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BMC Ophthalmology

BioMed Central -I '#G D>  
Page 1 of 7 =J<3B H^m  
(page number not for citation purposes) M;-PrJdyt  
BMC Ophthalmology UM3}7|  
Research article Open Access SwXVa/9a"  
Comparison of age-specific cataract prevalence in two 6 -N 442  
population-based surveys 6 years apart Rcc9Tx(zvQ  
Ava Grace Tan†, Jie Jin Wang*†, Elena Rochtchina† and Paul Mitchell†  l| j  
Address: Centre for Vision Research, Westmead Millennium Institute, Department of Ophthalmology, University of Sydney, Westmead Hospital, O,x[6P54P  
Westmead, NSW, Australia Vo"Wr>F  
Email: Ava Grace Tan - ava_tan@wmi.usyd.edu.au; Jie Jin Wang* - jiejin_wang@wmi.usyd.edu.au; l1l=52r   
Elena Rochtchina - elena_rochtchina@wmi.usyd.edu.au; Paul Mitchell - paul_mitchell@wmi.usyd.edu.au ]{s0/(EA  
* Corresponding author †Equal contributors Qzt'ZK  
Abstract _Dr9 w&;<  
Background: In this study, we aimed to compare age-specific cortical, nuclear and posterior 3K!(/,`  
subcapsular (PSC) cataract prevalence in two surveys 6 years apart. OD]` oJ|  
Methods: The Blue Mountains Eye Study examined 3654 participants (82.4% of those eligible) in X6 *4IE  
cross-section I (1992–4) and 3509 participants (75.1% of survivors and 85.2% of newly eligible) in g[';1}/B4  
cross-section II (1997–2000, 66.5% overlap with cross-section I). Cataract was assessed from lens /W9(}Id6  
photographs following the Wisconsin Cataract Grading System. Cortical cataract was defined if ti'B}bH>'  
cortical opacity comprised ≥ 5% of lens area. Nuclear cataract was defined if nuclear opacity ≥ %;_94!(hC  
Wisconsin standard 4. PSC was defined if any present. Any cataract was defined to include persons cD6S;PSg  
who had previous cataract surgery. Weighted kappa for inter-grader reliability was 0.82, 0.55 and @Q teC@k  
0.82 for cortical, nuclear and PSC cataract, respectively. We assessed age-specific prevalence using l0 =[MXM4  
an interval of 5 years, so that participants within each age group were independent between the s|I Y t^  
two surveys. _NefzZWUJ  
Results: Age and gender distributions were similar between the two populations. The age-specific hh8Grl;  
prevalence of cortical (23.8% in 1st, 23.7% in 2nd) and PSC cataract (6.3%, 6.0%) was similar. The ;NU-\<Q{  
prevalence of nuclear cataract increased slightly from 18.7% to 23.9%. After age standardization, o1`\*]A7J  
the similar prevalence of cortical (23.8%, 23.5%) and PSC cataract (6.3%, 5.9%), and the increased aD]! eP/)  
prevalence of nuclear cataract (18.7%, 24.2%) remained. i/j53towe  
Conclusion: In two surveys of two population-based samples with similar age and gender Z<^;Ybw{`Z  
distributions, we found a relatively stable cortical and PSC cataract prevalence over a 6-year period. HS[($  
The increased prevalence of nuclear cataract deserves further study. vd?Bk_d9k,  
Background .7]P-]uOZ  
Age-related cataract is the leading cause of reversible visual H2H`7 +I,  
impairment in older persons [1-6]. In Australia, it is ,qx^D  
estimated that by the year 2021, the number of people o^XDG^35`  
affected by cataract will increase by 63%, due to population 85YUqVi9  
aging [7]. Surgical intervention is an effective treatment gk6UV2nE?  
for cataract and normal vision (> 20/40) can usually 8Qo'[+4;  
be restored with intraocular lens (IOL) implantation. `^52I kM)  
Cataract surgery with IOL implantation is currently the  D|) a7_  
most commonly performed, and is, arguably, the most %x N${4)6  
cost effective surgical procedure worldwide. Performance |>yWkq   
Published: 20 April 2006 ')U~a  
BMC Ophthalmology 2006, 6:17 doi:10.1186/1471-2415-6-17 ! !A0K"h  
Received: 14 December 2005 V(_1q  
Accepted: 20 April 2006 y(o)} m*0  
This article is available from: http://www.biomedcentral.com/1471-2415/6/17 RN[I%^$"  
© 2006 Tan et al; licensee BioMed Central Ltd. Keozn*fzI  
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), ; xZjt4M1  
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 8 q@Z  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 PD)"od  
Page 2 of 7 0^lWy+  
(page number not for citation purposes) 0V4B Q:v  
of this surgical procedure has been continuously increasing .E<nQWz 8  
in the last two decades. Data from the Australian fes s6=k  
Health Insurance Commission has shown a steady  G 5;6q  
increase in Medicare claims for cataract surgery [8]. A 2.6- 3''S x8p  
fold increase in the total number of cataract procedures hq)1YO  
from 1985 to 1994 has been documented in Australia [9]. ZEAUoC1E1  
The rate of cataract surgery per thousand persons aged 65 ;f =m+QXU  
years or older has doubled in the last 20 years [8,9]. In the j{@6y  
Blue Mountains Eye Study population, we observed a onethird d ~Z\%4  
increase in cataract surgery prevalence over a mean f#\YX tR,k  
6-year interval, from 6% to nearly 8% in two cross-sectional l~6K}g?  
