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BMC Ophthalmology

BioMed Central XK3]AYH  
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(page number not for citation purposes) q @Kk\m  
BMC Ophthalmology 7u%a/<  
Research article Open Access 4UCwT1  
Comparison of age-specific cataract prevalence in two hYvNcOSks  
population-based surveys 6 years apart g5R,% 6  
Ava Grace Tan†, Jie Jin Wang*†, Elena Rochtchina† and Paul Mitchell† CM 9P"-  
Address: Centre for Vision Research, Westmead Millennium Institute, Department of Ophthalmology, University of Sydney, Westmead Hospital, g37q/nEv  
Westmead, NSW, Australia 5-p.MGso  
Email: Ava Grace Tan - ava_tan@wmi.usyd.edu.au; Jie Jin Wang* - jiejin_wang@wmi.usyd.edu.au; ?vu|o'$T,  
Elena Rochtchina - elena_rochtchina@wmi.usyd.edu.au; Paul Mitchell - paul_mitchell@wmi.usyd.edu.au A^pW]r=Xtk  
* Corresponding author †Equal contributors oeN zHp_  
Abstract agY5Dg7  
Background: In this study, we aimed to compare age-specific cortical, nuclear and posterior h PPB45^  
subcapsular (PSC) cataract prevalence in two surveys 6 years apart. P3$,ca'  
Methods: The Blue Mountains Eye Study examined 3654 participants (82.4% of those eligible) in ^gm>!-Gx  
cross-section I (1992–4) and 3509 participants (75.1% of survivors and 85.2% of newly eligible) in 5^F]tRz-  
cross-section II (1997–2000, 66.5% overlap with cross-section I). Cataract was assessed from lens 1l]C5P}E  
photographs following the Wisconsin Cataract Grading System. Cortical cataract was defined if G^KC&  
cortical opacity comprised ≥ 5% of lens area. Nuclear cataract was defined if nuclear opacity ≥ u{+!& 2}k  
Wisconsin standard 4. PSC was defined if any present. Any cataract was defined to include persons R92R}=G!  
who had previous cataract surgery. Weighted kappa for inter-grader reliability was 0.82, 0.55 and YKq0f=Ij  
0.82 for cortical, nuclear and PSC cataract, respectively. We assessed age-specific prevalence using !w=,p.?V=  
an interval of 5 years, so that participants within each age group were independent between the `e*61k5  
two surveys.  QT_^M1%  
Results: Age and gender distributions were similar between the two populations. The age-specific BvI 0v:  
prevalence of cortical (23.8% in 1st, 23.7% in 2nd) and PSC cataract (6.3%, 6.0%) was similar. The [0(mFMC`  
prevalence of nuclear cataract increased slightly from 18.7% to 23.9%. After age standardization, /#IH -2N  
the similar prevalence of cortical (23.8%, 23.5%) and PSC cataract (6.3%, 5.9%), and the increased {r{>?)O  
prevalence of nuclear cataract (18.7%, 24.2%) remained. ]Da4.s*mW  
Conclusion: In two surveys of two population-based samples with similar age and gender u7u~  
distributions, we found a relatively stable cortical and PSC cataract prevalence over a 6-year period. S| " TP\o  
The increased prevalence of nuclear cataract deserves further study. uH] m]t  
Background Cn/q=  
Age-related cataract is the leading cause of reversible visual DCK_F8  
impairment in older persons [1-6]. In Australia, it is q06@SD$   
estimated that by the year 2021, the number of people 'F<Sf:?.p  
affected by cataract will increase by 63%, due to population U 5clQiow  
aging [7]. Surgical intervention is an effective treatment dL(4mR8  
for cataract and normal vision (> 20/40) can usually th9 0O|;  
be restored with intraocular lens (IOL) implantation. qAbd xd[  
Cataract surgery with IOL implantation is currently the (Otur  
most commonly performed, and is, arguably, the most 4NI ' (#l  
cost effective surgical procedure worldwide. Performance WSSaZ9 =  
Published: 20 April 2006 rSbQ}O4V  
BMC Ophthalmology 2006, 6:17 doi:10.1186/1471-2415-6-17 Qv74?B@  
Received: 14 December 2005 Mi;Tn;3er  
Accepted: 20 April 2006 Hj1k-Bs&'w  
This article is available from: http://www.biomedcentral.com/1471-2415/6/17 s7AI:Zv  
© 2006 Tan et al; licensee BioMed Central Ltd. w[|y0jtw  
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), `} ZL'\G  
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ,qYf#fU#7  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 )y5iH){ !  
