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 Xdn&%5rI  
Page 1 of 7 i!a!qE.1  
(page number not for citation purposes) o%_-u +  
BMC Ophthalmology "V[j&B)P  
Research article Open Access " .7@  
Comparison of age-specific cataract prevalence in two =t, oj6P~  
population-based surveys 6 years apart `i`P}W!F  
Ava Grace Tan†, Jie Jin Wang*†, Elena Rochtchina† and Paul Mitchell† dcf,a<K\  
Address: Centre for Vision Research, Westmead Millennium Institute, Department of Ophthalmology, University of Sydney, Westmead Hospital, o<nM-"yWb  
Westmead, NSW, Australia ^T&{ORWz  
Email: Ava Grace Tan - ava_tan@wmi.usyd.edu.au; Jie Jin Wang* - jiejin_wang@wmi.usyd.edu.au; #:?:gY<  
Elena Rochtchina - elena_rochtchina@wmi.usyd.edu.au; Paul Mitchell - paul_mitchell@wmi.usyd.edu.au hkPMu@BI  
* Corresponding author †Equal contributors 2 5~Z%_?  
Abstract k6#$Nb606  
Background: In this study, we aimed to compare age-specific cortical, nuclear and posterior F$UL.`X _/  
subcapsular (PSC) cataract prevalence in two surveys 6 years apart. RvR.t"8  
Methods: The Blue Mountains Eye Study examined 3654 participants (82.4% of those eligible) in WOO3z5 La  
cross-section I (1992–4) and 3509 participants (75.1% of survivors and 85.2% of newly eligible) in |>ztx}\  
cross-section II (1997–2000, 66.5% overlap with cross-section I). Cataract was assessed from lens mZiKA-t  
photographs following the Wisconsin Cataract Grading System. Cortical cataract was defined if y3;M$Jr  
cortical opacity comprised ≥ 5% of lens area. Nuclear cataract was defined if nuclear opacity ≥ JZ}zXv   
Wisconsin standard 4. PSC was defined if any present. Any cataract was defined to include persons @fA{;@N  
who had previous cataract surgery. Weighted kappa for inter-grader reliability was 0.82, 0.55 and AWcbbj6Nd  
0.82 for cortical, nuclear and PSC cataract, respectively. We assessed age-specific prevalence using k~ )CJ6}  
an interval of 5 years, so that participants within each age group were independent between the ]G i&:k  
two surveys. dQ*^WNUB  
Results: Age and gender distributions were similar between the two populations. The age-specific NnAIL;WS  
prevalence of cortical (23.8% in 1st, 23.7% in 2nd) and PSC cataract (6.3%, 6.0%) was similar. The 7)U ik}0  
prevalence of nuclear cataract increased slightly from 18.7% to 23.9%. After age standardization, o} =*E  
the similar prevalence of cortical (23.8%, 23.5%) and PSC cataract (6.3%, 5.9%), and the increased ,~3rY,y-  
prevalence of nuclear cataract (18.7%, 24.2%) remained. GJdL1ptc  
Conclusion: In two surveys of two population-based samples with similar age and gender jTS8 qu  
distributions, we found a relatively stable cortical and PSC cataract prevalence over a 6-year period. @v`.^L{P  
The increased prevalence of nuclear cataract deserves further study. ]U#of O  
Background /[?} LrDO  
Age-related cataract is the leading cause of reversible visual Gd|kAC g  
impairment in older persons [1-6]. In Australia, it is S0StC$$1  
estimated that by the year 2021, the number of people zHKP$k8  
affected by cataract will increase by 63%, due to population r], %:imGr  
aging [7]. Surgical intervention is an effective treatment a( ~X  
for cataract and normal vision (> 20/40) can usually Y-8BL  
be restored with intraocular lens (IOL) implantation. 8d$|JN;)  
Cataract surgery with IOL implantation is currently the E-1u_7  
most commonly performed, and is, arguably, the most }bRn&)e  
cost effective surgical procedure worldwide. Performance (Q*x"G#4>  
Published: 20 April 2006 R1 SFMI   
BMC Ophthalmology 2006, 6:17 doi:10.1186/1471-2415-6-17 ];CIo> b_(  
Received: 14 December 2005 A3.I|/  
Accepted: 20 April 2006 xyo~p,(~t  
This article is available from: http://www.biomedcentral.com/1471-2415/6/17 :ek^M (  
© 2006 Tan et al; licensee BioMed Central Ltd. /t`|3Mw  
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), 0Sk~m4fj(  
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 1?w=v|b:P)  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 b5MU$}:  
Page 2 of 7 '0 ~?zP  
(page number not for citation purposes) =p5]r:9 W  
of this surgical procedure has been continuously increasing KaMg [ G  
in the last two decades. Data from the Australian 4<tbZP3/6)  
Health Insurance Commission has shown a steady >VZxDJ$R  
increase in Medicare claims for cataract surgery [8]. A 2.6- W{J e)N  
fold increase in the total number of cataract procedures x~uDCbL  
