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 kB@gy}  
Page 1 of 7 .\$A7DD+A  
(page number not for citation purposes) QD%xmP  
BMC Ophthalmology cu>(;=  
Research article Open Access %( 7##f_  
Comparison of age-specific cataract prevalence in two If'2 m_  
population-based surveys 6 years apart '-A;B.GV%  
Ava Grace Tan†, Jie Jin Wang*†, Elena Rochtchina† and Paul Mitchell† ^*fD  
Address: Centre for Vision Research, Westmead Millennium Institute, Department of Ophthalmology, University of Sydney, Westmead Hospital, |1CX?8)b=  
Westmead, NSW, Australia c?CfM>  
Email: Ava Grace Tan - ava_tan@wmi.usyd.edu.au; Jie Jin Wang* - jiejin_wang@wmi.usyd.edu.au; &X:;B'   
Elena Rochtchina - elena_rochtchina@wmi.usyd.edu.au; Paul Mitchell - paul_mitchell@wmi.usyd.edu.au Y910\h@V  
* Corresponding author †Equal contributors -B-G$ii  
Abstract >(P(!^[f  
Background: In this study, we aimed to compare age-specific cortical, nuclear and posterior 39O rY  
subcapsular (PSC) cataract prevalence in two surveys 6 years apart. qZF&^pCF}  
Methods: The Blue Mountains Eye Study examined 3654 participants (82.4% of those eligible) in r }qDvC D  
cross-section I (1992–4) and 3509 participants (75.1% of survivors and 85.2% of newly eligible) in AHn!>w,  
cross-section II (1997–2000, 66.5% overlap with cross-section I). Cataract was assessed from lens  mhrF9&s  
photographs following the Wisconsin Cataract Grading System. Cortical cataract was defined if |Io:D:  
cortical opacity comprised ≥ 5% of lens area. Nuclear cataract was defined if nuclear opacity ≥ ]:LlOv$  
Wisconsin standard 4. PSC was defined if any present. Any cataract was defined to include persons P]n0L4c  
who had previous cataract surgery. Weighted kappa for inter-grader reliability was 0.82, 0.55 and Z:^#9D{  
0.82 for cortical, nuclear and PSC cataract, respectively. We assessed age-specific prevalence using 'i$. _Tx  
an interval of 5 years, so that participants within each age group were independent between the o3+s.7 "  
two surveys. vrb@::sy0T  
Results: Age and gender distributions were similar between the two populations. The age-specific v3cMPN  
prevalence of cortical (23.8% in 1st, 23.7% in 2nd) and PSC cataract (6.3%, 6.0%) was similar. The BA1H)%  
prevalence of nuclear cataract increased slightly from 18.7% to 23.9%. After age standardization, /UK?&+1qE  
the similar prevalence of cortical (23.8%, 23.5%) and PSC cataract (6.3%, 5.9%), and the increased RK- bsf  
prevalence of nuclear cataract (18.7%, 24.2%) remained. *K_8=TIA*  
Conclusion: In two surveys of two population-based samples with similar age and gender v#{Nh8n  
distributions, we found a relatively stable cortical and PSC cataract prevalence over a 6-year period. k^|z.$+  
The increased prevalence of nuclear cataract deserves further study. ]wDqdD y7S  
Background 7+f6?  
