加入VIP 上传考博资料 您的流量 增加流量 考博报班 每日签到
   
主题 : BMC Ophthalmology
级别: 禁止发言
显示用户信息 
楼主  发表于: 2009-06-04   

BMC Ophthalmology

BioMed Central \^jRMIM==  
Page 1 of 7 Sl@Ucc31  
(page number not for citation purposes) zJ@^Bw;A^@  
BMC Ophthalmology l kyK  
Research article Open Access !0F+qzGG7  
Comparison of age-specific cataract prevalence in two Q X-n l~  
population-based surveys 6 years apart  M+:9U&>  
Ava Grace Tan†, Jie Jin Wang*†, Elena Rochtchina† and Paul Mitchell† +d(|Jid  
Address: Centre for Vision Research, Westmead Millennium Institute, Department of Ophthalmology, University of Sydney, Westmead Hospital, $dA]GWW5A  
Westmead, NSW, Australia 9Hd_sNUu\  
Email: Ava Grace Tan - ava_tan@wmi.usyd.edu.au; Jie Jin Wang* - jiejin_wang@wmi.usyd.edu.au; <Y$( l szT  
Elena Rochtchina - elena_rochtchina@wmi.usyd.edu.au; Paul Mitchell - paul_mitchell@wmi.usyd.edu.au `PSjk F(  
* Corresponding author †Equal contributors +(^H L3  
Abstract h[Uo6`  
Background: In this study, we aimed to compare age-specific cortical, nuclear and posterior ?nWzJ5w3  
subcapsular (PSC) cataract prevalence in two surveys 6 years apart. |=MhI5gsx  
Methods: The Blue Mountains Eye Study examined 3654 participants (82.4% of those eligible) in 5}c8v2R:B  
cross-section I (1992–4) and 3509 participants (75.1% of survivors and 85.2% of newly eligible) in nd7g8P9p  
cross-section II (1997–2000, 66.5% overlap with cross-section I). Cataract was assessed from lens ? Dn}  
photographs following the Wisconsin Cataract Grading System. Cortical cataract was defined if \-f/\P/ w  
cortical opacity comprised ≥ 5% of lens area. Nuclear cataract was defined if nuclear opacity ≥ `*U$pg  
Wisconsin standard 4. PSC was defined if any present. Any cataract was defined to include persons P +wpX  
who had previous cataract surgery. Weighted kappa for inter-grader reliability was 0.82, 0.55 and b};o:  
0.82 for cortical, nuclear and PSC cataract, respectively. We assessed age-specific prevalence using {^1''  
an interval of 5 years, so that participants within each age group were independent between the sx}S,aIU  
two surveys. Vjw u:M  
Results: Age and gender distributions were similar between the two populations. The age-specific KHgn  
prevalence of cortical (23.8% in 1st, 23.7% in 2nd) and PSC cataract (6.3%, 6.0%) was similar. The ]}p<P):hO  
prevalence of nuclear cataract increased slightly from 18.7% to 23.9%. After age standardization, $2RSYI`py  
the similar prevalence of cortical (23.8%, 23.5%) and PSC cataract (6.3%, 5.9%), and the increased Aa4Tq2G  
prevalence of nuclear cataract (18.7%, 24.2%) remained. R<(xWH  
Conclusion: In two surveys of two population-based samples with similar age and gender  K[LuvS  
distributions, we found a relatively stable cortical and PSC cataract prevalence over a 6-year period. u05Yy&(f  
The increased prevalence of nuclear cataract deserves further study. '+27_j  
Background Hmt2~>FI[  
Age-related cataract is the leading cause of reversible visual -;J6S  
impairment in older persons [1-6]. In Australia, it is +jyGRSo  
estimated that by the year 2021, the number of people 7 nFOV Z  
affected by cataract will increase by 63%, due to population Jazgn5  
aging [7]. Surgical intervention is an effective treatment %OHZOs  
for cataract and normal vision (> 20/40) can usually E)ZL+(  
be restored with intraocular lens (IOL) implantation. aWJj@',_  
Cataract surgery with IOL implantation is currently the o:fe`#t  
most commonly performed, and is, arguably, the most CxZh^V8LP  
cost effective surgical procedure worldwide. Performance G\TO ]c  
Published: 20 April 2006 6a9$VGInU  
BMC Ophthalmology 2006, 6:17 doi:10.1186/1471-2415-6-17 /XEW]/4  
Received: 14 December 2005 ?Ve I lD  
Accepted: 20 April 2006 K +3=gBU*w  
This article is available from: http://www.biomedcentral.com/1471-2415/6/17 3RT\G0?8f  
© 2006 Tan et al; licensee BioMed Central Ltd. lg~7[=%k#  
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), v{fcQb  
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. >3Q|k{97  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 \r[u >7I  
Page 2 of 7 ;% B9mM#p~  
(page number not for citation purposes) -p.\fvip  
of this surgical procedure has been continuously increasing 5UO+c( T  
in the last two decades. Data from the Australian ^}B,0yUu'  
Health Insurance Commission has shown a steady .8Bo5)q$a-  
increase in Medicare claims for cataract surgery [8]. A 2.6- MA6 Vy  
fold increase in the total number of cataract procedures tmooS7\a  
from 1985 to 1994 has been documented in Australia [9]. 4]ni-u0*  
The rate of cataract surgery per thousand persons aged 65 J5I@*f)l  
years or older has doubled in the last 20 years [8,9]. In the dkZe.pv$j  
Blue Mountains Eye Study population, we observed a onethird U5OX.0  
increase in cataract surgery prevalence over a mean ^hmV?a:Y  
6-year interval, from 6% to nearly 8% in two cross-sectional J-5>+E,nZ  
population-based samples with a similar age range 0)332}Oh  
[10]. Further increases in cataract surgery performance  p;w&}l{{  
would be expected as a result of improved surgical skills .4)oZ  
and technique, together with extending cataract surgical 7|DG1p9C  
benefits to a greater number of older people and an o g5VB  
increased number of persons with surgery performed on 1 _?8OU  
both eyes. >|E]??v  
Both the prevalence and incidence of age-related cataract |Ev|A9J!  