from 1985 to 1994 has been documented in Australia [9]. J|hVD  
The rate of cataract surgery per thousand persons aged 65 p2(ha3PW  
years or older has doubled in the last 20 years [8,9]. In the Y5 ;a  
Blue Mountains Eye Study population, we observed a onethird R|}4H*N  
increase in cataract surgery prevalence over a mean 66-\}8f8a  
6-year interval, from 6% to nearly 8% in two cross-sectional iVnMn1h  
population-based samples with a similar age range >Q<XyAH~  
[10]. Further increases in cataract surgery performance %5+X   
would be expected as a result of improved surgical skills fe<7D\Sp@  
and technique, together with extending cataract surgical 4$, W\d  
benefits to a greater number of older people and an F5+F O^3E  
increased number of persons with surgery performed on .fqy[qrM  
both eyes. Ih K SwT  
Both the prevalence and incidence of age-related cataract ,[ppETz  
link directly to the demand for, and the outcome of, cataract \VEnP=*:W  
surgery and eye health care provision. This report qZ E3T:S  
aimed to assess temporal changes in the prevalence of cortical z&n2JpLY7  
and nuclear cataract and posterior subcapsular cataract Fab]'#1q4  
(PSC) in two cross-sectional population-based x0% m}P/  
surveys 6 years apart. q9_AL8_  
Methods M]k  Q{(  
The Blue Mountains Eye Study (BMES) is a populationbased N LQ".mM+  
cohort study of common eye diseases and other AfhJ6cSIE  
health outcomes. The study involved eligible permanent $Bncdf  
residents aged 49 years and older, living in two postcode t}I@Rmso  
areas in the Blue Mountains, west of Sydney, Australia. oV['%Z'  
Participants were identified through a census and were :4 z\Q]  
invited to participate. The study was approved at each [O^/"Qk  
stage of the data collection by the Human Ethics Committees a;KdkykG  
of the University of Sydney and the Western Sydney ?[bE/Ya+S  
Area Health Service and adhered to the recommendations 3f^jy(  
of the Declaration of Helsinki. Written informed consent F4-rPv  
was obtained from each participant. "3]}V=L<5  
Details of the methods used in this study have been #r"|%nOfY  
described previously [11]. The baseline examinations V.$tq  
(BMES cross-section I) were conducted during 1992– 3^&`E} r  
1994 and included 3654 (82.4%) of 4433 eligible residents. "XV@O jr E  
Follow-up examinations (BMES IIA) were conducted SD*q+Si,1U  
during 1997–1999, with 2335 (75.0% of BMES 6~ y'  
cross section I survivors) participating. A repeat census of Hicd -'  
the same area was performed in 1999 and identified 1378 k kD#Bb  
newly eligible residents who moved into the area or the />I5,D'h  
eligible age group. During 1999–2000, 1174 (85.2%) of MUZ]*n&0  
this group participated in an extension study (BMES IIB). 3t.!5 L  
BMES cross-section II thus includes BMES IIA (66.5%) uSI@Cjp  
and BMES IIB (33.5%) participants (n = 3509). S}h d,"I  
Similar procedures were used for all stages of data collection EI?8/c  
at both surveys. A questionnaire was administered IFr"IOr'l  
including demographic, family and medical history. A !D{z. KO  
detailed eye examination included subjective refraction, Jia@HrLR  
slit-lamp (Topcon SL-7e camera, Topcon Optical Co, 3k>#z%//  
Tokyo, Japan) and retroillumination (Neitz CT-R camera, 1V[Zk lS  
Neitz Instrument Co, Tokyo, Japan) photography of the [ R8BcO(  
lens. Grading of lens photographs in the BMES has been 7;'UC','  
previously described [12]. Briefly, masked grading was BB3 a8  
performed on the lens photographs using the Wisconsin Z)~ ?foe'  
Cataract Grading System [13]. Cortical cataract and PSC &,P A+#  
were assessed from the retroillumination photographs by bxxLAWQ(  
estimating the percentage of the circular grid involved. B[YyA  
Cortical cataract was defined when cortical opacity yyu-y0_  
involved at least 5% of the total lens area. PSC was defined hTZ6@i/pS  
when opacity comprised at least 1% of the total lens area. O,^s)>c  
Slit-lamp photographs were used to assess nuclear cataract v_%6Ly  
using the Wisconsin standard set of four lens photographs yr>J^Et%_  
[13]. Nuclear cataract was defined when nuclear opacity =z9,=rR4  
was at least as great as the standard 4 photograph. Any cataract af6<w.i  
was defined to include persons who had previous #WG;p(?:  
cataract surgery as well as those with any of three cataract t'W6Fmwkx  
types. Inter-grader reliability was high, with weighted [D+PDR  
kappa 0.82 for cortical cataract, 0.55 (simple kappa 0.75) <x ;g9Z>(  
