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 OcIJT1  
Page 1 of 7 `Y$LXF~,Om  
(page number not for citation purposes) Z*kg= hs^  
BMC Ophthalmology OyTBgS G?a  
Research article Open Access 69CH W&  
Comparison of age-specific cataract prevalence in two J 9>uLz  
population-based surveys 6 years apart <5q:mG88  
Ava Grace Tan†, Jie Jin Wang*†, Elena Rochtchina† and Paul Mitchell† 9jJ&QACn  
Address: Centre for Vision Research, Westmead Millennium Institute, Department of Ophthalmology, University of Sydney, Westmead Hospital, {n |Ra[9_  
Westmead, NSW, Australia Mi:$<fEX  
Email: Ava Grace Tan - ava_tan@wmi.usyd.edu.au; Jie Jin Wang* - jiejin_wang@wmi.usyd.edu.au; +tlTH K  
Elena Rochtchina - elena_rochtchina@wmi.usyd.edu.au; Paul Mitchell - paul_mitchell@wmi.usyd.edu.au Elm/T]6  
* Corresponding author †Equal contributors a^~l[HSF  
Abstract Gu&zplB  
Background: In this study, we aimed to compare age-specific cortical, nuclear and posterior {:'e H  
subcapsular (PSC) cataract prevalence in two surveys 6 years apart. <Gs)~T#'  
Methods: The Blue Mountains Eye Study examined 3654 participants (82.4% of those eligible) in = V%s^  
cross-section I (1992–4) and 3509 participants (75.1% of survivors and 85.2% of newly eligible) in &Zq43~  
cross-section II (1997–2000, 66.5% overlap with cross-section I). Cataract was assessed from lens /GfC/)1_  
photographs following the Wisconsin Cataract Grading System. Cortical cataract was defined if 64`V+Hd  
cortical opacity comprised ≥ 5% of lens area. Nuclear cataract was defined if nuclear opacity ≥ xZbm,. v  
Wisconsin standard 4. PSC was defined if any present. Any cataract was defined to include persons )2 u=U9  
who had previous cataract surgery. Weighted kappa for inter-grader reliability was 0.82, 0.55 and =f=MtH?0y  
0.82 for cortical, nuclear and PSC cataract, respectively. We assessed age-specific prevalence using |.)dOk,o  
an interval of 5 years, so that participants within each age group were independent between the wD}[XE?S  
two surveys. ~kw[Aw3?D\  
Results: Age and gender distributions were similar between the two populations. The age-specific 4vGkg H<,  
prevalence of cortical (23.8% in 1st, 23.7% in 2nd) and PSC cataract (6.3%, 6.0%) was similar. The V5%B ,.d:  
prevalence of nuclear cataract increased slightly from 18.7% to 23.9%. After age standardization, i wQ'=M  
the similar prevalence of cortical (23.8%, 23.5%) and PSC cataract (6.3%, 5.9%), and the increased Ah) _mxK  
prevalence of nuclear cataract (18.7%, 24.2%) remained. l 0jjLqm:  
Conclusion: In two surveys of two population-based samples with similar age and gender ;' YM@n  
distributions, we found a relatively stable cortical and PSC cataract prevalence over a 6-year period. >mi%L3Pk  
The increased prevalence of nuclear cataract deserves further study. fQ 'P2$  
Background ,]42v?  
Age-related cataract is the leading cause of reversible visual bu,Z'  
impairment in older persons [1-6]. In Australia, it is lm o>z'<  
estimated that by the year 2021, the number of people & tkkn2t  
affected by cataract will increase by 63%, due to population -Q<3Q_  
aging [7]. Surgical intervention is an effective treatment o5 @ l!NQ  
for cataract and normal vision (> 20/40) can usually !2>gC"$nv  
be restored with intraocular lens (IOL) implantation. <RKh%4#~  
Cataract surgery with IOL implantation is currently the =YR/X@&  
most commonly performed, and is, arguably, the most "=MRzSke3  
cost effective surgical procedure worldwide. Performance dNB56E)5`J  
Published: 20 April 2006 #Kyb9Qg  
BMC Ophthalmology 2006, 6:17 doi:10.1186/1471-2415-6-17 %19TJn%J$  
Received: 14 December 2005 %($sj| _l  
Accepted: 20 April 2006 #E3Y; b%v  
This article is available from: http://www.biomedcentral.com/1471-2415/6/17 9(dbou  
© 2006 Tan et al; licensee BioMed Central Ltd. RM|<(kq  
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), 5Y"JRWC  
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. X8~ cWW  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 r77?s?  