Age-related cataract is the leading cause of reversible visual zZPWE "u}  
impairment in older persons [1-6]. In Australia, it is xdbzp U  
estimated that by the year 2021, the number of people D~ 3@v+d  
affected by cataract will increase by 63%, due to population ?XdvZf $  
aging [7]. Surgical intervention is an effective treatment xP~GpVhLF  
for cataract and normal vision (> 20/40) can usually V  H`_  
be restored with intraocular lens (IOL) implantation. @yb'h`f]  
Cataract surgery with IOL implantation is currently the ?bM%#x{e  
most commonly performed, and is, arguably, the most Wjq9f;  
cost effective surgical procedure worldwide. Performance :'%|LB c0  
Published: 20 April 2006 {sB-"NR`K  
BMC Ophthalmology 2006, 6:17 doi:10.1186/1471-2415-6-17 Y>aVnixx<  
Received: 14 December 2005 Q8Ek}O\MC  
Accepted: 20 April 2006 B!J?,SB  
This article is available from: http://www.biomedcentral.com/1471-2415/6/17 _ZavY<6  
© 2006 Tan et al; licensee BioMed Central Ltd. |)To 0Z  
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), l-W)? d  
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Gi-pi=#&cs  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 KO 8vUR*2R  
Page 2 of 7 T_2'=7  
(page number not for citation purposes)  !{V`N|0  
of this surgical procedure has been continuously increasing |0 F o{  
in the last two decades. Data from the Australian }N -UlL(  
Health Insurance Commission has shown a steady 9$v\D3<Z  
increase in Medicare claims for cataract surgery [8]. A 2.6- QE"$Lc)  
fold increase in the total number of cataract procedures @A8y!<  
from 1985 to 1994 has been documented in Australia [9]. i/ o  
The rate of cataract surgery per thousand persons aged 65 w7~]c,$y.  
years or older has doubled in the last 20 years [8,9]. In the jo"+_)]  
Blue Mountains Eye Study population, we observed a onethird ]b}3f<  
increase in cataract surgery prevalence over a mean %O%;\t  
6-year interval, from 6% to nearly 8% in two cross-sectional PNLlJlYlP  
population-based samples with a similar age range nq7)0F%e  
[10]. Further increases in cataract surgery performance J.2B By  
would be expected as a result of improved surgical skills P >0S ZP  
and technique, together with extending cataract surgical ]lJ#|zd8o  
benefits to a greater number of older people and an =#TQXm']Gi  
increased number of persons with surgery performed on -$s1k~o  
both eyes. T2W^4 )  
Both the prevalence and incidence of age-related cataract b2F1^]p  
link directly to the demand for, and the outcome of, cataract m|cRj{xZF  
surgery and eye health care provision. This report 2 (ux  
aimed to assess temporal changes in the prevalence of cortical Q4ii25]*  
and nuclear cataract and posterior subcapsular cataract ,V4pFQzL  
(PSC) in two cross-sectional population-based cEJ_z(\=hr  
surveys 6 years apart. OB,T>o@  
Methods _["97>q  
The Blue Mountains Eye Study (BMES) is a populationbased I GcR5/3  
cohort study of common eye diseases and other 0Z %<H\Z  
health outcomes. The study involved eligible permanent A^c5CJ_  
residents aged 49 years and older, living in two postcode nzYFa J+  
areas in the Blue Mountains, west of Sydney, Australia.  H<b4B$/  
Participants were identified through a census and were y7*^ H  
invited to participate. The study was approved at each SLd9-N}T  
stage of the data collection by the Human Ethics Committees hU2 N{Ac  
of the University of Sydney and the Western Sydney @D<Q'7mLh  
Area Health Service and adhered to the recommendations Y50$ 2%kM  
of the Declaration of Helsinki. Written informed consent  -gS/  
was obtained from each participant. 7xT<|3 I  
Details of the methods used in this study have been 1G8t=IA%D  
described previously [11]. The baseline examinations gD fVY%[Z  
(BMES cross-section I) were conducted during 1992– 1hp@.Fv  
1994 and included 3654 (82.4%) of 4433 eligible residents. q%^gG03.  
Follow-up examinations (BMES IIA) were conducted U(qM( E  
during 1997–1999, with 2335 (75.0% of BMES {la ^useg[  
cross section I survivors) participating. A repeat census of 0P5 3dF  
the same area was performed in 1999 and identified 1378  *JOv  
newly eligible residents who moved into the area or the {gi"ktgk  
eligible age group. During 1999–2000, 1174 (85.2%) of `Op ";E88  
this group participated in an extension study (BMES IIB). oq<#   
BMES cross-section II thus includes BMES IIA (66.5%) )'< zC  
and BMES IIB (33.5%) participants (n = 3509). N4 mQN90t  
Similar procedures were used for all stages of data collection h; unbz  
at both surveys. A questionnaire was administered @fYA{-ZC  
including demographic, family and medical history. A %F/tbXy{  
detailed eye examination included subjective refraction, >"nk}@  
slit-lamp (Topcon SL-7e camera, Topcon Optical Co, XJ NKM~  
Tokyo, Japan) and retroillumination (Neitz CT-R camera, Em.?  
