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 [ncOtDE  
Page 1 of 7 {t<U:*n2  
(page number not for citation purposes) a$'= a09  
BMC Ophthalmology TZ%u;tBH:  
Research article Open Access F;_L/8Ov1  
Comparison of age-specific cataract prevalence in two F m{`?!  
population-based surveys 6 years apart A!j6JY.w  
Ava Grace Tan†, Jie Jin Wang*†, Elena Rochtchina† and Paul Mitchell† /I3>u  
Address: Centre for Vision Research, Westmead Millennium Institute, Department of Ophthalmology, University of Sydney, Westmead Hospital, YDr/Cw>J  
Westmead, NSW, Australia fo30f =^Gi  
Email: Ava Grace Tan - ava_tan@wmi.usyd.edu.au; Jie Jin Wang* - jiejin_wang@wmi.usyd.edu.au; RA~%Cw4t  
Elena Rochtchina - elena_rochtchina@wmi.usyd.edu.au; Paul Mitchell - paul_mitchell@wmi.usyd.edu.au 5//.q;z  
* Corresponding author †Equal contributors N!&$fhY)  
Abstract @I^LmB 9*  
Background: In this study, we aimed to compare age-specific cortical, nuclear and posterior ' |>  
subcapsular (PSC) cataract prevalence in two surveys 6 years apart. S+EC!;@Xg  
Methods: The Blue Mountains Eye Study examined 3654 participants (82.4% of those eligible) in _PeBV<  
cross-section I (1992–4) and 3509 participants (75.1% of survivors and 85.2% of newly eligible) in {qHf%y&[  
cross-section II (1997–2000, 66.5% overlap with cross-section I). Cataract was assessed from lens 4^mpQ.]lO  
photographs following the Wisconsin Cataract Grading System. Cortical cataract was defined if HO(9 )sK  
cortical opacity comprised ≥ 5% of lens area. Nuclear cataract was defined if nuclear opacity ≥ 8}kY^"*&X  
Wisconsin standard 4. PSC was defined if any present. Any cataract was defined to include persons A<zSh }eh6  
who had previous cataract surgery. Weighted kappa for inter-grader reliability was 0.82, 0.55 and EJrn4QOs  
0.82 for cortical, nuclear and PSC cataract, respectively. We assessed age-specific prevalence using ?lYi![.o  
an interval of 5 years, so that participants within each age group were independent between the c`(]j w  
two surveys. '8 ~E  
Results: Age and gender distributions were similar between the two populations. The age-specific b4$-?f?V  
prevalence of cortical (23.8% in 1st, 23.7% in 2nd) and PSC cataract (6.3%, 6.0%) was similar. The /~Q2SrYH  
prevalence of nuclear cataract increased slightly from 18.7% to 23.9%. After age standardization, 6R+m;'  
the similar prevalence of cortical (23.8%, 23.5%) and PSC cataract (6.3%, 5.9%), and the increased pZ,P_?  
prevalence of nuclear cataract (18.7%, 24.2%) remained. C= 6Vd  
Conclusion: In two surveys of two population-based samples with similar age and gender ]_yk,}88d  
distributions, we found a relatively stable cortical and PSC cataract prevalence over a 6-year period. OJUH".o  
The increased prevalence of nuclear cataract deserves further study. 4epE!`z_&  
Background *LbRLwt  
Age-related cataract is the leading cause of reversible visual IZV D.1  
impairment in older persons [1-6]. In Australia, it is DV(^h$1_  
estimated that by the year 2021, the number of people p<\yp<g  
affected by cataract will increase by 63%, due to population b NBpt}$  
aging [7]. Surgical intervention is an effective treatment '{:WxGgi  
for cataract and normal vision (> 20/40) can usually )/u?_)b4"  
be restored with intraocular lens (IOL) implantation. 0?]*-wvp  
Cataract surgery with IOL implantation is currently the UGNFWZ c  
most commonly performed, and is, arguably, the most Azun"F_f  
cost effective surgical procedure worldwide. Performance I |?zSFa  
Published: 20 April 2006 &>I4-D[  
BMC Ophthalmology 2006, 6:17 doi:10.1186/1471-2415-6-17 :_%  
Received: 14 December 2005 \ 7QAk4I~  
Accepted: 20 April 2006  opK=Z  
This article is available from: http://www.biomedcentral.com/1471-2415/6/17 x;,H>!r"i  
© 2006 Tan et al; licensee BioMed Central Ltd. `CP}1W>  
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), * _puW x  
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 3_JxpQg  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 R&13P&:g  
Page 2 of 7 XY]|OZ7(  
(page number not for citation purposes) "=0#pH1o  
of this surgical procedure has been continuously increasing #\kYGr-G)  
in the last two decades. Data from the Australian [:geDk9O#'  
Health Insurance Commission has shown a steady ~ l~ai>/  
increase in Medicare claims for cataract surgery [8]. A 2.6-  hfpSxL  
fold increase in the total number of cataract procedures :zk69P3  
from 1985 to 1994 has been documented in Australia [9]. \e%H5W x  
The rate of cataract surgery per thousand persons aged 65 zK`z*\  
years or older has doubled in the last 20 years [8,9]. In the }v[*V   
Blue Mountains Eye Study population, we observed a onethird v%(2l|M  
increase in cataract surgery prevalence over a mean VY)! bjW.  