link directly to the demand for, and the outcome of, cataract &aLTy&8Fv  
surgery and eye health care provision. This report m-vn5OX  
aimed to assess temporal changes in the prevalence of cortical l< f9$l^U  
and nuclear cataract and posterior subcapsular cataract <\~v$=G  
(PSC) in two cross-sectional population-based t]$n~!  
surveys 6 years apart. ew~Z/ A   
Methods P1Hab2%+  
The Blue Mountains Eye Study (BMES) is a populationbased g Ed A hfx  
cohort study of common eye diseases and other Z8 #nu  
health outcomes. The study involved eligible permanent \yr9j$  
residents aged 49 years and older, living in two postcode XB7Aa)  
areas in the Blue Mountains, west of Sydney, Australia. b&:v6#i  
Participants were identified through a census and were u}[ a  
invited to participate. The study was approved at each mgAjD.  
stage of the data collection by the Human Ethics Committees /?'~`4!(  
of the University of Sydney and the Western Sydney h;gc5"mG  
Area Health Service and adhered to the recommendations l{{,D57J  
of the Declaration of Helsinki. Written informed consent ]y_ :+SHc  
was obtained from each participant. A@}5'LzL  
Details of the methods used in this study have been Vp/XVyL}R  
described previously [11]. The baseline examinations :y-;V  
(BMES cross-section I) were conducted during 1992– ,|A^ <R`  
1994 and included 3654 (82.4%) of 4433 eligible residents. -V/y~/]J  
Follow-up examinations (BMES IIA) were conducted I2[Z0G@&=  
during 1997–1999, with 2335 (75.0% of BMES L 4j#0I]lq  
cross section I survivors) participating. A repeat census of E>bkEm  
the same area was performed in 1999 and identified 1378 pU7;!u:c4%  
newly eligible residents who moved into the area or the 8z`ZHn3=  
eligible age group. During 1999–2000, 1174 (85.2%) of * ,a F-  
this group participated in an extension study (BMES IIB). wQ+pVu?6_  
BMES cross-section II thus includes BMES IIA (66.5%) g0B] ;Y>(  
and BMES IIB (33.5%) participants (n = 3509). 0/R;g~q@  
Similar procedures were used for all stages of data collection 4/ _jrZO  
at both surveys. A questionnaire was administered 1K Fd ~U  
including demographic, family and medical history. A YSP\+ZZ  
detailed eye examination included subjective refraction, !85bpQ.  
slit-lamp (Topcon SL-7e camera, Topcon Optical Co, m _)-  
Tokyo, Japan) and retroillumination (Neitz CT-R camera, &-=~8  
Neitz Instrument Co, Tokyo, Japan) photography of the %1i:*~g  
lens. Grading of lens photographs in the BMES has been R-Edht|{  
previously described [12]. Briefly, masked grading was W.j^ L;  
performed on the lens photographs using the Wisconsin }yT/UlU  
Cataract Grading System [13]. Cortical cataract and PSC %'K RbY  
were assessed from the retroillumination photographs by a|t~&\@  
estimating the percentage of the circular grid involved. w%])  
Cortical cataract was defined when cortical opacity t\Vng0  
involved at least 5% of the total lens area. PSC was defined vb>F)X?b_  
when opacity comprised at least 1% of the total lens area. H$I~Vz[\yb  
Slit-lamp photographs were used to assess nuclear cataract * :L"#20:R  
using the Wisconsin standard set of four lens photographs 7KI ekL  
[13]. Nuclear cataract was defined when nuclear opacity r&LZH.$oh  
was at least as great as the standard 4 photograph. Any cataract vMz|'-rm$  
was defined to include persons who had previous u "0{) ,  
cataract surgery as well as those with any of three cataract nah?V" ?Y  
types. Inter-grader reliability was high, with weighted IW\^-LI.  