Neitz Instrument Co, Tokyo, Japan) photography of the @',;/j80  
lens. Grading of lens photographs in the BMES has been 2Uk8{d  
previously described [12]. Briefly, masked grading was ,zyrBO0 Eq  
performed on the lens photographs using the Wisconsin g%[Ruugu  
Cataract Grading System [13]. Cortical cataract and PSC BR%:`uiQ<  
were assessed from the retroillumination photographs by n*xNMw1x"T  
estimating the percentage of the circular grid involved. BPOWo8TqD^  
Cortical cataract was defined when cortical opacity 3a S>U #  
involved at least 5% of the total lens area. PSC was defined ! O>mu6:Rf  
when opacity comprised at least 1% of the total lens area. e O}mZN  
Slit-lamp photographs were used to assess nuclear cataract FxT [4  
using the Wisconsin standard set of four lens photographs #sHP\|rA  
[13]. Nuclear cataract was defined when nuclear opacity O&0R ~<n  
was at least as great as the standard 4 photograph. Any cataract fj JIF%  
was defined to include persons who had previous s`2o\]  
cataract surgery as well as those with any of three cataract u@3w$"Pv1  
types. Inter-grader reliability was high, with weighted V+q RDQ  
kappa 0.82 for cortical cataract, 0.55 (simple kappa 0.75) ;D7jE+  
for nuclear cataract and 0.82 for PSC grading. The intragrader (qr T0D6  
reliability for nuclear cataract was assessed with ;sf/tX  
simple kappa 0.83 for the senior grader who graded 3PGyqt(   
nuclear cataract at both surveys. All PSC cases were confirmed y()( 8L  
by an ophthalmologist (PM). Y4O L 82Y  
In cross-section I, 219 persons (6.0%) had missing or '3Ie0QO]"%  
ungradable Neitz photographs, leaving 3435 with photographs /WfxI>v  
available for cortical cataract and PSC assessment, v2'J L(=  
while 1153 (31.6%) had randomly missing or ungradable h(-&.Sm")H  
Topcon photographs due to a camera malfunction, leaving CmOb+:4@K  
2501 with photographs available for nuclear cataract 8E+l; 2   
assessment. Comparison of characteristics between participants %-Z~f~<?  
with and without Neitz or Topcon photographs in *@nUas 2"  
cross-section I showed no statistically significant differences i`$rzXcS  
between the two groups, as reported previously 08a|]li  
[12]. In cross-section II, 441 persons (12.5%) had missing @\?f77O f6  
or ungradable Neitz photographs, leaving 3068 for cortical |Y11sDa9h  
cataract and PSC assessment, and 648 (18.5%) had p/~kw:I  
missing or ungradable Topcon photographs, leaving 2860 ~~,<+X:  
for nuclear cataract assessment. l0{DnQA>I  
Data analysis was performed using the Statistical Analysis {@Ac L:Eit  
System (SAS, SAS Institute, Cary, NC, USA). Age-adjusted *lAdS]I  
prevalence was calculated using direct standardization of ZZ*k 3Ce  
the cross-section II population to the cross-section I population. }HorR2(`N  
We assessed age-specific prevalence using an [@Y q^.6t  
interval of 5 years, so that participants within each age (K6S tNtN  
group were independent between the two cross-sectional V&H8-,7z  
surveys. zP}v2  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 3H2;mqq  
Page 3 of 7 ^6>|!  