6-year interval, from 6% to nearly 8% in two cross-sectional c!Gnd*!?-  
population-based samples with a similar age range 0GW(?7ZC  
[10]. Further increases in cataract surgery performance %/17K2g  
would be expected as a result of improved surgical skills 1*{ ` .  
and technique, together with extending cataract surgical \hpD  
benefits to a greater number of older people and an kYwk'\s  
increased number of persons with surgery performed on Vk/CV2  
both eyes. *Z*4L|zT  
Both the prevalence and incidence of age-related cataract }Wf\\  
link directly to the demand for, and the outcome of, cataract "V!y"yQ  
surgery and eye health care provision. This report 8<}f:9/  
aimed to assess temporal changes in the prevalence of cortical @[M5$,"  
and nuclear cataract and posterior subcapsular cataract 1df }gG  
(PSC) in two cross-sectional population-based M#II,z>q  
surveys 6 years apart. qP<wf=wY  
Methods wehZ7eqm  
The Blue Mountains Eye Study (BMES) is a populationbased  PDaD:}9  
cohort study of common eye diseases and other -g'[1  
health outcomes. The study involved eligible permanent #Jt9U 1WbF  
residents aged 49 years and older, living in two postcode :hYV\8 $  
areas in the Blue Mountains, west of Sydney, Australia. .Cfi/  
Participants were identified through a census and were Rckqr7q  
invited to participate. The study was approved at each )h-Qi#{  
stage of the data collection by the Human Ethics Committees b]s.h8+v;  
of the University of Sydney and the Western Sydney MY1 1 5%  
Area Health Service and adhered to the recommendations fI@4 v\  
of the Declaration of Helsinki. Written informed consent ..RCR_DIp  
was obtained from each participant. }Z5#{Sd  
Details of the methods used in this study have been 0U'g2F>{  
described previously [11]. The baseline examinations IM:*uv  
(BMES cross-section I) were conducted during 1992– ||TKo967]  
1994 and included 3654 (82.4%) of 4433 eligible residents. iXpLcHi  
Follow-up examinations (BMES IIA) were conducted A;E7~qOG  
during 1997–1999, with 2335 (75.0% of BMES P+r -t8  
cross section I survivors) participating. A repeat census of Y <;A989D  
the same area was performed in 1999 and identified 1378 , Q~C F;qe  
newly eligible residents who moved into the area or the _&s37A&\  
eligible age group. During 1999–2000, 1174 (85.2%) of S~auwY,<  
this group participated in an extension study (BMES IIB). _l}"gUtiw  
BMES cross-section II thus includes BMES IIA (66.5%) 4O Lq  
and BMES IIB (33.5%) participants (n = 3509). zRDBl02v$T  
Similar procedures were used for all stages of data collection wmu#@Hf/[h  
at both surveys. A questionnaire was administered }{<@wE%s  
including demographic, family and medical history. A i}mvKV?!|1  
detailed eye examination included subjective refraction, 0mj^Tms  
slit-lamp (Topcon SL-7e camera, Topcon Optical Co, Y/Yp+W6n  
Tokyo, Japan) and retroillumination (Neitz CT-R camera, F6 ?4E"d  
Neitz Instrument Co, Tokyo, Japan) photography of the ooa>~!91P  
lens. Grading of lens photographs in the BMES has been -DgJkyt+<  
previously described [12]. Briefly, masked grading was F.:B_t  
performed on the lens photographs using the Wisconsin "_Wv,CYmNr  
Cataract Grading System [13]. Cortical cataract and PSC ! Ff/RRo  
were assessed from the retroillumination photographs by u Ey>7I  
estimating the percentage of the circular grid involved. Cf#[E~24  
Cortical cataract was defined when cortical opacity k!Y7 Rc{"  
involved at least 5% of the total lens area. PSC was defined -A}U^-'a}  
when opacity comprised at least 1% of the total lens area. P~Cx#`#(V  
Slit-lamp photographs were used to assess nuclear cataract 9\F:<Bf$#  
using the Wisconsin standard set of four lens photographs #kD8U#  
[13]. Nuclear cataract was defined when nuclear opacity E:,V{&tLK  
was at least as great as the standard 4 photograph. Any cataract 5v:c@n  
was defined to include persons who had previous ~3YN;St-  
cataract surgery as well as those with any of three cataract 0'ha!4h3Z  
types. Inter-grader reliability was high, with weighted $`L!2  
kappa 0.82 for cortical cataract, 0.55 (simple kappa 0.75) "PO>@tY  
for nuclear cataract and 0.82 for PSC grading. The intragrader dD _(MbTt  
reliability for nuclear cataract was assessed with Dk$[b9b  
simple kappa 0.83 for the senior grader who graded 8 /3`rEW  
nuclear cataract at both surveys. All PSC cases were confirmed pJ*x[y  
by an ophthalmologist (PM). 04eE\%?  
