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 8ap%?  
Page 1 of 7 YwjKAyLU  
(page number not for citation purposes) Yp^rR }N  
BMC Ophthalmology rE.;g^4p  
Research article Open Access ]H+8rY%+  
Comparison of age-specific cataract prevalence in two klT@cO-9  
population-based surveys 6 years apart .uMn0PE   
Ava Grace Tan†, Jie Jin Wang*†, Elena Rochtchina† and Paul Mitchell† 2{H@(Vgpbr  
Address: Centre for Vision Research, Westmead Millennium Institute, Department of Ophthalmology, University of Sydney, Westmead Hospital, c7x ~{V8  
Westmead, NSW, Australia *Doa* wQ  
Email: Ava Grace Tan - ava_tan@wmi.usyd.edu.au; Jie Jin Wang* - jiejin_wang@wmi.usyd.edu.au; RAgg: 3^  
Elena Rochtchina - elena_rochtchina@wmi.usyd.edu.au; Paul Mitchell - paul_mitchell@wmi.usyd.edu.au Ch <[l8;K  
* Corresponding author †Equal contributors BBwy,\o#  
Abstract 1W^t aJH]  
Background: In this study, we aimed to compare age-specific cortical, nuclear and posterior 1mOh{:1u  
subcapsular (PSC) cataract prevalence in two surveys 6 years apart. nrub*BuA  
Methods: The Blue Mountains Eye Study examined 3654 participants (82.4% of those eligible) in e> e}vZlX  
cross-section I (1992–4) and 3509 participants (75.1% of survivors and 85.2% of newly eligible) in Nfrw0b  
cross-section II (1997–2000, 66.5% overlap with cross-section I). Cataract was assessed from lens >UiYL}'br6  
photographs following the Wisconsin Cataract Grading System. Cortical cataract was defined if K * LlW@  
cortical opacity comprised ≥ 5% of lens area. Nuclear cataract was defined if nuclear opacity ≥ ib#KpEk  
Wisconsin standard 4. PSC was defined if any present. Any cataract was defined to include persons Z>:NPZODf  
who had previous cataract surgery. Weighted kappa for inter-grader reliability was 0.82, 0.55 and CQF:Rnb  
0.82 for cortical, nuclear and PSC cataract, respectively. We assessed age-specific prevalence using Lt?lv2k=L  
an interval of 5 years, so that participants within each age group were independent between the ~ =M7 3U#  
two surveys. qouhuH_WtJ  
Results: Age and gender distributions were similar between the two populations. The age-specific ,8U &?8l  
prevalence of cortical (23.8% in 1st, 23.7% in 2nd) and PSC cataract (6.3%, 6.0%) was similar. The x<tb  
prevalence of nuclear cataract increased slightly from 18.7% to 23.9%. After age standardization, wh$sn:J  
the similar prevalence of cortical (23.8%, 23.5%) and PSC cataract (6.3%, 5.9%), and the increased UZ\u;/}  
prevalence of nuclear cataract (18.7%, 24.2%) remained. V_ :1EBzz  
Conclusion: In two surveys of two population-based samples with similar age and gender +%yfcyZ.  
distributions, we found a relatively stable cortical and PSC cataract prevalence over a 6-year period. 4tRYw0f47  
The increased prevalence of nuclear cataract deserves further study. Xv ]W(f1  
Background N)uSG&S:  
Age-related cataract is the leading cause of reversible visual I0D(F i  
impairment in older persons [1-6]. In Australia, it is i1ixi\P{0  
estimated that by the year 2021, the number of people 'N (:@]4N  
affected by cataract will increase by 63%, due to population |mxDjgq  
aging [7]. Surgical intervention is an effective treatment <=zQ NBtx  
for cataract and normal vision (> 20/40) can usually u^@f&BIG]:  
be restored with intraocular lens (IOL) implantation. h5*JkRm  
Cataract surgery with IOL implantation is currently the hgYZOwQ  
most commonly performed, and is, arguably, the most &FMc?wq  
cost effective surgical procedure worldwide. Performance + nrbShV  
Published: 20 April 2006 PS)4 I&;U  
BMC Ophthalmology 2006, 6:17 doi:10.1186/1471-2415-6-17 7OcW C-<  
Received: 14 December 2005 *'Sd/%8{  
Accepted: 20 April 2006 %<\vGqsM  
This article is available from: http://www.biomedcentral.com/1471-2415/6/17 N({MPO9  
© 2006 Tan et al; licensee BioMed Central Ltd. DrKP%BnS  
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), F&4rO\aC"/  
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. } MJy +Z8&  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 hQ,ch[j'  
Page 2 of 7 [<Mx2<8f  
(page number not for citation purposes) ne>pOK<vZ  
of this surgical procedure has been continuously increasing >!eAM )  
in the last two decades. Data from the Australian ((YMVe  
Health Insurance Commission has shown a steady RD!&LFz/}  
increase in Medicare claims for cataract surgery [8]. A 2.6- LC,F <>w1  
fold increase in the total number of cataract procedures pj\u9 L_  
from 1985 to 1994 has been documented in Australia [9]. 29;?I3< *  
The rate of cataract surgery per thousand persons aged 65 H*d9l2,KZS  
years or older has doubled in the last 20 years [8,9]. In the [T8WThs  
Blue Mountains Eye Study population, we observed a onethird NH[kNi'  
increase in cataract surgery prevalence over a mean 1T"`v tR  
6-year interval, from 6% to nearly 8% in two cross-sectional Y z<3JRw  
population-based samples with a similar age range ]0Y4U7W  
[10]. Further increases in cataract surgery performance Y>dF5&(kb  
would be expected as a result of improved surgical skills 3atBX5  
and technique, together with extending cataract surgical 5#HW2"7  
benefits to a greater number of older people and an .M qP_Z',  
increased number of persons with surgery performed on ;;! yC  
both eyes. J4k=A7^N  
Both the prevalence and incidence of age-related cataract P}Gj %4/G  
link directly to the demand for, and the outcome of, cataract R|6Cv3:  
surgery and eye health care provision. This report tZ]?^_Y1  
aimed to assess temporal changes in the prevalence of cortical )MtF23k)g  
and nuclear cataract and posterior subcapsular cataract b:U$x20n$  
(PSC) in two cross-sectional population-based Xc =Y  
surveys 6 years apart. :">!r.Q  
Methods pd:WEI ,  
The Blue Mountains Eye Study (BMES) is a populationbased K%,2=.  