kappa 0.82 for cortical cataract, 0.55 (simple kappa 0.75) 3yx[*'e$  
for nuclear cataract and 0.82 for PSC grading. The intragrader 0 1mu6)  
reliability for nuclear cataract was assessed with cO5F=ZxR  
simple kappa 0.83 for the senior grader who graded q1rj!7  
nuclear cataract at both surveys. All PSC cases were confirmed 9Q9{>d#"  
by an ophthalmologist (PM). AS;Sz/YP  
In cross-section I, 219 persons (6.0%) had missing or &PC6C<<f  
ungradable Neitz photographs, leaving 3435 with photographs V lx.C~WYn  
available for cortical cataract and PSC assessment, 6_`Bo%  
while 1153 (31.6%) had randomly missing or ungradable R'gd/.[e  
Topcon photographs due to a camera malfunction, leaving _[[0rn$  
2501 with photographs available for nuclear cataract 4Fp[94 b  
assessment. Comparison of characteristics between participants lAnq2j|  
with and without Neitz or Topcon photographs in 7T/BzXr,B  
cross-section I showed no statistically significant differences T<*)Cdid  
between the two groups, as reported previously /si<Fp)z  
[12]. In cross-section II, 441 persons (12.5%) had missing utmJ>GW SI  
or ungradable Neitz photographs, leaving 3068 for cortical gXI-{R7Me  
cataract and PSC assessment, and 648 (18.5%) had D9+qT<ojN  
missing or ungradable Topcon photographs, leaving 2860 [63\2{_^v  
for nuclear cataract assessment. (utP@d^  
Data analysis was performed using the Statistical Analysis ~ky;[  
System (SAS, SAS Institute, Cary, NC, USA). Age-adjusted 6 /<Hx@r (  
prevalence was calculated using direct standardization of r|l?2 eO~  
the cross-section II population to the cross-section I population. ec ;  
We assessed age-specific prevalence using an I0x)d`  
interval of 5 years, so that participants within each age 1 *' /B  
group were independent between the two cross-sectional W.^zN'a  
surveys. O7 ;=g!j  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 2OoANiX  
Page 3 of 7 1Le8W)J  
(page number not for citation purposes) tMw65Xei6b  
Results 9]v,3'QI  
Characteristics of the two survey populations have been )B]s.w  
previously compared [14] and showed that age and sex kTH"" h{  
distributions were similar. Table 1 compares participant CcUF)$kz  
characteristics between the two cross-sections. Cross-section PE5*]+lW.  
II participants generally had higher rates of diabetes, zg ,=A?  
hypertension, myopia and more users of inhaled steroids. ;j9%D`u<  
Cataract prevalence rates in cross-sections I and II are B& @ pZYl  
shown in Figure 1. The overall prevalence of cortical cataract ,f^fr&6jb  
was 23.8% and 23.7% in cross-sections I and II, (2eS:1+'8  
respectively (age-sex adjusted P = 0.81). Corresponding poAJl;T  
prevalence of PSC was 6.3% and 6.0% for the two crosssections ry|a_3X(I  
(age-sex adjusted P = 0.60). There was an XQ=%a5w  
increased prevalence of nuclear cataract, from 18.7% in U@q 5`4-!8  
cross-section I to 23.9% in cross-section II over the 6-year "m{i`<,  
period (age-sex adjusted P < 0.001). Prevalence of any cataract oaQW~R`_  
(including persons who had cataract surgery), however, {F wvuk  
was relatively stable (46.9% and 46.8% in crosssections !:xycLdfUp  
I and II, respectively). s[8M$YBf  
After age-standardization, these prevalence rates remained B:X%k/{  
stable for cortical cataract (23.8% and 23.5% in the two j1`<+YT<#  
surveys) and PSC (6.3% and 5.9%). The slightly increased 693"Pg8b  
prevalence of nuclear cataract (from 18.7% to 24.2%) was @Y`Z3LiR$  
not altered. ]A}ZaXd  
Table 2 shows the age-specific prevalence rates for cortical q6pHL  
cataract, PSC and nuclear cataract in cross-sections I and ' ds2\gN  
II. A similar trend of increasing cataract prevalence with 3ibQbk  
increasing age was evident for all three types of cataract in : j kO  
both surveys. Comparing the age-specific prevalence vLxaZWr  
between the two surveys, a reduction in PSC prevalence in +F q_w  