population-based samples with a similar age range KwuucY  
[10]. Further increases in cataract surgery performance ]mTBD<3\  
would be expected as a result of improved surgical skills >Icr4?zq  
and technique, together with extending cataract surgical |_V(^b}  
benefits to a greater number of older people and an VPe0\?!d  
increased number of persons with surgery performed on =l/6-j^  
both eyes. s/E|Z1pg3  
Both the prevalence and incidence of age-related cataract v1 .3gzR  
link directly to the demand for, and the outcome of, cataract JE=t e(a  
surgery and eye health care provision. This report  .Q{RT p  
aimed to assess temporal changes in the prevalence of cortical |eqBCZn  
and nuclear cataract and posterior subcapsular cataract ^[M{s(b  
(PSC) in two cross-sectional population-based *doNPp)m  
surveys 6 years apart. n HseA  
Methods .ZpOYhk  
The Blue Mountains Eye Study (BMES) is a populationbased M:S-%aQ_<y  
cohort study of common eye diseases and other J ^'El^F  
health outcomes. The study involved eligible permanent ~r1pO#r-  
residents aged 49 years and older, living in two postcode }LzBo\  
areas in the Blue Mountains, west of Sydney, Australia. b 7UJ  
Participants were identified through a census and were apvcWF%  
invited to participate. The study was approved at each ]A*}Dem*5  
stage of the data collection by the Human Ethics Committees 0MG>77  
of the University of Sydney and the Western Sydney =[6^NR(  
Area Health Service and adhered to the recommendations !+l'<*8V  
of the Declaration of Helsinki. Written informed consent  is'V%q  
was obtained from each participant. T(b9b,ov)  
Details of the methods used in this study have been ;G[V:.o-  
described previously [11]. The baseline examinations IG7 81:,/  
(BMES cross-section I) were conducted during 1992– jvzioFCt  
1994 and included 3654 (82.4%) of 4433 eligible residents. )t6]F6!_  
Follow-up examinations (BMES IIA) were conducted I6>J.6luF9  
during 1997–1999, with 2335 (75.0% of BMES $l7^-SK`E  
cross section I survivors) participating. A repeat census of _P>YG<*"kQ  
the same area was performed in 1999 and identified 1378 IGlR,tw_/  
newly eligible residents who moved into the area or the TdtV (  
eligible age group. During 1999–2000, 1174 (85.2%) of 8nz({Mb9Z  
this group participated in an extension study (BMES IIB). } M#e\neii  
BMES cross-section II thus includes BMES IIA (66.5%) S@qp_!  
and BMES IIB (33.5%) participants (n = 3509). -dntV=  
Similar procedures were used for all stages of data collection ~+q1g[6  
at both surveys. A questionnaire was administered ><V*`{bD9)  
including demographic, family and medical history. A hW^,' m  
detailed eye examination included subjective refraction, %)ho<z:7U  
slit-lamp (Topcon SL-7e camera, Topcon Optical Co, 3DU1c?M:  
Tokyo, Japan) and retroillumination (Neitz CT-R camera, 6{Wo5O{!\  
Neitz Instrument Co, Tokyo, Japan) photography of the 8|u 4xf<  
lens. Grading of lens photographs in the BMES has been Up9{aX  
previously described [12]. Briefly, masked grading was %fS9F^AK  
performed on the lens photographs using the Wisconsin zWsr|= [  
Cataract Grading System [13]. Cortical cataract and PSC OM*_%UF  
were assessed from the retroillumination photographs by 0I}e>]:I  
estimating the percentage of the circular grid involved. m[hL GD'Fi  
Cortical cataract was defined when cortical opacity oA1_W).wJ  
involved at least 5% of the total lens area. PSC was defined Nw;qJ58@  
when opacity comprised at least 1% of the total lens area. 7& M-^Ev  
Slit-lamp photographs were used to assess nuclear cataract q=1 N&#R G  
using the Wisconsin standard set of four lens photographs   f XD+  
[13]. Nuclear cataract was defined when nuclear opacity }Zhe%M=}G  
was at least as great as the standard 4 photograph. Any cataract GES}o9?#  
was defined to include persons who had previous _Q V=3UWP  
cataract surgery as well as those with any of three cataract U82a]i0  
types. Inter-grader reliability was high, with weighted eP{srP3 9  
kappa 0.82 for cortical cataract, 0.55 (simple kappa 0.75) ^-o{3Q(w  
for nuclear cataract and 0.82 for PSC grading. The intragrader %mI0*YRma  
reliability for nuclear cataract was assessed with FX:`7c]:9  
simple kappa 0.83 for the senior grader who graded `e[S Zj\  
nuclear cataract at both surveys. All PSC cases were confirmed c*USA eP  
by an ophthalmologist (PM). qxL\ G &~  
In cross-section I, 219 persons (6.0%) had missing or !_I1=yi  