(page number not for citation purposes) -<]_:Kf{;&  
Results /8\&f %E  
Characteristics of the two survey populations have been FSs$ ] d;  
previously compared [14] and showed that age and sex d/rz0L  
distributions were similar. Table 1 compares participant L$ Ar]O)  
characteristics between the two cross-sections. Cross-section @(fY4]K  
II participants generally had higher rates of diabetes, 3>)BI(Wl  
hypertension, myopia and more users of inhaled steroids. ItE~MJ5p  
Cataract prevalence rates in cross-sections I and II are h\\2r>  
shown in Figure 1. The overall prevalence of cortical cataract $ywh%OEH  
was 23.8% and 23.7% in cross-sections I and II, xGv,%'u\  
respectively (age-sex adjusted P = 0.81). Corresponding j YID44$  
prevalence of PSC was 6.3% and 6.0% for the two crosssections @]wem  
(age-sex adjusted P = 0.60). There was an W;]U P$5l  
increased prevalence of nuclear cataract, from 18.7% in #'J7Wy  
cross-section I to 23.9% in cross-section II over the 6-year -G#@BtB2+  
period (age-sex adjusted P < 0.001). Prevalence of any cataract P3ev 4DL  
(including persons who had cataract surgery), however, [k 7N+W8  
was relatively stable (46.9% and 46.8% in crosssections 8;f<qu|w  
I and II, respectively). nk$V{(FJ  
After age-standardization, these prevalence rates remained gdFoTcHgO|  
stable for cortical cataract (23.8% and 23.5% in the two "|r^l  
surveys) and PSC (6.3% and 5.9%). The slightly increased !XA%[u  
prevalence of nuclear cataract (from 18.7% to 24.2%) was ?WtG|w  
not altered. 5@t uo`k  
Table 2 shows the age-specific prevalence rates for cortical @TPgA(5NR  
cataract, PSC and nuclear cataract in cross-sections I and K(KP3Q  
II. A similar trend of increasing cataract prevalence with \{=`F`oB=  
increasing age was evident for all three types of cataract in FoD/Q  
both surveys. Comparing the age-specific prevalence qb&N S4#  
between the two surveys, a reduction in PSC prevalence in s]<r  
cross-section II was observed in the older age groups (≥ 75 mImbS)V  
years). In contrast, increased nuclear cataract prevalence HZ<f(  
in cross-section II was observed in the older age groups (≥ &c?hJ8"  
70 years). Age-specific cortical cataract prevalence was relatively ivUsMhx>S,  
consistent between the two surveys, except for a uyRA`<&w  
reduction in prevalence observed in the 80–84 age group L8w76|  
and an increasing prevalence in the older age groups (≥ 85 ,dj* p ,J  
years). p1VahjRE-  
Similar gender differences in cataract prevalence were 'UvS3]bSYW  
observed in both surveys (Table 3). Higher prevalence of n:^"[Le  
cortical and nuclear cataract in women than men was evident !ga (L3vf  
but the difference was only significant for cortical Y K?*7  
cataract (age-adjusted odds ratio, OR, for women 1.3, Y0u'@l_[F  
95% confidence intervals, CI, 1.1–1.5 in cross-section I FH`'1iVH  
and OR 1.4, 95% CI 1.1–1.6 in cross-section II). In con- B`?N0t%X  
Table 1: Participant characteristics. x#j\"$dla  
Characteristics Cross-section I Cross-section II SC $`  
n % n % u_6BHsU  
Age (mean) (66.2) (66.7) .KU SNrs'  
50–54 485 13.3 350 10.0 9"HmHy&:E  
55–59 534 14.6 580 16.5 lA.;ZD!  
60–64 638 17.5 600 17.1 g<rKV+$6  
65–69 671 18.4 639 18.2 )p!*c,  
70–74 538 14.7 572 16.3 7Js>!KR  
75–79 422 11.6 407 11.6 E &];>3C  
80–84 230 6.3 226 6.4 0Y6q$h>4  
85–89 100 2.7 110 3.1 ,\S pjE  
90+ 36 1.0 24 0.7 %7NsBR!y  
Female 2072 56.7 1998 57.0 G+hF [b44'  
Ever Smokers 1784 51.2 1789 51.2 MS st  
Use of inhaled steroids 370 10.94 478 13.8^ F%PwIB~cy  
History of:  %K%^ ]{  
Diabetes 284 7.8 347 9.9^ 7>'uj7r]=  
Hypertension 1669 46.0 1825 52.2^ j!lAxlOX  
Emmetropia* 1558 42.9 1478 42.2 ^nHB1"OCV  
Myopia* 442 12.2 495 14.1^ d1~_?V'r]  
Hyperopia* 1633 45.0 1532 43.7 E7X!cm/2<  
n = number of persons affected ? o~:'Z  
* best spherical equivalent refraction correction 9^ >M>f"  
^ P < 0.01 fg9?3x Z  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 =ze FK_S!  