for nuclear cataract and 0.82 for PSC grading. The intragrader xZ2 1i QeN  
reliability for nuclear cataract was assessed with @(x]+*)  
simple kappa 0.83 for the senior grader who graded < T.R%Jys  
nuclear cataract at both surveys. All PSC cases were confirmed ^qC.bv]&  
by an ophthalmologist (PM). sP@XV/`3L6  
In cross-section I, 219 persons (6.0%) had missing or }>y~P~`S:  
ungradable Neitz photographs, leaving 3435 with photographs ~v/` `s  
available for cortical cataract and PSC assessment, 3bC-B!{;g  
while 1153 (31.6%) had randomly missing or ungradable UDJ#P9uy  
Topcon photographs due to a camera malfunction, leaving :Zq?V`+M  
2501 with photographs available for nuclear cataract ~/SLGyu  
assessment. Comparison of characteristics between participants ;*Y+.?>a  
with and without Neitz or Topcon photographs in Qqb%^}Xx'u  
cross-section I showed no statistically significant differences 3~WI3ZIR  
between the two groups, as reported previously ]NWcd~"b!Z  
[12]. In cross-section II, 441 persons (12.5%) had missing Oa@SyroF=  
or ungradable Neitz photographs, leaving 3068 for cortical qB$QC  
cataract and PSC assessment, and 648 (18.5%) had E'8XXV^I?P  
missing or ungradable Topcon photographs, leaving 2860 ~k 6V?z}  
for nuclear cataract assessment. @{<^rLt  
Data analysis was performed using the Statistical Analysis Z$Qwn  
System (SAS, SAS Institute, Cary, NC, USA). Age-adjusted  UiK)m:NU  
prevalence was calculated using direct standardization of +W[{UC4b  
the cross-section II population to the cross-section I population. 1)N#  
We assessed age-specific prevalence using an @1pfH\m  
interval of 5 years, so that participants within each age )&)tX.  
group were independent between the two cross-sectional T0@<u  
surveys. gK *=T  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 \)Mz UOZn  
Page 3 of 7 @v /Ae_q!  
(page number not for citation purposes) pwVGe|h%,  
Results G-o6~"J\  
Characteristics of the two survey populations have been &)!N 5Veb  
previously compared [14] and showed that age and sex PEKXPF N  
distributions were similar. Table 1 compares participant rXGaav9  
characteristics between the two cross-sections. Cross-section a(`"qS  
II participants generally had higher rates of diabetes, NPE 4@c_a@  
hypertension, myopia and more users of inhaled steroids. iN L>TVUM  
Cataract prevalence rates in cross-sections I and II are ="g9 >  
shown in Figure 1. The overall prevalence of cortical cataract 1yc$b+TH  
was 23.8% and 23.7% in cross-sections I and II, m{yq.H[X  
respectively (age-sex adjusted P = 0.81). Corresponding 2rf#Bq?7  
prevalence of PSC was 6.3% and 6.0% for the two crosssections ~ Bt >Y  
(age-sex adjusted P = 0.60). There was an [XA:pj;rg'  
increased prevalence of nuclear cataract, from 18.7% in }qhND-9#@  
cross-section I to 23.9% in cross-section II over the 6-year )b|xzj @  
period (age-sex adjusted P < 0.001). Prevalence of any cataract d8^S~7  
(including persons who had cataract surgery), however, 91FVe  
was relatively stable (46.9% and 46.8% in crosssections BDi+ *8  
I and II, respectively). TPi{c_ ]  
After age-standardization, these prevalence rates remained kh"APxQ79  
stable for cortical cataract (23.8% and 23.5% in the two wr6(C:  
surveys) and PSC (6.3% and 5.9%). The slightly increased dhr-tw  
prevalence of nuclear cataract (from 18.7% to 24.2%) was t1o_x}z4.  
not altered. ;Z&w"oSJ  
Table 2 shows the age-specific prevalence rates for cortical )EsFy6K:  
cataract, PSC and nuclear cataract in cross-sections I and C^ ~[b o  
II. A similar trend of increasing cataract prevalence with rWuqlx#  
increasing age was evident for all three types of cataract in kl5Y{![/&f  
both surveys. Comparing the age-specific prevalence ","to  
between the two surveys, a reduction in PSC prevalence in QLH6N mk  
cross-section II was observed in the older age groups (≥ 75 }Szs9-Wns  
years). In contrast, increased nuclear cataract prevalence Qy'-3GB  
in cross-section II was observed in the older age groups (≥ )!l1   
70 years). Age-specific cortical cataract prevalence was relatively fj y2\J!  
consistent between the two surveys, except for a d((,R@N'  
reduction in prevalence observed in the 80–84 age group n_t.l<V  
and an increasing prevalence in the older age groups (≥ 85 T'%R kag>  
years). F#l!LER^1g  
Similar gender differences in cataract prevalence were 0F[+rh"x  
observed in both surveys (Table 3). Higher prevalence of @9h6D<?  