Page 2 of 7 sAf9rZt*'  
(page number not for citation purposes) Mru~<:9  
of this surgical procedure has been continuously increasing hg!x_Eq|  
in the last two decades. Data from the Australian $F<%Jl7_Z  
Health Insurance Commission has shown a steady <'V A=orD  
increase in Medicare claims for cataract surgery [8]. A 2.6- 0;'j!`l9  
fold increase in the total number of cataract procedures *?s/Ho &'  
from 1985 to 1994 has been documented in Australia [9]. wX@H &)<s  
The rate of cataract surgery per thousand persons aged 65 P: jDB{  
years or older has doubled in the last 20 years [8,9]. In the 01'y^`\xQ  
Blue Mountains Eye Study population, we observed a onethird uF.Q ",<  
increase in cataract surgery prevalence over a mean Ug%<b  
6-year interval, from 6% to nearly 8% in two cross-sectional wbn^R'  
population-based samples with a similar age range -Cg`x=G;z  
[10]. Further increases in cataract surgery performance /vMQF+  
would be expected as a result of improved surgical skills "tEj`eR  
and technique, together with extending cataract surgical J{a Q1)  
benefits to a greater number of older people and an &E} I  
increased number of persons with surgery performed on AEiWL.*.  
both eyes. )*"T  
Both the prevalence and incidence of age-related cataract 7uWJ6Wk  
link directly to the demand for, and the outcome of, cataract m 4wPuW  
surgery and eye health care provision. This report i7Y s_8A"9  
aimed to assess temporal changes in the prevalence of cortical IptB.bYc  
and nuclear cataract and posterior subcapsular cataract &\CJg'D:m  
(PSC) in two cross-sectional population-based 3'|Uqf8  
surveys 6 years apart. ez{P-qB  
Methods #RCZA4>  
The Blue Mountains Eye Study (BMES) is a populationbased oAIY=z  
cohort study of common eye diseases and other g6x/f<2x  
health outcomes. The study involved eligible permanent JNU"5sB  
residents aged 49 years and older, living in two postcode W)G2Cs?p  
areas in the Blue Mountains, west of Sydney, Australia. ::^qy^n  
Participants were identified through a census and were s8`}x_k=  
invited to participate. The study was approved at each )&b}^1  
stage of the data collection by the Human Ethics Committees kMfc"JXF  
of the University of Sydney and the Western Sydney 'qD'PLV  
Area Health Service and adhered to the recommendations (9WL+S  
of the Declaration of Helsinki. Written informed consent (Von;U  
was obtained from each participant. s= -WB0E  
Details of the methods used in this study have been nm{'HH-4  
described previously [11]. The baseline examinations |IyM"UH  
(BMES cross-section I) were conducted during 1992– -$sl!%HO%  
1994 and included 3654 (82.4%) of 4433 eligible residents. iMOPD}`IX  
Follow-up examinations (BMES IIA) were conducted T6/$pJ l  
during 1997–1999, with 2335 (75.0% of BMES \S|VkPv  
cross section I survivors) participating. A repeat census of ( Fjs N5  
the same area was performed in 1999 and identified 1378 =Ov;'MC  
newly eligible residents who moved into the area or the |)|vG_  
eligible age group. During 1999–2000, 1174 (85.2%) of O|^6UH  
this group participated in an extension study (BMES IIB). oJ4mxi@|#  
BMES cross-section II thus includes BMES IIA (66.5%) 5W:Gl?$S}  
and BMES IIB (33.5%) participants (n = 3509). k`iq<b  
Similar procedures were used for all stages of data collection $@ T6g  
at both surveys. A questionnaire was administered n41\y:CAo  
including demographic, family and medical history. A ^)%wq@Hi  
detailed eye examination included subjective refraction, <Vr] 2mw  
slit-lamp (Topcon SL-7e camera, Topcon Optical Co, ] fwTi(4y  
Tokyo, Japan) and retroillumination (Neitz CT-R camera, LzEE]i  
Neitz Instrument Co, Tokyo, Japan) photography of the x9{Sl[2&  
lens. Grading of lens photographs in the BMES has been C7fi 1~  
previously described [12]. Briefly, masked grading was +gD)Yd  
performed on the lens photographs using the Wisconsin o}AqNw60v  
Cataract Grading System [13]. Cortical cataract and PSC 9cw4tqTm  