Page 4 of 7 5:Yck<  
(page number not for citation purposes) V&Xi> X8  
t 4GG1E. z}  
rast, men had slightly higher PSC prevalence than women 87QZun%  
in both cross-sections but the difference was not significant eecw]P_?  
(OR 1.1, 95% CI 0.8–1.4 for men in cross-section I kCima/+_  
and OR 1.2, 95% 0.9–1.6 in cross-section II). *0%4l_i  
Discussion UF@IBb}0  
Findings from two surveys of BMES cross-sectional populations 9o-!ecx}  
with similar age and gender distribution showed 3g4e' ]t  
that the prevalence of cortical cataract and PSC remained dCB&c ^  
stable, while the prevalence of nuclear cataract appeared QJx9I_  
to have increased. Comparison of age-specific prevalence,  X ?tj$  
with totally independent samples within each age group, yh S#&)O  
confirmed the robustness of our findings from the two mO#I nTO  
survey samples. Although lens photographs taken from p1+7 <Y:  
the two surveys were graded for nuclear cataract by the xN6>2e  
same graders, who documented a high inter- and intragrader F[5S(7M 7  
reliability, we cannot exclude the possibility that g^1r0.Sp{8  
variations in photography, performed by different photographers, BsKbn@'uC  
may have contributed to the observed difference sF y]+DB  
in nuclear cataract prevalence. However, the overall MFv Si  
Table 2: Age-specific prevalence of cataract types in cross sections I and II. PC|'yAN:  
Cataract type Age (years) Cross-section I Cross-section II ?4,@, ae&  
n % (95% CL)* n % (95% CL)* J==}QEhQ{  
Cortical 50–54 473 4.4 (2.6–6.3) 338 7.4 (4.6–10.2) f3 !n$lj  
55–59 522 9.2 (6.7–11.7) 542 9.0 (6.6–11.5) kfXS_\@iW1  
60–64 615 16.4 (13.5–19.4) 556 16.7 (13.6–19.8) D3y>iQd   
65–69 653 26.2 (22.8–29.6) 581 23.6 (20.1–27.0) S/VA~,KCe;  
70–74 516 31.2 (27.2–35.2) 514 35.4 (31.3–39.6) \*uugw,\y  
75–79 366 40.2 (35.1–45.2) 332 39.8 (34.5–45.1) pajy#0 U  
80–84 194 58.8 (51.8–65.8) 163 42.9 (35.3–50.6) u#FXW_-TK  
85–89 74 52.7 (41.1–64.4) 73 54.8 (43.1–66.5) ijF V<P  
90+ 22 68.2 (47.0–89.3) 14 78.6 (54.0–103.2) >60"p~t  
PSC 50–54 474 2.7 (1.3–4.2) 338 2.4 (0.7–4.0) !N1J@LT5h  
55–59 522 2.9 (1.4–4.3) 541 2.6 (1.3–3.9) +C_*Vs@4  
60–64 616 4.6 (2.9–6.2) 548 5.7 (3.7–7.6) ~T02._E  
65–69 655 6.3 (4.4–8.1) 573 4.5 (2.8–6.3) -D#5o,]3  
70–74 517 6.8 (4.6–8.9) 505 9.7 (7.1–12.3) 9`BEi(z  
75–79 367 11.4 (8.2–14.7) 327 9.5 (6.3–12.7) 9 ZGV%Tw  
80–84 196 12.2 (7.6–16.9) 155 10.3 (5.5–15.2) WNa3^K/W{  
85–89 74 18.9 (9.8–28.1) 69 11.6 (3.9–19.4) ^wJEfac  
90+ 23 21.7 (3.5–40.0) 11 0.0 v U}: U)S  
Nuclear 50–54 323 1.6 (0.2–2.9) 331 0.9 (–0.2–1.9) hM>*a!)U  
55–59 386 2.3 (0.8–3.8) 507 3.6 (1.9–5.2) "15=ET  
60–64 453 5.3 (3.2–7.4) 501 11.6 (8.8–14.4) 59i]  
65–69 478 17.2 (13.8–20.1) 534 18.5 (15.2–21.9) x> \Bxa8  
70–74 392 27.6 (23.1–32.0) 453 36.0 (31.6–40.4) <Oa9oM},d  
75–79 255 45.1 (39.0–51.3) 302 55.6 (50.0–61.3) 2r;GcjezH  
80–84 146 54.1 (45.9–62.3) 147 73.5 (66.3–80.7) [))JX"a  
85–89 50 64.0 (50.2–77.8) 70 80.0 (70.4–89.6) K/|   
90+ 18 72.2 (49.3–95.1) 15 73.3 (48.0–98.7) 3ji:O T  
n = number of persons l.oBcg[  
* 95% Confidence Limits yW("G-Nm  
