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 F ^m;xy  
Page 1 of 7 C0>L<*C  
(page number not for citation purposes) X+N8r^&  
BMC Ophthalmology 6['o^>\}f  
Research article Open Access 41Ab,  
Comparison of age-specific cataract prevalence in two kjOkPp  
population-based surveys 6 years apart QR<<O  
Ava Grace Tan†, Jie Jin Wang*†, Elena Rochtchina† and Paul Mitchell† 0h{&k7T<7  
Address: Centre for Vision Research, Westmead Millennium Institute, Department of Ophthalmology, University of Sydney, Westmead Hospital, e nw*[D !  
Westmead, NSW, Australia /xB O;'rR  
Email: Ava Grace Tan - ava_tan@wmi.usyd.edu.au; Jie Jin Wang* - jiejin_wang@wmi.usyd.edu.au; 5ci1ce  
Elena Rochtchina - elena_rochtchina@wmi.usyd.edu.au; Paul Mitchell - paul_mitchell@wmi.usyd.edu.au 58eO|c(  
* Corresponding author †Equal contributors 8]bLp  
Abstract #)iPvV'  
Background: In this study, we aimed to compare age-specific cortical, nuclear and posterior $H&:R&Us  
subcapsular (PSC) cataract prevalence in two surveys 6 years apart. ,"YTG*ky  
Methods: The Blue Mountains Eye Study examined 3654 participants (82.4% of those eligible) in +c__U Qx  
cross-section I (1992–4) and 3509 participants (75.1% of survivors and 85.2% of newly eligible) in ),^pi?  
cross-section II (1997–2000, 66.5% overlap with cross-section I). Cataract was assessed from lens K}'?#a(aX=  
photographs following the Wisconsin Cataract Grading System. Cortical cataract was defined if _c}# f\ +_  
cortical opacity comprised ≥ 5% of lens area. Nuclear cataract was defined if nuclear opacity ≥ FJT0lC  
Wisconsin standard 4. PSC was defined if any present. Any cataract was defined to include persons n8`WU3&  
who had previous cataract surgery. Weighted kappa for inter-grader reliability was 0.82, 0.55 and <|w(Sn  
0.82 for cortical, nuclear and PSC cataract, respectively. We assessed age-specific prevalence using ksUF(lYk  
an interval of 5 years, so that participants within each age group were independent between the ^uPg71r:  
two surveys. Ynp#3 r  
Results: Age and gender distributions were similar between the two populations. The age-specific J@#rOOu  
prevalence of cortical (23.8% in 1st, 23.7% in 2nd) and PSC cataract (6.3%, 6.0%) was similar. The }02(Y!Gh  
prevalence of nuclear cataract increased slightly from 18.7% to 23.9%. After age standardization, n9-WZsc1  
the similar prevalence of cortical (23.8%, 23.5%) and PSC cataract (6.3%, 5.9%), and the increased 8xkLfN|N=  
prevalence of nuclear cataract (18.7%, 24.2%) remained. 2^f7GP  
Conclusion: In two surveys of two population-based samples with similar age and gender 5du xW>D  
distributions, we found a relatively stable cortical and PSC cataract prevalence over a 6-year period. 6qWWfm/6  
The increased prevalence of nuclear cataract deserves further study. jdx T662q  
Background M Ih\z7gW  
Age-related cataract is the leading cause of reversible visual C;.,+(G  
impairment in older persons [1-6]. In Australia, it is Eh$1p iJG  
estimated that by the year 2021, the number of people G&"O)$h  
affected by cataract will increase by 63%, due to population _KkP{g,Y  
aging [7]. Surgical intervention is an effective treatment Kx?8 HA[5  
for cataract and normal vision (> 20/40) can usually ?/my G{E  
be restored with intraocular lens (IOL) implantation.  'S:$4j  
Cataract surgery with IOL implantation is currently the \NKQ:F1  
most commonly performed, and is, arguably, the most Z[eWey_  
cost effective surgical procedure worldwide. Performance |"+Uf w^  
Published: 20 April 2006 l[rK)PM   
BMC Ophthalmology 2006, 6:17 doi:10.1186/1471-2415-6-17 j0s$}FPUI  
Received: 14 December 2005 dlIYzO<  
Accepted: 20 April 2006 @PctBS<s  
This article is available from: http://www.biomedcentral.com/1471-2415/6/17 /'b7q y  
© 2006 Tan et al; licensee BioMed Central Ltd. 7R# }AQ   
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),  Lw%_xRn)  
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. K9y~  e  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 g 4952u  
Page 2 of 7 4I&Mdt<^D  
(page number not for citation purposes) l5\V4  
of this surgical procedure has been continuously increasing EdkIT|c{  
in the last two decades. Data from the Australian .J O1kt  
Health Insurance Commission has shown a steady Vjw u:M  
increase in Medicare claims for cataract surgery [8]. A 2.6- mCG&=Fx  
fold increase in the total number of cataract procedures k%Vprc  
from 1985 to 1994 has been documented in Australia [9]. Z!7xRy  
The rate of cataract surgery per thousand persons aged 65 >?rMMR+A  
years or older has doubled in the last 20 years [8,9]. In the &/WE{W  
Blue Mountains Eye Study population, we observed a onethird x0:BxRx*  
increase in cataract surgery prevalence over a mean .{} 8mFi 1  
6-year interval, from 6% to nearly 8% in two cross-sectional NzTF2ve(  
population-based samples with a similar age range Z# bO}!  