cohort study of common eye diseases and other @D]5civm_  
health outcomes. The study involved eligible permanent <ykU6=  
residents aged 49 years and older, living in two postcode b(,M1.[qt  
areas in the Blue Mountains, west of Sydney, Australia. j@AIK+0Qc  
Participants were identified through a census and were @bi}W`  
invited to participate. The study was approved at each =-0/k;^  
stage of the data collection by the Human Ethics Committees 9>= ;FY  
of the University of Sydney and the Western Sydney G'nmllB`]  
Area Health Service and adhered to the recommendations 034iK[ib"  
of the Declaration of Helsinki. Written informed consent TtK[nP  
was obtained from each participant. #oS<E1  
Details of the methods used in this study have been KKb,d0T[  
described previously [11]. The baseline examinations L 8c0lx}Nn  
(BMES cross-section I) were conducted during 1992– 6, ^>mNm  
1994 and included 3654 (82.4%) of 4433 eligible residents. a1g,@0s  
Follow-up examinations (BMES IIA) were conducted ](Xb _xMf  
during 1997–1999, with 2335 (75.0% of BMES ML}J\7R  
cross section I survivors) participating. A repeat census of \Q {m9fE  
the same area was performed in 1999 and identified 1378 [xK3F+  
newly eligible residents who moved into the area or the 'S20\hwt-  
eligible age group. During 1999–2000, 1174 (85.2%) of 6gkV*|U,e  
this group participated in an extension study (BMES IIB). 1Rt33\1J0  
BMES cross-section II thus includes BMES IIA (66.5%) 48J@C vU  
and BMES IIB (33.5%) participants (n = 3509). '<gI8W</  
Similar procedures were used for all stages of data collection *zaQx+L  
at both surveys. A questionnaire was administered :W"~ {~#?  
including demographic, family and medical history. A `A,-@`p  
detailed eye examination included subjective refraction, t DO=P c  
slit-lamp (Topcon SL-7e camera, Topcon Optical Co, 3>3Kwc~E  
Tokyo, Japan) and retroillumination (Neitz CT-R camera, Ij 79~pn  
Neitz Instrument Co, Tokyo, Japan) photography of the l.(v^3:X  
lens. Grading of lens photographs in the BMES has been  FK^p")i  
previously described [12]. Briefly, masked grading was FW;m\vu  
performed on the lens photographs using the Wisconsin OP;v bZ  
Cataract Grading System [13]. Cortical cataract and PSC j9m_jv  
were assessed from the retroillumination photographs by u6J8"< -W  
estimating the percentage of the circular grid involved. W4 t;{b  
Cortical cataract was defined when cortical opacity  nI[os  
involved at least 5% of the total lens area. PSC was defined ;Y)w@ bNt@  
when opacity comprised at least 1% of the total lens area. #`~C)=-  
Slit-lamp photographs were used to assess nuclear cataract r^2p*nr}  
using the Wisconsin standard set of four lens photographs @MoKWfc  
[13]. Nuclear cataract was defined when nuclear opacity .[YuRLGz  
was at least as great as the standard 4 photograph. Any cataract Plc-4y1  
was defined to include persons who had previous &g#@3e1>  
cataract surgery as well as those with any of three cataract "x%Htq@  
types. Inter-grader reliability was high, with weighted %J#YM'g  
kappa 0.82 for cortical cataract, 0.55 (simple kappa 0.75)  pD(j'[  
for nuclear cataract and 0.82 for PSC grading. The intragrader 5b5x!do  
reliability for nuclear cataract was assessed with L]yS[UN$  
simple kappa 0.83 for the senior grader who graded 1v#%Ei$6`t  
nuclear cataract at both surveys. All PSC cases were confirmed Cwr~HY  
by an ophthalmologist (PM). 5CuuG<0  
In cross-section I, 219 persons (6.0%) had missing or {ba q+  
ungradable Neitz photographs, leaving 3435 with photographs U1Q:= yD  
available for cortical cataract and PSC assessment, vp1941P  
while 1153 (31.6%) had randomly missing or ungradable 6e(Qwt  
Topcon photographs due to a camera malfunction, leaving rW<KKGsRWQ  
2501 with photographs available for nuclear cataract ysJQb~2q  
assessment. Comparison of characteristics between participants )S3\,S-.  