Page 2 of 7 ff**)Xdh  
(page number not for citation purposes) H5j~<@STC  
of this surgical procedure has been continuously increasing osB[KRT>("  
in the last two decades. Data from the Australian cfyN)#9  
Health Insurance Commission has shown a steady 4E}]>  
increase in Medicare claims for cataract surgery [8]. A 2.6-  )f>s\T  
fold increase in the total number of cataract procedures zHw[`"[  
from 1985 to 1994 has been documented in Australia [9]. RcitW;{|Kg  
The rate of cataract surgery per thousand persons aged 65 /m%i"kki  
years or older has doubled in the last 20 years [8,9]. In the m/r4f279  
Blue Mountains Eye Study population, we observed a onethird Sp: `Z1kH  
increase in cataract surgery prevalence over a mean a]|P rjPI  
6-year interval, from 6% to nearly 8% in two cross-sectional t5G@M&d4Eo  
population-based samples with a similar age range #8z2>&:|  
[10]. Further increases in cataract surgery performance !>W _3Ea  
would be expected as a result of improved surgical skills g|tnYN  
and technique, together with extending cataract surgical B v /]>Z  
benefits to a greater number of older people and an %?1k}(qUeY  
increased number of persons with surgery performed on [vV]lWOp'  
both eyes. M^DYzJ  
Both the prevalence and incidence of age-related cataract +K,]#$k  
link directly to the demand for, and the outcome of, cataract `O ?61YUQH  
surgery and eye health care provision. This report 422d4Zu  
aimed to assess temporal changes in the prevalence of cortical '+LC.lM  
and nuclear cataract and posterior subcapsular cataract {>'GE16x  
(PSC) in two cross-sectional population-based >u? pq6;  
surveys 6 years apart. 8%q:lI  
Methods 60(j[d-$p  
The Blue Mountains Eye Study (BMES) is a populationbased E9JxntX  
cohort study of common eye diseases and other [Zc8tE2oN  
health outcomes. The study involved eligible permanent N# $ob 9  
residents aged 49 years and older, living in two postcode aGY R:jR$  
areas in the Blue Mountains, west of Sydney, Australia. _3v6c  
Participants were identified through a census and were J3`a}LyDf  
invited to participate. The study was approved at each 5nC#<EE  
stage of the data collection by the Human Ethics Committees %X)w$}WH  
of the University of Sydney and the Western Sydney xe9E</M_  
Area Health Service and adhered to the recommendations =Ji+GJ <,9  
of the Declaration of Helsinki. Written informed consent ,`kag~bZ  
was obtained from each participant. t+7|/GLs2  
Details of the methods used in this study have been |hHj7X <?k  
described previously [11]. The baseline examinations n$]78\C  
(BMES cross-section I) were conducted during 1992– R.nAD{>h*  
1994 and included 3654 (82.4%) of 4433 eligible residents. $=&a 0O#  
Follow-up examinations (BMES IIA) were conducted !j8.JP}!)  
during 1997–1999, with 2335 (75.0% of BMES r:rM~``  
cross section I survivors) participating. A repeat census of {yj8LxX^  
the same area was performed in 1999 and identified 1378 &|6 A 8,  
newly eligible residents who moved into the area or the ?xkw~3Yfi  
eligible age group. During 1999–2000, 1174 (85.2%) of NJ%>|`FEi7  
this group participated in an extension study (BMES IIB). LsW7JIQd  
BMES cross-section II thus includes BMES IIA (66.5%) ^~dBO %M^  
and BMES IIB (33.5%) participants (n = 3509). `LroH>_  
Similar procedures were used for all stages of data collection VK)vb.:  
at both surveys. A questionnaire was administered kJP` C\4}f  
including demographic, family and medical history. A 3haR/Y N  
detailed eye examination included subjective refraction, =qWcw7!"  
slit-lamp (Topcon SL-7e camera, Topcon Optical Co,  m[>pv1o  
Tokyo, Japan) and retroillumination (Neitz CT-R camera, p+.xye U(  
Neitz Instrument Co, Tokyo, Japan) photography of the EOj.Jrs~  
lens. Grading of lens photographs in the BMES has been D(X:dB50@  
previously described [12]. Briefly, masked grading was jx=5 E6(h  
performed on the lens photographs using the Wisconsin )(/Bw&$  
Cataract Grading System [13]. Cortical cataract and PSC 6?`3zdOeO  
were assessed from the retroillumination photographs by , tEd>  
estimating the percentage of the circular grid involved. f,(@K%  
Cortical cataract was defined when cortical opacity 0F5QAR O  
involved at least 5% of the total lens area. PSC was defined y 1I(^<qO=  
when opacity comprised at least 1% of the total lens area. F'^y?UP[  
Slit-lamp photographs were used to assess nuclear cataract kJ_XG;8  
using the Wisconsin standard set of four lens photographs hpBn_  
[13]. Nuclear cataract was defined when nuclear opacity Hw\hTTK  
was at least as great as the standard 4 photograph. Any cataract eZbT;  
was defined to include persons who had previous _8{6&AmIw  
cataract surgery as well as those with any of three cataract 3E$h  W  
types. Inter-grader reliability was high, with weighted G0mvrc- (  
kappa 0.82 for cortical cataract, 0.55 (simple kappa 0.75) 8(@ Y@`/  
for nuclear cataract and 0.82 for PSC grading. The intragrader 3bK=Q3N  
reliability for nuclear cataract was assessed with 5M= S7B3=  
simple kappa 0.83 for the senior grader who graded k%K\~U8"  
nuclear cataract at both surveys. All PSC cases were confirmed # n\|Q\W  
by an ophthalmologist (PM). +9NI=s6  
In cross-section I, 219 persons (6.0%) had missing or jlM %Y ZC  
ungradable Neitz photographs, leaving 3435 with photographs BnPL>11Y  
available for cortical cataract and PSC assessment, +V,Ld&r  
while 1153 (31.6%) had randomly missing or ungradable <=gf|(  
Topcon photographs due to a camera malfunction, leaving ;yDXo\g m  
2501 with photographs available for nuclear cataract Y}hz UKJ  
assessment. Comparison of characteristics between participants <xaB$}R  
with and without Neitz or Topcon photographs in EWp'zbWP  
cross-section I showed no statistically significant differences  rT!9{uK  
between the two groups, as reported previously kT ,2eel  
[12]. In cross-section II, 441 persons (12.5%) had missing ^SJa/I EZ.  