[10]. Further increases in cataract surgery performance ,wXmJ)/WZ  
would be expected as a result of improved surgical skills B?- poB&  
and technique, together with extending cataract surgical !?/:p.  
benefits to a greater number of older people and an ,v,rY'  
increased number of persons with surgery performed on cD}]4  
both eyes. |_>^vW1 f  
Both the prevalence and incidence of age-related cataract @un+y9m[C  
link directly to the demand for, and the outcome of, cataract Z7RBJK7|.  
surgery and eye health care provision. This report K,$rG%c zX  
aimed to assess temporal changes in the prevalence of cortical : -d_  
and nuclear cataract and posterior subcapsular cataract x3Y)l1gh  
(PSC) in two cross-sectional population-based XWyP'\  
surveys 6 years apart. 4=MjyH|[Jx  
Methods 8/BMFR J  
The Blue Mountains Eye Study (BMES) is a populationbased qq]Iy=  
cohort study of common eye diseases and other nS*Y+Q^9a  
health outcomes. The study involved eligible permanent F_jHi0A  
residents aged 49 years and older, living in two postcode vIbM@Y4 '?  
areas in the Blue Mountains, west of Sydney, Australia. Z>Mv$F"p:  
Participants were identified through a census and were |=m.eU  
invited to participate. The study was approved at each 7K:V<vX5  
stage of the data collection by the Human Ethics Committees %kjG[C  
of the University of Sydney and the Western Sydney uMS+,dXy  
Area Health Service and adhered to the recommendations G+t:]\  
of the Declaration of Helsinki. Written informed consent U/QgO  
was obtained from each participant. hN &?x5aC>  
Details of the methods used in this study have been O9(z"c  
described previously [11]. The baseline examinations 4^F%bXJ)  
(BMES cross-section I) were conducted during 1992– t'l4$}(  
1994 and included 3654 (82.4%) of 4433 eligible residents. ~<m^  
Follow-up examinations (BMES IIA) were conducted Mz p<s<BX  
during 1997–1999, with 2335 (75.0% of BMES "J1A9|  
cross section I survivors) participating. A repeat census of 89g a+#7  
the same area was performed in 1999 and identified 1378 _9 ]:0bDUo  
newly eligible residents who moved into the area or the \7r0]& _  
eligible age group. During 1999–2000, 1174 (85.2%) of )Y7H@e\1  
this group participated in an extension study (BMES IIB). LV^^Bd8Ct  
BMES cross-section II thus includes BMES IIA (66.5%) c MXv  
and BMES IIB (33.5%) participants (n = 3509). ^{4BcM7eH  
Similar procedures were used for all stages of data collection vSH,fS-n  
at both surveys. A questionnaire was administered ^w60AqR8  
including demographic, family and medical history. A * 9^8NY]  
detailed eye examination included subjective refraction, `$B?TNuch7  
slit-lamp (Topcon SL-7e camera, Topcon Optical Co, =9GA LoGL  
Tokyo, Japan) and retroillumination (Neitz CT-R camera, $^ee~v;m4  
Neitz Instrument Co, Tokyo, Japan) photography of the  $3^M-w  
lens. Grading of lens photographs in the BMES has been -3{Q`@F  
previously described [12]. Briefly, masked grading was <l{oE? N  
performed on the lens photographs using the Wisconsin [a2]_]E%  
Cataract Grading System [13]. Cortical cataract and PSC ]#)(D- i  
were assessed from the retroillumination photographs by q? ' 4&  
estimating the percentage of the circular grid involved. .| 4P :r  
Cortical cataract was defined when cortical opacity ,a?)O6?/  
involved at least 5% of the total lens area. PSC was defined eiKY az  
when opacity comprised at least 1% of the total lens area. PR %)3  
Slit-lamp photographs were used to assess nuclear cataract xsZG(Tz  
using the Wisconsin standard set of four lens photographs :?6HG_9X  
[13]. Nuclear cataract was defined when nuclear opacity ,8@<sF B'  
was at least as great as the standard 4 photograph. Any cataract J:@gmo`M;V  
was defined to include persons who had previous kpgA2u7  
cataract surgery as well as those with any of three cataract L 4j#0I]lq  
types. Inter-grader reliability was high, with weighted 3Z XAAV  
kappa 0.82 for cortical cataract, 0.55 (simple kappa 0.75) ,hn#DJ)  
for nuclear cataract and 0.82 for PSC grading. The intragrader z &EDW 5I  
reliability for nuclear cataract was assessed with NUV">i.(  
simple kappa 0.83 for the senior grader who graded Lh[0B.g<  
nuclear cataract at both surveys. All PSC cases were confirmed fDy*dp4z  
by an ophthalmologist (PM). 46>rvy.r  
In cross-section I, 219 persons (6.0%) had missing or Msqqjhoy  
ungradable Neitz photographs, leaving 3435 with photographs *9\j1Nd  
available for cortical cataract and PSC assessment, xt^1,V4Ei~  
while 1153 (31.6%) had randomly missing or ungradable ZmsYRk~@-  
Topcon photographs due to a camera malfunction, leaving //63|;EEkl  
2501 with photographs available for nuclear cataract (47?lw &  
assessment. Comparison of characteristics between participants >(RkoExO/  
with and without Neitz or Topcon photographs in 'nTlCYT  
cross-section I showed no statistically significant differences :r q~5hK  
between the two groups, as reported previously 50_[hC&C)  
[12]. In cross-section II, 441 persons (12.5%) had missing ]Y [N=G  
or ungradable Neitz photographs, leaving 3068 for cortical w%])  
cataract and PSC assessment, and 648 (18.5%) had ;J W ]b]  
missing or ungradable Topcon photographs, leaving 2860 clvg5{^q[  
for nuclear cataract assessment. o/{`\4  
Data analysis was performed using the Statistical Analysis VIAq$iu7  
System (SAS, SAS Institute, Cary, NC, USA). Age-adjusted mjD^iu8?  