with and without Neitz or Topcon photographs in {]*c 29b>  
cross-section I showed no statistically significant differences :1^LsLr5  
between the two groups, as reported previously ,Z aRy$?  
[12]. In cross-section II, 441 persons (12.5%) had missing czA5n  
or ungradable Neitz photographs, leaving 3068 for cortical N1Ng^aY0  
cataract and PSC assessment, and 648 (18.5%) had v>:Ur}u!D  
missing or ungradable Topcon photographs, leaving 2860 imo$-}A  
for nuclear cataract assessment. ( )2I#  
Data analysis was performed using the Statistical Analysis 7X`l&7IXP  
System (SAS, SAS Institute, Cary, NC, USA). Age-adjusted ~Uj=^leYO  
prevalence was calculated using direct standardization of :Hn6b$Vy8  
the cross-section II population to the cross-section I population. i=ea ?eT`  
We assessed age-specific prevalence using an 5:\},n+VE  
interval of 5 years, so that participants within each age C\\~E9+  
group were independent between the two cross-sectional >/g#lS 5  
surveys. Z.c'Hs+;  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 d<% z 1Dj2  
Page 3 of 7 "76 ]u)  
(page number not for citation purposes) %u?>#  
Results ?iPC*  
Characteristics of the two survey populations have been //* fSF   
previously compared [14] and showed that age and sex l-fi%Z7C  
distributions were similar. Table 1 compares participant |)nZ^Cc  
characteristics between the two cross-sections. Cross-section 7zA'ri3w  
II participants generally had higher rates of diabetes, ={_C&57N1  
hypertension, myopia and more users of inhaled steroids. ~F7 -HaQJ  
Cataract prevalence rates in cross-sections I and II are mi ik%7>W  
shown in Figure 1. The overall prevalence of cortical cataract fg s!v7  
was 23.8% and 23.7% in cross-sections I and II, f) znTJL  
respectively (age-sex adjusted P = 0.81). Corresponding gaQdG=G8$  
prevalence of PSC was 6.3% and 6.0% for the two crosssections ?u-|>N>  
(age-sex adjusted P = 0.60). There was an 7/!8e.M\  
increased prevalence of nuclear cataract, from 18.7% in 5)FJ :1-  
cross-section I to 23.9% in cross-section II over the 6-year io _1Y]N  
period (age-sex adjusted P < 0.001). Prevalence of any cataract x8wD0D  
(including persons who had cataract surgery), however, Vc_'hz]Z  
was relatively stable (46.9% and 46.8% in crosssections FQm`~rA~zt  
I and II, respectively). V}bjK8$$  
After age-standardization, these prevalence rates remained j!_;1++q  
stable for cortical cataract (23.8% and 23.5% in the two A$<.a'&T!  
surveys) and PSC (6.3% and 5.9%). The slightly increased &{ay=Mj  
prevalence of nuclear cataract (from 18.7% to 24.2%) was ./,/y"x  
not altered. qo p^;~  
Table 2 shows the age-specific prevalence rates for cortical GO8GJ;B-U  
cataract, PSC and nuclear cataract in cross-sections I and , 0imiv  
II. A similar trend of increasing cataract prevalence with os,* 3WO  
increasing age was evident for all three types of cataract in y603$Cv  
both surveys. Comparing the age-specific prevalence /~}}"zx&  
between the two surveys, a reduction in PSC prevalence in ~$ng^D  
cross-section II was observed in the older age groups (≥ 75 ?6Jx@Sh  
years). In contrast, increased nuclear cataract prevalence Ai:BEPKe  
in cross-section II was observed in the older age groups (≥ ]gm exa=(i  
70 years). Age-specific cortical cataract prevalence was relatively :ZTc7 }  
consistent between the two surveys, except for a wLmhy,  
reduction in prevalence observed in the 80–84 age group plUZ"Tr  
and an increasing prevalence in the older age groups (≥ 85 b6}H$Sx~  
years). ?kWC}k{  
Similar gender differences in cataract prevalence were u xW~uEh  
observed in both surveys (Table 3). Higher prevalence of WP?TX b`5  
cortical and nuclear cataract in women than men was evident hn^<;av=  
but the difference was only significant for cortical {6"Ph(I1  
cataract (age-adjusted odds ratio, OR, for women 1.3, eAXc:222  
95% confidence intervals, CI, 1.1–1.5 in cross-section I (&}i`}v_  