Cataract FMioguunrtea i1n ps rEeyvea lSetnucdey in cross-sections I and II of the Blue %S`ik!K"I  
Cataract prevalence in cross-sections I and II of the Blue azX`oU,l  
Mountains Eye Study. lKWr=k~  
0 ?Y3@"rdR  
10 .zS D`v@[  
20 Spgg+; 9  
30 sRq U]i8l  
40 jBpVxv  
50 0S.?E.-&0  
cortical PSC nuclear any >a=d;  
cataract <HQ&-jx  
Cataract type "'A"U  
% % {Q-8w!  
Cross-section I JJ5C}`(  
Cross-section II cNj*E =~;  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 -t4 [oB  
Page 5 of 7 &&PgOFD  
(page number not for citation purposes) 4* M@]J "  
prevalence of any cataract (including cataract surgery) was r7I B{}>-  
relatively stable over the 6-year period. If'2rE7J  
Although different population-based studies used different mP-2s;q  
grading systems to assess cataract [15], the overall de YyaV  
prevalence of the three cataract types were similar across <LA^%2jT  
different study populations [12,16-23]. Most studies have H?U't 09  
suggested that nuclear cataract is the most prevalent type DJP 6TFT&G  
of cataract, followed by cortical cataract [16-20]. Ours and ~HDdO3  
other studies reported that cortical cataract was the most _/ Os^>R  
prevalent type [12,21-23]. @ yxt($G  
Our age-specific prevalence data show a reduction of )+Y&4Qu  
15.9% in cortical cataract prevalence for the 80–84 year ]rW8y%yD  
age group, concordant with an increase in cataract surgery +t]Xj1Q  
prevalence by 9% in those aged 80+ years observed in the Sz0+ <F#5  
same study population [10]. Although cortical cataract is cZQu*K^j  
thought to be the least likely cataract type leading to a cataract ek)Xrp:2  
surgery, this may not be the case in all older persons. kh?. K#  
A relatively stable cortical cataract and PSC prevalence I/p] DT  
over the 6-year period is expected. We cannot offer a 8tQ|-l *  
definitive explanation for the increase in nuclear cataract H_B~P%E@]  
prevalence. A possible explanation could be that a moderate kRot7-7I|  
level of nuclear cataract causes less visual disturbance F?4Sz#  
than the other two types of cataract, thus for the oldest age r nBOj#N  
groups, persons with nuclear cataract could have been less *Bw#c j  
likely to have surgery unless it is very dense or co-existing 5py R ~+  
with cortical cataract or PSC. Previous studies have shown Q}P-$X+/ n  
that functional vision and reading performance were high 0HbJKix!  
in patients undergoing cataract surgery who had nuclear ~A >o O-0K  
cataract only compared to those with mixed type of cataract XxO n3i  
(nuclear and cortical) or PSC [24,25]. In addition, the XO wiHW{  
overall prevalence of any cataract (including cataract surgery) u~'OcO  
was similar in the two cross-sections, which appears d=F-L  
to support our speculation that in the oldest age group, ")M;+<c"l  
nuclear cataract may have been less likely to be operated -P#nT 2  
than the other two types of cataract. This could have - 1 W  
resulted in an increased nuclear cataract prevalence (due ,F: =(21  
to less being operated), compensated by the decreased "{( [!  