ungradable Neitz photographs, leaving 3435 with photographs Zxk~X}K\P  
available for cortical cataract and PSC assessment, s%[F,hQRk  
while 1153 (31.6%) had randomly missing or ungradable 5 Qgu:)}  
Topcon photographs due to a camera malfunction, leaving i~B?p[  
2501 with photographs available for nuclear cataract 0G%9 @^B  
assessment. Comparison of characteristics between participants n#_B4UqW%  
with and without Neitz or Topcon photographs in Ky3mz w|  
cross-section I showed no statistically significant differences o3WOp80hz  
between the two groups, as reported previously ,H7X_KbFD4  
[12]. In cross-section II, 441 persons (12.5%) had missing dQ:,pe7A  
or ungradable Neitz photographs, leaving 3068 for cortical ,p2UshOmd  
cataract and PSC assessment, and 648 (18.5%) had _3IT3mb2n  
missing or ungradable Topcon photographs, leaving 2860 'nmGHorp  
for nuclear cataract assessment. I8#2+$Be+@  
Data analysis was performed using the Statistical Analysis t}t(fJHY`  
System (SAS, SAS Institute, Cary, NC, USA). Age-adjusted .)E#*kLWR  
prevalence was calculated using direct standardization of vHaM yA-  
the cross-section II population to the cross-section I population. jkeerU6  
We assessed age-specific prevalence using an pn"!wqg  
interval of 5 years, so that participants within each age j?T'N:Qd  
group were independent between the two cross-sectional 5(;Y&?k  
surveys. p.8bX  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 v>X!/if<y  
Page 3 of 7 DYX{v`>f^  
(page number not for citation purposes) 4KPn V+h"b  
Results kUBE+a6#  
Characteristics of the two survey populations have been m:BzIcW<\  
previously compared [14] and showed that age and sex Jv~R /qaaD  
distributions were similar. Table 1 compares participant i?L=8+9f  
characteristics between the two cross-sections. Cross-section b42%^E  
II participants generally had higher rates of diabetes, Lg4|6.Ez|P  
hypertension, myopia and more users of inhaled steroids. ?XKX&ws  
Cataract prevalence rates in cross-sections I and II are \((MoQ9Qk  
shown in Figure 1. The overall prevalence of cortical cataract FDo PW~+[  
was 23.8% and 23.7% in cross-sections I and II, Z% +$< J  
respectively (age-sex adjusted P = 0.81). Corresponding lHiWzt u  
prevalence of PSC was 6.3% and 6.0% for the two crosssections Y S3~sA  
(age-sex adjusted P = 0.60). There was an -TD\?Q  
increased prevalence of nuclear cataract, from 18.7% in (bm^R-SbB  
cross-section I to 23.9% in cross-section II over the 6-year VQIvu)I  
period (age-sex adjusted P < 0.001). Prevalence of any cataract TX)W.2u=  
(including persons who had cataract surgery), however, Q#MB=:0 {  
was relatively stable (46.9% and 46.8% in crosssections &l6@C3N$  
I and II, respectively). &C'^YF_^0  
After age-standardization, these prevalence rates remained |JkfAnrN$I  
stable for cortical cataract (23.8% and 23.5% in the two *eg0^ByeD  
surveys) and PSC (6.3% and 5.9%). The slightly increased _2KIe(,;  
prevalence of nuclear cataract (from 18.7% to 24.2%) was 8T+9 fh]I  
not altered. (wj:Gc  
Table 2 shows the age-specific prevalence rates for cortical d==0 @`  
cataract, PSC and nuclear cataract in cross-sections I and NX\AQVy9  
II. A similar trend of increasing cataract prevalence with 5V 2ZAYV  
increasing age was evident for all three types of cataract in 'VV U-)(8  
both surveys. Comparing the age-specific prevalence |!FQQ(1b  
between the two surveys, a reduction in PSC prevalence in }NDl~5  
cross-section II was observed in the older age groups (≥ 75  Z 9:  
years). In contrast, increased nuclear cataract prevalence 20I`F>-*  
in cross-section II was observed in the older age groups (≥ k"#gSCW$  
70 years). Age-specific cortical cataract prevalence was relatively ILr=< j  
consistent between the two surveys, except for a +cfcr*  
reduction in prevalence observed in the 80–84 age group rC@VMe|0  
and an increasing prevalence in the older age groups (≥ 85 G:*vV#K  
years). $e1.y b%  
Similar gender differences in cataract prevalence were pPa]@ z~O  
observed in both surveys (Table 3). Higher prevalence of B*_ K}5UO  
cortical and nuclear cataract in women than men was evident RP$u/x"b  
but the difference was only significant for cortical ZK;/~9KU  
cataract (age-adjusted odds ratio, OR, for women 1.3, t U}6^yc  
95% confidence intervals, CI, 1.1–1.5 in cross-section I ,>aa2  
and OR 1.4, 95% CI 1.1–1.6 in cross-section II). In con- CHTK.%AQH!  