cortical and nuclear cataract in women than men was evident pIvr*UzY  
but the difference was only significant for cortical RV6|sN[x>  
cataract (age-adjusted odds ratio, OR, for women 1.3, I- WR6s=  
95% confidence intervals, CI, 1.1–1.5 in cross-section I h_xzqElZu  
and OR 1.4, 95% CI 1.1–1.6 in cross-section II). In con- f:/"OCig  
Table 1: Participant characteristics. >L88`  
Characteristics Cross-section I Cross-section II Wg=4`&F^  
n % n % :stA]JB# w  
Age (mean) (66.2) (66.7) x@,B))WlGr  
50–54 485 13.3 350 10.0 |F?/L>  
55–59 534 14.6 580 16.5 %`^{Hh`  
60–64 638 17.5 600 17.1  u~j&g  
65–69 671 18.4 639 18.2 "v5jYz5M  
70–74 538 14.7 572 16.3 9 IY1"j0O  
75–79 422 11.6 407 11.6 #w]@yL]|is  
80–84 230 6.3 226 6.4 2g_ 2$)2  
85–89 100 2.7 110 3.1 8H2A<&3i  
90+ 36 1.0 24 0.7 =s h]H$  
Female 2072 56.7 1998 57.0 G}gmkp]z  
Ever Smokers 1784 51.2 1789 51.2 '645Fr[lg  
Use of inhaled steroids 370 10.94 478 13.8^ rsC^Re:*jr  
History of: aA&}=lm  
Diabetes 284 7.8 347 9.9^ 1A;f[Rze  
Hypertension 1669 46.0 1825 52.2^ -!pg1w06  
Emmetropia* 1558 42.9 1478 42.2 #)EVi7UP  
Myopia* 442 12.2 495 14.1^ jL9to6 Hmr  
Hyperopia* 1633 45.0 1532 43.7 jij-pDQnv  
n = number of persons affected gqQ"'SRw  
* best spherical equivalent refraction correction  f|-%.,  
^ P < 0.01 R7~#7qKQB  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 J:Ncy}AO  
Page 4 of 7 "o>gX'm*  
(page number not for citation purposes) p;YS`*!s  
t W>(p4m  
rast, men had slightly higher PSC prevalence than women I 7s}{pG  
in both cross-sections but the difference was not significant @6:J$B~)u  
(OR 1.1, 95% CI 0.8–1.4 for men in cross-section I w2e 9Ue~WH  
and OR 1.2, 95% 0.9–1.6 in cross-section II). :x/L.Bz  
Discussion k&S I -jxj  
Findings from two surveys of BMES cross-sectional populations Ob>M]udn  
with similar age and gender distribution showed M|uWSG  
that the prevalence of cortical cataract and PSC remained U fAN)SE"  
stable, while the prevalence of nuclear cataract appeared 5t-dvYgU  
to have increased. Comparison of age-specific prevalence, |\_d^U &`  
with totally independent samples within each age group, e:kd0)9  
confirmed the robustness of our findings from the two 76rRF   
survey samples. Although lens photographs taken from Z/w "zCd  
the two surveys were graded for nuclear cataract by the Ed=]RR 4R  
same graders, who documented a high inter- and intragrader EoD[,:*  
reliability, we cannot exclude the possibility that STY\c5  
variations in photography, performed by different photographers,  i#W0  
may have contributed to the observed difference hAv.rjhw_  
in nuclear cataract prevalence. However, the overall t;e+WZkV  
Table 2: Age-specific prevalence of cataract types in cross sections I and II. X9 oxni#  
Cataract type Age (years) Cross-section I Cross-section II -^+!:0';  
n % (95% CL)* n % (95% CL)* ^jx V  
Cortical 50–54 473 4.4 (2.6–6.3) 338 7.4 (4.6–10.2) gV-x1s+  
55–59 522 9.2 (6.7–11.7) 542 9.0 (6.6–11.5) X=U>r  
60–64 615 16.4 (13.5–19.4) 556 16.7 (13.6–19.8) + Ip C  
65–69 653 26.2 (22.8–29.6) 581 23.6 (20.1–27.0) Gcz@z1a=n  
70–74 516 31.2 (27.2–35.2) 514 35.4 (31.3–39.6) e;ej/)no`  
75–79 366 40.2 (35.1–45.2) 332 39.8 (34.5–45.1) i1E~F  
80–84 194 58.8 (51.8–65.8) 163 42.9 (35.3–50.6) }u aRS9d  
85–89 74 52.7 (41.1–64.4) 73 54.8 (43.1–66.5) vOKWi:-U  
90+ 22 68.2 (47.0–89.3) 14 78.6 (54.0–103.2) G^Q8B^Lg  
PSC 50–54 474 2.7 (1.3–4.2) 338 2.4 (0.7–4.0) <B %s9Zy  
55–59 522 2.9 (1.4–4.3) 541 2.6 (1.3–3.9) t'pY~a9F  
60–64 616 4.6 (2.9–6.2) 548 5.7 (3.7–7.6) '**dD2 n  
65–69 655 6.3 (4.4–8.1) 573 4.5 (2.8–6.3) ,|r%tNh<8$  
70–74 517 6.8 (4.6–8.9) 505 9.7 (7.1–12.3) E0o?rgfdq  
75–79 367 11.4 (8.2–14.7) 327 9.5 (6.3–12.7) ~7}aW#  
80–84 196 12.2 (7.6–16.9) 155 10.3 (5.5–15.2) fi.[a8w:W  
85–89 74 18.9 (9.8–28.1) 69 11.6 (3.9–19.4) 5!p of\/a  