In cross-section I, 219 persons (6.0%) had missing or $ f`\TKlN  
ungradable Neitz photographs, leaving 3435 with photographs o/uA_19  
available for cortical cataract and PSC assessment, 3\J-=U  
while 1153 (31.6%) had randomly missing or ungradable pa1.+~)  
Topcon photographs due to a camera malfunction, leaving W-9?|ei  
2501 with photographs available for nuclear cataract _&0_@  
assessment. Comparison of characteristics between participants S%ULGX:@ga  
with and without Neitz or Topcon photographs in -8;@NAUa  
cross-section I showed no statistically significant differences rdK=f<I]  
between the two groups, as reported previously laVqI|0q  
[12]. In cross-section II, 441 persons (12.5%) had missing lCmT m  
or ungradable Neitz photographs, leaving 3068 for cortical :q6j{C(  
cataract and PSC assessment, and 648 (18.5%) had !)1r{u  
missing or ungradable Topcon photographs, leaving 2860 p$r=jF&  
for nuclear cataract assessment. DIx!S w7EC  
Data analysis was performed using the Statistical Analysis ?f{{{0$S  
System (SAS, SAS Institute, Cary, NC, USA). Age-adjusted sC ,[CN:b  
prevalence was calculated using direct standardization of w}*2Hz&Q!  
the cross-section II population to the cross-section I population. yht|0mZV  
We assessed age-specific prevalence using an RzPqtN  
interval of 5 years, so that participants within each age 4`(b(DL]  
group were independent between the two cross-sectional 5[^pU$Y  
surveys. 3LT[?C]H$  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 t[L0kF9en  
Page 3 of 7 ,Mt/* ^|  
(page number not for citation purposes) x8L$T (^  
Results s*A#;  
Characteristics of the two survey populations have been .Sz<%d7XIQ  
previously compared [14] and showed that age and sex # tN#_<W  
distributions were similar. Table 1 compares participant >]DnEF&  
characteristics between the two cross-sections. Cross-section :Taequ k  
II participants generally had higher rates of diabetes, AQCU\E  
hypertension, myopia and more users of inhaled steroids. u 3&9R)J1  
Cataract prevalence rates in cross-sections I and II are xj/Iq<'R*O  
shown in Figure 1. The overall prevalence of cortical cataract zqd_^  
was 23.8% and 23.7% in cross-sections I and II, {5<3./5O  
respectively (age-sex adjusted P = 0.81). Corresponding AOvn <Q  
prevalence of PSC was 6.3% and 6.0% for the two crosssections 4g^nhJP$  
(age-sex adjusted P = 0.60). There was an %<4ZU!2L  
increased prevalence of nuclear cataract, from 18.7% in X?p. U  
cross-section I to 23.9% in cross-section II over the 6-year 'IR2H{Q  
period (age-sex adjusted P < 0.001). Prevalence of any cataract (%` R{Y  
(including persons who had cataract surgery), however, Gag=GHG  
was relatively stable (46.9% and 46.8% in crosssections zkFx2(Hq-f  
I and II, respectively). r-Nv<oH;  
After age-standardization, these prevalence rates remained XeGtge/}T  
stable for cortical cataract (23.8% and 23.5% in the two )U>JFgpIW  
surveys) and PSC (6.3% and 5.9%). The slightly increased #q[k"x=c  
prevalence of nuclear cataract (from 18.7% to 24.2%) was *U[Nn5#?  
not altered. v61'fQ1Qg!  
Table 2 shows the age-specific prevalence rates for cortical K'Gv+UC*6  
cataract, PSC and nuclear cataract in cross-sections I and 0vu$d xb[  
II. A similar trend of increasing cataract prevalence with Vh%=JL sK  
increasing age was evident for all three types of cataract in 9DAk|K   
both surveys. Comparing the age-specific prevalence F_Pv\?35z  
between the two surveys, a reduction in PSC prevalence in U{^~X_?  
cross-section II was observed in the older age groups (≥ 75 v6Vd V.BI  
years). In contrast, increased nuclear cataract prevalence s]tBd !~  
in cross-section II was observed in the older age groups (≥ h3}gg@Fm  
70 years). Age-specific cortical cataract prevalence was relatively Zx%ib8| j  
consistent between the two surveys, except for a WAzYnl'p  
reduction in prevalence observed in the 80–84 age group A7|CG[wZ  
and an increasing prevalence in the older age groups (≥ 85 |U~m8e&:  
years). L<GF1I)  
Similar gender differences in cataract prevalence were E{Gkq:  
observed in both surveys (Table 3). Higher prevalence of R:Pw@   
cortical and nuclear cataract in women than men was evident yu<'-)T.?  
but the difference was only significant for cortical Mya l3UF  
cataract (age-adjusted odds ratio, OR, for women 1.3, Q9Y$x{R&  
95% confidence intervals, CI, 1.1–1.5 in cross-section I `{1&*4!  