or ungradable Neitz photographs, leaving 3068 for cortical InfUH8./t  
cataract and PSC assessment, and 648 (18.5%) had >YP ]IQ  
missing or ungradable Topcon photographs, leaving 2860 1Jn: huV2  
for nuclear cataract assessment. %q5iy0~P  
Data analysis was performed using the Statistical Analysis ba"a!#wA  
System (SAS, SAS Institute, Cary, NC, USA). Age-adjusted 8+U':xR  
prevalence was calculated using direct standardization of K0\Wty0  
the cross-section II population to the cross-section I population. ^`Qh*:T$  
We assessed age-specific prevalence using an x|IG'R1:Y  
interval of 5 years, so that participants within each age pgU4>tyD  
group were independent between the two cross-sectional ,';+A{aV  
surveys. _=oNQ  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 D[iIj_CKQ  
Page 3 of 7 !>L+q@l)  
(page number not for citation purposes) 26\*x  
Results ne\N1`AU  
Characteristics of the two survey populations have been B\ a#Vtyut  
previously compared [14] and showed that age and sex QWWoj[d#  
distributions were similar. Table 1 compares participant h8uDs|O9n  
characteristics between the two cross-sections. Cross-section BA+:}81&<q  
II participants generally had higher rates of diabetes, -?AaRwZ,  
hypertension, myopia and more users of inhaled steroids. 3((53@s98  
Cataract prevalence rates in cross-sections I and II are B(%b Bhs  
shown in Figure 1. The overall prevalence of cortical cataract .cX,"2;n  
was 23.8% and 23.7% in cross-sections I and II, sP NAG  
respectively (age-sex adjusted P = 0.81). Corresponding jn;b{*Lf  
prevalence of PSC was 6.3% and 6.0% for the two crosssections 7F{=bL  
(age-sex adjusted P = 0.60). There was an ]m(5>h#  
increased prevalence of nuclear cataract, from 18.7% in >MIp r  
cross-section I to 23.9% in cross-section II over the 6-year m'%Z53&  
period (age-sex adjusted P < 0.001). Prevalence of any cataract r,4V SyZF\  
(including persons who had cataract surgery), however, jdYv*/^  
was relatively stable (46.9% and 46.8% in crosssections )>LC*_v  
I and II, respectively). {&c%VVZb:Z  
After age-standardization, these prevalence rates remained ,b@0Qa"  
stable for cortical cataract (23.8% and 23.5% in the two NB&u^8b  
surveys) and PSC (6.3% and 5.9%). The slightly increased *X;g Y  
prevalence of nuclear cataract (from 18.7% to 24.2%) was "A:wWb< m  
not altered. LE Y Y{G?  
Table 2 shows the age-specific prevalence rates for cortical Ac.z6]p  
cataract, PSC and nuclear cataract in cross-sections I and <][|,9mw  
II. A similar trend of increasing cataract prevalence with 7q|(ZZa  
increasing age was evident for all three types of cataract in 7@vc Qv kC  
both surveys. Comparing the age-specific prevalence r\[HR ^`  
between the two surveys, a reduction in PSC prevalence in U & Ay3/  
cross-section II was observed in the older age groups (≥ 75 EW4XFP4 c  
years). In contrast, increased nuclear cataract prevalence &nn.h@zje  
in cross-section II was observed in the older age groups (≥ (p14{  
70 years). Age-specific cortical cataract prevalence was relatively ;g m){ g  
consistent between the two surveys, except for a {=g-zsc]K  
reduction in prevalence observed in the 80–84 age group v:6b&wS L3  
and an increasing prevalence in the older age groups (≥ 85 C [2tH2*#  
years). ydns_Z  
Similar gender differences in cataract prevalence were Op%^dwVG(v  
observed in both surveys (Table 3). Higher prevalence of KH KqE6  
cortical and nuclear cataract in women than men was evident N%B#f\N  
but the difference was only significant for cortical  Uero!+_  
cataract (age-adjusted odds ratio, OR, for women 1.3, n1ED _9  
95% confidence intervals, CI, 1.1–1.5 in cross-section I <01B\t7  
and OR 1.4, 95% CI 1.1–1.6 in cross-section II). In con- <![T~<.  