prevalence was calculated using direct standardization of Bp^LLH  
the cross-section II population to the cross-section I population. eo]nkyYDP  
We assessed age-specific prevalence using an |m's)  
interval of 5 years, so that participants within each age Mq0MtC6-  
group were independent between the two cross-sectional '4'Z  
surveys. 0F)v9EK(W4  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 |=q~X}DA  
Page 3 of 7 HyzSHI  
(page number not for citation purposes) T1Py6Q,-  
Results irlFB #..  
Characteristics of the two survey populations have been i9ySD  
previously compared [14] and showed that age and sex 0qN`-0Yk  
distributions were similar. Table 1 compares participant T,!EL +o4  
characteristics between the two cross-sections. Cross-section GN_L"|#)=  
II participants generally had higher rates of diabetes, Au2?f~#Fv  
hypertension, myopia and more users of inhaled steroids. 9^/Y7Wp/@  
Cataract prevalence rates in cross-sections I and II are lAnq2j|  
shown in Figure 1. The overall prevalence of cortical cataract 7T/BzXr,B  
was 23.8% and 23.7% in cross-sections I and II, T<*)Cdid  
respectively (age-sex adjusted P = 0.81). Corresponding /si<Fp)z  
prevalence of PSC was 6.3% and 6.0% for the two crosssections Ck/44Wfej  
(age-sex adjusted P = 0.60). There was an rO#w(]   
increased prevalence of nuclear cataract, from 18.7% in i|{psA  
cross-section I to 23.9% in cross-section II over the 6-year sywuS  
period (age-sex adjusted P < 0.001). Prevalence of any cataract LuySa2 ,  
(including persons who had cataract surgery), however, h\!8*e;RAW  
was relatively stable (46.9% and 46.8% in crosssections `t/j6 e]  
I and II, respectively). Pg}QRCB@  
After age-standardization, these prevalence rates remained nXn@|J&z~U  
stable for cortical cataract (23.8% and 23.5% in the two ;O7"!\  
surveys) and PSC (6.3% and 5.9%). The slightly increased H4ie$/[$8  
prevalence of nuclear cataract (from 18.7% to 24.2%) was Pm%xX ~H  
not altered. uzH MQp  
Table 2 shows the age-specific prevalence rates for cortical 'xta/@Sq  
cataract, PSC and nuclear cataract in cross-sections I and 1'/ [x(/]d  
II. A similar trend of increasing cataract prevalence with ~Eg]Auk7  
increasing age was evident for all three types of cataract in vb[ 0H{TT2  
both surveys. Comparing the age-specific prevalence jSpj6:@B  
between the two surveys, a reduction in PSC prevalence in w1I07 (  
cross-section II was observed in the older age groups (≥ 75 Z5xQ -T`  
years). In contrast, increased nuclear cataract prevalence "SN*hzs"]`  
in cross-section II was observed in the older age groups (≥ *OA(v^@tx7  
70 years). Age-specific cortical cataract prevalence was relatively 81E EYf  
consistent between the two surveys, except for a Gy \ ]j  
reduction in prevalence observed in the 80–84 age group GeJ}myD O  
and an increasing prevalence in the older age groups (≥ 85 `qJJ{<1&U  
years). f$FO 1B)  
Similar gender differences in cataract prevalence were Stw g[K0<  
observed in both surveys (Table 3). Higher prevalence of E0I/]0  
cortical and nuclear cataract in women than men was evident D9TjjA|zS  
but the difference was only significant for cortical K+|XI|1p  
cataract (age-adjusted odds ratio, OR, for women 1.3, aB6/-T+ u  
95% confidence intervals, CI, 1.1–1.5 in cross-section I -r,v3n  