and OR 1.4, 95% CI 1.1–1.6 in cross-section II). In con- _kgGz@/p  
Table 1: Participant characteristics. %[l*:05  
Characteristics Cross-section I Cross-section II lur$?_gt  
n % n % hI&ugdf  
Age (mean) (66.2) (66.7) k|O?qE1hP  
50–54 485 13.3 350 10.0 U c6]]Bbc  
55–59 534 14.6 580 16.5 W(C\lSE0  
60–64 638 17.5 600 17.1 Lq-Di|6q  
65–69 671 18.4 639 18.2 -zzM!1@F  
70–74 538 14.7 572 16.3 cz2guUu  
75–79 422 11.6 407 11.6 aMUy^>  
80–84 230 6.3 226 6.4 4 ^=qc99  
85–89 100 2.7 110 3.1 yq?7!X  
90+ 36 1.0 24 0.7 C4#EN}  
Female 2072 56.7 1998 57.0 rO_|_nV[  
Ever Smokers 1784 51.2 1789 51.2 r35'U#VMk?  
Use of inhaled steroids 370 10.94 478 13.8^ o(2tRDT\_b  
History of: 6I)1[tU  
Diabetes 284 7.8 347 9.9^ 3eqVY0q  
Hypertension 1669 46.0 1825 52.2^ #Cwzk{p(  
Emmetropia* 1558 42.9 1478 42.2 l$i^e|*  
Myopia* 442 12.2 495 14.1^ "Yk3K^`1T.  
Hyperopia* 1633 45.0 1532 43.7 m((A  
n = number of persons affected !Q`vOVSUD  
* best spherical equivalent refraction correction 3#IU^6l:1S  
^ P < 0.01 q,<AW>  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 Ar+<n 2;[  
Page 4 of 7 ,%|$# g 0  
(page number not for citation purposes) 1j_ x51p  
t 5 M.KF;P  
rast, men had slightly higher PSC prevalence than women -:5]*zVp+-  
in both cross-sections but the difference was not significant U?MKZL7  
(OR 1.1, 95% CI 0.8–1.4 for men in cross-section I oic}Go  
and OR 1.2, 95% 0.9–1.6 in cross-section II). hhS]wM?B  
Discussion A YC22(  
Findings from two surveys of BMES cross-sectional populations m&'z|eN  
with similar age and gender distribution showed o9tvf|+z  
that the prevalence of cortical cataract and PSC remained J!%cHqR  
stable, while the prevalence of nuclear cataract appeared \Ty%E<  
to have increased. Comparison of age-specific prevalence, Dn[iA~  
with totally independent samples within each age group, b&Dc DX  
confirmed the robustness of our findings from the two '' @upZBJ  
survey samples. Although lens photographs taken from G 4jaHpPi  
the two surveys were graded for nuclear cataract by the BjT0m k"P  
same graders, who documented a high inter- and intragrader aZe[Nos  
reliability, we cannot exclude the possibility that Jy,Dcl  
variations in photography, performed by different photographers, u6~|].j R  
may have contributed to the observed difference ` "Gd/  
in nuclear cataract prevalence. However, the overall k)2L <Lmn  
Table 2: Age-specific prevalence of cataract types in cross sections I and II. K%Sy~6iD&  
Cataract type Age (years) Cross-section I Cross-section II I|6wPV?  
n % (95% CL)* n % (95% CL)* [6bK>w"v  
Cortical 50–54 473 4.4 (2.6–6.3) 338 7.4 (4.6–10.2) k5>K/;*9  
55–59 522 9.2 (6.7–11.7) 542 9.0 (6.6–11.5) uZyR{~-C  
60–64 615 16.4 (13.5–19.4) 556 16.7 (13.6–19.8) #&Zb8HAj  
65–69 653 26.2 (22.8–29.6) 581 23.6 (20.1–27.0) u&iMY3=  
70–74 516 31.2 (27.2–35.2) 514 35.4 (31.3–39.6) zh hH A9  
75–79 366 40.2 (35.1–45.2) 332 39.8 (34.5–45.1) w$JG:y#  
80–84 194 58.8 (51.8–65.8) 163 42.9 (35.3–50.6) { r9fKA  
85–89 74 52.7 (41.1–64.4) 73 54.8 (43.1–66.5) it2@hZc5  
90+ 22 68.2 (47.0–89.3) 14 78.6 (54.0–103.2) -U6" Ce  
PSC 50–54 474 2.7 (1.3–4.2) 338 2.4 (0.7–4.0) QyJ2P{z  
55–59 522 2.9 (1.4–4.3) 541 2.6 (1.3–3.9) axTvA(k9  
60–64 616 4.6 (2.9–6.2) 548 5.7 (3.7–7.6) & yKUf  
65–69 655 6.3 (4.4–8.1) 573 4.5 (2.8–6.3) {+V1>6  
70–74 517 6.8 (4.6–8.9) 505 9.7 (7.1–12.3) ,0^:q)_  
75–79 367 11.4 (8.2–14.7) 327 9.5 (6.3–12.7) _,h hO  