Table 1: Participant characteristics. v}_$9&|S  
Characteristics Cross-section I Cross-section II THu a?,oyW  
n % n % ./g0T{&  
Age (mean) (66.2) (66.7) 0"QE,pLe4  
50–54 485 13.3 350 10.0 m&q;.|W  
55–59 534 14.6 580 16.5 +Xp;T`,v  
60–64 638 17.5 600 17.1 6bGD8 ;  
65–69 671 18.4 639 18.2 ,7(/Il 9  
70–74 538 14.7 572 16.3 l 3K8{HY  
75–79 422 11.6 407 11.6 b{rmxtx  
80–84 230 6.3 226 6.4 ,ln uu  
85–89 100 2.7 110 3.1 $ZRN#x@  
90+ 36 1.0 24 0.7 t}7wR TG  
Female 2072 56.7 1998 57.0  ~^S-  
Ever Smokers 1784 51.2 1789 51.2 qM0MSwvC=  
Use of inhaled steroids 370 10.94 478 13.8^ ECScx02  
History of: EVFfXv^  
Diabetes 284 7.8 347 9.9^ 2YKM9Ks  
Hypertension 1669 46.0 1825 52.2^ fhmr*E'J  
Emmetropia* 1558 42.9 1478 42.2 .;b> T  
Myopia* 442 12.2 495 14.1^ hYn'uL^~[  
Hyperopia* 1633 45.0 1532 43.7 VK;x6*Y  
n = number of persons affected @<G/H|f  
* best spherical equivalent refraction correction Wts{tb  
^ P < 0.01 (NdgF+'=  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 <6C9R>  
Page 4 of 7 fWyDWU  
(page number not for citation purposes) iyYY)roB  
t P|4E1O  
rast, men had slightly higher PSC prevalence than women ^Nw]'e3  
in both cross-sections but the difference was not significant N[bN"'U/1  
(OR 1.1, 95% CI 0.8–1.4 for men in cross-section I rR@n> Xx  
and OR 1.2, 95% 0.9–1.6 in cross-section II). *\KMkx  
Discussion \GvY`kt3  
Findings from two surveys of BMES cross-sectional populations `E=rh3 L0o  
with similar age and gender distribution showed xm|4\H&Bg  
that the prevalence of cortical cataract and PSC remained 'c0'P%[5A  
stable, while the prevalence of nuclear cataract appeared SU  O;  
to have increased. Comparison of age-specific prevalence, yvWzc uL#  
with totally independent samples within each age group, BhW]Oq&  
confirmed the robustness of our findings from the two ;"Y;l=9_  
survey samples. Although lens photographs taken from 8EG8!,\I  
the two surveys were graded for nuclear cataract by the 3>9dJx4I  
same graders, who documented a high inter- and intragrader mK40 f  
reliability, we cannot exclude the possibility that s.;KVy,=Bu  
variations in photography, performed by different photographers, qH%L"J  
may have contributed to the observed difference .8qzU47E  
in nuclear cataract prevalence. However, the overall 92aDHECo  
Table 2: Age-specific prevalence of cataract types in cross sections I and II.  K-5"#  
Cataract type Age (years) Cross-section I Cross-section II B N*,!fx  
n % (95% CL)* n % (95% CL)* _`@Xy!Ye  
Cortical 50–54 473 4.4 (2.6–6.3) 338 7.4 (4.6–10.2) jaO#><f  
55–59 522 9.2 (6.7–11.7) 542 9.0 (6.6–11.5) K~Au?\{  
60–64 615 16.4 (13.5–19.4) 556 16.7 (13.6–19.8) ?Y0$X>nm  
65–69 653 26.2 (22.8–29.6) 581 23.6 (20.1–27.0) }8V;s-1  
70–74 516 31.2 (27.2–35.2) 514 35.4 (31.3–39.6) W|H4i;u  
75–79 366 40.2 (35.1–45.2) 332 39.8 (34.5–45.1) FJjF*2 .  
80–84 194 58.8 (51.8–65.8) 163 42.9 (35.3–50.6) TtwJ,&b  
85–89 74 52.7 (41.1–64.4) 73 54.8 (43.1–66.5) &FJU%tFA  
90+ 22 68.2 (47.0–89.3) 14 78.6 (54.0–103.2) P96Cw~<Q?  