prevalence of cortical cataract and PSC (due to these being kp`0erJqw  
more likely to be operated), leading to stable overall prevalence V2Y$yV8g1  
of any cataract.  cht  
Possible selection bias arising from selective survival 0QoLS|voA/  
among persons without cataract could have led to underestimation ./.=Rw  
of cataract prevalence in both surveys. We Dl\d_:+  
assume that such an underestimation occurred equally in xOIg|2^8  
both surveys, and thus should not have influenced our wLMvC{5  
assessment of temporal changes. W5/};K\.  
Measurement error could also have partially contributed q6&67u0  
to the observed difference in nuclear cataract prevalence. b *9-}g:  
Assessment of nuclear cataract from photographs is a )ddsyFGW  
potentially subjective process that can be influenced by \7 Mq $d  
variations in photography (light exposure, focus and the BD'NuI  
slit-lamp angle when the photograph was taken) and q{@P+2<wF  
grading. Although we used the same Topcon slit-lamp %EoH4LzT  
camera and the same two graders who graded photos cY~M4:vgT  
from both surveys, we are still not able to exclude the possibility +2y&B,L_Wh  
of a partial influence from photographic variation n?Zf/T  
on this result. [R\=M'  
A similar gender difference (women having a higher rate % $.vOFP9  
than men) in cortical cataract prevalence was observed in %,;gP.dh7  
both surveys. Our findings are in keeping with observations G"C ;A`6  
from the Beaver Dam Eye Study [18], the Barbados 1M/$< kQ-N  
Eye Study [22] and the Lens Opacities Case-Control 6Pijvx^0  
Group [26]. It has been suggested that the difference ol#yjrv  
could be related to hormonal factors [18,22]. A previous idz9YpW  
study on biochemical factors and cataract showed that a dq2@6xd  
lower level of iron was associated with an increased risk of _<2 RYXBC  
cortical cataract [27]. No interaction between sex and biochemical gi 5XP]z  
factors were detected and no gender difference %HVD^. V  
was assessed in this study [27]. The gender difference seen b?>VPuyBb  
in cortical cataract could be related to relatively low iron <b'1#Pd>0  
levels and low hemoglobin concentration usually seen in &~}@u[=ux  
women [28]. Diabetes is a known risk factor for cortical /D 8EI   
Table 3: Gender distribution of cataract types in cross-sections I and II. k|5k8CRX  
Cataract type Gender Cross-section I Cross-section II nAvs~J  
n % (95% CL)* n % (95% CL)* EFD?di)s  
Cortical Male 1496 21.1 (19.0–23.1) 1328 20.4 (18.2–22.6) >-eS&rma  
Female 1939 25.9 (23.9–27.8) 1785 26.2 (24.2–28.3) eZ A6D\  
PSC Male 1500 6.5 (5.2–7.7) 1314 6.4 (5.1–7.7) \D ^7Z97  
Female 1944 6.2 (5.1–7.2) 1753 5.7 (4.6–6.7) ;)P5#S!n-  
Nuclear Male 1106 17.6 (15.4–19.9) 1225 22.5 (20.1–24.8) \:h0w;34O  
Female 1395 19.5 (17.4–21.6) 1635 25.0 (22.9–27.1) _=6vW^ s  
n = number of persons vyujC`61d  
* 95% Confidence Limits k5q(7&C  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 Z rA Um  
Page 6 of 7 3eJ\aVI>pE  
(page number not for citation purposes) J#+Op/mmo  
cataract but in this particular population diabetes is more pTN%;`) {  
prevalent in men than women in all age groups [29]. Differential [@x  
exposures to cataract risk factors or different dietary $f9 ,##/  
or lifestyle patterns between men and women may *u58l(&`8  
also be related to these observations and warrant further Q:kwQg:~  
study. U-ERhm>uk  
Conclusion L(W%~UGN V  