80–84 196 12.2 (7.6–16.9) 155 10.3 (5.5–15.2) g-c\ ;  
85–89 74 18.9 (9.8–28.1) 69 11.6 (3.9–19.4) )V!dmVQq{g  
90+ 23 21.7 (3.5–40.0) 11 0.0 PvzB, 2":  
Nuclear 50–54 323 1.6 (0.2–2.9) 331 0.9 (–0.2–1.9) JW!SrM xF  
55–59 386 2.3 (0.8–3.8) 507 3.6 (1.9–5.2) zwAkXj  
60–64 453 5.3 (3.2–7.4) 501 11.6 (8.8–14.4) 7o$4ov;T  
65–69 478 17.2 (13.8–20.1) 534 18.5 (15.2–21.9) tHhA _  
70–74 392 27.6 (23.1–32.0) 453 36.0 (31.6–40.4) ?#F}mOVAa  
75–79 255 45.1 (39.0–51.3) 302 55.6 (50.0–61.3) Q3Sw W  
80–84 146 54.1 (45.9–62.3) 147 73.5 (66.3–80.7) 9JHu{r"M  
85–89 50 64.0 (50.2–77.8) 70 80.0 (70.4–89.6) .P[ %t=W  
90+ 18 72.2 (49.3–95.1) 15 73.3 (48.0–98.7) . bh>_ W_h  
n = number of persons 9/LI[{  
* 95% Confidence Limits hJ0)"OA5  
Cataract FMioguunrtea i1n ps rEeyvea lSetnucdey in cross-sections I and II of the Blue Te`Z Qqb  
Cataract prevalence in cross-sections I and II of the Blue ;J3az`  
Mountains Eye Study. x\vb@!BZ  
0 kve{CO*  
10 JFx=X=C  
20 |BD]K0  
30 7d0E9t;W  
40 oWVlHAPj  
50 0z g\thL  
cortical PSC nuclear any *N"bn'>3  
cataract n237%LH[  
Cataract type iVM{ L  
% i)V-q9\  
Cross-section I jV^Dj  
Cross-section II \*#9Ry^f  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 `vJ+ sRf  
Page 5 of 7 Z']D8>d  
(page number not for citation purposes) XJ;kyEx3=O  
prevalence of any cataract (including cataract surgery) was h5 Y3 v  
relatively stable over the 6-year period. ~y{(&7sM  
Although different population-based studies used different 3\ 6 UH  
grading systems to assess cataract [15], the overall rt5UT~  
prevalence of the three cataract types were similar across =4 &/P r  
different study populations [12,16-23]. Most studies have |y@TI  
suggested that nuclear cataract is the most prevalent type F"9 f6<ge  
of cataract, followed by cortical cataract [16-20]. Ours and iq`y  
other studies reported that cortical cataract was the most u]P0:)tS.  
prevalent type [12,21-23]. UO}Kk*  
Our age-specific prevalence data show a reduction of kWL\JDZ`.  
15.9% in cortical cataract prevalence for the 80–84 year <{.o+~k  
age group, concordant with an increase in cataract surgery >l qWni  
prevalence by 9% in those aged 80+ years observed in the sb Oa] 5]  
same study population [10]. Although cortical cataract is Zs!)w9y&V  
thought to be the least likely cataract type leading to a cataract ni gp83:  
surgery, this may not be the case in all older persons. "V:B-q  
A relatively stable cortical cataract and PSC prevalence {{ M?+]p,^  
over the 6-year period is expected. We cannot offer a b9HE #*d,  
definitive explanation for the increase in nuclear cataract J ?$4Yf  
prevalence. A possible explanation could be that a moderate w5|az6wZB!  
level of nuclear cataract causes less visual disturbance $53I%.  
than the other two types of cataract, thus for the oldest age G8"L #[~  
groups, persons with nuclear cataract could have been less ;<%~g8:XL  
likely to have surgery unless it is very dense or co-existing $@q)IK%FDL  
with cortical cataract or PSC. Previous studies have shown &O(z|-&| x  
that functional vision and reading performance were high f+Nq?GvwBQ  
in patients undergoing cataract surgery who had nuclear |{]\n/M  
cataract only compared to those with mixed type of cataract N. 3 x[%:  
(nuclear and cortical) or PSC [24,25]. In addition, the ptGM'  
overall prevalence of any cataract (including cataract surgery) Q~]#x![u0  
was similar in the two cross-sections, which appears a;m-Vu!  