90+ 23 21.7 (3.5–40.0) 11 0.0 3r]:k) J  
Nuclear 50–54 323 1.6 (0.2–2.9) 331 0.9 (–0.2–1.9) l9eCsVQ~V  
55–59 386 2.3 (0.8–3.8) 507 3.6 (1.9–5.2) fd<a%nSD  
60–64 453 5.3 (3.2–7.4) 501 11.6 (8.8–14.4) wG\ +C'&~  
65–69 478 17.2 (13.8–20.1) 534 18.5 (15.2–21.9) " A}S92  
70–74 392 27.6 (23.1–32.0) 453 36.0 (31.6–40.4) nGqD{!i<  
75–79 255 45.1 (39.0–51.3) 302 55.6 (50.0–61.3) AsOkOS3  
80–84 146 54.1 (45.9–62.3) 147 73.5 (66.3–80.7) sD!)=t_  
85–89 50 64.0 (50.2–77.8) 70 80.0 (70.4–89.6) E9"P~ nz  
90+ 18 72.2 (49.3–95.1) 15 73.3 (48.0–98.7) ..5rW0lr  
n = number of persons 4|#@41\ B  
* 95% Confidence Limits =>kE`"{!  
Cataract FMioguunrtea i1n ps rEeyvea lSetnucdey in cross-sections I and II of the Blue ;;#_[Zl  
Cataract prevalence in cross-sections I and II of the Blue 2`?58&  
Mountains Eye Study. 7`c\~_Df_  
0 b,tf]Z-  
10 Fzc8)*w  
20 pp2,d`01[L  
30 !)1gGXRY  
40 Us.")GiHE  
50 L xg,BZV  
cortical PSC nuclear any lzE{e6  
cataract =G9 9U/  
Cataract type BIk0n;Kz<L  
% C;UqLMrOI  
Cross-section I %lbDcEsf9  
Cross-section II `Nnaw+<]  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 Nf!g1D"U  
Page 5 of 7 b:M1P&R  
(page number not for citation purposes) Y_gMoo  
prevalence of any cataract (including cataract surgery) was <y}9Twdy  
relatively stable over the 6-year period. J_|LG rt})  
Although different population-based studies used different 2YbI."o b  
grading systems to assess cataract [15], the overall $5]}]  
prevalence of the three cataract types were similar across 4!</JZX~$  
different study populations [12,16-23]. Most studies have ^c-8~r|y,  
suggested that nuclear cataract is the most prevalent type Pss$[ %  
of cataract, followed by cortical cataract [16-20]. Ours and d$H   
other studies reported that cortical cataract was the most IrMUw$  
prevalent type [12,21-23]. AbExJ~JV\g  
Our age-specific prevalence data show a reduction of a$AR   
15.9% in cortical cataract prevalence for the 80–84 year vmj'X>Q  
age group, concordant with an increase in cataract surgery x<'<E@jpU;  
prevalence by 9% in those aged 80+ years observed in the K7-z.WTUR  
same study population [10]. Although cortical cataract is hE;|VSdo  
thought to be the least likely cataract type leading to a cataract w:VD[\h  
surgery, this may not be the case in all older persons. M/mm2?4  
A relatively stable cortical cataract and PSC prevalence &Yklf?EZ>Q  
over the 6-year period is expected. We cannot offer a DuMzK%  
definitive explanation for the increase in nuclear cataract _yRD*2 !;  
prevalence. A possible explanation could be that a moderate DP8%/CV!*  
level of nuclear cataract causes less visual disturbance `6:B0-r  
than the other two types of cataract, thus for the oldest age Z_h-5VU-  
groups, persons with nuclear cataract could have been less jf^BEz5  
likely to have surgery unless it is very dense or co-existing (uVL!%61k  
with cortical cataract or PSC. Previous studies have shown KDS} "/  
that functional vision and reading performance were high _M) G  
in patients undergoing cataract surgery who had nuclear zMXQfR   
cataract only compared to those with mixed type of cataract % aqP{mOO  
(nuclear and cortical) or PSC [24,25]. In addition, the bgYUsc*uR  
overall prevalence of any cataract (including cataract surgery) &\y`9QpVF  
was similar in the two cross-sections, which appears ^~;"$=Wf  
to support our speculation that in the oldest age group, cSTF$62E  
nuclear cataract may have been less likely to be operated TjE'X2/  
than the other two types of cataract. This could have *>h|<|T'  
resulted in an increased nuclear cataract prevalence (due z*UgRLKZD  
to less being operated), compensated by the decreased IG Ax+3V  
prevalence of cortical cataract and PSC (due to these being ?2%;VKN4  
more likely to be operated), leading to stable overall prevalence i IM\_<?  
