes in Refraction over 10 Years in an Adult Population: The Beaver Dam Eye Study Invest. Ophthalmol. Vis. Sci., August 1, 2002; 43(8): 2566 - 2571. [Abstract] [Full Text] [PDF] |
||||
![]() |
S.-M. Saw, W.-H. Chua, C.-Y. Hong, H.-M. Wu, W.-Y. Chan, K.-S. Chia, R. A. Stone, and D. Tan Nearwork in Early-Onset Myopia Invest. Ophthalmol. Vis. Sci., February 1, 2002; 43(2): 332 - 339. [Abstract] [Full Text] [PDF] |
||||
![]() |
N G Congdon, P J Foster, S Wamsley, J Gutmark, W Nolan, S K Seah, G J Johnson, and A T Broman Biometric gonioscopy and the effects of age, race, and sex on the anterior chamber angle Br. J. Ophthalmol., January 1, 2002; 86(1): 18 - 22. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Y. Wong, P. J. Foster, G. J. Johnson, B. E. K. Klein, and S. K. L. Seah The Relationship between Ocular Dimensions and Refraction with Adult Stature: The Tanjong Pagar Survey Invest. Ophthalmol. Vis. Sci., May 1, 2001; 42(6): 1237 - 1242. [Abstract] [Full Text] |
||||
![]() |
B. Seet, T. Y. Wong, D. T H Tan, S. M. Saw, V. Balakrishnan, L. K H Lee, and A. S M Lim Myopia in Singapore: taking a public health approach Br. J. Ophthalmol., May 1, 2001; 85(5): 521 - 526. [Full Text] |
||||
| ||||||||||||||||||||||||||||||||||||