PSC 50–54 474 2.7 (1.3–4.2) 338 2.4 (0.7–4.0) y13CR2t6  
55–59 522 2.9 (1.4–4.3) 541 2.6 (1.3–3.9) !QQ<Ai!E  
60–64 616 4.6 (2.9–6.2) 548 5.7 (3.7–7.6) .}$`+h8W T  
65–69 655 6.3 (4.4–8.1) 573 4.5 (2.8–6.3) Pzk[^z$C  
70–74 517 6.8 (4.6–8.9) 505 9.7 (7.1–12.3) @dE 3  
75–79 367 11.4 (8.2–14.7) 327 9.5 (6.3–12.7) OP|.I._I  
80–84 196 12.2 (7.6–16.9) 155 10.3 (5.5–15.2) 8V=HyF#  
85–89 74 18.9 (9.8–28.1) 69 11.6 (3.9–19.4) [al(>Wr9  
90+ 23 21.7 (3.5–40.0) 11 0.0 Y uw E 0  
Nuclear 50–54 323 1.6 (0.2–2.9) 331 0.9 (–0.2–1.9) L_ Xn ,  
55–59 386 2.3 (0.8–3.8) 507 3.6 (1.9–5.2) GFQG(7G9  
60–64 453 5.3 (3.2–7.4) 501 11.6 (8.8–14.4) [NCXn>Z  
65–69 478 17.2 (13.8–20.1) 534 18.5 (15.2–21.9) s]F?=yEp  
70–74 392 27.6 (23.1–32.0) 453 36.0 (31.6–40.4) [.#p  
75–79 255 45.1 (39.0–51.3) 302 55.6 (50.0–61.3) {p#l!P/  
80–84 146 54.1 (45.9–62.3) 147 73.5 (66.3–80.7) H;TOPtt2  
85–89 50 64.0 (50.2–77.8) 70 80.0 (70.4–89.6) gfdPx:7^  
90+ 18 72.2 (49.3–95.1) 15 73.3 (48.0–98.7) ' FPcAW^8  
n = number of persons =A0"0D{\  
* 95% Confidence Limits xP{H jONu  
Cataract FMioguunrtea i1n ps rEeyvea lSetnucdey in cross-sections I and II of the Blue mc0sdb,c$  
Cataract prevalence in cross-sections I and II of the Blue nJldz;  
Mountains Eye Study. .\ ;l-U  
0 L;.VEz!  
10 c]s (u+i  
20 B&%L`v2[  
30 @MN}^umx`  
40 *tTP8ZCQ[  
50 2p$n*|T&c  
cortical PSC nuclear any .KT 7le<Zm  
cataract k8InbX[  
Cataract type {+ @ms$z  
% 7.7Cluh5,  
Cross-section I $?]@_=  
Cross-section II 4B:\  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 #6*V7@9]3|  
Page 5 of 7 oJlN.Q#u&  
(page number not for citation purposes) ~=`f]IL  
prevalence of any cataract (including cataract surgery) was G ]L0eV  
relatively stable over the 6-year period. cwH,l$  
Although different population-based studies used different ppwd-^f3j  
grading systems to assess cataract [15], the overall >VRo|o<D  
prevalence of the three cataract types were similar across 4'+d"Ok  
different study populations [12,16-23]. Most studies have 0=N4O!X9  
suggested that nuclear cataract is the most prevalent type  'P@=/  
of cataract, followed by cortical cataract [16-20]. Ours and w"fCI 13  
other studies reported that cortical cataract was the most a6;gBoV  
prevalent type [12,21-23]. v t^r1j  
Our age-specific prevalence data show a reduction of q1N4X7<_  
15.9% in cortical cataract prevalence for the 80–84 year Q9` s_4  
age group, concordant with an increase in cataract surgery L\QQjI{  
prevalence by 9% in those aged 80+ years observed in the rER~P \-  
same study population [10]. Although cortical cataract is B"~U<6s0  
thought to be the least likely cataract type leading to a cataract YEg .  
surgery, this may not be the case in all older persons. y.jS{r".  
A relatively stable cortical cataract and PSC prevalence RM)1*l`!E  
over the 6-year period is expected. We cannot offer a Sv.KI{;v$  
definitive explanation for the increase in nuclear cataract M NkKy(Za  
prevalence. A possible explanation could be that a moderate WEno+Z~=1'  
level of nuclear cataract causes less visual disturbance R|/Wz/$1A  
than the other two types of cataract, thus for the oldest age Z$Z`@&U=  
groups, persons with nuclear cataract could have been less ].LJt['%8  
likely to have surgery unless it is very dense or co-existing DG_}9M!DW@  
with cortical cataract or PSC. Previous studies have shown #N; $  
that functional vision and reading performance were high 4+)Z k$E  
in patients undergoing cataract surgery who had nuclear |p;4dL  
cataract only compared to those with mixed type of cataract #]"/{Z  
(nuclear and cortical) or PSC [24,25]. In addition, the !>\9t9  
overall prevalence of any cataract (including cataract surgery) ty':`)  
was similar in the two cross-sections, which appears O ,l\e 3;  
to support our speculation that in the oldest age group, i"/r)>"b  
nuclear cataract may have been less likely to be operated H1Q''$}Z.  