cross-section II was observed in the older age groups (≥ 75 ,y'6vW`%g9  
years). In contrast, increased nuclear cataract prevalence sSfP.R  
in cross-section II was observed in the older age groups (≥ D7nK"]HG;l  
70 years). Age-specific cortical cataract prevalence was relatively -ysNo4#e&  
consistent between the two surveys, except for a 3Qd/X&P  
reduction in prevalence observed in the 80–84 age group c$,1j%[)  
and an increasing prevalence in the older age groups (≥ 85  omg#[  
years). -BP10-V  
Similar gender differences in cataract prevalence were OIj.K@Kr  
observed in both surveys (Table 3). Higher prevalence of Z$INmo6  
cortical and nuclear cataract in women than men was evident 3#'8 S_  
but the difference was only significant for cortical g%Tokl  
cataract (age-adjusted odds ratio, OR, for women 1.3, D N)o|p  
95% confidence intervals, CI, 1.1–1.5 in cross-section I Rd7U5MBEF  
and OR 1.4, 95% CI 1.1–1.6 in cross-section II). In con- $)@D(m,ybd  
Table 1: Participant characteristics. ;=$;h6W0  
Characteristics Cross-section I Cross-section II !&Q?ASJH  
n % n % f.$[?Fi  
Age (mean) (66.2) (66.7) C{$iuus0  
50–54 485 13.3 350 10.0 %y9sC1 T  
55–59 534 14.6 580 16.5 5qH*"i+|s  
60–64 638 17.5 600 17.1 w>cqsTq  
65–69 671 18.4 639 18.2 [uGsF0#e  
70–74 538 14.7 572 16.3 ~C^:SND7  
75–79 422 11.6 407 11.6 \,Ws=9f  
80–84 230 6.3 226 6.4 Pb;c:HeI/  
85–89 100 2.7 110 3.1 E,tdn#_|  
90+ 36 1.0 24 0.7 "[P3b"=gW  
Female 2072 56.7 1998 57.0 O'IU1sU  
Ever Smokers 1784 51.2 1789 51.2 L!*+: L DL  
Use of inhaled steroids 370 10.94 478 13.8^ vE^tdzAG  
History of: &~+QPnI>Pm  
Diabetes 284 7.8 347 9.9^ n"RV! {&  
Hypertension 1669 46.0 1825 52.2^ r!f UMDS  
Emmetropia* 1558 42.9 1478 42.2 ou-UR5  
Myopia* 442 12.2 495 14.1^ ?[Y(JO#  
Hyperopia* 1633 45.0 1532 43.7 I4jRz*Ufe?  
n = number of persons affected $2h%IK>#G  
* best spherical equivalent refraction correction Gqd|F>  
^ P < 0.01 t}_ #N'`  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 #PD6LO  
Page 4 of 7 k2v:F  
(page number not for citation purposes) 8lpAe0p(Z  
t #}y8hzS$  
rast, men had slightly higher PSC prevalence than women 9r]|P}yuS  
in both cross-sections but the difference was not significant SdYf^@%}F  
(OR 1.1, 95% CI 0.8–1.4 for men in cross-section I Qh&Qsyo%  
and OR 1.2, 95% 0.9–1.6 in cross-section II). ?p@J7{a  
Discussion P!|Z%H  
Findings from two surveys of BMES cross-sectional populations @p*)^D6E\  
with similar age and gender distribution showed RX>P-vp  
that the prevalence of cortical cataract and PSC remained @5nFa~*K%  
stable, while the prevalence of nuclear cataract appeared KCTX2eNN&h  
to have increased. Comparison of age-specific prevalence,  '?9zL*  
with totally independent samples within each age group, O<cP1TF  
confirmed the robustness of our findings from the two 4c< s"2F  
survey samples. Although lens photographs taken from 0h@FHw2d  
the two surveys were graded for nuclear cataract by the X-HE9PT.  
same graders, who documented a high inter- and intragrader G@H!D[wd  
reliability, we cannot exclude the possibility that [oTe8^@[  
variations in photography, performed by different photographers, 12n:)yQy  
may have contributed to the observed difference /J#(8p  
in nuclear cataract prevalence. However, the overall TsTc3  
Table 2: Age-specific prevalence of cataract types in cross sections I and II. <P pvVDy3  
Cataract type Age (years) Cross-section I Cross-section II G7CeWfS  
n % (95% CL)* n % (95% CL)* /g<Oh{o8  
Cortical 50–54 473 4.4 (2.6–6.3) 338 7.4 (4.6–10.2) uatUo  
55–59 522 9.2 (6.7–11.7) 542 9.0 (6.6–11.5) &j 4pC$Dj  
60–64 615 16.4 (13.5–19.4) 556 16.7 (13.6–19.8) -x//@8"   
65–69 653 26.2 (22.8–29.6) 581 23.6 (20.1–27.0) "Q.*  
70–74 516 31.2 (27.2–35.2) 514 35.4 (31.3–39.6) X .t4;  
75–79 366 40.2 (35.1–45.2) 332 39.8 (34.5–45.1) /d3Jd .l!  