to support our speculation that in the oldest age group, VN|P(S6  
nuclear cataract may have been less likely to be operated ~h?zK 1  
than the other two types of cataract. This could have 9>d$a2 nc  
resulted in an increased nuclear cataract prevalence (due :<Y,^V(  
to less being operated), compensated by the decreased LX4S}QXw  
prevalence of cortical cataract and PSC (due to these being C/ow{MxA  
more likely to be operated), leading to stable overall prevalence )Z0pU \  
of any cataract. r8+{HknB;  
Possible selection bias arising from selective survival hT9fqH  
among persons without cataract could have led to underestimation FVsV Y1  
of cataract prevalence in both surveys. We F)) +a&O  
assume that such an underestimation occurred equally in >F6'^9|  
both surveys, and thus should not have influenced our zCj]mH`es'  
assessment of temporal changes. }'a}s0h  
Measurement error could also have partially contributed bTE%p0  
to the observed difference in nuclear cataract prevalence. >}GtmnF  
Assessment of nuclear cataract from photographs is a QRhR.:M\  
potentially subjective process that can be influenced by a_w# ,^/P  
variations in photography (light exposure, focus and the 3J~Q pw0<  
slit-lamp angle when the photograph was taken) and I/rq@27o  
grading. Although we used the same Topcon slit-lamp ] 7_ f'M1F  
camera and the same two graders who graded photos xR q|W4ay  
from both surveys, we are still not able to exclude the possibility ^aN;M\  
of a partial influence from photographic variation K/KZ}PI-O  
on this result. y[oc^Zuo  
A similar gender difference (women having a higher rate i5w  
than men) in cortical cataract prevalence was observed in #GT/Q3{C  
both surveys. Our findings are in keeping with observations J,%v`A~ N  
from the Beaver Dam Eye Study [18], the Barbados rePJ4i [y  
Eye Study [22] and the Lens Opacities Case-Control yNi/JM  
Group [26]. It has been suggested that the difference .Ebg>j:\  
could be related to hormonal factors [18,22]. A previous R}>xpU1  
study on biochemical factors and cataract showed that a Tn< <i  
lower level of iron was associated with an increased risk of _@;t^j+l  
cortical cataract [27]. No interaction between sex and biochemical yt}Ve6  m  
factors were detected and no gender difference [U.3rcT"N  
was assessed in this study [27]. The gender difference seen D/^yAfI  
in cortical cataract could be related to relatively low iron Lqq RuKi  
levels and low hemoglobin concentration usually seen in Pp3<K649  
women [28]. Diabetes is a known risk factor for cortical -61{ MMiA  
Table 3: Gender distribution of cataract types in cross-sections I and II. {D J!T  
Cataract type Gender Cross-section I Cross-section II =7wI/5iN  
n % (95% CL)* n % (95% CL)* ?j9J6=2  
Cortical Male 1496 21.1 (19.0–23.1) 1328 20.4 (18.2–22.6) =~6A c}$  
Female 1939 25.9 (23.9–27.8) 1785 26.2 (24.2–28.3) / E}L%OvE  
PSC Male 1500 6.5 (5.2–7.7) 1314 6.4 (5.1–7.7) 3cfW|J  
Female 1944 6.2 (5.1–7.2) 1753 5.7 (4.6–6.7) 0F> ils  
Nuclear Male 1106 17.6 (15.4–19.9) 1225 22.5 (20.1–24.8) _ dEc? R}  
Female 1395 19.5 (17.4–21.6) 1635 25.0 (22.9–27.1) EKo!vie G  
n = number of persons ui%B|b&&  
* 95% Confidence Limits >?>@&A/  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17  B C*62m  
Page 6 of 7 uNSaw['0j  
(page number not for citation purposes) djJD'JL  
cataract but in this particular population diabetes is more F|pM$Kd`  
prevalent in men than women in all age groups [29]. Differential |`vwykhezO  
exposures to cataract risk factors or different dietary EZnXS"z  
or lifestyle patterns between men and women may -!i1xR (;h  
also be related to these observations and warrant further 1oU/gm$7\q  
study. GPV=(}z  
Conclusion !jlLF:v|1A  
In summary, in two population-based surveys 6 years mbT4K8<^  
apart, we have documented a relatively stable prevalence t 7GK\B8:  
of cortical cataract and PSC over the period. The observed jHjap:i`cI  
overall increased nuclear cataract prevalence by 5% over a h;" 9.  