and OR 1.4, 95% CI 1.1–1.6 in cross-section II). In con- w<H2#d>5!@  
Table 1: Participant characteristics. wb9(aS4  
Characteristics Cross-section I Cross-section II Pd+*syOM  
n % n % a+HK fK  
Age (mean) (66.2) (66.7) S(CkA\[rz  
50–54 485 13.3 350 10.0 3UXZ|!-  
55–59 534 14.6 580 16.5 x:0 swZ5Z  
60–64 638 17.5 600 17.1 v)np.j0V7  
65–69 671 18.4 639 18.2 YZ<z lU  
70–74 538 14.7 572 16.3 8o+:|V~X  
75–79 422 11.6 407 11.6 AS]8rH  
80–84 230 6.3 226 6.4 Lxv;[2XsW)  
85–89 100 2.7 110 3.1 o@N[O^Q V  
90+ 36 1.0 24 0.7 w2xD1oK~o  
Female 2072 56.7 1998 57.0 +%j27~ R>D  
Ever Smokers 1784 51.2 1789 51.2 3|!3R'g/ >  
Use of inhaled steroids 370 10.94 478 13.8^ 2H w7V3q  
History of: ~] ?s A{  
Diabetes 284 7.8 347 9.9^ Q3%]  
Hypertension 1669 46.0 1825 52.2^ sCw>J#@2>  
Emmetropia* 1558 42.9 1478 42.2 x%`YV):*  
Myopia* 442 12.2 495 14.1^ Io*H}$Gf  
Hyperopia* 1633 45.0 1532 43.7 ##BbR  
n = number of persons affected `Y.~eE  
* best spherical equivalent refraction correction ,+ IFV  
^ P < 0.01 OqS!y( (  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 I5E =Ujc_  
Page 4 of 7 ;_SSR8uHv  
(page number not for citation purposes) ,9d]-CuP;  
t N@tKgx  
rast, men had slightly higher PSC prevalence than women _BA; H+M  
in both cross-sections but the difference was not significant EPn!6W5^  
(OR 1.1, 95% CI 0.8–1.4 for men in cross-section I l0^cdl-  
and OR 1.2, 95% 0.9–1.6 in cross-section II). -a@e28Y  
Discussion n= 4  
Findings from two surveys of BMES cross-sectional populations E,tdn#_|  
with similar age and gender distribution showed z H-a%$5  
that the prevalence of cortical cataract and PSC remained d'Bxi"K  
stable, while the prevalence of nuclear cataract appeared TW>G YGz  
to have increased. Comparison of age-specific prevalence, &*" *b\  
with totally independent samples within each age group, O!nS3%De  
confirmed the robustness of our findings from the two p%meuWV%5  
survey samples. Although lens photographs taken from $m#^0%  
the two surveys were graded for nuclear cataract by the m-azd ~r[  
same graders, who documented a high inter- and intragrader ]i(/T$?~  
reliability, we cannot exclude the possibility that }R 16WY_'  
variations in photography, performed by different photographers, jr0j0$BF  
may have contributed to the observed difference OS;  T;  
in nuclear cataract prevalence. However, the overall AvrvBz[  
Table 2: Age-specific prevalence of cataract types in cross sections I and II. h_#=f(.'j  
Cataract type Age (years) Cross-section I Cross-section II 2kDY+AN;  
n % (95% CL)* n % (95% CL)* G`n $A/ 9Q  
Cortical 50–54 473 4.4 (2.6–6.3) 338 7.4 (4.6–10.2) 8 5ET$YV  
55–59 522 9.2 (6.7–11.7) 542 9.0 (6.6–11.5) 8O]`3oa>  
60–64 615 16.4 (13.5–19.4) 556 16.7 (13.6–19.8) B2j1G JEO  
65–69 653 26.2 (22.8–29.6) 581 23.6 (20.1–27.0) DNq(\@x[!  
70–74 516 31.2 (27.2–35.2) 514 35.4 (31.3–39.6) l[:Aq&[o3  
75–79 366 40.2 (35.1–45.2) 332 39.8 (34.5–45.1) y& yf&p  
80–84 194 58.8 (51.8–65.8) 163 42.9 (35.3–50.6) AcuF0KWw/  
85–89 74 52.7 (41.1–64.4) 73 54.8 (43.1–66.5) seEo)m`d  
90+ 22 68.2 (47.0–89.3) 14 78.6 (54.0–103.2) {>1FZsR49t  
PSC 50–54 474 2.7 (1.3–4.2) 338 2.4 (0.7–4.0) ~>(~2083*;  
55–59 522 2.9 (1.4–4.3) 541 2.6 (1.3–3.9) GqRXNs!  
60–64 616 4.6 (2.9–6.2) 548 5.7 (3.7–7.6) I)'bf/6?  