were assessed from the retroillumination photographs by ?[L0LL?ce  
estimating the percentage of the circular grid involved. no\}aTx  
Cortical cataract was defined when cortical opacity +=29y@c  
involved at least 5% of the total lens area. PSC was defined yrK-- C8  
when opacity comprised at least 1% of the total lens area. Ig?.*j ]  
Slit-lamp photographs were used to assess nuclear cataract )lngef /D_  
using the Wisconsin standard set of four lens photographs ][>M<J  
[13]. Nuclear cataract was defined when nuclear opacity ~1wdAq`'a  
was at least as great as the standard 4 photograph. Any cataract M@ LaD 5  
was defined to include persons who had previous iw]B QjK  
cataract surgery as well as those with any of three cataract me}Gb a  
types. Inter-grader reliability was high, with weighted ,*}g r  
kappa 0.82 for cortical cataract, 0.55 (simple kappa 0.75) X-2S*L'  
for nuclear cataract and 0.82 for PSC grading. The intragrader ZZ.0'   
reliability for nuclear cataract was assessed with J/P@m_Yx  
simple kappa 0.83 for the senior grader who graded 0.+Z;j  
nuclear cataract at both surveys. All PSC cases were confirmed W0?Y%Da(4m  
by an ophthalmologist (PM). 5)zh@aJ@  
In cross-section I, 219 persons (6.0%) had missing or 'r?HL;,q  
ungradable Neitz photographs, leaving 3435 with photographs Jv{"R!e"P  
available for cortical cataract and PSC assessment, =x.v*W]F`  
while 1153 (31.6%) had randomly missing or ungradable "62Ysapq+  
Topcon photographs due to a camera malfunction, leaving <n2{+eO  
2501 with photographs available for nuclear cataract v.^ 'x  
assessment. Comparison of characteristics between participants 63dtO{:4  
with and without Neitz or Topcon photographs in @. ]K6qC  
cross-section I showed no statistically significant differences )1yUV*6  
between the two groups, as reported previously `::(jW.KO  
[12]. In cross-section II, 441 persons (12.5%) had missing g #<?OFl  
or ungradable Neitz photographs, leaving 3068 for cortical Cq;K,B9  
cataract and PSC assessment, and 648 (18.5%) had BMsy}08dQ  
missing or ungradable Topcon photographs, leaving 2860 LVcy.kU@]  
for nuclear cataract assessment. {aa,#B] i  
Data analysis was performed using the Statistical Analysis xA1pDrfC/  
System (SAS, SAS Institute, Cary, NC, USA). Age-adjusted Gqz)='  
prevalence was calculated using direct standardization of hE`%1j2(  
the cross-section II population to the cross-section I population. \]:NOmI^'  
We assessed age-specific prevalence using an U,3K6AZA 7  
interval of 5 years, so that participants within each age L5|;VH  
group were independent between the two cross-sectional 2i'-lM=  
surveys. \c^jaK5  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 Dq1XZ%8  
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Results P*=3$-`  
Characteristics of the two survey populations have been b0Cao SWo  
previously compared [14] and showed that age and sex #Lt+6sa]2@  
distributions were similar. Table 1 compares participant lSv;wwEg  
characteristics between the two cross-sections. Cross-section c] 9CN  
II participants generally had higher rates of diabetes, ill'K Py  
hypertension, myopia and more users of inhaled steroids. [*E.G~IS`  
Cataract prevalence rates in cross-sections I and II are ~l(tl[  
shown in Figure 1. The overall prevalence of cortical cataract ^7<mlr  
was 23.8% and 23.7% in cross-sections I and II, EF{'J8AQ  
respectively (age-sex adjusted P = 0.81). Corresponding /'^>-!8_1  
prevalence of PSC was 6.3% and 6.0% for the two crosssections 6y!?xot  
(age-sex adjusted P = 0.60). There was an Mp}NUQHE  
increased prevalence of nuclear cataract, from 18.7% in gxtbu$  
cross-section I to 23.9% in cross-section II over the 6-year AsF`A"Cdw<  
period (age-sex adjusted P < 0.001). Prevalence of any cataract W%QtJB1)  
(including persons who had cataract surgery), however, Gl:T  
was relatively stable (46.9% and 46.8% in crosssections rZ4<*Zegv  
I and II, respectively). Pu*UZcXY  