and OR 1.4, 95% CI 1.1–1.6 in cross-section II). In con- AmaT0tzJC  
Table 1: Participant characteristics. 'ixwD^x  
Characteristics Cross-section I Cross-section II x97 j  
n % n % , 8:(OB|a  
Age (mean) (66.2) (66.7) e<=cdze  
50–54 485 13.3 350 10.0 iM IlZ  
55–59 534 14.6 580 16.5 /4c\K-Z;  
60–64 638 17.5 600 17.1 :,Pn3xl  
65–69 671 18.4 639 18.2 My<snmr2d  
70–74 538 14.7 572 16.3 <%maDM^_\(  
75–79 422 11.6 407 11.6 [21 =5S   
80–84 230 6.3 226 6.4 99}(~B  
85–89 100 2.7 110 3.1 gUxP>hB  
90+ 36 1.0 24 0.7 t" k*PA  
Female 2072 56.7 1998 57.0 E0u~i59Z  
Ever Smokers 1784 51.2 1789 51.2 U4gF(Q  
Use of inhaled steroids 370 10.94 478 13.8^ (@t(?Js  
History of: \<y`!"c  
Diabetes 284 7.8 347 9.9^ q0$ !y!~  
Hypertension 1669 46.0 1825 52.2^ _acE :H  
Emmetropia* 1558 42.9 1478 42.2 )^4\,u\@  
Myopia* 442 12.2 495 14.1^ 11<Qxu$rL  
Hyperopia* 1633 45.0 1532 43.7 Z0o~+Ct$  
n = number of persons affected }&n<uUDH  
* best spherical equivalent refraction correction x/;buW-  
^ P < 0.01 P5 K' p5}#  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 bKrhIU[  
Page 4 of 7 Z$0 uH*h  
(page number not for citation purposes) GG@ md_  
t x9;gT&@H  
rast, men had slightly higher PSC prevalence than women }RHn)}+  
in both cross-sections but the difference was not significant (xVsDAp=@  
(OR 1.1, 95% CI 0.8–1.4 for men in cross-section I Q(<)KZIK  
and OR 1.2, 95% 0.9–1.6 in cross-section II). ^go7_y  
Discussion F8;dKyT?q  
Findings from two surveys of BMES cross-sectional populations 7VMvF/ap]u  
with similar age and gender distribution showed &_~+(  
that the prevalence of cortical cataract and PSC remained \>C YC|  
stable, while the prevalence of nuclear cataract appeared B>GE 9y5  
to have increased. Comparison of age-specific prevalence, &_"]5/"(  
with totally independent samples within each age group, hO'; {Nl/$  
confirmed the robustness of our findings from the two |1b_3?e  
survey samples. Although lens photographs taken from ]3g?hM6  
the two surveys were graded for nuclear cataract by the GDD '[;  
same graders, who documented a high inter- and intragrader tQ H+)*  
reliability, we cannot exclude the possibility that q-c=nkN3  
variations in photography, performed by different photographers, Y=?yhAw  
may have contributed to the observed difference ,t`Kv1  
in nuclear cataract prevalence. However, the overall co9 .wB@  
Table 2: Age-specific prevalence of cataract types in cross sections I and II. ~ug= {b  
Cataract type Age (years) Cross-section I Cross-section II E;1Jh(58)b  
n % (95% CL)* n % (95% CL)* {W]=~*w  
Cortical 50–54 473 4.4 (2.6–6.3) 338 7.4 (4.6–10.2) Sp}tD<V  
55–59 522 9.2 (6.7–11.7) 542 9.0 (6.6–11.5) F0:A]`|  
60–64 615 16.4 (13.5–19.4) 556 16.7 (13.6–19.8) cOPB2\,  
65–69 653 26.2 (22.8–29.6) 581 23.6 (20.1–27.0) lKlU-4  
70–74 516 31.2 (27.2–35.2) 514 35.4 (31.3–39.6) /r-aPJX  
75–79 366 40.2 (35.1–45.2) 332 39.8 (34.5–45.1) $dA-2e1 0  
80–84 194 58.8 (51.8–65.8) 163 42.9 (35.3–50.6) cCa|YW^j  
85–89 74 52.7 (41.1–64.4) 73 54.8 (43.1–66.5) kI:}| _  
90+ 22 68.2 (47.0–89.3) 14 78.6 (54.0–103.2) vq!_^F<  
PSC 50–54 474 2.7 (1.3–4.2) 338 2.4 (0.7–4.0) M?[h0{ ^K  
55–59 522 2.9 (1.4–4.3) 541 2.6 (1.3–3.9) Tp0bS  
60–64 616 4.6 (2.9–6.2) 548 5.7 (3.7–7.6) SF5@Vg  
65–69 655 6.3 (4.4–8.1) 573 4.5 (2.8–6.3) $2u 'N:o  
70–74 517 6.8 (4.6–8.9) 505 9.7 (7.1–12.3) A0Zt8>w  
75–79 367 11.4 (8.2–14.7) 327 9.5 (6.3–12.7) 8 O67  
80–84 196 12.2 (7.6–16.9) 155 10.3 (5.5–15.2) H6&J;yT}  
85–89 74 18.9 (9.8–28.1) 69 11.6 (3.9–19.4) \TF!S"V  
90+ 23 21.7 (3.5–40.0) 11 0.0 !YP@m~  
Nuclear 50–54 323 1.6 (0.2–2.9) 331 0.9 (–0.2–1.9) L a@ +>  
55–59 386 2.3 (0.8–3.8) 507 3.6 (1.9–5.2) V=lfl1Ev0J  
60–64 453 5.3 (3.2–7.4) 501 11.6 (8.8–14.4) r)i>06Hd  
65–69 478 17.2 (13.8–20.1) 534 18.5 (15.2–21.9) U-:ieao@  
70–74 392 27.6 (23.1–32.0) 453 36.0 (31.6–40.4) QjC22lW-  
75–79 255 45.1 (39.0–51.3) 302 55.6 (50.0–61.3) J@OB`2?Zv  
80–84 146 54.1 (45.9–62.3) 147 73.5 (66.3–80.7) m~dC3}e8/?  