80–84 194 58.8 (51.8–65.8) 163 42.9 (35.3–50.6) :skR6J  
85–89 74 52.7 (41.1–64.4) 73 54.8 (43.1–66.5) hN-@_XSw<I  
90+ 22 68.2 (47.0–89.3) 14 78.6 (54.0–103.2) 3 ~v 17  
PSC 50–54 474 2.7 (1.3–4.2) 338 2.4 (0.7–4.0) $,4h\>1WP  
55–59 522 2.9 (1.4–4.3) 541 2.6 (1.3–3.9) GI %&.Vd  
60–64 616 4.6 (2.9–6.2) 548 5.7 (3.7–7.6) Z4] n<~o  
65–69 655 6.3 (4.4–8.1) 573 4.5 (2.8–6.3) !ZBtX t#P  
70–74 517 6.8 (4.6–8.9) 505 9.7 (7.1–12.3) rpT.n-H>%A  
75–79 367 11.4 (8.2–14.7) 327 9.5 (6.3–12.7) /5ZX6YkeH  
80–84 196 12.2 (7.6–16.9) 155 10.3 (5.5–15.2) VPUVPq~ &  
85–89 74 18.9 (9.8–28.1) 69 11.6 (3.9–19.4) &~,4$& _  
90+ 23 21.7 (3.5–40.0) 11 0.0 (>v'0 RA  
Nuclear 50–54 323 1.6 (0.2–2.9) 331 0.9 (–0.2–1.9) ukWn@q*  
55–59 386 2.3 (0.8–3.8) 507 3.6 (1.9–5.2) BN_h3|)  
60–64 453 5.3 (3.2–7.4) 501 11.6 (8.8–14.4) ~ nsb  
65–69 478 17.2 (13.8–20.1) 534 18.5 (15.2–21.9)  $GJT  
70–74 392 27.6 (23.1–32.0) 453 36.0 (31.6–40.4) '.mepxf< f  
75–79 255 45.1 (39.0–51.3) 302 55.6 (50.0–61.3) XIW0Z C   
80–84 146 54.1 (45.9–62.3) 147 73.5 (66.3–80.7) oh9 ;_~  
85–89 50 64.0 (50.2–77.8) 70 80.0 (70.4–89.6) >@YefNX6  
90+ 18 72.2 (49.3–95.1) 15 73.3 (48.0–98.7) ,EB}IG ]  
n = number of persons 9njl,Q:  
* 95% Confidence Limits Ke$_l]}  
Cataract FMioguunrtea i1n ps rEeyvea lSetnucdey in cross-sections I and II of the Blue $]2)r[eA)  
Cataract prevalence in cross-sections I and II of the Blue r\Nfq(w  
Mountains Eye Study. y0* rY  
0 gYKz,$  
10 / A=w`[<  
20 Y=Vbs x  
30 >Fel) a  
40 >L7s[vKn  
50 t'qYM5  
cortical PSC nuclear any 9j,g&G.K  
cataract .w2ID  
Cataract type 22\!Z2@T/  
% 1\.$=N  
Cross-section I ;a:H-iC  
Cross-section II rd%%NnT"  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 'Uok<;  
Page 5 of 7 M^ FY6TT4O  
(page number not for citation purposes) rO1!h%&o"  
prevalence of any cataract (including cataract surgery) was w:~*wv  
relatively stable over the 6-year period. D& @]  
Although different population-based studies used different YG p+[|'  
grading systems to assess cataract [15], the overall C* 7/iRe  
prevalence of the three cataract types were similar across #/)t]&n  
different study populations [12,16-23]. Most studies have A4K.,bZ   
suggested that nuclear cataract is the most prevalent type ).k DY ?s  
of cataract, followed by cortical cataract [16-20]. Ours and -yYdj1y;  
other studies reported that cortical cataract was the most je4l3Hl  
prevalent type [12,21-23]. f:T?oR>2  
Our age-specific prevalence data show a reduction of 'M90Yia  
15.9% in cortical cataract prevalence for the 80–84 year J=4>zQLW  
age group, concordant with an increase in cataract surgery Q?{%c[s  
prevalence by 9% in those aged 80+ years observed in the 1<@SMcj>  
same study population [10]. Although cortical cataract is E8Dh;j  
thought to be the least likely cataract type leading to a cataract ']]d-~:  
surgery, this may not be the case in all older persons. 39pG-otJ  
A relatively stable cortical cataract and PSC prevalence \bA Yic  
over the 6-year period is expected. We cannot offer a 9>""xt  
definitive explanation for the increase in nuclear cataract gL;Kie6Z  
prevalence. A possible explanation could be that a moderate 2iAC_"n  
level of nuclear cataract causes less visual disturbance 7*/{m K)  
than the other two types of cataract, thus for the oldest age B@,9Cx564  
groups, persons with nuclear cataract could have been less D28`?B9 (  
likely to have surgery unless it is very dense or co-existing OMGggg  
with cortical cataract or PSC. Previous studies have shown a QH6akH  
that functional vision and reading performance were high azcPeAe  
in patients undergoing cataract surgery who had nuclear +Y\:Q<eMFg  
cataract only compared to those with mixed type of cataract PT"}2sR)  
(nuclear and cortical) or PSC [24,25]. In addition, the 4#U}bN  
overall prevalence of any cataract (including cataract surgery) #;!&8iH  
was similar in the two cross-sections, which appears 1^ iBS  
to support our speculation that in the oldest age group, xU *:a[g  
nuclear cataract may have been less likely to be operated B.z$0=b  
than the other two types of cataract. This could have 4<s.|W`  
resulted in an increased nuclear cataract prevalence (due )?n'ZhsX  
to less being operated), compensated by the decreased "gM^o  
prevalence of cortical cataract and PSC (due to these being Z$oy;j99y  
more likely to be operated), leading to stable overall prevalence R1jl<=  
of any cataract. >1y6DC  
Possible selection bias arising from selective survival ?Ua,ba*  
among persons without cataract could have led to underestimation #-hO\ QdC  
of cataract prevalence in both surveys. We K^- 1M?  