65–69 655 6.3 (4.4–8.1) 573 4.5 (2.8–6.3) \wA:58 -j  
70–74 517 6.8 (4.6–8.9) 505 9.7 (7.1–12.3) b*?u+tWP_  
75–79 367 11.4 (8.2–14.7) 327 9.5 (6.3–12.7) K{ar)_V/  
80–84 196 12.2 (7.6–16.9) 155 10.3 (5.5–15.2) To>,8E+GAb  
85–89 74 18.9 (9.8–28.1) 69 11.6 (3.9–19.4) 0uDD aFS  
90+ 23 21.7 (3.5–40.0) 11 0.0 @/<UhnI  
Nuclear 50–54 323 1.6 (0.2–2.9) 331 0.9 (–0.2–1.9) =p'+kS+  
55–59 386 2.3 (0.8–3.8) 507 3.6 (1.9–5.2) oVy{~D=  
60–64 453 5.3 (3.2–7.4) 501 11.6 (8.8–14.4) '3672wF/  
65–69 478 17.2 (13.8–20.1) 534 18.5 (15.2–21.9) p5#x7*xR6  
70–74 392 27.6 (23.1–32.0) 453 36.0 (31.6–40.4) WSHPh hM  
75–79 255 45.1 (39.0–51.3) 302 55.6 (50.0–61.3) }aRib{L  
80–84 146 54.1 (45.9–62.3) 147 73.5 (66.3–80.7) A0)^I:&  
85–89 50 64.0 (50.2–77.8) 70 80.0 (70.4–89.6) h) Wp  
90+ 18 72.2 (49.3–95.1) 15 73.3 (48.0–98.7) &Pr\n&9A  
n = number of persons h`|04Q  
* 95% Confidence Limits } jj)  
Cataract FMioguunrtea i1n ps rEeyvea lSetnucdey in cross-sections I and II of the Blue !CYC7HeF  
Cataract prevalence in cross-sections I and II of the Blue _Ub `\ytx  
Mountains Eye Study. _f[Q\gK  
0 ^OY]Y+S`Ox  
10 ~(d {j}M>  
20 5YD~l(,S1]  
30 sApix=Lr  
40 C27:ty V  
50 W*C~Xba<  
cortical PSC nuclear any _B^zm-}8|B  
cataract WBE>0L  
Cataract type vamZKm~p  
% >7> I1  
Cross-section I eQbHf  
Cross-section II F[jE#M=k  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 5BhR4+1J  
Page 5 of 7 ;/K2h_=3z  
(page number not for citation purposes) )dT@0Ys%  
prevalence of any cataract (including cataract surgery) was @ma(py  
relatively stable over the 6-year period. 9"P|Csj  
Although different population-based studies used different <gp?}Lk  
grading systems to assess cataract [15], the overall 11=$] K>  
prevalence of the three cataract types were similar across  j#](Q!  
different study populations [12,16-23]. Most studies have ZL!u$)(V  
suggested that nuclear cataract is the most prevalent type t2N W$ -E  
of cataract, followed by cortical cataract [16-20]. Ours and 5f-b>=02  
other studies reported that cortical cataract was the most Zl9@E;|=  
prevalent type [12,21-23]. qyH -Z@  
Our age-specific prevalence data show a reduction of `R[Hxi  
15.9% in cortical cataract prevalence for the 80–84 year Aedf (L7\  
age group, concordant with an increase in cataract surgery L:G #>  
prevalence by 9% in those aged 80+ years observed in the -#|D>  
same study population [10]. Although cortical cataract is Mbi]EZ  
thought to be the least likely cataract type leading to a cataract ?{ir $M  
surgery, this may not be the case in all older persons. j6rNt|  
A relatively stable cortical cataract and PSC prevalence tb3V qFx  
over the 6-year period is expected. We cannot offer a !J`lA  
definitive explanation for the increase in nuclear cataract * DL7p8  
prevalence. A possible explanation could be that a moderate v,KKn\X  
level of nuclear cataract causes less visual disturbance 4DA34m(  
than the other two types of cataract, thus for the oldest age `Fy-"Uf  
groups, persons with nuclear cataract could have been less isQ(O  
likely to have surgery unless it is very dense or co-existing ?"B] "%M&  
with cortical cataract or PSC. Previous studies have shown uw)7N(os\`  
that functional vision and reading performance were high 3N7H7(IR  
in patients undergoing cataract surgery who had nuclear d1 j9{  
cataract only compared to those with mixed type of cataract Tg\bpLk0=  
(nuclear and cortical) or PSC [24,25]. In addition, the "W|A^@r}  
overall prevalence of any cataract (including cataract surgery) bF'rK'',  
was similar in the two cross-sections, which appears 4fEDg{T  
to support our speculation that in the oldest age group, m>>.N?  