of any cataract. zP&D  
Possible selection bias arising from selective survival .b? Aq^i8  
among persons without cataract could have led to underestimation f_2(`T#  
of cataract prevalence in both surveys. We X;1yQ |su  
assume that such an underestimation occurred equally in dmWCNeja.  
both surveys, and thus should not have influenced our 5eiKMKW[  
assessment of temporal changes. .JOZ2QWm<  
Measurement error could also have partially contributed $^_6,uBM[  
to the observed difference in nuclear cataract prevalence. q B IekQT  
Assessment of nuclear cataract from photographs is a fx-8mf3  
potentially subjective process that can be influenced by l,*5*1lM  
variations in photography (light exposure, focus and the 15S& ,$ 1&  
slit-lamp angle when the photograph was taken) and 6e8 gFQ"w2  
grading. Although we used the same Topcon slit-lamp Bi2 c5[3  
camera and the same two graders who graded photos gyb99c,)  
from both surveys, we are still not able to exclude the possibility Bf.iRh0Q5  
of a partial influence from photographic variation \wD L oR  
on this result. <F8e? xy  
A similar gender difference (women having a higher rate j9rxu$N+  
than men) in cortical cataract prevalence was observed in ! B92W  
both surveys. Our findings are in keeping with observations *7E#=xb  
from the Beaver Dam Eye Study [18], the Barbados zn>+ \  
Eye Study [22] and the Lens Opacities Case-Control e=nvm'[h  
Group [26]. It has been suggested that the difference Mg2e0}{  
could be related to hormonal factors [18,22]. A previous 1BEs> Sm  
study on biochemical factors and cataract showed that a 8ok=&Gq4  
lower level of iron was associated with an increased risk of KZTLIZxI-  
cortical cataract [27]. No interaction between sex and biochemical b8_F2  
factors were detected and no gender difference LP=y$B  
was assessed in this study [27]. The gender difference seen t>AOF\  
in cortical cataract could be related to relatively low iron y%X! l(gQ  
levels and low hemoglobin concentration usually seen in 9|lLce$  
women [28]. Diabetes is a known risk factor for cortical 0QT:@v2R  
Table 3: Gender distribution of cataract types in cross-sections I and II. Gx8!AmeX  
Cataract type Gender Cross-section I Cross-section II YVwpqOE.=  
n % (95% CL)* n % (95% CL)*  |iI dm  
Cortical Male 1496 21.1 (19.0–23.1) 1328 20.4 (18.2–22.6) <zL_6Y2  
Female 1939 25.9 (23.9–27.8) 1785 26.2 (24.2–28.3) .>eRX%  
PSC Male 1500 6.5 (5.2–7.7) 1314 6.4 (5.1–7.7) P1Z"}Qw  
Female 1944 6.2 (5.1–7.2) 1753 5.7 (4.6–6.7) Scx!h.\5  
Nuclear Male 1106 17.6 (15.4–19.9) 1225 22.5 (20.1–24.8) e`S\-t?Z  
Female 1395 19.5 (17.4–21.6) 1635 25.0 (22.9–27.1) /IG{j}  
n = number of persons D*Zj oU  
* 95% Confidence Limits $L 8>Ha}  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 L2,2Sn*4i  
Page 6 of 7 !8[T*'LJ-  
(page number not for citation purposes) W-l+%T!  
cataract but in this particular population diabetes is more @ <{%r  
prevalent in men than women in all age groups [29]. Differential "qNFDr(WM  
exposures to cataract risk factors or different dietary VaY#_80$s  
or lifestyle patterns between men and women may 5, ,~k=  
also be related to these observations and warrant further NX,m6u  
study. jkx>o?s)z  
Conclusion &F uPd}F  
In summary, in two population-based surveys 6 years rP3tFvOH  
apart, we have documented a relatively stable prevalence 7%i'F=LzT  
of cortical cataract and PSC over the period. The observed [M[<'+^*  
overall increased nuclear cataract prevalence by 5% over a )0-A;X2  
6-year period needs confirmation by future studies, and !:!(=(4$P  
reasons for such an increase deserve further study. \ saV8U7B  
Competing interests BV B2$&eJ  
The author(s) declare that they have no competing interests. !xfDWbvHV  
Authors' contributions % -!%n= P  
AGT graded the photographs, performed literature search |y U!d %  
and wrote the first draft of the manuscript. JJW graded the T0tX%_6`  
photographs, critically reviewed and modified the manuscript. <#h,_WP*  