After age-standardization, these prevalence rates remained J~`%Nj 5>  
stable for cortical cataract (23.8% and 23.5% in the two ee[NZz  
surveys) and PSC (6.3% and 5.9%). The slightly increased Y\S^DJy  
prevalence of nuclear cataract (from 18.7% to 24.2%) was ,QAp5I%3=  
not altered. Oj\mkg  
Table 2 shows the age-specific prevalence rates for cortical e!'u{>u  
cataract, PSC and nuclear cataract in cross-sections I and 6;V 1PK>9  
II. A similar trend of increasing cataract prevalence with m(] IxI  
increasing age was evident for all three types of cataract in ?MB nnyo6  
both surveys. Comparing the age-specific prevalence ^C T}i'  
between the two surveys, a reduction in PSC prevalence in "b7C0NE  
cross-section II was observed in the older age groups (≥ 75 b;ZAz  
years). In contrast, increased nuclear cataract prevalence ^<+heX  
in cross-section II was observed in the older age groups (≥ TnAX;+u  
70 years). Age-specific cortical cataract prevalence was relatively (LPD  
consistent between the two surveys, except for a 6GvnyJ{[  
reduction in prevalence observed in the 80–84 age group 7?#32B Gr  
and an increasing prevalence in the older age groups (≥ 85 4 tTJE<y  
years). @U5>w\  
Similar gender differences in cataract prevalence were mr.DP~O:9p  
observed in both surveys (Table 3). Higher prevalence of DJUtuex  
cortical and nuclear cataract in women than men was evident 4f,x@:Jw  
but the difference was only significant for cortical lNAHn<ht  
cataract (age-adjusted odds ratio, OR, for women 1.3, i(rY'o2 BN  
95% confidence intervals, CI, 1.1–1.5 in cross-section I $vz%   
and OR 1.4, 95% CI 1.1–1.6 in cross-section II). In con- =Y[Ae7e  
Table 1: Participant characteristics. N4-J !r@#~  
Characteristics Cross-section I Cross-section II U7?ez  
n % n % F{tSfKy2  
Age (mean) (66.2) (66.7) #C mBgxg+M  
50–54 485 13.3 350 10.0 ?Q2pD!L{  
55–59 534 14.6 580 16.5 @Iu-F4YT  
60–64 638 17.5 600 17.1 W9"I++~f  
65–69 671 18.4 639 18.2 *Cw2h  
70–74 538 14.7 572 16.3 t;3.;  
75–79 422 11.6 407 11.6 ow "Xv  
80–84 230 6.3 226 6.4 Y2EN!{YU  
85–89 100 2.7 110 3.1 M='Kjc>e  
90+ 36 1.0 24 0.7 qZe"'"3M  
Female 2072 56.7 1998 57.0 Ip0q&i<6  
Ever Smokers 1784 51.2 1789 51.2 $}fA;BP  
Use of inhaled steroids 370 10.94 478 13.8^ |sz9l/,lG  
History of: .EO1{2=  
Diabetes 284 7.8 347 9.9^ _L":Wux  
Hypertension 1669 46.0 1825 52.2^ "Cb<~Dy  
Emmetropia* 1558 42.9 1478 42.2  ~A/_\-  
Myopia* 442 12.2 495 14.1^ iY-dM(_:]  
Hyperopia* 1633 45.0 1532 43.7 HV@:!zM  
n = number of persons affected Hik[pV K@  
* best spherical equivalent refraction correction c+=&5=i[3  
^ P < 0.01 Fm "$W^H  
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t }8HLyK,4  
rast, men had slightly higher PSC prevalence than women ,tZwXP{  
in both cross-sections but the difference was not significant 7 <xxOY>y  
(OR 1.1, 95% CI 0.8–1.4 for men in cross-section I \!r^6'A   
and OR 1.2, 95% 0.9–1.6 in cross-section II). ` ;;!>rm  
Discussion {\B!Rjt[T  
Findings from two surveys of BMES cross-sectional populations #^Y,,GA  
with similar age and gender distribution showed c,@6MeKHq  
that the prevalence of cortical cataract and PSC remained ZAE;$pkP  
stable, while the prevalence of nuclear cataract appeared H|Ems}b  
to have increased. Comparison of age-specific prevalence, {Fj`'0Xu;  
with totally independent samples within each age group, )7^jq|  
confirmed the robustness of our findings from the two ze- iDd_y  
survey samples. Although lens photographs taken from $IHa]9 {  
the two surveys were graded for nuclear cataract by the E O 5Vg  
same graders, who documented a high inter- and intragrader 157X0&EX  
reliability, we cannot exclude the possibility that y3x_B@}BY  
variations in photography, performed by different photographers, c0@v`-9  
may have contributed to the observed difference 5q\]]LV>  
in nuclear cataract prevalence. However, the overall C<3An_Dy  
Table 2: Age-specific prevalence of cataract types in cross sections I and II. V{][{ 5SR  