assume that such an underestimation occurred equally in #6sz@XfV  
both surveys, and thus should not have influenced our :yay:3qv  
assessment of temporal changes. 6iC>CY3CG  
Measurement error could also have partially contributed sFU< PgV  
to the observed difference in nuclear cataract prevalence. &H(yLd[  
Assessment of nuclear cataract from photographs is a A_9WSXR  
potentially subjective process that can be influenced by )7q$Pc Y  
variations in photography (light exposure, focus and the > mGH4{H  
slit-lamp angle when the photograph was taken) and ZbnAAbfKH  
grading. Although we used the same Topcon slit-lamp Uj@th  
camera and the same two graders who graded photos K!|eN_1A  
from both surveys, we are still not able to exclude the possibility 8&<:(mAP  
of a partial influence from photographic variation 7Q 3!= b  
on this result. 9>}&dQ8  
A similar gender difference (women having a higher rate cx}Yu8  
than men) in cortical cataract prevalence was observed in Daf|.5>(@  
both surveys. Our findings are in keeping with observations 4W T[(  
from the Beaver Dam Eye Study [18], the Barbados U>5^:%3  
Eye Study [22] and the Lens Opacities Case-Control ?HEqv$ n  
Group [26]. It has been suggested that the difference ldv@C6+J  
could be related to hormonal factors [18,22]. A previous -Cf)`/  
study on biochemical factors and cataract showed that a oOFTQB_6  
lower level of iron was associated with an increased risk of )'shpRB;1  
cortical cataract [27]. No interaction between sex and biochemical 6F\ 6,E  
factors were detected and no gender difference blc?[ [,!  
was assessed in this study [27]. The gender difference seen U ?[ (  
in cortical cataract could be related to relatively low iron <'Q6\R}:vC  
levels and low hemoglobin concentration usually seen in U S^% $Z:  
women [28]. Diabetes is a known risk factor for cortical jP@ @<dt  
Table 3: Gender distribution of cataract types in cross-sections I and II. a`O'ZY  
Cataract type Gender Cross-section I Cross-section II G|i0n   
n % (95% CL)* n % (95% CL)* 4,RPidv%O  
Cortical Male 1496 21.1 (19.0–23.1) 1328 20.4 (18.2–22.6) )e(<YST  
Female 1939 25.9 (23.9–27.8) 1785 26.2 (24.2–28.3) ^F^g(|(K  
PSC Male 1500 6.5 (5.2–7.7) 1314 6.4 (5.1–7.7) -jH|L{Iyq}  
Female 1944 6.2 (5.1–7.2) 1753 5.7 (4.6–6.7) 1M ?BSH{  
Nuclear Male 1106 17.6 (15.4–19.9) 1225 22.5 (20.1–24.8) mc{z  
Female 1395 19.5 (17.4–21.6) 1635 25.0 (22.9–27.1) 3(YvqPp&  
n = number of persons IZVP-  
* 95% Confidence Limits {3Inj8a=?A  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 ZmK=8iN9J  
Page 6 of 7 ||+~8z#+,  
(page number not for citation purposes) YQ0#j'}/  
cataract but in this particular population diabetes is more @ @[xTyA  
prevalent in men than women in all age groups [29]. Differential "*vrrY  
exposures to cataract risk factors or different dietary vCa8` m  
or lifestyle patterns between men and women may *l5?_tF  
also be related to these observations and warrant further NuZ2,<~9  
study. )O'LE&kQ|  
Conclusion Gxr\a2Z&r%  
In summary, in two population-based surveys 6 years ( /y8KG 3  
apart, we have documented a relatively stable prevalence J8i;E 4R  
of cortical cataract and PSC over the period. The observed b]u$!W  
overall increased nuclear cataract prevalence by 5% over a *%xbn8  
6-year period needs confirmation by future studies, and 4m*)("H  
reasons for such an increase deserve further study. c^}G=Z1@  
Competing interests ^O|f w?,  
The author(s) declare that they have no competing interests. "vGh/sXW  
Authors' contributions i/:L^SQAq  
AGT graded the photographs, performed literature search ]4aPn  
and wrote the first draft of the manuscript. JJW graded the w8lr pbLh  
photographs, critically reviewed and modified the manuscript. JFv70rBe  
ER performed the statistical analysis and critically 'LgRdtO6  
reviewed the manuscript. PM designed and directed the Y?^liI`#  
study, adjudicated cataract cases and critically reviewed W3:j Z:  
and modified the manuscript. All authors read and {4_s:+v0  
approved the final manuscript. B=A!hXNa  
Acknowledgements n#!c!EfG  
This study was supported by the Australian National Health & Medical 8}n< 3_  
Research Council, Canberra, Australia (Grant Nos 974159, 991407). The f' A$':Y  
abstract was presented at the Association for Research in Vision and Ophthalmology ElO|6kOBYG  
(ARVO) meeting in Fort Lauderdale, Florida, USA, May 2005. yaz6?,)  
References ~n=DI/AJ@-  
1. Congdon N, O'Colmain B, Klaver CC, Klein R, Munoz B, Friedman Ysm RY=3  
DS, Kempen J, Taylor HR, Mitchell P: Causes and prevalence of HK )m^!=  
visual impairment among adults in the United States. Arch nJI2IPZ  
Ophthalmol 2004, 122(4):477-485. 4t*%(  
2. Rahmani B, Tielsch JM, Katz J, Gottsch J, Quigley H, Javitt J, Sommer jNj;#C)  
A: The cause-specific prevalence of visual impairment in an |WB-Ng  
urban population. The Baltimore Eye Survey. Ophthalmology 8N&' n  
1996, 103:1721-1726. XG|N$~N+2  
3. Keeffe JE, Konyama K, Taylor HR: Vision impairment in the Kx9u|fp5  
Pacific region. Br J Ophthalmol 2002, 86:605-610. @)>Z+g  
4. Reidy A, Minassian DC, Vafidis G, Joseph J, Farrow S, Wu J, Desai P, @c^ Dl  
Connolly A: Prevalence of serious eye disease and visual C1 ^%!)  