Table 1: Participant characteristics. 1\}XL=BE  
Characteristics Cross-section I Cross-section II (Y'cxwj%  
n % n % ?98!2:'{9  
Age (mean) (66.2) (66.7) j^=Eu r/  
50–54 485 13.3 350 10.0 frUs'j/bZ  
55–59 534 14.6 580 16.5 !p$p 7   
60–64 638 17.5 600 17.1 t Aq0Z)  
65–69 671 18.4 639 18.2 .K84"Gdx  
70–74 538 14.7 572 16.3 ^mn!;nu  
75–79 422 11.6 407 11.6 ;N#}3lpLqg  
80–84 230 6.3 226 6.4 ^"O>EY':  
85–89 100 2.7 110 3.1 7tWC<#  
90+ 36 1.0 24 0.7 {@CQ (  
Female 2072 56.7 1998 57.0 uGz)Vz&3  
Ever Smokers 1784 51.2 1789 51.2 8\68NG6o  
Use of inhaled steroids 370 10.94 478 13.8^ 6!>p<p"Ns  
History of: 5IUdA?  
Diabetes 284 7.8 347 9.9^ A :ts_*  
Hypertension 1669 46.0 1825 52.2^ , r*Kxy  
Emmetropia* 1558 42.9 1478 42.2 sJx_X8  
Myopia* 442 12.2 495 14.1^ zHA::6OgPN  
Hyperopia* 1633 45.0 1532 43.7 l6#Y}<tq  
n = number of persons affected .O"a:^i  
* best spherical equivalent refraction correction "LlQl3"=  
^ P < 0.01 4/~x+tdc  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 C]2-V1,ZX  
Page 4 of 7 )1!<<;@0  
(page number not for citation purposes) 27N;>   
t M>Q ZN  
rast, men had slightly higher PSC prevalence than women ~2\Sn-`  
in both cross-sections but the difference was not significant 1Sz tN3'q  
(OR 1.1, 95% CI 0.8–1.4 for men in cross-section I f$QkzWvr  
and OR 1.2, 95% 0.9–1.6 in cross-section II). V K6D  
Discussion D(ItNMc Ku  
Findings from two surveys of BMES cross-sectional populations BW)-F (v   
with similar age and gender distribution showed %B\x %e ;P  
that the prevalence of cortical cataract and PSC remained z |llf7:  
stable, while the prevalence of nuclear cataract appeared :=y5713  
to have increased. Comparison of age-specific prevalence, Ez~5ax7x  
with totally independent samples within each age group, *JDz0M4f  
confirmed the robustness of our findings from the two z*h:Nt%.  
survey samples. Although lens photographs taken from OM0r*<D"!  
the two surveys were graded for nuclear cataract by the _M/N_Fm  
same graders, who documented a high inter- and intragrader z.8nYL5^}  
reliability, we cannot exclude the possibility that $,@}%NlHc  
variations in photography, performed by different photographers, pZ'q_Oux  
may have contributed to the observed difference ,i6E L  
in nuclear cataract prevalence. However, the overall =( |%%,3  
Table 2: Age-specific prevalence of cataract types in cross sections I and II. Q// @5m_  
Cataract type Age (years) Cross-section I Cross-section II 53{\H&q  
n % (95% CL)* n % (95% CL)* l SdA7  
Cortical 50–54 473 4.4 (2.6–6.3) 338 7.4 (4.6–10.2) 'Wnh1|z  
55–59 522 9.2 (6.7–11.7) 542 9.0 (6.6–11.5) r\Y,*e  
60–64 615 16.4 (13.5–19.4) 556 16.7 (13.6–19.8) xg/(  
65–69 653 26.2 (22.8–29.6) 581 23.6 (20.1–27.0) _aevaWtEx  
70–74 516 31.2 (27.2–35.2) 514 35.4 (31.3–39.6) neM.M )0  
75–79 366 40.2 (35.1–45.2) 332 39.8 (34.5–45.1) Jm<NDE~rw  
80–84 194 58.8 (51.8–65.8) 163 42.9 (35.3–50.6) 1<'z)r4  
85–89 74 52.7 (41.1–64.4) 73 54.8 (43.1–66.5) /al56n  
90+ 22 68.2 (47.0–89.3) 14 78.6 (54.0–103.2) :Q DkaA  
PSC 50–54 474 2.7 (1.3–4.2) 338 2.4 (0.7–4.0) 4Y?2u  
55–59 522 2.9 (1.4–4.3) 541 2.6 (1.3–3.9) )). =MTk  
60–64 616 4.6 (2.9–6.2) 548 5.7 (3.7–7.6) SX"|~Pi(  
65–69 655 6.3 (4.4–8.1) 573 4.5 (2.8–6.3) ,5 ka{Q`K  
70–74 517 6.8 (4.6–8.9) 505 9.7 (7.1–12.3) 0a89<yX  
75–79 367 11.4 (8.2–14.7) 327 9.5 (6.3–12.7) g)czJ=T2  
80–84 196 12.2 (7.6–16.9) 155 10.3 (5.5–15.2) dP_Q kO  
85–89 74 18.9 (9.8–28.1) 69 11.6 (3.9–19.4) CWkWW/ZI  
90+ 23 21.7 (3.5–40.0) 11 0.0 k_]'?f7Z  
Nuclear 50–54 323 1.6 (0.2–2.9) 331 0.9 (–0.2–1.9) !6=s{V&r1  
55–59 386 2.3 (0.8–3.8) 507 3.6 (1.9–5.2) _MC',p&  
60–64 453 5.3 (3.2–7.4) 501 11.6 (8.8–14.4) DQY1oM)D !  