Cataract type Age (years) Cross-section I Cross-section II 6Pz\6DU,I  
n % (95% CL)* n % (95% CL)* Pu=YQ #F'  
Cortical 50–54 473 4.4 (2.6–6.3) 338 7.4 (4.6–10.2) K$4Ky&89  
55–59 522 9.2 (6.7–11.7) 542 9.0 (6.6–11.5) Af;$ }P  
60–64 615 16.4 (13.5–19.4) 556 16.7 (13.6–19.8) j9%=^ZoQj  
65–69 653 26.2 (22.8–29.6) 581 23.6 (20.1–27.0) >1YJETysO  
70–74 516 31.2 (27.2–35.2) 514 35.4 (31.3–39.6) /wQDcz  
75–79 366 40.2 (35.1–45.2) 332 39.8 (34.5–45.1) oZQu& O'  
80–84 194 58.8 (51.8–65.8) 163 42.9 (35.3–50.6) Z',pQ{rD  
85–89 74 52.7 (41.1–64.4) 73 54.8 (43.1–66.5) 3oh(d. Z  
90+ 22 68.2 (47.0–89.3) 14 78.6 (54.0–103.2) &W1cc#(  
PSC 50–54 474 2.7 (1.3–4.2) 338 2.4 (0.7–4.0) T!8,R{V]4  
55–59 522 2.9 (1.4–4.3) 541 2.6 (1.3–3.9) RJ`F2b sYN  
60–64 616 4.6 (2.9–6.2) 548 5.7 (3.7–7.6) Kg 56.$  
65–69 655 6.3 (4.4–8.1) 573 4.5 (2.8–6.3) :p89J\  
70–74 517 6.8 (4.6–8.9) 505 9.7 (7.1–12.3) zFlW\wc  
75–79 367 11.4 (8.2–14.7) 327 9.5 (6.3–12.7) e7-U0rrE  
80–84 196 12.2 (7.6–16.9) 155 10.3 (5.5–15.2) Au9Rr3n  
85–89 74 18.9 (9.8–28.1) 69 11.6 (3.9–19.4) T{Av[>M  
90+ 23 21.7 (3.5–40.0) 11 0.0 'Je;3"@  
Nuclear 50–54 323 1.6 (0.2–2.9) 331 0.9 (–0.2–1.9) HN\9 d  
55–59 386 2.3 (0.8–3.8) 507 3.6 (1.9–5.2) yTv#T(of  
60–64 453 5.3 (3.2–7.4) 501 11.6 (8.8–14.4) 3{CXIS  
65–69 478 17.2 (13.8–20.1) 534 18.5 (15.2–21.9) "~XAD(T6  
70–74 392 27.6 (23.1–32.0) 453 36.0 (31.6–40.4) (<|,LagTuc  
75–79 255 45.1 (39.0–51.3) 302 55.6 (50.0–61.3) -GH>12YP  
80–84 146 54.1 (45.9–62.3) 147 73.5 (66.3–80.7) !Eu}ro.}  
85–89 50 64.0 (50.2–77.8) 70 80.0 (70.4–89.6) Tv!zqx#E  
90+ 18 72.2 (49.3–95.1) 15 73.3 (48.0–98.7) r3'0{Nn+  
n = number of persons G@s rQum(  
* 95% Confidence Limits *y0TtEd;  
Cataract FMioguunrtea i1n ps rEeyvea lSetnucdey in cross-sections I and II of the Blue /C}u,dBf  
Cataract prevalence in cross-sections I and II of the Blue b-,4< H8m  
Mountains Eye Study. + JsMYv  
0 \<TWy&2&  
10 y2KR^/LN|Y  
20 OQ&l/|{O0?  
30 G .NGS%v  
40 }"Clv /3_  
50 1aDx 6Mq  
cortical PSC nuclear any $i1$nc8  
cataract g=n{G@*N  
Cataract type g%TOYZr!X  
% xPCRT *Pd  
Cross-section I A` 71L V%  
Cross-section II lha)4d  
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Page 5 of 7 jl9hFubwW  
(page number not for citation purposes) !y+uQ_IS@  
prevalence of any cataract (including cataract surgery) was 5/8=Do](  
relatively stable over the 6-year period. Np7+g`nG  
Although different population-based studies used different OY Sq)!:  
grading systems to assess cataract [15], the overall B`|f"+.  
prevalence of the three cataract types were similar across ,<k%'a!B  
different study populations [12,16-23]. Most studies have H-\Ym}BGu  
suggested that nuclear cataract is the most prevalent type 9fm9xTL  
of cataract, followed by cortical cataract [16-20]. Ours and #lR-?Uh  
other studies reported that cortical cataract was the most 1oe,>\\  
prevalent type [12,21-23]. F/x2}'  
Our age-specific prevalence data show a reduction of A3)"+`&PUl  
15.9% in cortical cataract prevalence for the 80–84 year LTxP@pr  
age group, concordant with an increase in cataract surgery )xq=V  
prevalence by 9% in those aged 80+ years observed in the 47N,jVt4  
same study population [10]. Although cortical cataract is &(oA/jFQ  
thought to be the least likely cataract type leading to a cataract \3OEC`  
surgery, this may not be the case in all older persons. BmKf%:l}  
A relatively stable cortical cataract and PSC prevalence VCfHm"'E8  
over the 6-year period is expected. We cannot offer a v4<W57oH  
definitive explanation for the increase in nuclear cataract 2xf #@`U  
prevalence. A possible explanation could be that a moderate (<YBvpt4>  
level of nuclear cataract causes less visual disturbance L&c & <+0T  
than the other two types of cataract, thus for the oldest age Qo)Da}uo20  
groups, persons with nuclear cataract could have been less 3CgID6[Sy  
likely to have surgery unless it is very dense or co-existing b{qN7X~>  
with cortical cataract or PSC. Previous studies have shown <pfl>Uf  