impairment in a north London population: population based, kQkc+sGJf  
cross sectional study. BMJ 1998, 316:1643-1646. GDSV:]hL  
5. Resnikoff S, Pascolini D, Etya'ale D, Kocur I, Pararajasegaram R, J9lZ1,22  
Pokharel GP, Mariotti SP: Global data on visual impairment in :#:|:q.]  
the year 2002. Bull World Health Organ 2004, 82:844-851. n])# <0  
6. Pascolini D, Mariotti SP, Pokharel GP, Pararajasegaram R, Etya'ale D, xn*$Ty+  
Negrel AD, Resnikoff S: 2002 global update of available data on oU|G74e6  
visual impairment: a compilation of population-based prevalence 4Y(@ KU b  
studies. Ophthalmic Epidemiol 2004, 11:67-115. +2`BZ}5y  
7. Rochtchina E, Mukesh BN, Wang JJ, McCarty CA, Taylor HR, Mitchell ~| j  eNT  
P: Projected prevalence of age-related cataract and cataract ?^voA.Bv<  
surgery in Australia for the years 2001 and 2021: pooled data ZiUb+;JA  
from two population-based surveys. Clin Experiment Ophthalmol Sf S3}Tn[  
2003, 31:233-236. Z3]I^i FI  
8. Medicare Benefits Schedule Statistics [http://www.medicar @1CXc"IgA  
eaustralia.gov.au/statistics/dyn_mbs/forms/mbs_tab4.shtml] *}\M!u{J  
9. Keeffe JE, Taylor HR: Cataract surgery in Australia 1985–94. d?7?tL2  
Aust N Z J Ophthalmol 1996, 24:313-317. l!*_[r   
10. Tan AG, Wang JJ, Rochtchina E, Jakobsen K, Mitchell P: Increase in t"$~o:U&)  
cataract surgery prevalence from 1992–1994 to 1997–2000: ;M?)-dpZ  
Analysis of two population cross-sections. Clin Experiment Ophthalmol rpKZ>S|7+)  
2004, 32:284-288. n^nE&'[?0g  
11. Mitchell P, Smith W, Attebo K, Wang JJ: Prevalence of age-related c|/HX%Y  
maculopathy in Australia. The Blue Mountains Eye Study. v@zi?D K  
Ophthalmology 1995, 102:1450-1460. 4]r_K2.cc  
12. Mitchell P, Cumming RG, Attebo K, Panchapakesan J: Prevalence of 2j+w5KvU  
cataract in Australia: the Blue Mountains eye study. Ophthalmology }xsO^K  
1997, 104:581-588. 2|;|C8C  
13. Klein BEK, Magli YL, Neider MW, Klein R: Wisconsin system for classification os 5$(  
of cataracts from photographs (protocol) Madison, WI; 1990. &Ym):pc  
14. Foran S, Wang JJ, Mitchell P: Causes of visual impairment in two V}V->j*  
older population cross-sections: the Blue Mountains Eye necY/&Ld-  
Study. Ophthalmic Epidemiol 2003, 10:215-225. W{;Qi&^ca  
15. Congdon N, Vingerling JR, Klein BE, West S, Friedman DS, Kempen J, 8R*;8y_  
O'Colmain B, Wu SY, Taylor HR: Prevalence of cataract and  Qx z[  
pseudophakia/aphakia among adults in the United States. d<-f:}^k0  
Arch Ophthalmol 2004, 122:487-494. kk78*s {6  
16. Sperduto RD, Hiller R: The prevalence of nuclear, cortical, and gBqDx|G  
posterior subcapsular lens opacities in a general population  rDFrreQP  
sample. Ophthalmology 1984, 91:815-818. y`RzcXblIZ  
17. Adamsons I, Munoz B, Enger C, Taylor HR: Prevalence of lens ;g0s1nz  
opacities in surgical and general populations. Arch Ophthalmol jf3Zy :*K  
1991, 109:993-997. 7 .29'  
18. Klein BE, Klein R, Linton KL: Prevalence of age-related lens 4vg3F(   
opacities in a population. The Beaver Dam Eye Study. Ophthalmology ehW[LRtq  
1992, 99:546-552. (1z"=NCp  
19. West SK, Munoz B, Schein OD, Duncan DD, Rubin GS: Racial differences ins(RWO  
in lens opacities: the Salisbury Eye Evaluation (SEE) 5az%yS  
project. Am J Epidemiol 1998, 148:1033-1039. rf0Z5.  