6-year period needs confirmation by future studies, and R|&jvG=|  
reasons for such an increase deserve further study. g{PEplk  
Competing interests 7p1f*N[X  
The author(s) declare that they have no competing interests. >_XC  
Authors' contributions (U@Ks )  
AGT graded the photographs, performed literature search 7m.#No>^  
and wrote the first draft of the manuscript. JJW graded the 7slpj8  
photographs, critically reviewed and modified the manuscript. WSEw:pln  
ER performed the statistical analysis and critically [vv $"$z  
reviewed the manuscript. PM designed and directed the ^]rPda#  
study, adjudicated cataract cases and critically reviewed Xz,fjKUnN  
and modified the manuscript. All authors read and oRkh>yj'  
approved the final manuscript. P;8nC:zL  
Acknowledgements KBC?SxJSJc  
This study was supported by the Australian National Health & Medical +H{TV#+r  
Research Council, Canberra, Australia (Grant Nos 974159, 991407). The m&MAA^I  
abstract was presented at the Association for Research in Vision and Ophthalmology G0%},Q/  
(ARVO) meeting in Fort Lauderdale, Florida, USA, May 2005. k~%j"%OB  
References i(qZ#oN  
1. Congdon N, O'Colmain B, Klaver CC, Klein R, Munoz B, Friedman c-VIpA1  
DS, Kempen J, Taylor HR, Mitchell P: Causes and prevalence of =;Q:z^S  
visual impairment among adults in the United States. Arch 5Z@0XI  
Ophthalmol 2004, 122(4):477-485. Z ".Xroq~  
2. Rahmani B, Tielsch JM, Katz J, Gottsch J, Quigley H, Javitt J, Sommer n58yR -"  
A: The cause-specific prevalence of visual impairment in an <N{wFvF  
urban population. The Baltimore Eye Survey. Ophthalmology d/Sw.=vq  
1996, 103:1721-1726. gNHS:k\"  
3. Keeffe JE, Konyama K, Taylor HR: Vision impairment in the oRZ98?Y\B  
Pacific region. Br J Ophthalmol 2002, 86:605-610. j:2TicHD C  
4. Reidy A, Minassian DC, Vafidis G, Joseph J, Farrow S, Wu J, Desai P, $GR rTC!  
Connolly A: Prevalence of serious eye disease and visual X5pb9zRq  
impairment in a north London population: population based, p'`?CJq8  
cross sectional study. BMJ 1998, 316:1643-1646. lqTc6@:D  
5. Resnikoff S, Pascolini D, Etya'ale D, Kocur I, Pararajasegaram R, )+Y"4?z~  
Pokharel GP, Mariotti SP: Global data on visual impairment in ZsNZ3;d@u(  
the year 2002. Bull World Health Organ 2004, 82:844-851. ZkJLq[:cM  
6. Pascolini D, Mariotti SP, Pokharel GP, Pararajasegaram R, Etya'ale D, "Zfm4Nx "  
Negrel AD, Resnikoff S: 2002 global update of available data on GT7&>}FJ)  
visual impairment: a compilation of population-based prevalence '%X29B5  
studies. Ophthalmic Epidemiol 2004, 11:67-115. Lb?WhjqZ  
7. Rochtchina E, Mukesh BN, Wang JJ, McCarty CA, Taylor HR, Mitchell ]Twy j  
P: Projected prevalence of age-related cataract and cataract ]Cs=EZr  
surgery in Australia for the years 2001 and 2021: pooled data 9W0*|!tQ,+  
from two population-based surveys. Clin Experiment Ophthalmol _7z]zy@PC5  
2003, 31:233-236. !w}b}+]GB  
8. Medicare Benefits Schedule Statistics [http://www.medicar hFo29oN  
eaustralia.gov.au/statistics/dyn_mbs/forms/mbs_tab4.shtml] bg!(B<!X  
9. Keeffe JE, Taylor HR: Cataract surgery in Australia 1985–94. m lxtey6H3  
Aust N Z J Ophthalmol 1996, 24:313-317. K {kd:pr  
10. Tan AG, Wang JJ, Rochtchina E, Jakobsen K, Mitchell P: Increase in  )m#Y^  
cataract surgery prevalence from 1992–1994 to 1997–2000: q_6fr$-Qh  
Analysis of two population cross-sections. Clin Experiment Ophthalmol :c|Om{;  
2004, 32:284-288. ufe |I  
11. Mitchell P, Smith W, Attebo K, Wang JJ: Prevalence of age-related 2-DG6\QX|  
maculopathy in Australia. The Blue Mountains Eye Study. sv!zY= 6  
Ophthalmology 1995, 102:1450-1460. c`/VYgcTqB  
12. Mitchell P, Cumming RG, Attebo K, Panchapakesan J: Prevalence of == E8^jYJw  
cataract in Australia: the Blue Mountains eye study. Ophthalmology _9]vlxgtG(  
1997, 104:581-588. z#Fel/L`O  
13. Klein BEK, Magli YL, Neider MW, Klein R: Wisconsin system for classification <S=( `D  
of cataracts from photographs (protocol) Madison, WI; 1990. oNIYO *[  
14. Foran S, Wang JJ, Mitchell P: Causes of visual impairment in two I-}ms  
older population cross-sections: the Blue Mountains Eye Qu1&$oO  
Study. Ophthalmic Epidemiol 2003, 10:215-225. Z.&/,UU:4  
15. Congdon N, Vingerling JR, Klein BE, West S, Friedman DS, Kempen J, >|c?ZqW  