that functional vision and reading performance were high h;,1BpbM  
in patients undergoing cataract surgery who had nuclear 6#7hMQ0&;O  
cataract only compared to those with mixed type of cataract [3"F$?e5  
(nuclear and cortical) or PSC [24,25]. In addition, the >MJ#|vO  
overall prevalence of any cataract (including cataract surgery) ?TeozhUY  
was similar in the two cross-sections, which appears 0KnL{Cj   
to support our speculation that in the oldest age group, g'KxjjYT,  
nuclear cataract may have been less likely to be operated ||JUP}eP  
than the other two types of cataract. This could have  tPQ|znB|  
resulted in an increased nuclear cataract prevalence (due VxBBZsZO~  
to less being operated), compensated by the decreased dpTsTU!\  
prevalence of cortical cataract and PSC (due to these being 5]>*0#C S  
more likely to be operated), leading to stable overall prevalence ._^}M<o L  
of any cataract. n74\{`8]o  
Possible selection bias arising from selective survival Sp492W+  
among persons without cataract could have led to underestimation 7b+r LyS0  
of cataract prevalence in both surveys. We :a6LfPEAX  
assume that such an underestimation occurred equally in UB.1xcI  
both surveys, and thus should not have influenced our 4d`YZNvZW/  
assessment of temporal changes. _;B wP  
Measurement error could also have partially contributed I )rO|  
to the observed difference in nuclear cataract prevalence. }:m/@LKB  
Assessment of nuclear cataract from photographs is a =SXdO)%2  
potentially subjective process that can be influenced by 0n{.96r0R  
variations in photography (light exposure, focus and the sq!$+ =1-X  
slit-lamp angle when the photograph was taken) and q7X#LYk  
grading. Although we used the same Topcon slit-lamp {1)A"lQu  
camera and the same two graders who graded photos B+K6(^j,,y  
from both surveys, we are still not able to exclude the possibility xj3 qOx$  
of a partial influence from photographic variation !&{rnK  
on this result. 9B!Sv/)y!r  
A similar gender difference (women having a higher rate QWk3y" 5n<  
than men) in cortical cataract prevalence was observed in rP:g `?*V  
both surveys. Our findings are in keeping with observations HU'Mi8xxy  
from the Beaver Dam Eye Study [18], the Barbados s*k)h,\  
Eye Study [22] and the Lens Opacities Case-Control t>[W]%op  
Group [26]. It has been suggested that the difference wM+1/[7  
could be related to hormonal factors [18,22]. A previous } ?j5V  
study on biochemical factors and cataract showed that a sp,-JZD  
lower level of iron was associated with an increased risk of YNr"]SA@;  
cortical cataract [27]. No interaction between sex and biochemical M7TLQqaF  
factors were detected and no gender difference /'sv7hg+  
was assessed in this study [27]. The gender difference seen $ln8Cpbca  
in cortical cataract could be related to relatively low iron d=D-s  
levels and low hemoglobin concentration usually seen in  >Uw:cq  
women [28]. Diabetes is a known risk factor for cortical !Y ,7%  
Table 3: Gender distribution of cataract types in cross-sections I and II. xDo0bR(  
Cataract type Gender Cross-section I Cross-section II 1&|]8=pG7  
n % (95% CL)* n % (95% CL)* *?FVLE  
Cortical Male 1496 21.1 (19.0–23.1) 1328 20.4 (18.2–22.6) Fi/iA%,  
Female 1939 25.9 (23.9–27.8) 1785 26.2 (24.2–28.3) NoiB9 8g  
PSC Male 1500 6.5 (5.2–7.7) 1314 6.4 (5.1–7.7) ,8e'<y  
Female 1944 6.2 (5.1–7.2) 1753 5.7 (4.6–6.7) aJ'Fn  
Nuclear Male 1106 17.6 (15.4–19.9) 1225 22.5 (20.1–24.8) #AJW-+1g.=  
Female 1395 19.5 (17.4–21.6) 1635 25.0 (22.9–27.1) W_W!v&@E=  
n = number of persons Rl Oy,/-<  
* 95% Confidence Limits BJjic%V  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 @IL04' \  
Page 6 of 7 `?z('FV  
(page number not for citation purposes) cibl j?"Wi  
cataract but in this particular population diabetes is more y\T$) XGV  
prevalent in men than women in all age groups [29]. Differential riIubX#  
exposures to cataract risk factors or different dietary `NIb? /!f  