85–89 50 64.0 (50.2–77.8) 70 80.0 (70.4–89.6) (%U@3._  
90+ 18 72.2 (49.3–95.1) 15 73.3 (48.0–98.7) 06Gt&_Q  
n = number of persons e#B#B  
* 95% Confidence Limits qVdwfT{1J  
Cataract FMioguunrtea i1n ps rEeyvea lSetnucdey in cross-sections I and II of the Blue 7^M9qTEHp  
Cataract prevalence in cross-sections I and II of the Blue >/#KI~}'N  
Mountains Eye Study. %J8|zKT5t  
0 @rHK( 25+d  
10 ;3 F"TH  
20 IJJ%$%F/  
30 u-1;'a  
40 (708H_  
50 fi+R2p~vs  
cortical PSC nuclear any 1lsLJ4P  
cataract 5'Q|EIL  
Cataract type KE1ao9H8wR  
% .^bft P\  
Cross-section I o0ZM[0@j  
Cross-section II qClHP)<  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 0A:n0[V:]  
Page 5 of 7 QaGlR`Y  
(page number not for citation purposes) OgcHS?  
prevalence of any cataract (including cataract surgery) was uHIiH@ S  
relatively stable over the 6-year period. QW_agm  
Although different population-based studies used different [Px'\ nVf  
grading systems to assess cataract [15], the overall %hN.ktZ/s  
prevalence of the three cataract types were similar across \]9.zlB  
different study populations [12,16-23]. Most studies have W- $a Y2  
suggested that nuclear cataract is the most prevalent type cE iu)2*e  
of cataract, followed by cortical cataract [16-20]. Ours and \ j.x0/;  
other studies reported that cortical cataract was the most 1 ^g t1o  
prevalent type [12,21-23]. =&dW(uyzY  
Our age-specific prevalence data show a reduction of $^ 'aCU0C  
15.9% in cortical cataract prevalence for the 80–84 year AOp/d(vx5i  
age group, concordant with an increase in cataract surgery =TP( UJ  
prevalence by 9% in those aged 80+ years observed in the Og %U  
same study population [10]. Although cortical cataract is j%V["?)  
thought to be the least likely cataract type leading to a cataract GFk1/ F  
surgery, this may not be the case in all older persons. .bD_R7Bi6  
A relatively stable cortical cataract and PSC prevalence -xg2q V\c  
over the 6-year period is expected. We cannot offer a >\<*4J$PZ  
definitive explanation for the increase in nuclear cataract }%TSGC4{  
prevalence. A possible explanation could be that a moderate S>q>K"j^!  
level of nuclear cataract causes less visual disturbance JIO$=+p  
than the other two types of cataract, thus for the oldest age utlpY1#q/  
groups, persons with nuclear cataract could have been less JM.XH7k  
likely to have surgery unless it is very dense or co-existing he+#Q 6  
with cortical cataract or PSC. Previous studies have shown "k$JP  
that functional vision and reading performance were high <uP^-bv;(  
in patients undergoing cataract surgery who had nuclear m+$ @'TbP  
cataract only compared to those with mixed type of cataract _ia!mT <  
(nuclear and cortical) or PSC [24,25]. In addition, the T:asm1BC[  
overall prevalence of any cataract (including cataract surgery) ']o od!  
was similar in the two cross-sections, which appears UFn8kBk  
to support our speculation that in the oldest age group, FZpKFsPx  
nuclear cataract may have been less likely to be operated [LM^), J?  
than the other two types of cataract. This could have Ix DWJ#k  
resulted in an increased nuclear cataract prevalence (due R@T6U:1  
to less being operated), compensated by the decreased BRG|Asg(  
prevalence of cortical cataract and PSC (due to these being 1D([@)^  
more likely to be operated), leading to stable overall prevalence E^ h=!RW{  
of any cataract. 6er(%4!  