nuclear cataract may have been less likely to be operated %bW_,b  
than the other two types of cataract. This could have 2eT?qCxqc  
resulted in an increased nuclear cataract prevalence (due ]MbPivM  
to less being operated), compensated by the decreased +.G"ool  
prevalence of cortical cataract and PSC (due to these being UO/sv2CN  
more likely to be operated), leading to stable overall prevalence .KsR48g8  
of any cataract. pSZ2>^";  
Possible selection bias arising from selective survival Gr"CHz/  
among persons without cataract could have led to underestimation QLA.;`HIE  
of cataract prevalence in both surveys. We Q?{%c[s  
assume that such an underestimation occurred equally in =OVDJ0ozZ  
both surveys, and thus should not have influenced our sV^:u^  
assessment of temporal changes. d:H'[l.F%  
Measurement error could also have partially contributed \bA Yic  
to the observed difference in nuclear cataract prevalence. RaZ>.5 D  
Assessment of nuclear cataract from photographs is a " qI99 e  
potentially subjective process that can be influenced by " \$^j#o  
variations in photography (light exposure, focus and the x-^6U  
slit-lamp angle when the photograph was taken) and  Dn- gP  
grading. Although we used the same Topcon slit-lamp %x)b Z= An  
camera and the same two graders who graded photos x3@-E  
from both surveys, we are still not able to exclude the possibility V5|ANt  
of a partial influence from photographic variation #;!&8iH  
on this result. u8e_Lqx?  
A similar gender difference (women having a higher rate rS8a/d~;0  
than men) in cortical cataract prevalence was observed in {Gxe%gu6 K  
both surveys. Our findings are in keeping with observations 9KSi-2?H  
from the Beaver Dam Eye Study [18], the Barbados Jh[0xb  
Eye Study [22] and the Lens Opacities Case-Control t [Q D#;  
Group [26]. It has been suggested that the difference n*4`Tduu^  
could be related to hormonal factors [18,22]. A previous 0=d2_YzSf  
study on biochemical factors and cataract showed that a ,d G.67  
lower level of iron was associated with an increased risk of 8^mE<  
cortical cataract [27]. No interaction between sex and biochemical CB@7XUR  
factors were detected and no gender difference W{p }N  
was assessed in this study [27]. The gender difference seen Bous d  
in cortical cataract could be related to relatively low iron Kg@'mG  
levels and low hemoglobin concentration usually seen in jm0p%%z  
women [28]. Diabetes is a known risk factor for cortical  7WJ \nK  
Table 3: Gender distribution of cataract types in cross-sections I and II. y@P%t9l  
Cataract type Gender Cross-section I Cross-section II > A#5` $i  
n % (95% CL)* n % (95% CL)* PK *W u<<  
Cortical Male 1496 21.1 (19.0–23.1) 1328 20.4 (18.2–22.6) 'H1 ~Zhv  
Female 1939 25.9 (23.9–27.8) 1785 26.2 (24.2–28.3) P8 X07IK  
PSC Male 1500 6.5 (5.2–7.7) 1314 6.4 (5.1–7.7) nF3}wCe)  
Female 1944 6.2 (5.1–7.2) 1753 5.7 (4.6–6.7) 16NHzAQ  
Nuclear Male 1106 17.6 (15.4–19.9) 1225 22.5 (20.1–24.8) F^ q{[Z  
Female 1395 19.5 (17.4–21.6) 1635 25.0 (22.9–27.1) R|; BO:S1  
n = number of persons <'y<8gpM  
* 95% Confidence Limits m*0YMS>Y |  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 -YoL.`s1   
Page 6 of 7 K;K0D@>]HR  
(page number not for citation purposes) I8H3*DE  
cataract but in this particular population diabetes is more k %I83,+  
prevalent in men than women in all age groups [29]. Differential ]HKt7 %,  
exposures to cataract risk factors or different dietary !V|{(>+<  
or lifestyle patterns between men and women may <o E Ay  
also be related to these observations and warrant further 72HA.!ry  
study. 1;B~n5C.   