65–69 478 17.2 (13.8–20.1) 534 18.5 (15.2–21.9) )1Bz0:  
70–74 392 27.6 (23.1–32.0) 453 36.0 (31.6–40.4) C{/U;Ie -b  
75–79 255 45.1 (39.0–51.3) 302 55.6 (50.0–61.3) ^5]9B<i[Y  
80–84 146 54.1 (45.9–62.3) 147 73.5 (66.3–80.7) zgjgEhnvU  
85–89 50 64.0 (50.2–77.8) 70 80.0 (70.4–89.6) |iUF3s|?  
90+ 18 72.2 (49.3–95.1) 15 73.3 (48.0–98.7) J.XkdGQ  
n = number of persons _m?i$5  
* 95% Confidence Limits A x8>  
Cataract FMioguunrtea i1n ps rEeyvea lSetnucdey in cross-sections I and II of the Blue tZ[9qms^_  
Cataract prevalence in cross-sections I and II of the Blue B bmw[Qf\  
Mountains Eye Study. mH$`)i8  
0 VgXT4gO!  
10 k?7"r4Vc)S  
20 ^Ak?2,xB#+  
30 uB"B{:Kz  
40 9<rs3 84  
50 OSO MFt  
cortical PSC nuclear any @Pc7$qD%  
cataract !q$VnqFk  
Cataract type A v>v\ :.>  
% 392(N(  
Cross-section I  Me z&@{  
Cross-section II #Db^*  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 C"n!mr{srt  
Page 5 of 7 )kjQ W&)g  
(page number not for citation purposes) ih)\P0wed  
prevalence of any cataract (including cataract surgery) was 92Gfxld\  
relatively stable over the 6-year period. -,*m\Fe}  
Although different population-based studies used different H5d@TB, `  
grading systems to assess cataract [15], the overall ,k.")  
prevalence of the three cataract types were similar across 7)D[}UXz  
different study populations [12,16-23]. Most studies have sQ\HIU%]  
suggested that nuclear cataract is the most prevalent type nT:<_'!  