than the other two types of cataract. This could have IT,"8 s  
resulted in an increased nuclear cataract prevalence (due SzRL}}I  
to less being operated), compensated by the decreased k 9cK b f@  
prevalence of cortical cataract and PSC (due to these being 6!@0VI&P  
more likely to be operated), leading to stable overall prevalence *8/VSs  
of any cataract. bS,etd  
Possible selection bias arising from selective survival |n)<4%i8J  
among persons without cataract could have led to underestimation 61G|?Aax  
of cataract prevalence in both surveys. We JW-|<CJ  
assume that such an underestimation occurred equally in "= FIFf  
both surveys, and thus should not have influenced our u]R$]&<  
assessment of temporal changes. av$  
Measurement error could also have partially contributed iL+y(]  
to the observed difference in nuclear cataract prevalence. P7'M],!9w  
Assessment of nuclear cataract from photographs is a {Wh BoD  
potentially subjective process that can be influenced by y!F:m=x<  
variations in photography (light exposure, focus and the f]c <9Q>*  
slit-lamp angle when the photograph was taken) and D_Guc8*  
grading. Although we used the same Topcon slit-lamp Ny]lvgu9X  
camera and the same two graders who graded photos FbmsN)mv!%  
from both surveys, we are still not able to exclude the possibility f0OgK<.>T  
of a partial influence from photographic variation KLW&bJ$|j  
on this result. (VEp~BW@-R  
A similar gender difference (women having a higher rate (,shiK[5f  
than men) in cortical cataract prevalence was observed in 'g2vX&=$A  
both surveys. Our findings are in keeping with observations ,^HS`!s[ E  
from the Beaver Dam Eye Study [18], the Barbados &"xQ~05  
Eye Study [22] and the Lens Opacities Case-Control ?H<~ac2e  
Group [26]. It has been suggested that the difference PFm\[2  
could be related to hormonal factors [18,22]. A previous 3Mur*tj#  
study on biochemical factors and cataract showed that a v O PMgEI  
lower level of iron was associated with an increased risk of Qd?CTYNsv  
cortical cataract [27]. No interaction between sex and biochemical - {0g#G  
factors were detected and no gender difference YlrB@mE0n$  
was assessed in this study [27]. The gender difference seen 8sH50jeP  
in cortical cataract could be related to relatively low iron ]  ;&"1A  
levels and low hemoglobin concentration usually seen in JS PW>W"  
women [28]. Diabetes is a known risk factor for cortical Tn /Ut}]O  
Table 3: Gender distribution of cataract types in cross-sections I and II. r  3|4gG  
Cataract type Gender Cross-section I Cross-section II %OEq,Tb  
n % (95% CL)* n % (95% CL)* x_k S g  
Cortical Male 1496 21.1 (19.0–23.1) 1328 20.4 (18.2–22.6) Hk~k@Wft  
Female 1939 25.9 (23.9–27.8) 1785 26.2 (24.2–28.3) VcrVaBw  
PSC Male 1500 6.5 (5.2–7.7) 1314 6.4 (5.1–7.7) <>n9 'i1  
Female 1944 6.2 (5.1–7.2) 1753 5.7 (4.6–6.7) ?d~]Wd!z  
Nuclear Male 1106 17.6 (15.4–19.9) 1225 22.5 (20.1–24.8) 8ZW?|-i  
Female 1395 19.5 (17.4–21.6) 1635 25.0 (22.9–27.1) (uRZxX  
n = number of persons qfa}3k8et  
* 95% Confidence Limits P2t_T'R}  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 )d:K:YXt  
Page 6 of 7 p&\K9hfi  
(page number not for citation purposes) K0oFPDJN  
cataract but in this particular population diabetes is more Fe5jdV<  
prevalent in men than women in all age groups [29]. Differential G0pBR]_5z$  
exposures to cataract risk factors or different dietary -p]>Be+^x  
or lifestyle patterns between men and women may c_Tzyh7l4  
also be related to these observations and warrant further BJgDo  
study. <}]{~y  
Conclusion rw]yKH  
In summary, in two population-based surveys 6 years Za0gs @$  
apart, we have documented a relatively stable prevalence 0E1=W 6UZ  
of cortical cataract and PSC over the period. The observed Je@kiE  