Conclusion fRp]  
In summary, in two population-based surveys 6 years *>fr'jj1$  
apart, we have documented a relatively stable prevalence TrI+F+;  
of cortical cataract and PSC over the period. The observed 1NYR8W]2  
overall increased nuclear cataract prevalence by 5% over a x}G:n[B7_V  
6-year period needs confirmation by future studies, and jIh1)*]054  
reasons for such an increase deserve further study. [ATJ! O  
Competing interests T(|'.&a  
The author(s) declare that they have no competing interests. 8SRR)O[)}  
Authors' contributions y oW ~  
AGT graded the photographs, performed literature search s$Vl">9#  
and wrote the first draft of the manuscript. JJW graded the q,v<:sS9T  
photographs, critically reviewed and modified the manuscript. m8n)sw,,  
ER performed the statistical analysis and critically 8Vu@awz{L  
reviewed the manuscript. PM designed and directed the =VC18yA  
study, adjudicated cataract cases and critically reviewed <2 U#U;  
and modified the manuscript. All authors read and VL%. maj  
approved the final manuscript. 7# AIX],  
Acknowledgements %;`Kd}CO  
This study was supported by the Australian National Health & Medical 2z>-H595az  
Research Council, Canberra, Australia (Grant Nos 974159, 991407). The x0j5D  
abstract was presented at the Association for Research in Vision and Ophthalmology G`!x+FB  
(ARVO) meeting in Fort Lauderdale, Florida, USA, May 2005. %QP[/5vQ  
References 161P%sGx2  
1. Congdon N, O'Colmain B, Klaver CC, Klein R, Munoz B, Friedman PMjNc_))  
DS, Kempen J, Taylor HR, Mitchell P: Causes and prevalence of ?(ORk|)kU  
visual impairment among adults in the United States. Arch M}] *j  
Ophthalmol 2004, 122(4):477-485. ~ l}f@@u  
2. Rahmani B, Tielsch JM, Katz J, Gottsch J, Quigley H, Javitt J, Sommer ^h?fr`  
A: The cause-specific prevalence of visual impairment in an >u=  
urban population. The Baltimore Eye Survey. Ophthalmology M 9)4ihK  
1996, 103:1721-1726. l7`{O/hN  
3. Keeffe JE, Konyama K, Taylor HR: Vision impairment in the x`E<]z*w}  
Pacific region. Br J Ophthalmol 2002, 86:605-610. pg{VKrT`  
4. Reidy A, Minassian DC, Vafidis G, Joseph J, Farrow S, Wu J, Desai P, -YNpHd/;,  
Connolly A: Prevalence of serious eye disease and visual yD"]:ts3  
impairment in a north London population: population based, HK )m^!=  
cross sectional study. BMJ 1998, 316:1643-1646. =lAjQt  
5. Resnikoff S, Pascolini D, Etya'ale D, Kocur I, Pararajasegaram R, FJn-cR.n  
Pokharel GP, Mariotti SP: Global data on visual impairment in =$OGHc  
the year 2002. Bull World Health Organ 2004, 82:844-851. X>I3N?5  
6. Pascolini D, Mariotti SP, Pokharel GP, Pararajasegaram R, Etya'ale D, .\_):j*  
Negrel AD, Resnikoff S: 2002 global update of available data on /3s&??{tv  
visual impairment: a compilation of population-based prevalence tz ;3  
studies. Ophthalmic Epidemiol 2004, 11:67-115. b8d0]YS  
7. Rochtchina E, Mukesh BN, Wang JJ, McCarty CA, Taylor HR, Mitchell <::lfPP  
P: Projected prevalence of age-related cataract and cataract 9#9 UzKX#  
surgery in Australia for the years 2001 and 2021: pooled data ^ ]9K>}  
from two population-based surveys. Clin Experiment Ophthalmol >YI Vi4''  
2003, 31:233-236. G&S2U=KdV%  
8. Medicare Benefits Schedule Statistics [http://www.medicar g8O6 b  
eaustralia.gov.au/statistics/dyn_mbs/forms/mbs_tab4.shtml] pGD@R=8  
9. Keeffe JE, Taylor HR: Cataract surgery in Australia 1985–94. }Xj25` x  
Aust N Z J Ophthalmol 1996, 24:313-317. "Not / 8J  
10. Tan AG, Wang JJ, Rochtchina E, Jakobsen K, Mitchell P: Increase in xM%4/QE+  
cataract surgery prevalence from 1992–1994 to 1997–2000: SIp)&  
Analysis of two population cross-sections. Clin Experiment Ophthalmol P<g(i 6]  
2004, 32:284-288. '=0}2sF>  
11. Mitchell P, Smith W, Attebo K, Wang JJ: Prevalence of age-related ~N!HxQ  
maculopathy in Australia. The Blue Mountains Eye Study. L/"MRQ"  
Ophthalmology 1995, 102:1450-1460. '3S~QN  
12. Mitchell P, Cumming RG, Attebo K, Panchapakesan J: Prevalence of AW5iwq6p  
cataract in Australia: the Blue Mountains eye study. Ophthalmology F*P0=DD  
1997, 104:581-588. s|p I`  
13. Klein BEK, Magli YL, Neider MW, Klein R: Wisconsin system for classification tA#Pc6zBuC  
of cataracts from photographs (protocol) Madison, WI; 1990. ^}+\52w  
14. Foran S, Wang JJ, Mitchell P: Causes of visual impairment in two G(t:s5:  
older population cross-sections: the Blue Mountains Eye B@F@,?K4%  