of cataract, followed by cortical cataract [16-20]. Ours and l@w\ Vxr  
other studies reported that cortical cataract was the most \'g7oV;>cI  
prevalent type [12,21-23]. Zt41fPQ  
Our age-specific prevalence data show a reduction of Z/ml ,4e  
15.9% in cortical cataract prevalence for the 80–84 year f8K0/z  
age group, concordant with an increase in cataract surgery %Qj$@.*:  
prevalence by 9% in those aged 80+ years observed in the ~a  V5  
same study population [10]. Although cortical cataract is lrkgsv6  
thought to be the least likely cataract type leading to a cataract 3`D*AFQc  
surgery, this may not be the case in all older persons. eCJ tNPd  
A relatively stable cortical cataract and PSC prevalence SefF Ci%4  
over the 6-year period is expected. We cannot offer a ;L76V$&  
definitive explanation for the increase in nuclear cataract g}6M+QNj  
prevalence. A possible explanation could be that a moderate \COoU ("  
level of nuclear cataract causes less visual disturbance Z! /_H($  
than the other two types of cataract, thus for the oldest age PU\xFt  
groups, persons with nuclear cataract could have been less V`/c#y||  
likely to have surgery unless it is very dense or co-existing iX2exJto  
with cortical cataract or PSC. Previous studies have shown ^Q0=Ggh  
that functional vision and reading performance were high TRgj`FG  
in patients undergoing cataract surgery who had nuclear X pK eN2=p  
cataract only compared to those with mixed type of cataract 6e,IjocsB  
(nuclear and cortical) or PSC [24,25]. In addition, the ~_CZ1  
overall prevalence of any cataract (including cataract surgery) ZBK)rmhMx  
was similar in the two cross-sections, which appears x^`P[>  
to support our speculation that in the oldest age group, Tsu\4 cL]  
nuclear cataract may have been less likely to be operated B|^=2 >8s  
than the other two types of cataract. This could have dZkKAK:v  
resulted in an increased nuclear cataract prevalence (due BUI#y `J  
to less being operated), compensated by the decreased |P9MhfN  
prevalence of cortical cataract and PSC (due to these being o<s~ 455m/  
more likely to be operated), leading to stable overall prevalence j~in%|^  
of any cataract. |1!OwQax  
Possible selection bias arising from selective survival `P|V&;}K  
among persons without cataract could have led to underestimation MnY}U",   
of cataract prevalence in both surveys. We r;waT@&C  
assume that such an underestimation occurred equally in A$zC$9{0I  
both surveys, and thus should not have influenced our ZI :wJU:f  
assessment of temporal changes. |ns9ziTDI  
Measurement error could also have partially contributed SrWmV@"y  
to the observed difference in nuclear cataract prevalence. 1TN+pmc}@  
Assessment of nuclear cataract from photographs is a oB!-JX9  
potentially subjective process that can be influenced by *$t=Lh  
variations in photography (light exposure, focus and the 4kNSF  
slit-lamp angle when the photograph was taken) and Q;z'"P   
grading. Although we used the same Topcon slit-lamp .'1]2/ad  
camera and the same two graders who graded photos (iO/@iw  
from both surveys, we are still not able to exclude the possibility YMwL(m1  
of a partial influence from photographic variation NQbgk+&wD  
on this result. EF6"P H+J@  
A similar gender difference (women having a higher rate <;Td8T;  
than men) in cortical cataract prevalence was observed in $4CsiZ6  
both surveys. Our findings are in keeping with observations c<)O#i@3/  
from the Beaver Dam Eye Study [18], the Barbados b:*( f#"q  
Eye Study [22] and the Lens Opacities Case-Control -A"0mS8L  
Group [26]. It has been suggested that the difference U4y ?z  
could be related to hormonal factors [18,22]. A previous 3)dtl!VMW[  
study on biochemical factors and cataract showed that a #|cr\\2*  
lower level of iron was associated with an increased risk of i"M$hXO  
cortical cataract [27]. No interaction between sex and biochemical ueJ_F#y  
factors were detected and no gender difference M ~6k[ew  
was assessed in this study [27]. The gender difference seen (=D^BXtH|  
in cortical cataract could be related to relatively low iron J35[GZ';D  
levels and low hemoglobin concentration usually seen in |0N1]Hf   
women [28]. Diabetes is a known risk factor for cortical 3%V VG~[  
Table 3: Gender distribution of cataract types in cross-sections I and II. {F$MZ2E  
Cataract type Gender Cross-section I Cross-section II &G!2T!xx  
n % (95% CL)* n % (95% CL)* 9Or  
Cortical Male 1496 21.1 (19.0–23.1) 1328 20.4 (18.2–22.6) [/eRc  
Female 1939 25.9 (23.9–27.8) 1785 26.2 (24.2–28.3) ]0@ J)Z09  
PSC Male 1500 6.5 (5.2–7.7) 1314 6.4 (5.1–7.7) X7fJ+C n  
Female 1944 6.2 (5.1–7.2) 1753 5.7 (4.6–6.7) v>p~y u+G  
Nuclear Male 1106 17.6 (15.4–19.9) 1225 22.5 (20.1–24.8) ~_yz\;#  
Female 1395 19.5 (17.4–21.6) 1635 25.0 (22.9–27.1) = M/($PA  
n = number of persons P'CDV3+  
* 95% Confidence Limits ,W&::/2<7  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 h*X u/aOg  
Page 6 of 7 dpcFS0  
(page number not for citation purposes) ;Quk%6;[N  
cataract but in this particular population diabetes is more YumHECej  