or lifestyle patterns between men and women may zG9FO/@av  
also be related to these observations and warrant further r8EJ@pOF2w  
study. 1CC0]pyHX  
Conclusion w){B$X  
In summary, in two population-based surveys 6 years `i`P}W!F  
apart, we have documented a relatively stable prevalence dcf,a<K\  
of cortical cataract and PSC over the period. The observed o<nM-"yWb  
overall increased nuclear cataract prevalence by 5% over a ^T&{ORWz  
6-year period needs confirmation by future studies, and fEBi'Ad  
reasons for such an increase deserve further study. JN 8Rh  
Competing interests c}@E@Y`@w  
The author(s) declare that they have no competing interests. z4YDngf=4  
Authors' contributions \'2rs152  
AGT graded the photographs, performed literature search sVh)Ofn  
and wrote the first draft of the manuscript. JJW graded the bc(MN8b]j  
photographs, critically reviewed and modified the manuscript. g:!U,<C^a  
ER performed the statistical analysis and critically z};|.N}  
reviewed the manuscript. PM designed and directed the \|>% /P  
study, adjudicated cataract cases and critically reviewed ~i1 jh:,  
and modified the manuscript. All authors read and X5o*8Bg4M  
approved the final manuscript. vv)q&,<c  
Acknowledgements N^QxqQ~  
This study was supported by the Australian National Health & Medical vd%AV(]<LJ  
Research Council, Canberra, Australia (Grant Nos 974159, 991407). The 2*sTU  
abstract was presented at the Association for Research in Vision and Ophthalmology a<-aE4wdm  
(ARVO) meeting in Fort Lauderdale, Florida, USA, May 2005. uihH")Mo  
References V?OTP&+J%  
1. Congdon N, O'Colmain B, Klaver CC, Klein R, Munoz B, Friedman ~C{:G;Iy0  
DS, Kempen J, Taylor HR, Mitchell P: Causes and prevalence of ;gL{*gR]S  
visual impairment among adults in the United States. Arch T'6`A <`3  
Ophthalmol 2004, 122(4):477-485. ]EK(k7nH  
2. Rahmani B, Tielsch JM, Katz J, Gottsch J, Quigley H, Javitt J, Sommer 5@RcAQb:  
A: The cause-specific prevalence of visual impairment in an &Sg]P  
urban population. The Baltimore Eye Survey. Ophthalmology Fug4u?-n  
1996, 103:1721-1726. +tk`$g  
3. Keeffe JE, Konyama K, Taylor HR: Vision impairment in the d%I7OBBx@  
Pacific region. Br J Ophthalmol 2002, 86:605-610. TFOx=_.%i  
4. Reidy A, Minassian DC, Vafidis G, Joseph J, Farrow S, Wu J, Desai P, ^U?Ac=  
Connolly A: Prevalence of serious eye disease and visual y f*'=q  
impairment in a north London population: population based, ;39b.v\^  
cross sectional study. BMJ 1998, 316:1643-1646. b ~UWFX#U  
5. Resnikoff S, Pascolini D, Etya'ale D, Kocur I, Pararajasegaram R, 1>[#./@  
Pokharel GP, Mariotti SP: Global data on visual impairment in J<L\IP?%  
the year 2002. Bull World Health Organ 2004, 82:844-851. CA|l| t^  
6. Pascolini D, Mariotti SP, Pokharel GP, Pararajasegaram R, Etya'ale D, WZ`i\s1#  
Negrel AD, Resnikoff S: 2002 global update of available data on @_t=0Rc  
visual impairment: a compilation of population-based prevalence N( 7(~D=)B  
studies. Ophthalmic Epidemiol 2004, 11:67-115. <}RD]Sc$1  
7. Rochtchina E, Mukesh BN, Wang JJ, McCarty CA, Taylor HR, Mitchell )^8[({r~  
P: Projected prevalence of age-related cataract and cataract LL);Ym9d  
surgery in Australia for the years 2001 and 2021: pooled data !e<5JO;c  
from two population-based surveys. Clin Experiment Ophthalmol :YRHO|  
2003, 31:233-236. #9s)fR  
8. Medicare Benefits Schedule Statistics [http://www.medicar 9{3_2CIL  
eaustralia.gov.au/statistics/dyn_mbs/forms/mbs_tab4.shtml] IG|u;PH<  
9. Keeffe JE, Taylor HR: Cataract surgery in Australia 1985–94. J;<dO7j5  
Aust N Z J Ophthalmol 1996, 24:313-317. D5xQ  
10. Tan AG, Wang JJ, Rochtchina E, Jakobsen K, Mitchell P: Increase in ]35`N<Ac  
cataract surgery prevalence from 1992–1994 to 1997–2000: j=U"t\{  
Analysis of two population cross-sections. Clin Experiment Ophthalmol v6DjNyg<x  
2004, 32:284-288. R`$Y]@i&B  
11. Mitchell P, Smith W, Attebo K, Wang JJ: Prevalence of age-related ?7pn%_S  
maculopathy in Australia. The Blue Mountains Eye Study. a~@f,b w  