Study. Ophthalmic Epidemiol 2003, 10:215-225. v@zi?D K  
15. Congdon N, Vingerling JR, Klein BE, West S, Friedman DS, Kempen J, c`<2&ke  
O'Colmain B, Wu SY, Taylor HR: Prevalence of cataract and #I=EYl=Vvi  
pseudophakia/aphakia among adults in the United States. "0HUaU,e  
Arch Ophthalmol 2004, 122:487-494. $e+sqgU  
16. Sperduto RD, Hiller R: The prevalence of nuclear, cortical, and (H_dZL  
posterior subcapsular lens opacities in a general population yX!u&  
sample. Ophthalmology 1984, 91:815-818. ! VR&HEru  
17. Adamsons I, Munoz B, Enger C, Taylor HR: Prevalence of lens x^K4&'</  
opacities in surgical and general populations. Arch Ophthalmol [oh06_rB  
1991, 109:993-997. nkHl;;WJ  
18. Klein BE, Klein R, Linton KL: Prevalence of age-related lens L"ho|v9:  
opacities in a population. The Beaver Dam Eye Study. Ophthalmology z_> ~=Mm  
1992, 99:546-552. n%3!)/$  
19. West SK, Munoz B, Schein OD, Duncan DD, Rubin GS: Racial differences C&z!="hMhR  
in lens opacities: the Salisbury Eye Evaluation (SEE) =2&\<Q_Fi  
project. Am J Epidemiol 1998, 148:1033-1039. S# ]] h/  
20. Congdon N, West SK, Buhrmann RR, Kouzis A, Munoz B, Mkocha H: 1h@qcom9K_  
Prevalence of the different types of age-related cataract in k3bQ32()  
an African population. Invest Ophthalmol Vis Sci 2001, *duG/?>P  
42:2478-2482. hi,=" /9  
21. Livingston PM, Guest CS, Stanislavsky Y, Lee S, Bayley S, Walker C, \9[vi +T  
McKean C, Taylor HR: A population-based estimate of cataract 6La[( )  
prevalence: the Melbourne Visual Impairment Project experience. d7^ `  
Dev Ophthalmol 1994, 26:1-6. <ww D*t  
22. Leske MC, Connell AM, Wu SY, Hyman L, Schachat A: Prevalence eKr>>4,-P  
of lens opacities in the Barbados Eye Study. Arch Ophthalmol {\5(aQ)Vi5  
1997, 115:105-111. published erratum appears in Arch Ophthalmol a{ST4d'T  
1997 Jul;115(7):931 1>e30Ri,g  
23. Seah SK, Wong TY, Foster PJ, Ng TP, Johnson GJ: Prevalence of o(ow{S@=4  
lens opacity in Chinese residents of Singapore: the tanjong !*v% s  
pagar survey. Ophthalmology 2002, 109:2058-2064. lfAy$qP"}  
24. Stifter E, Sacu S, Weghaupt H, Konig F, Richter-Muksch S, Thaler A, #ksDU  
Velikay-Parel M, Radner W: Reading performance depending on Ubu&$4a  
the type of cataract and its predictability on the visual outcome. 9(]_so24,  
J Cataract Refract Surg 2004, 30:1259-1267. ]KuM's  
25. Stifter E, Sacu S, Weghaupt H: Functional vision with cataracts of 437Wy+Q|e  
different morphologies: comparative study. J Cataract Refract .6gx|V+  
Surg 2004, 30:1883-1891. k*A(7qQA`4  
26. Leske MC, Chylack LT Jr, Wu SY: The Lens Opacities Case-Control @_`r*Tb)dM  
Study. Risk factors for cataract. Arch Ophthalmol 1991, g/C 7wc  
109:244-251. "\*)KH`C  
27. Leske MC, Wu SY, Hyman L, Sperduto R, Underwood B, Chylack LT, 6 :4GI  
Milton RC, Srivastava S, Ansari N: Biochemical factors in the lens u [qy1M0  
opacities. Case-control study. The Lens Opacities Case-Control 3@=<4$  
Study Group. Arch Ophthalmol 1995, 113:1113-1119. 4&NB xe  
28. Yip R, Johnson C, Dallman PR: Age-related changes in laboratory ,P <I<QYu  
values used in the diagnosis of anemia and iron deficiency. -}m  
Am J Clin Nutr 1984, 39:427-436. HJr/N)d  
29. Mitchell P, Smith W, Wang JJ, Cumming RG, Leeder SR, Burnett L: G5qsnTxUJ  
Diabetes in an older Australian population. Diabetes Res Clin b!g)/%C  
Pract 1998, 41:177-184. oRd{?I&NY  
Pre-publication history sA6Hk B.  
The pre-publication history for this paper can be accessed iY>x x~V  
here: !$HuH6_[  
Publish with BioMed Central and every 8GxT!  
scientist can read your work free of charge }|h-=T '  
"BioMed Central will be the most significant development for !& c%! *  
disseminating the results of biomedical research in our lifetime." pjO  
Sir Paul Nurse, Cancer Research UK 9I 6^-m@:  
Your research papers will be: RCqL~7C+ k  
available free of charge to the entire biomedical community \nOV2(FAT  
peer reviewed and published immediately upon acceptance NHZMH!=4:n  
cited in PubMed and archived on PubMed Central Ew}GPJ  
yours — you keep the copyright ,=!s;+lu{  
Submit your manuscript here: a:|]F|  
http://www.biomedcentral.com/info/publishing_adv.asp _6FDuCVD-  
BioMedcentral /_fZ 2$/  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 LzXIqj'H7T  
Page 7 of 7 IwFf8? 3  
(page number not for citation purposes) >VjtKSN  
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