20. Congdon N, West SK, Buhrmann RR, Kouzis A, Munoz B, Mkocha H: g}%ODa !H  
Prevalence of the different types of age-related cataract in p -$C*0{  
an African population. Invest Ophthalmol Vis Sci 2001, qy|bOl  
42:2478-2482. -H%v6E%yh  
21. Livingston PM, Guest CS, Stanislavsky Y, Lee S, Bayley S, Walker C, ( }b~}X9  
McKean C, Taylor HR: A population-based estimate of cataract y11^q*}  
prevalence: the Melbourne Visual Impairment Project experience. s* GZOz  
Dev Ophthalmol 1994, 26:1-6.  ]~;*9`:  
22. Leske MC, Connell AM, Wu SY, Hyman L, Schachat A: Prevalence k^}[+IFJ  
of lens opacities in the Barbados Eye Study. Arch Ophthalmol SNqSp.>-U"  
1997, 115:105-111. published erratum appears in Arch Ophthalmol ~DD _n  
1997 Jul;115(7):931 kZF]BPh.  
23. Seah SK, Wong TY, Foster PJ, Ng TP, Johnson GJ: Prevalence of ;"&?Okz  
lens opacity in Chinese residents of Singapore: the tanjong i6paNHi*  
pagar survey. Ophthalmology 2002, 109:2058-2064. !EIH"`>!  
24. Stifter E, Sacu S, Weghaupt H, Konig F, Richter-Muksch S, Thaler A, Y @ v][Q  
Velikay-Parel M, Radner W: Reading performance depending on Vs 5 &X+k  
the type of cataract and its predictability on the visual outcome. JM;bNW8  
J Cataract Refract Surg 2004, 30:1259-1267. IX+Jf? &^  
25. Stifter E, Sacu S, Weghaupt H: Functional vision with cataracts of 4PVg?  
different morphologies: comparative study. J Cataract Refract /K!)}f( 6  
Surg 2004, 30:1883-1891. <l1/lm<#  
26. Leske MC, Chylack LT Jr, Wu SY: The Lens Opacities Case-Control TzC(YWt  
Study. Risk factors for cataract. Arch Ophthalmol 1991,  _ %mm  
109:244-251. ),{3LIr  
27. Leske MC, Wu SY, Hyman L, Sperduto R, Underwood B, Chylack LT, /eHf 8l  
Milton RC, Srivastava S, Ansari N: Biochemical factors in the lens Q3>qT84  
opacities. Case-control study. The Lens Opacities Case-Control : fmV||Q  
Study Group. Arch Ophthalmol 1995, 113:1113-1119. N,w6  
28. Yip R, Johnson C, Dallman PR: Age-related changes in laboratory #xmiUN,|  
values used in the diagnosis of anemia and iron deficiency. ^RnQX#+  
Am J Clin Nutr 1984, 39:427-436. )%jS9e{d  
29. Mitchell P, Smith W, Wang JJ, Cumming RG, Leeder SR, Burnett L: s-*N_Dv  
Diabetes in an older Australian population. Diabetes Res Clin `x=kb;  
Pract 1998, 41:177-184. ,;6%s>Cvd(  
Pre-publication history 7eq.U yUxs  
The pre-publication history for this paper can be accessed CH+%q+I  
here: jEKa9rt  
Publish with BioMed Central and every 5M\0t\uEn  
scientist can read your work free of charge 2^s&#@n3t  
"BioMed Central will be the most significant development for 2;]tItd1  
disseminating the results of biomedical research in our lifetime." 8;=?F>]xn  
Sir Paul Nurse, Cancer Research UK lU|ltnU  
Your research papers will be: 7# 'j>]  
available free of charge to the entire biomedical community M/V"Ke"N  
peer reviewed and published immediately upon acceptance Q9y|1Wg1W  
cited in PubMed and archived on PubMed Central Nt+UL/ 1]  
yours — you keep the copyright fo}@B &=4  
Submit your manuscript here: .WOF:Nu4  
http://www.biomedcentral.com/info/publishing_adv.asp q&ed4{H<  
BioMedcentral ve#[LBOC8  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 ;F_&h#D]3  
Page 7 of 7 s5 Fn("h]n  
(page number not for citation purposes) L%9yFg%u  
http://www.biomedcentral.com/1471-2415/6/17/prepub
评价一下你浏览此帖子的感受

精彩

感动

搞笑

开心

愤怒

无聊

灌水

  
描述
快速回复

验证问题:
2+6=? 正确答案:8
按"Ctrl+Enter"直接提交