Ophthalmology 1995, 102:1450-1460. #5h_{q4l  
12. Mitchell P, Cumming RG, Attebo K, Panchapakesan J: Prevalence of f99"~)B|  
cataract in Australia: the Blue Mountains eye study. Ophthalmology @"h4S*U  
1997, 104:581-588. lH?jqp  
13. Klein BEK, Magli YL, Neider MW, Klein R: Wisconsin system for classification Ax\d{0/oL2  
of cataracts from photographs (protocol) Madison, WI; 1990. l z"o( %D  
14. Foran S, Wang JJ, Mitchell P: Causes of visual impairment in two Z  #  
older population cross-sections: the Blue Mountains Eye b 1.S21  
Study. Ophthalmic Epidemiol 2003, 10:215-225. &,8Q e;  
15. Congdon N, Vingerling JR, Klein BE, West S, Friedman DS, Kempen J, F0&ubspt\  
O'Colmain B, Wu SY, Taylor HR: Prevalence of cataract and 9;I%Dv  
pseudophakia/aphakia among adults in the United States. Rs{8vV  
Arch Ophthalmol 2004, 122:487-494. 9i 9 ,X^=  
16. Sperduto RD, Hiller R: The prevalence of nuclear, cortical, and 4~A$u^scn  
posterior subcapsular lens opacities in a general population  |15!D  
sample. Ophthalmology 1984, 91:815-818. Gjq7@F'  
17. Adamsons I, Munoz B, Enger C, Taylor HR: Prevalence of lens 4D n&+=fq  
opacities in surgical and general populations. Arch Ophthalmol K_ymA,&()  
1991, 109:993-997. bh5P98 s  
18. Klein BE, Klein R, Linton KL: Prevalence of age-related lens  ID`C  
opacities in a population. The Beaver Dam Eye Study. Ophthalmology j 7:r8? G  
1992, 99:546-552. I+t wI&GS  
19. West SK, Munoz B, Schein OD, Duncan DD, Rubin GS: Racial differences k7@QFw4 j  
in lens opacities: the Salisbury Eye Evaluation (SEE) dHiir&Rd9`  
project. Am J Epidemiol 1998, 148:1033-1039. ,<K+.7,)E  
20. Congdon N, West SK, Buhrmann RR, Kouzis A, Munoz B, Mkocha H: oB!Y)f6H1  
Prevalence of the different types of age-related cataract in (y?F8]TfM  
an African population. Invest Ophthalmol Vis Sci 2001, l i?@BHEf  
42:2478-2482. Iv3yDL;  
21. Livingston PM, Guest CS, Stanislavsky Y, Lee S, Bayley S, Walker C, Jb$G  
McKean C, Taylor HR: A population-based estimate of cataract |uz<)  
prevalence: the Melbourne Visual Impairment Project experience. o ~y{9Q  
Dev Ophthalmol 1994, 26:1-6. b'SP,}s5"  
22. Leske MC, Connell AM, Wu SY, Hyman L, Schachat A: Prevalence aB (pdW4  
of lens opacities in the Barbados Eye Study. Arch Ophthalmol ~vpF|4Zn5  
1997, 115:105-111. published erratum appears in Arch Ophthalmol mE{QTZS  
1997 Jul;115(7):931 T ?[;ej:  
23. Seah SK, Wong TY, Foster PJ, Ng TP, Johnson GJ: Prevalence of s&o9LdL  
lens opacity in Chinese residents of Singapore: the tanjong h*JN0O<b  
pagar survey. Ophthalmology 2002, 109:2058-2064. !nJl.Y$  
24. Stifter E, Sacu S, Weghaupt H, Konig F, Richter-Muksch S, Thaler A, CDtL.a\  
Velikay-Parel M, Radner W: Reading performance depending on ^J-Xy\ X  
the type of cataract and its predictability on the visual outcome. #l&*&R~>  
J Cataract Refract Surg 2004, 30:1259-1267. rxol7"2l  
25. Stifter E, Sacu S, Weghaupt H: Functional vision with cataracts of D9P,[: "  
different morphologies: comparative study. J Cataract Refract _~CJitR3  
Surg 2004, 30:1883-1891. /@ g 8MUq7  
26. Leske MC, Chylack LT Jr, Wu SY: The Lens Opacities Case-Control =,ax"C?pR  
Study. Risk factors for cataract. Arch Ophthalmol 1991, a""9%./B  
109:244-251. KK >j V  
27. Leske MC, Wu SY, Hyman L, Sperduto R, Underwood B, Chylack LT, }oG6XI9  
Milton RC, Srivastava S, Ansari N: Biochemical factors in the lens PCgr`($U  
opacities. Case-control study. The Lens Opacities Case-Control +?3RC$jyw  
Study Group. Arch Ophthalmol 1995, 113:1113-1119. E$:2AK{*  
28. Yip R, Johnson C, Dallman PR: Age-related changes in laboratory ZHeue_~x4  
values used in the diagnosis of anemia and iron deficiency. fk?!0M6d  
Am J Clin Nutr 1984, 39:427-436. ?(B}w*G~  
29. Mitchell P, Smith W, Wang JJ, Cumming RG, Leeder SR, Burnett L: !.V_?aYi8  
Diabetes in an older Australian population. Diabetes Res Clin N#-. [9!  
Pract 1998, 41:177-184. }D)eS |B  
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