prevalent in men than women in all age groups [29]. Differential 3S WO_  
exposures to cataract risk factors or different dietary ;AK@Kb  
or lifestyle patterns between men and women may srfM"Lb'  
also be related to these observations and warrant further #1` lJ  
study. 6(.]TEu0  
Conclusion 3a]Omuu|=  
In summary, in two population-based surveys 6 years N|L Ey  
apart, we have documented a relatively stable prevalence q`DilZ]S  
of cortical cataract and PSC over the period. The observed s+yX82Y  
overall increased nuclear cataract prevalence by 5% over a 1K'.QRZMb9  
6-year period needs confirmation by future studies, and 2OJ=Xb1  
reasons for such an increase deserve further study. Yy:Q/zw o  
Competing interests PE-P(T3s[8  
The author(s) declare that they have no competing interests. %4rPkPAtrp  
Authors' contributions F)g.xQ  
AGT graded the photographs, performed literature search KD5}Nk)t  
and wrote the first draft of the manuscript. JJW graded the =W~K_jE5lo  
photographs, critically reviewed and modified the manuscript. Pq:GvM`  
ER performed the statistical analysis and critically <MH| <hP  
reviewed the manuscript. PM designed and directed the c p7Rpqg  
study, adjudicated cataract cases and critically reviewed fhZD#D  
and modified the manuscript. All authors read and 'YcoF;&[C  
approved the final manuscript. * -Kf  
Acknowledgements Tv{X$`%  
This study was supported by the Australian National Health & Medical H/Fq'FsQB  
Research Council, Canberra, Australia (Grant Nos 974159, 991407). The y-iu Ozq4  
abstract was presented at the Association for Research in Vision and Ophthalmology BiUOjQC#  
(ARVO) meeting in Fort Lauderdale, Florida, USA, May 2005. &_EjP hZ  
References `/mcjKQ&9y  
1. Congdon N, O'Colmain B, Klaver CC, Klein R, Munoz B, Friedman do:3aP'S,  
DS, Kempen J, Taylor HR, Mitchell P: Causes and prevalence of i2EXE0;  
visual impairment among adults in the United States. Arch dm&vLQVS  
Ophthalmol 2004, 122(4):477-485.  5 `B ! 1  
2. Rahmani B, Tielsch JM, Katz J, Gottsch J, Quigley H, Javitt J, Sommer )NwIEk>Tf  
A: The cause-specific prevalence of visual impairment in an k2xOu9ncEj  
urban population. The Baltimore Eye Survey. Ophthalmology {T]^C  
1996, 103:1721-1726. j'V# =vH  
3. Keeffe JE, Konyama K, Taylor HR: Vision impairment in the m};Qng]  
Pacific region. Br J Ophthalmol 2002, 86:605-610. :Sx !jx>W  
4. Reidy A, Minassian DC, Vafidis G, Joseph J, Farrow S, Wu J, Desai P, #UcqKq  
Connolly A: Prevalence of serious eye disease and visual |X6]#&g7  
impairment in a north London population: population based, 3UIR^Rh+  
cross sectional study. BMJ 1998, 316:1643-1646. luyU!  
5. Resnikoff S, Pascolini D, Etya'ale D, Kocur I, Pararajasegaram R, ;c'9Xyl-  
Pokharel GP, Mariotti SP: Global data on visual impairment in +a%Vp!y  
the year 2002. Bull World Health Organ 2004, 82:844-851. YJlpP0;++  
6. Pascolini D, Mariotti SP, Pokharel GP, Pararajasegaram R, Etya'ale D, KMxP%dV/=  
Negrel AD, Resnikoff S: 2002 global update of available data on AiT&:'<UT  
visual impairment: a compilation of population-based prevalence ]8|cV GMa  
studies. Ophthalmic Epidemiol 2004, 11:67-115. \k{UqU+s  
7. Rochtchina E, Mukesh BN, Wang JJ, McCarty CA, Taylor HR, Mitchell /N`l z>^~  
P: Projected prevalence of age-related cataract and cataract i9.~cnk  
surgery in Australia for the years 2001 and 2021: pooled data Gu-*@C:^&  
from two population-based surveys. Clin Experiment Ophthalmol D2`tWRm0  
2003, 31:233-236. K0#kW \4`  
8. Medicare Benefits Schedule Statistics [http://www.medicar !vU$^>zo~  
eaustralia.gov.au/statistics/dyn_mbs/forms/mbs_tab4.shtml] ^<8 c`k )e  
9. Keeffe JE, Taylor HR: Cataract surgery in Australia 1985–94. m]yt6b4  
Aust N Z J Ophthalmol 1996, 24:313-317. NzmVQ-4  
10. Tan AG, Wang JJ, Rochtchina E, Jakobsen K, Mitchell P: Increase in +UxhSF U  
cataract surgery prevalence from 1992–1994 to 1997–2000: gHLBtl/  
Analysis of two population cross-sections. Clin Experiment Ophthalmol un4q,Ac~0  
2004, 32:284-288. F)we^'X  
11. Mitchell P, Smith W, Attebo K, Wang JJ: Prevalence of age-related G: f\wK[  
maculopathy in Australia. The Blue Mountains Eye Study. J`T1 88  
Ophthalmology 1995, 102:1450-1460. W|K"0ab  
12. Mitchell P, Cumming RG, Attebo K, Panchapakesan J: Prevalence of &C eG4_Mi  
cataract in Australia: the Blue Mountains eye study. Ophthalmology nR7 usL  
1997, 104:581-588. x/NR_~Rnk  
13. Klein BEK, Magli YL, Neider MW, Klein R: Wisconsin system for classification oyGO!j  
of cataracts from photographs (protocol) Madison, WI; 1990. )P:r;a'  
14. Foran S, Wang JJ, Mitchell P: Causes of visual impairment in two pKf]&?FX  
older population cross-sections: the Blue Mountains Eye r)P^CZm  
Study. Ophthalmic Epidemiol 2003, 10:215-225. g">E it*[  
15. Congdon N, Vingerling JR, Klein BE, West S, Friedman DS, Kempen J, =9UR~-`d\  
O'Colmain B, Wu SY, Taylor HR: Prevalence of cataract and  rO]7 g  
pseudophakia/aphakia among adults in the United States. ;2||g8'  
Arch Ophthalmol 2004, 122:487-494. C WJGr:}&  
16. Sperduto RD, Hiller R: The prevalence of nuclear, cortical, and `I(#.*  
posterior subcapsular lens opacities in a general population &uwj&-u?  