O'Colmain B, Wu SY, Taylor HR: Prevalence of cataract and I-/>M/66  
pseudophakia/aphakia among adults in the United States. m94PFD@N  
Arch Ophthalmol 2004, 122:487-494. OX'V  
16. Sperduto RD, Hiller R: The prevalence of nuclear, cortical, and <{k` K[)  
posterior subcapsular lens opacities in a general population <T?-A}0uO  
sample. Ophthalmology 1984, 91:815-818. \I:27:iAL  
17. Adamsons I, Munoz B, Enger C, Taylor HR: Prevalence of lens 6lCpf1>6@  
opacities in surgical and general populations. Arch Ophthalmol mZ2CG O R  
1991, 109:993-997. z bYv}q  
18. Klein BE, Klein R, Linton KL: Prevalence of age-related lens L {P'mG=4  
opacities in a population. The Beaver Dam Eye Study. Ophthalmology .hu7JM+  
1992, 99:546-552. zt: !hM/Vt  
19. West SK, Munoz B, Schein OD, Duncan DD, Rubin GS: Racial differences |,@D <  
in lens opacities: the Salisbury Eye Evaluation (SEE) -Uy)=]Zae  
project. Am J Epidemiol 1998, 148:1033-1039. y~\ujp_5w  
20. Congdon N, West SK, Buhrmann RR, Kouzis A, Munoz B, Mkocha H: nKzm.D gt_  
Prevalence of the different types of age-related cataract in r&m49N,d  
an African population. Invest Ophthalmol Vis Sci 2001, |YsR;=6wT  
42:2478-2482. >z qaV@T  
21. Livingston PM, Guest CS, Stanislavsky Y, Lee S, Bayley S, Walker C, LT<2 n.S  
McKean C, Taylor HR: A population-based estimate of cataract {daX?N|V  
prevalence: the Melbourne Visual Impairment Project experience. Et!J*{s  
Dev Ophthalmol 1994, 26:1-6. W,NqevXo:  
22. Leske MC, Connell AM, Wu SY, Hyman L, Schachat A: Prevalence ':fp|m)M  
of lens opacities in the Barbados Eye Study. Arch Ophthalmol \894 Jqh  
1997, 115:105-111. published erratum appears in Arch Ophthalmol w.w{L=p:<"  
1997 Jul;115(7):931 72d|Jbd  
23. Seah SK, Wong TY, Foster PJ, Ng TP, Johnson GJ: Prevalence of 5PO_qr= Hx  
lens opacity in Chinese residents of Singapore: the tanjong tO{{ci$-T  
pagar survey. Ophthalmology 2002, 109:2058-2064. : c~SH/qS  
24. Stifter E, Sacu S, Weghaupt H, Konig F, Richter-Muksch S, Thaler A, KR#,6  
Velikay-Parel M, Radner W: Reading performance depending on RbL?(  
the type of cataract and its predictability on the visual outcome. @KK6JyOTQ  
J Cataract Refract Surg 2004, 30:1259-1267. v']_)  
25. Stifter E, Sacu S, Weghaupt H: Functional vision with cataracts of ySr,HXz  
different morphologies: comparative study. J Cataract Refract >^~^#MT  
Surg 2004, 30:1883-1891. wx*?@f>u^  
26. Leske MC, Chylack LT Jr, Wu SY: The Lens Opacities Case-Control H[u9C:}9b  
Study. Risk factors for cataract. Arch Ophthalmol 1991, `Y:]&w  
109:244-251. (M$0'BV0  
27. Leske MC, Wu SY, Hyman L, Sperduto R, Underwood B, Chylack LT, KMwV;r  
Milton RC, Srivastava S, Ansari N: Biochemical factors in the lens U`q keNd  
opacities. Case-control study. The Lens Opacities Case-Control =$J(]KPv!?  
Study Group. Arch Ophthalmol 1995, 113:1113-1119. + f67y  
28. Yip R, Johnson C, Dallman PR: Age-related changes in laboratory ;stuTj@vH  
values used in the diagnosis of anemia and iron deficiency. %3a-@!|1<  
Am J Clin Nutr 1984, 39:427-436. @e)}#kN.  
29. Mitchell P, Smith W, Wang JJ, Cumming RG, Leeder SR, Burnett L: pq{`WgA^  
Diabetes in an older Australian population. Diabetes Res Clin !:|*!  
Pract 1998, 41:177-184. A4tk</A  
Pre-publication history @wcF#?J  
The pre-publication history for this paper can be accessed mLuNl^)3  
here: _p*9LsN$L  
Publish with BioMed Central and every /Sj~lHh  
scientist can read your work free of charge zL yI|%KH  
"BioMed Central will be the most significant development for G]=z ![$  
disseminating the results of biomedical research in our lifetime." E%`J =C}  
Sir Paul Nurse, Cancer Research UK Q~(Gll;  
Your research papers will be: wmr?ANk  
available free of charge to the entire biomedical community P4[kW}R  
peer reviewed and published immediately upon acceptance mw 28E\U  
cited in PubMed and archived on PubMed Central uxf,95<g)  
yours — you keep the copyright dTg`z,^F  
Submit your manuscript here: jo:Z  
http://www.biomedcentral.com/info/publishing_adv.asp eq6O6-  
BioMedcentral Bg~]u+c*  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 tY)L^.*7  
Page 7 of 7 Cb;6yE)!Z  
(page number not for citation purposes) Pp_ 4B  
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:
freekaobo官方微信订阅号 正确答案:考博
按"Ctrl+Enter"直接提交