ER performed the statistical analysis and critically ZPmqoR[  
reviewed the manuscript. PM designed and directed the -/pz3n  
study, adjudicated cataract cases and critically reviewed G0UaE1n  
and modified the manuscript. All authors read and F<,pAxl~@  
approved the final manuscript. T;92M}\  
Acknowledgements R^.PKT2E  
This study was supported by the Australian National Health & Medical YCD |lL#  
Research Council, Canberra, Australia (Grant Nos 974159, 991407). The ;DuVb2~+  
abstract was presented at the Association for Research in Vision and Ophthalmology Vc(4d-d5  
(ARVO) meeting in Fort Lauderdale, Florida, USA, May 2005. y''~j<'  
References 5v)^4( )  
1. Congdon N, O'Colmain B, Klaver CC, Klein R, Munoz B, Friedman _u[tv,  
DS, Kempen J, Taylor HR, Mitchell P: Causes and prevalence of OJcS%-~  
visual impairment among adults in the United States. Arch yjjq&Cn  
Ophthalmol 2004, 122(4):477-485. .t_t)'L  
2. Rahmani B, Tielsch JM, Katz J, Gottsch J, Quigley H, Javitt J, Sommer !i;6!w  
A: The cause-specific prevalence of visual impairment in an N:<$]x>  
urban population. The Baltimore Eye Survey. Ophthalmology ty,oj33  
1996, 103:1721-1726. ^aSb~lce  
3. Keeffe JE, Konyama K, Taylor HR: Vision impairment in the sG`x |%t  
Pacific region. Br J Ophthalmol 2002, 86:605-610. \ASt&'E  
4. Reidy A, Minassian DC, Vafidis G, Joseph J, Farrow S, Wu J, Desai P, Keh=>K)T  
Connolly A: Prevalence of serious eye disease and visual iwK.*07+  
impairment in a north London population: population based, m.K cTM%j  
cross sectional study. BMJ 1998, 316:1643-1646. xsH1)  
5. Resnikoff S, Pascolini D, Etya'ale D, Kocur I, Pararajasegaram R, |T|m5V'l  
Pokharel GP, Mariotti SP: Global data on visual impairment in ZA(u"T~  
the year 2002. Bull World Health Organ 2004, 82:844-851. +Uq|Yh'Q  
6. Pascolini D, Mariotti SP, Pokharel GP, Pararajasegaram R, Etya'ale D, #d@wjQ0DW  
Negrel AD, Resnikoff S: 2002 global update of available data on A<+Dx  
visual impairment: a compilation of population-based prevalence aJ+V]WmA  
studies. Ophthalmic Epidemiol 2004, 11:67-115. ;:6\w!fc  
7. Rochtchina E, Mukesh BN, Wang JJ, McCarty CA, Taylor HR, Mitchell Z mJ<h&  
P: Projected prevalence of age-related cataract and cataract nQiZ6[L  
surgery in Australia for the years 2001 and 2021: pooled data z5jw\jBD  
from two population-based surveys. Clin Experiment Ophthalmol e(t}$Q=  
2003, 31:233-236. zgwe z$  
8. Medicare Benefits Schedule Statistics [http://www.medicar ' h7Faj  
eaustralia.gov.au/statistics/dyn_mbs/forms/mbs_tab4.shtml] ;QBS0x \f@  
9. Keeffe JE, Taylor HR: Cataract surgery in Australia 1985–94. VhO%4[Jl  
Aust N Z J Ophthalmol 1996, 24:313-317. |oPRP1F-;e  
10. Tan AG, Wang JJ, Rochtchina E, Jakobsen K, Mitchell P: Increase in K?uZIDo  
cataract surgery prevalence from 1992–1994 to 1997–2000: CYaN;HV@_  
Analysis of two population cross-sections. Clin Experiment Ophthalmol b}K,wAx  
2004, 32:284-288. @su<h\)  
11. Mitchell P, Smith W, Attebo K, Wang JJ: Prevalence of age-related y \skke]  
maculopathy in Australia. The Blue Mountains Eye Study. gQeQy  
Ophthalmology 1995, 102:1450-1460. L2XhrLK.|  
12. Mitchell P, Cumming RG, Attebo K, Panchapakesan J: Prevalence of "`% ,l|D  
cataract in Australia: the Blue Mountains eye study. Ophthalmology Cab.a)o  
1997, 104:581-588. P{o)Ir8Tt  
13. Klein BEK, Magli YL, Neider MW, Klein R: Wisconsin system for classification 0-Mzb{n5  
of cataracts from photographs (protocol) Madison, WI; 1990. 4LTm&+(5  
14. Foran S, Wang JJ, Mitchell P: Causes of visual impairment in two ;iKLf~a a  
older population cross-sections: the Blue Mountains Eye Xz^nm\  
Study. Ophthalmic Epidemiol 2003, 10:215-225. JN wI{  
15. Congdon N, Vingerling JR, Klein BE, West S, Friedman DS, Kempen J, \W*L9azr  
O'Colmain B, Wu SY, Taylor HR: Prevalence of cataract and G[k3`  
pseudophakia/aphakia among adults in the United States. pAy4%|(  
Arch Ophthalmol 2004, 122:487-494. b? ); D  
16. Sperduto RD, Hiller R: The prevalence of nuclear, cortical, and l'"nU6B&  