Possible selection bias arising from selective survival T9y;OG  
among persons without cataract could have led to underestimation ~bA,GfSn0  
of cataract prevalence in both surveys. We #$'"cfRxc  
assume that such an underestimation occurred equally in ? S=W&  
both surveys, and thus should not have influenced our Ln#a<Rx.E7  
assessment of temporal changes. \94jrr  
Measurement error could also have partially contributed V`a+Hi<P\  
to the observed difference in nuclear cataract prevalence. 17UK1Jx,  
Assessment of nuclear cataract from photographs is a ,qFA\cO*  
potentially subjective process that can be influenced by ?H;{~n?  
variations in photography (light exposure, focus and the zDBD.5R;  
slit-lamp angle when the photograph was taken) and ddpl Pzm#  
grading. Although we used the same Topcon slit-lamp ?KN:r E  
camera and the same two graders who graded photos KHj6Tg;)  
from both surveys, we are still not able to exclude the possibility m^Lj+=Z"  
of a partial influence from photographic variation j64 4V|z  
on this result. MR9/Y:Nm  
A similar gender difference (women having a higher rate }N3`gCy9eN  
than men) in cortical cataract prevalence was observed in ] V G?+  
both surveys. Our findings are in keeping with observations A]y*so!)>  
from the Beaver Dam Eye Study [18], the Barbados z& 'f/w8  
Eye Study [22] and the Lens Opacities Case-Control #Q6w+"  
Group [26]. It has been suggested that the difference B\<ydN  
could be related to hormonal factors [18,22]. A previous 1i?=JAFfM  
study on biochemical factors and cataract showed that a Yw"P)Zp  
lower level of iron was associated with an increased risk of L{PH0Jf  
cortical cataract [27]. No interaction between sex and biochemical m6so]xr  
factors were detected and no gender difference Y1r ,2k  
was assessed in this study [27]. The gender difference seen V/H@vKN2  
in cortical cataract could be related to relatively low iron @l,{x|00  
levels and low hemoglobin concentration usually seen in g X/NtO %  
women [28]. Diabetes is a known risk factor for cortical k:0P+d  
Table 3: Gender distribution of cataract types in cross-sections I and II. r{"uv=,`  
Cataract type Gender Cross-section I Cross-section II rt.[,m  
n % (95% CL)* n % (95% CL)* 9.8,q  
Cortical Male 1496 21.1 (19.0–23.1) 1328 20.4 (18.2–22.6) M.k|bh8  
Female 1939 25.9 (23.9–27.8) 1785 26.2 (24.2–28.3) G2@KI-  
PSC Male 1500 6.5 (5.2–7.7) 1314 6.4 (5.1–7.7) d^SE)/j  
Female 1944 6.2 (5.1–7.2) 1753 5.7 (4.6–6.7) C={mi#G[/  
Nuclear Male 1106 17.6 (15.4–19.9) 1225 22.5 (20.1–24.8) h ]}`@M"  
Female 1395 19.5 (17.4–21.6) 1635 25.0 (22.9–27.1) %c0z)R~  
n = number of persons E4m:1=Nd~]  
* 95% Confidence Limits ]PVt o\B=  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 $ 'u \B  
Page 6 of 7 nt`<y0ta  
(page number not for citation purposes) Qdm(q:w  
cataract but in this particular population diabetes is more ?d,M.o{0]  
prevalent in men than women in all age groups [29]. Differential XW:%vJu^`  
exposures to cataract risk factors or different dietary  V.fp/jhj  
or lifestyle patterns between men and women may 4(sttd_  
also be related to these observations and warrant further $[w|oAwi  
study. H oS|f0  
Conclusion aZxO/b^j  
In summary, in two population-based surveys 6 years k) 3s?  