overall increased nuclear cataract prevalence by 5% over a !LiQ 1`V{  
6-year period needs confirmation by future studies, and EX+,:l\^  
reasons for such an increase deserve further study. <6R"h -u"  
Competing interests GG+5/hU  
The author(s) declare that they have no competing interests. y1#O%=g  
Authors' contributions 79wLT \&  
AGT graded the photographs, performed literature search 4w;~4#ZPp  
and wrote the first draft of the manuscript. JJW graded the cQn)^jx=  
photographs, critically reviewed and modified the manuscript. "wINBya'M  
ER performed the statistical analysis and critically A0>x9XSkJ  
reviewed the manuscript. PM designed and directed the )88nMH-  
study, adjudicated cataract cases and critically reviewed 0bSz4<}  
and modified the manuscript. All authors read and 3~<}bee5|q  
approved the final manuscript. G0/>8_Q>Nr  
Acknowledgements ^j=bObaX  
This study was supported by the Australian National Health & Medical dyO E6Ex  
Research Council, Canberra, Australia (Grant Nos 974159, 991407). The @)b^^Fp  
abstract was presented at the Association for Research in Vision and Ophthalmology r.<JDdj  
(ARVO) meeting in Fort Lauderdale, Florida, USA, May 2005. />F.Nsujy  
References /AR]dcL@76  
1. Congdon N, O'Colmain B, Klaver CC, Klein R, Munoz B, Friedman Q6x%  
DS, Kempen J, Taylor HR, Mitchell P: Causes and prevalence of CKd 3w8;  
visual impairment among adults in the United States. Arch m|1n x  
Ophthalmol 2004, 122(4):477-485. Up|f=@=  
2. Rahmani B, Tielsch JM, Katz J, Gottsch J, Quigley H, Javitt J, Sommer 4 | f}F  
A: The cause-specific prevalence of visual impairment in an H TR1)b  
urban population. The Baltimore Eye Survey. Ophthalmology uLK(F B  
1996, 103:1721-1726. tN2 W8d  
3. Keeffe JE, Konyama K, Taylor HR: Vision impairment in the &D*8l?A/1f  
Pacific region. Br J Ophthalmol 2002, 86:605-610. N"1 QX6  
4. Reidy A, Minassian DC, Vafidis G, Joseph J, Farrow S, Wu J, Desai P, 'HB~Dbq`V  
Connolly A: Prevalence of serious eye disease and visual &O*ENpF  
impairment in a north London population: population based, u]bz42]  
cross sectional study. BMJ 1998, 316:1643-1646. ET+'Pj3  
5. Resnikoff S, Pascolini D, Etya'ale D, Kocur I, Pararajasegaram R, RUX8qT(Z  
Pokharel GP, Mariotti SP: Global data on visual impairment in ? d5h9}B  
the year 2002. Bull World Health Organ 2004, 82:844-851. q~h:<,5  
6. Pascolini D, Mariotti SP, Pokharel GP, Pararajasegaram R, Etya'ale D, ^*>n4U  
Negrel AD, Resnikoff S: 2002 global update of available data on ZAeQ~ j~  
visual impairment: a compilation of population-based prevalence n1 v,#GE  
studies. Ophthalmic Epidemiol 2004, 11:67-115. OoM_q/oI  
7. Rochtchina E, Mukesh BN, Wang JJ, McCarty CA, Taylor HR, Mitchell RH~sbnZ)F  
P: Projected prevalence of age-related cataract and cataract Hg whe=P  
surgery in Australia for the years 2001 and 2021: pooled data uP6-cs  
from two population-based surveys. Clin Experiment Ophthalmol TvM24Orct  
2003, 31:233-236. k>>`fE\K  
8. Medicare Benefits Schedule Statistics [http://www.medicar 74]a/'4  
eaustralia.gov.au/statistics/dyn_mbs/forms/mbs_tab4.shtml] v.b5iv5  
9. Keeffe JE, Taylor HR: Cataract surgery in Australia 1985–94. )!a$#"'  
Aust N Z J Ophthalmol 1996, 24:313-317. zX~}]?|9  
10. Tan AG, Wang JJ, Rochtchina E, Jakobsen K, Mitchell P: Increase in 7E(%9W6P  
cataract surgery prevalence from 1992–1994 to 1997–2000: Qi:j)uDW  
Analysis of two population cross-sections. Clin Experiment Ophthalmol $?$9y ^\  
2004, 32:284-288. LzE/g)>  
11. Mitchell P, Smith W, Attebo K, Wang JJ: Prevalence of age-related ZqP7@fO_%  
maculopathy in Australia. The Blue Mountains Eye Study. =qX*]  
Ophthalmology 1995, 102:1450-1460. L=m:/qQL  
12. Mitchell P, Cumming RG, Attebo K, Panchapakesan J: Prevalence of |[ocyUsxX  
cataract in Australia: the Blue Mountains eye study. Ophthalmology N8 M'0i?  