posterior subcapsular lens opacities in a general population /QQRy_Z1)  
sample. Ophthalmology 1984, 91:815-818. 23?u_?+4i  
17. Adamsons I, Munoz B, Enger C, Taylor HR: Prevalence of lens ;I4vPh5Q  
opacities in surgical and general populations. Arch Ophthalmol KuP#i]Na  
1991, 109:993-997. g#$ C8k  
18. Klein BE, Klein R, Linton KL: Prevalence of age-related lens [.}qi[=n  
opacities in a population. The Beaver Dam Eye Study. Ophthalmology n#">k%bD  
1992, 99:546-552. T~E;@weR  
19. West SK, Munoz B, Schein OD, Duncan DD, Rubin GS: Racial differences nCq'=L,m  
in lens opacities: the Salisbury Eye Evaluation (SEE) ;^ME  
project. Am J Epidemiol 1998, 148:1033-1039. 5&n:i,  
20. Congdon N, West SK, Buhrmann RR, Kouzis A, Munoz B, Mkocha H: _.JQ h   
Prevalence of the different types of age-related cataract in hL3up]pZ  
an African population. Invest Ophthalmol Vis Sci 2001, 3RtVFDIZA"  
42:2478-2482. :`N&BV  
21. Livingston PM, Guest CS, Stanislavsky Y, Lee S, Bayley S, Walker C, )E.AY  
McKean C, Taylor HR: A population-based estimate of cataract }eLApFHEDg  
prevalence: the Melbourne Visual Impairment Project experience. L/u|90) L  
Dev Ophthalmol 1994, 26:1-6. eX$KH;M  
22. Leske MC, Connell AM, Wu SY, Hyman L, Schachat A: Prevalence X;!*D  
of lens opacities in the Barbados Eye Study. Arch Ophthalmol 7rd mj[vu  
1997, 115:105-111. published erratum appears in Arch Ophthalmol 4#(/{6J  
1997 Jul;115(7):931 I2/am8!u%  
23. Seah SK, Wong TY, Foster PJ, Ng TP, Johnson GJ: Prevalence of % G!!0V!  
lens opacity in Chinese residents of Singapore: the tanjong fK7 ?"^`/  
pagar survey. Ophthalmology 2002, 109:2058-2064. "bej#'M#  
24. Stifter E, Sacu S, Weghaupt H, Konig F, Richter-Muksch S, Thaler A, 8[@,i|kgg0  
Velikay-Parel M, Radner W: Reading performance depending on ajycYk9<m  
the type of cataract and its predictability on the visual outcome. Cj>HMB}  
J Cataract Refract Surg 2004, 30:1259-1267. }Cu:BD.zQ  
25. Stifter E, Sacu S, Weghaupt H: Functional vision with cataracts of w,IJ44f ^%  
different morphologies: comparative study. J Cataract Refract RJ?)O#}  
Surg 2004, 30:1883-1891. qXtC7uNj$  
26. Leske MC, Chylack LT Jr, Wu SY: The Lens Opacities Case-Control Sd6O?&(  
Study. Risk factors for cataract. Arch Ophthalmol 1991, G+=G c(J  
109:244-251. "7sv@I_j  
27. Leske MC, Wu SY, Hyman L, Sperduto R, Underwood B, Chylack LT, QP(d77 n  
Milton RC, Srivastava S, Ansari N: Biochemical factors in the lens Sv#MlS>  
opacities. Case-control study. The Lens Opacities Case-Control ZW?h\0Hh  
Study Group. Arch Ophthalmol 1995, 113:1113-1119. \8#[AD*@s2  
28. Yip R, Johnson C, Dallman PR: Age-related changes in laboratory N@PuC>  
values used in the diagnosis of anemia and iron deficiency. #_ulmB;  
Am J Clin Nutr 1984, 39:427-436. \L>XF'o  
29. Mitchell P, Smith W, Wang JJ, Cumming RG, Leeder SR, Burnett L: 3fLdceT  
Diabetes in an older Australian population. Diabetes Res Clin :'r* 5EX  
Pract 1998, 41:177-184. /[ m7~B]QE  
Pre-publication history yPmo1|'X>d  
The pre-publication history for this paper can be accessed npeL1zO-$  
here: \X %#-y  
Publish with BioMed Central and every ?n<F?~  
scientist can read your work free of charge to13&#o  
"BioMed Central will be the most significant development for %(s|  
disseminating the results of biomedical research in our lifetime." \@PMj"p|:  
Sir Paul Nurse, Cancer Research UK MNU7O X<  
Your research papers will be: (f"Qz~R|6_  
available free of charge to the entire biomedical community )*%uG{h  
peer reviewed and published immediately upon acceptance zecM|S_  
cited in PubMed and archived on PubMed Central ]pNM~,  
yours — you keep the copyright =_&,^h@'3e  
Submit your manuscript here: tY#&_%W  
http://www.biomedcentral.com/info/publishing_adv.asp zk }SEt-  
BioMedcentral !rgXB(  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 &7kLSb&|;  
Page 7 of 7 0R unex[  
(page number not for citation purposes) 3q'nO-KJ  
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