apart, we have documented a relatively stable prevalence Wa}"SqYr h  
of cortical cataract and PSC over the period. The observed HYFN?~G  
overall increased nuclear cataract prevalence by 5% over a $$~a=q,P[  
6-year period needs confirmation by future studies, and x {vIT- f  
reasons for such an increase deserve further study. /[L)tj7B  
Competing interests ytob/tc  
The author(s) declare that they have no competing interests. Ir>2sTrm  
Authors' contributions mR!rn^<l  
AGT graded the photographs, performed literature search #\0TxG5'QA  
and wrote the first draft of the manuscript. JJW graded the Jbkt'Z(&J  
photographs, critically reviewed and modified the manuscript. PgTDjEo  
ER performed the statistical analysis and critically i U,/!IQ  
reviewed the manuscript. PM designed and directed the e+x*psQ  
study, adjudicated cataract cases and critically reviewed cPm~` Zd  
and modified the manuscript. All authors read and b<8q 92F  
approved the final manuscript. CBIT`k.+  
Acknowledgements z=[l.Af_  
This study was supported by the Australian National Health & Medical wyNC|P;j$g  
Research Council, Canberra, Australia (Grant Nos 974159, 991407). The ,Z?m`cx  
abstract was presented at the Association for Research in Vision and Ophthalmology (A2U~j?Ry}  
(ARVO) meeting in Fort Lauderdale, Florida, USA, May 2005. ` -yhl3si  
References OoE9W  
1. Congdon N, O'Colmain B, Klaver CC, Klein R, Munoz B, Friedman G}s;JJax  
DS, Kempen J, Taylor HR, Mitchell P: Causes and prevalence of #*+;B93 )  
visual impairment among adults in the United States. Arch TdNsyr}JG  
Ophthalmol 2004, 122(4):477-485. 1x8(I&i  
2. Rahmani B, Tielsch JM, Katz J, Gottsch J, Quigley H, Javitt J, Sommer <Ak:8&$O  
A: The cause-specific prevalence of visual impairment in an eS* *L 3  
urban population. The Baltimore Eye Survey. Ophthalmology W3"vTZJF  
1996, 103:1721-1726. 9x4wk*z  
3. Keeffe JE, Konyama K, Taylor HR: Vision impairment in the MkkA{p  
Pacific region. Br J Ophthalmol 2002, 86:605-610. i_|h{JK)  
4. Reidy A, Minassian DC, Vafidis G, Joseph J, Farrow S, Wu J, Desai P, D\n>*x  
Connolly A: Prevalence of serious eye disease and visual ;g&7*1E  
impairment in a north London population: population based, LH bZjZ2  
cross sectional study. BMJ 1998, 316:1643-1646. is64)2F](  
5. Resnikoff S, Pascolini D, Etya'ale D, Kocur I, Pararajasegaram R, ]aREQ?ma&z  
Pokharel GP, Mariotti SP: Global data on visual impairment in q$ bHO  
the year 2002. Bull World Health Organ 2004, 82:844-851. )J{.Cx<E  
6. Pascolini D, Mariotti SP, Pokharel GP, Pararajasegaram R, Etya'ale D, aeLBaS  
Negrel AD, Resnikoff S: 2002 global update of available data on [^h/(a`  
visual impairment: a compilation of population-based prevalence 6-D%)Z(  
studies. Ophthalmic Epidemiol 2004, 11:67-115. hgF21Oj9  
7. Rochtchina E, Mukesh BN, Wang JJ, McCarty CA, Taylor HR, Mitchell =ltbSf7  
P: Projected prevalence of age-related cataract and cataract <{3q{VW*  
surgery in Australia for the years 2001 and 2021: pooled data 0 =3FO}[u  
from two population-based surveys. Clin Experiment Ophthalmol wa9'2a1?  
2003, 31:233-236. y.L|rRe@P  
8. Medicare Benefits Schedule Statistics [http://www.medicar 9OE_?R0c!  
eaustralia.gov.au/statistics/dyn_mbs/forms/mbs_tab4.shtml] r0rJ.}!  
9. Keeffe JE, Taylor HR: Cataract surgery in Australia 1985–94. T3=-UYx]  
Aust N Z J Ophthalmol 1996, 24:313-317. gvow\9{|C  
10. Tan AG, Wang JJ, Rochtchina E, Jakobsen K, Mitchell P: Increase in BiVd ka  
cataract surgery prevalence from 1992–1994 to 1997–2000: ZE5-i@1  
Analysis of two population cross-sections. Clin Experiment Ophthalmol KfJ c  
2004, 32:284-288. (:tTx>V#  
11. Mitchell P, Smith W, Attebo K, Wang JJ: Prevalence of age-related S jC)6mo  
maculopathy in Australia. The Blue Mountains Eye Study. V\e13cL]  
Ophthalmology 1995, 102:1450-1460. <z~2 d  
12. Mitchell P, Cumming RG, Attebo K, Panchapakesan J: Prevalence of Oc^6u  
cataract in Australia: the Blue Mountains eye study. Ophthalmology 8u7K$Q  
1997, 104:581-588. v@}1WGY  
13. Klein BEK, Magli YL, Neider MW, Klein R: Wisconsin system for classification S)Ub/`f{s  
of cataracts from photographs (protocol) Madison, WI; 1990. Kt/+PS  
14. Foran S, Wang JJ, Mitchell P: Causes of visual impairment in two 3Vb=6-|  
older population cross-sections: the Blue Mountains Eye USHlb#*  
Study. Ophthalmic Epidemiol 2003, 10:215-225. Q]2sj:  