sample. Ophthalmology 1984, 91:815-818. B+G,v:)R6z  
17. Adamsons I, Munoz B, Enger C, Taylor HR: Prevalence of lens :3k&[W*  
opacities in surgical and general populations. Arch Ophthalmol DPuz'e*  
1991, 109:993-997. zGrUl|j  
18. Klein BE, Klein R, Linton KL: Prevalence of age-related lens rixP[`!]x  
opacities in a population. The Beaver Dam Eye Study. Ophthalmology __p\`3(,'  
1992, 99:546-552. CmaV>  
19. West SK, Munoz B, Schein OD, Duncan DD, Rubin GS: Racial differences 8(R%?> 8  
in lens opacities: the Salisbury Eye Evaluation (SEE) {C>.fg%t  
project. Am J Epidemiol 1998, 148:1033-1039. V[f-Nj Kf  
20. Congdon N, West SK, Buhrmann RR, Kouzis A, Munoz B, Mkocha H: UUy% :t  
Prevalence of the different types of age-related cataract in Z:3N*YkL  
an African population. Invest Ophthalmol Vis Sci 2001, y5_`<lFv  
42:2478-2482. ]3@6o*R;  
21. Livingston PM, Guest CS, Stanislavsky Y, Lee S, Bayley S, Walker C, I@VhxJh  
McKean C, Taylor HR: A population-based estimate of cataract *vn^ W  
prevalence: the Melbourne Visual Impairment Project experience. kTG4h@w  
Dev Ophthalmol 1994, 26:1-6. 1JIL6w _  
22. Leske MC, Connell AM, Wu SY, Hyman L, Schachat A: Prevalence TRwlUC3hQ  
of lens opacities in the Barbados Eye Study. Arch Ophthalmol 1:<=zqh0  
1997, 115:105-111. published erratum appears in Arch Ophthalmol >$=-0?.  
1997 Jul;115(7):931 3 w9 j~s  
23. Seah SK, Wong TY, Foster PJ, Ng TP, Johnson GJ: Prevalence of )X{x\ /N  
lens opacity in Chinese residents of Singapore: the tanjong )Lht}I ]:  
pagar survey. Ophthalmology 2002, 109:2058-2064. J+f .r|?  
24. Stifter E, Sacu S, Weghaupt H, Konig F, Richter-Muksch S, Thaler A, ;seD{y7!  
Velikay-Parel M, Radner W: Reading performance depending on rj[2XIO  
the type of cataract and its predictability on the visual outcome. :fI|>I ~  
J Cataract Refract Surg 2004, 30:1259-1267. m9bR %j  
25. Stifter E, Sacu S, Weghaupt H: Functional vision with cataracts of 1{N73]-M:  
different morphologies: comparative study. J Cataract Refract :TU;%@7  
Surg 2004, 30:1883-1891. z-|gw.y  
26. Leske MC, Chylack LT Jr, Wu SY: The Lens Opacities Case-Control 8Xpf|? .  
Study. Risk factors for cataract. Arch Ophthalmol 1991, 44 bTx y  
109:244-251. ~m^.&mv3/  
27. Leske MC, Wu SY, Hyman L, Sperduto R, Underwood B, Chylack LT, sg"J00  
Milton RC, Srivastava S, Ansari N: Biochemical factors in the lens L3:dANG  
opacities. Case-control study. The Lens Opacities Case-Control Xd%c00"U  
Study Group. Arch Ophthalmol 1995, 113:1113-1119. w~J 7|8Y  
28. Yip R, Johnson C, Dallman PR: Age-related changes in laboratory oh+Q}Fa:  
values used in the diagnosis of anemia and iron deficiency. )1Rn;(j9Re  
Am J Clin Nutr 1984, 39:427-436. xU$A/!oK  
29. Mitchell P, Smith W, Wang JJ, Cumming RG, Leeder SR, Burnett L: {awv= s  
Diabetes in an older Australian population. Diabetes Res Clin P7GuFn/p~2  
Pract 1998, 41:177-184. 6<sd6SM  
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