1997, 104:581-588. G4m4k  
13. Klein BEK, Magli YL, Neider MW, Klein R: Wisconsin system for classification {,Fcd(MU  
of cataracts from photographs (protocol) Madison, WI; 1990. .+vd6Uc5a  
14. Foran S, Wang JJ, Mitchell P: Causes of visual impairment in two -5xCQJ[  
older population cross-sections: the Blue Mountains Eye pn s+y  
Study. Ophthalmic Epidemiol 2003, 10:215-225.  ob]dZ  
15. Congdon N, Vingerling JR, Klein BE, West S, Friedman DS, Kempen J, o\60 n  
O'Colmain B, Wu SY, Taylor HR: Prevalence of cataract and avBua6i'  
pseudophakia/aphakia among adults in the United States. H+R7X71{  
Arch Ophthalmol 2004, 122:487-494. 4Cd#sQ  
16. Sperduto RD, Hiller R: The prevalence of nuclear, cortical, and ~lk@6{`l|1  
posterior subcapsular lens opacities in a general population ]?# #))RUS  
sample. Ophthalmology 1984, 91:815-818. - `4Ty*K  
17. Adamsons I, Munoz B, Enger C, Taylor HR: Prevalence of lens ^r4|{  
opacities in surgical and general populations. Arch Ophthalmol VWD.J  
1991, 109:993-997. ctK65h{Eo  
18. Klein BE, Klein R, Linton KL: Prevalence of age-related lens RF!'K ko  
opacities in a population. The Beaver Dam Eye Study. Ophthalmology #]X2^ND4 7  
1992, 99:546-552. 9fMSAB+c%  
19. West SK, Munoz B, Schein OD, Duncan DD, Rubin GS: Racial differences Q]T BQ&  
in lens opacities: the Salisbury Eye Evaluation (SEE) U3N(cFXn  
project. Am J Epidemiol 1998, 148:1033-1039. Ju4.@  
20. Congdon N, West SK, Buhrmann RR, Kouzis A, Munoz B, Mkocha H: SXh?U,5u  
Prevalence of the different types of age-related cataract in p_9g|B0D  
an African population. Invest Ophthalmol Vis Sci 2001, C/y(E |zC$  
42:2478-2482. q- H&5K  
21. Livingston PM, Guest CS, Stanislavsky Y, Lee S, Bayley S, Walker C, mZE8.`  
McKean C, Taylor HR: A population-based estimate of cataract "4RQ`.S R  
prevalence: the Melbourne Visual Impairment Project experience. ]'e A O  
Dev Ophthalmol 1994, 26:1-6. iU XM( ]  
22. Leske MC, Connell AM, Wu SY, Hyman L, Schachat A: Prevalence ZqFUPHc  
of lens opacities in the Barbados Eye Study. Arch Ophthalmol 8J):\jAZ6  
1997, 115:105-111. published erratum appears in Arch Ophthalmol `$M et Q  
1997 Jul;115(7):931 ([tG y  
23. Seah SK, Wong TY, Foster PJ, Ng TP, Johnson GJ: Prevalence of 'xk1o,;  
lens opacity in Chinese residents of Singapore: the tanjong VRB~7\A5<)  
pagar survey. Ophthalmology 2002, 109:2058-2064. M_; w %FV  
24. Stifter E, Sacu S, Weghaupt H, Konig F, Richter-Muksch S, Thaler A, @ce3%`c_  
Velikay-Parel M, Radner W: Reading performance depending on oAaf)?8  
the type of cataract and its predictability on the visual outcome. P|8e%P  
J Cataract Refract Surg 2004, 30:1259-1267. ^H-QYuz:T0  
25. Stifter E, Sacu S, Weghaupt H: Functional vision with cataracts of 6$DG.p  
different morphologies: comparative study. J Cataract Refract u X> PefR  
Surg 2004, 30:1883-1891. boIVU`F-!  
26. Leske MC, Chylack LT Jr, Wu SY: The Lens Opacities Case-Control MorW\7-}  
Study. Risk factors for cataract. Arch Ophthalmol 1991, n{ 3| E3  
109:244-251. (<n>EF#  
27. Leske MC, Wu SY, Hyman L, Sperduto R, Underwood B, Chylack LT, @| P3  
Milton RC, Srivastava S, Ansari N: Biochemical factors in the lens @T_O6TcY  
opacities. Case-control study. The Lens Opacities Case-Control &62` Wr0C  
Study Group. Arch Ophthalmol 1995, 113:1113-1119. ^h`!f vyH  
28. Yip R, Johnson C, Dallman PR: Age-related changes in laboratory $=lJG(2%  
values used in the diagnosis of anemia and iron deficiency. O8iu+}]/6  
Am J Clin Nutr 1984, 39:427-436. &`m~o/  
29. Mitchell P, Smith W, Wang JJ, Cumming RG, Leeder SR, Burnett L: VSx%8IM+X  
Diabetes in an older Australian population. Diabetes Res Clin \ x:_*`fU  
Pract 1998, 41:177-184. +H[Q~P8'[  
Pre-publication history 5vYsA1Z   
The pre-publication history for this paper can be accessed ??q!jm-m  
here: vrQFx~ZztH  
Publish with BioMed Central and every EmF]W+!z%  
scientist can read your work free of charge "i}Z(_7yr  
"BioMed Central will be the most significant development for C CLfvex  
disseminating the results of biomedical research in our lifetime." 7L1\1E:!  
Sir Paul Nurse, Cancer Research UK 2Qw )-EB  
Your research papers will be: xcsFODx~  
available free of charge to the entire biomedical community N"&$b_u[  
peer reviewed and published immediately upon acceptance MM=W9#  
cited in PubMed and archived on PubMed Central fp,1qzU[k  
yours — you keep the copyright kbD*=d}3{  
Submit your manuscript here: 4S^  
http://www.biomedcentral.com/info/publishing_adv.asp O7! fI'R  
BioMedcentral zsHG= Ee*  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 *;>V2!N=U  
Page 7 of 7 R (t!xf  
(page number not for citation purposes) ^)(G(=-Rf  
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:
4+6=? 正确答案:10
按"Ctrl+Enter"直接提交