15. Congdon N, Vingerling JR, Klein BE, West S, Friedman DS, Kempen J, &deZ  
O'Colmain B, Wu SY, Taylor HR: Prevalence of cataract and P!>{>r4  
pseudophakia/aphakia among adults in the United States. U_ N5~#9   
Arch Ophthalmol 2004, 122:487-494. JsWq._O{/  
16. Sperduto RD, Hiller R: The prevalence of nuclear, cortical, and GDNh?R  
posterior subcapsular lens opacities in a general population 8VAYIxRv  
sample. Ophthalmology 1984, 91:815-818. 5;sQ@  
17. Adamsons I, Munoz B, Enger C, Taylor HR: Prevalence of lens e$FAhwpo n  
opacities in surgical and general populations. Arch Ophthalmol ^J*G%*  
1991, 109:993-997. ib""Fv7{  
18. Klein BE, Klein R, Linton KL: Prevalence of age-related lens p'uqh e X  
opacities in a population. The Beaver Dam Eye Study. Ophthalmology +UpMMh q  
1992, 99:546-552. >TQBRA;'  
19. West SK, Munoz B, Schein OD, Duncan DD, Rubin GS: Racial differences yjM@/b  
in lens opacities: the Salisbury Eye Evaluation (SEE) ^! v}  
project. Am J Epidemiol 1998, 148:1033-1039. a|6x!p2X  
20. Congdon N, West SK, Buhrmann RR, Kouzis A, Munoz B, Mkocha H: zvK5Zxl  
Prevalence of the different types of age-related cataract in |)72E[lL  
an African population. Invest Ophthalmol Vis Sci 2001, KWn1%oGJ  
42:2478-2482. _:fO)gs|1  
21. Livingston PM, Guest CS, Stanislavsky Y, Lee S, Bayley S, Walker C, GJ^]ER-K  
McKean C, Taylor HR: A population-based estimate of cataract 9,EaN{GM  
prevalence: the Melbourne Visual Impairment Project experience. L->f= 8L  
Dev Ophthalmol 1994, 26:1-6. dbq{a  
22. Leske MC, Connell AM, Wu SY, Hyman L, Schachat A: Prevalence ]zwqGA  
of lens opacities in the Barbados Eye Study. Arch Ophthalmol wMPw/a;  
1997, 115:105-111. published erratum appears in Arch Ophthalmol mZ0oa-Iy  
1997 Jul;115(7):931 mJDKxgGK  
23. Seah SK, Wong TY, Foster PJ, Ng TP, Johnson GJ: Prevalence of BtNW5'^  
lens opacity in Chinese residents of Singapore: the tanjong ]Re~V{uh  
pagar survey. Ophthalmology 2002, 109:2058-2064. mP$G 9R  
24. Stifter E, Sacu S, Weghaupt H, Konig F, Richter-Muksch S, Thaler A, V.gY1   
Velikay-Parel M, Radner W: Reading performance depending on P VkN3J  
the type of cataract and its predictability on the visual outcome. 64 \5v?C  
J Cataract Refract Surg 2004, 30:1259-1267. `j!2uRFe>  
25. Stifter E, Sacu S, Weghaupt H: Functional vision with cataracts of `2(R}zUHN  
different morphologies: comparative study. J Cataract Refract Va |9)m  
Surg 2004, 30:1883-1891.  ZV q  
26. Leske MC, Chylack LT Jr, Wu SY: The Lens Opacities Case-Control _9-D3_P[3  
Study. Risk factors for cataract. Arch Ophthalmol 1991, ,8"[ /@  
109:244-251. c>i*HN}Z|  
27. Leske MC, Wu SY, Hyman L, Sperduto R, Underwood B, Chylack LT, ^B!?;\4IM  
Milton RC, Srivastava S, Ansari N: Biochemical factors in the lens u g:G9vjQ  
opacities. Case-control study. The Lens Opacities Case-Control j.'"CU  
Study Group. Arch Ophthalmol 1995, 113:1113-1119. =Wy`X0h  
28. Yip R, Johnson C, Dallman PR: Age-related changes in laboratory F/od,w9_  
values used in the diagnosis of anemia and iron deficiency. -^jLU FC  
Am J Clin Nutr 1984, 39:427-436. hHl-;%#  
29. Mitchell P, Smith W, Wang JJ, Cumming RG, Leeder SR, Burnett L: CygV_q  
Diabetes in an older Australian population. Diabetes Res Clin x^O2Lj,w\  
Pract 1998, 41:177-184. ~B*\k^t`  
Pre-publication history ;{q) |GRF  
The pre-publication history for this paper can be accessed X>GY*XU  
here: AUjTcu>i  
Publish with BioMed Central and every Y7V&zF{  
scientist can read your work free of charge %V1T !<  
"BioMed Central will be the most significant development for 8(/f!~  
disseminating the results of biomedical research in our lifetime." OZ14-}Lr5  
Sir Paul Nurse, Cancer Research UK yqb <<4I  
Your research papers will be: zu*G4?]~h  
available free of charge to the entire biomedical community 6N+)LF}P b  
peer reviewed and published immediately upon acceptance g#%FY1xp  
cited in PubMed and archived on PubMed Central r\ Yur  
yours — you keep the copyright dlzamoS@AR  
Submit your manuscript here: /N{@g.edL  
http://www.biomedcentral.com/info/publishing_adv.asp Cl.T'A$  
BioMedcentral A}Dpw[Q2@8  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 EM w(%}8w  
Page 7 of 7 5"~^;O  
(page number not for citation purposes) ]bE?n.NwZ  
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:
免费考博网网址是什么? 正确答案:freekaobo.com
按"Ctrl+Enter"直接提交