In summary, in two population-based surveys 6 years i[mC3ghM6,  
apart, we have documented a relatively stable prevalence <1 TlW ~q<  
of cortical cataract and PSC over the period. The observed 2-QuT"Gkd  
overall increased nuclear cataract prevalence by 5% over a d~w}NK[(  
6-year period needs confirmation by future studies, and &~z+R="=  
reasons for such an increase deserve further study. ys:1Z\$P  
Competing interests 6s> sj7  
The author(s) declare that they have no competing interests. _3s~!2  
Authors' contributions wgC??Be;ut  
AGT graded the photographs, performed literature search b #o}=m  
and wrote the first draft of the manuscript. JJW graded the |Ba4 G`  
photographs, critically reviewed and modified the manuscript. 53g8T+`\(  
ER performed the statistical analysis and critically #j(q/ T{x  
reviewed the manuscript. PM designed and directed the j<`I\Pmv  
study, adjudicated cataract cases and critically reviewed e[d7UV[Knn  
and modified the manuscript. All authors read and IKNFYe[9e  
approved the final manuscript. $O;N/N:m  
Acknowledgements (mD-FR@#  
This study was supported by the Australian National Health & Medical r[C3u[  
Research Council, Canberra, Australia (Grant Nos 974159, 991407). The {hW +^  
abstract was presented at the Association for Research in Vision and Ophthalmology clPZd  
(ARVO) meeting in Fort Lauderdale, Florida, USA, May 2005. gJ)h9e*m^  
References / K2.V@T  
1. Congdon N, O'Colmain B, Klaver CC, Klein R, Munoz B, Friedman  [%gK^Zt  
DS, Kempen J, Taylor HR, Mitchell P: Causes and prevalence of pIU#c&%<9  
visual impairment among adults in the United States. Arch *IMF4 x 5M  
Ophthalmol 2004, 122(4):477-485. a"v"n$  
2. Rahmani B, Tielsch JM, Katz J, Gottsch J, Quigley H, Javitt J, Sommer F^%{ ;  
A: The cause-specific prevalence of visual impairment in an *@$($<pY&  
urban population. The Baltimore Eye Survey. Ophthalmology e)ZyTuj  
1996, 103:1721-1726. Egjk^:@  
3. Keeffe JE, Konyama K, Taylor HR: Vision impairment in the _D7HQ  
Pacific region. Br J Ophthalmol 2002, 86:605-610. IGF37';;  
4. Reidy A, Minassian DC, Vafidis G, Joseph J, Farrow S, Wu J, Desai P, R:pBbA7E  
Connolly A: Prevalence of serious eye disease and visual 1?e>x91  
impairment in a north London population: population based, E,ZB;  
cross sectional study. BMJ 1998, 316:1643-1646. kMJQeo79  
5. Resnikoff S, Pascolini D, Etya'ale D, Kocur I, Pararajasegaram R, ^w&5@3d  
Pokharel GP, Mariotti SP: Global data on visual impairment in &}L36|A:  
the year 2002. Bull World Health Organ 2004, 82:844-851. ~Uwr68 9N  
6. Pascolini D, Mariotti SP, Pokharel GP, Pararajasegaram R, Etya'ale D, AK*mcTr  
Negrel AD, Resnikoff S: 2002 global update of available data on xsY>{/C  
visual impairment: a compilation of population-based prevalence +,{Wcb  
studies. Ophthalmic Epidemiol 2004, 11:67-115. >zfZw"mEP  
7. Rochtchina E, Mukesh BN, Wang JJ, McCarty CA, Taylor HR, Mitchell %Zv(gI`A  
P: Projected prevalence of age-related cataract and cataract Q'Q72Fg  
surgery in Australia for the years 2001 and 2021: pooled data 0c\|S>g [  
from two population-based surveys. Clin Experiment Ophthalmol YjIED,eRv  
2003, 31:233-236. NZ%~n:/V#  
8. Medicare Benefits Schedule Statistics [http://www.medicar '7O{*=`oj  
eaustralia.gov.au/statistics/dyn_mbs/forms/mbs_tab4.shtml] Fy(nu-W  
9. Keeffe JE, Taylor HR: Cataract surgery in Australia 1985–94. hI>rtaY_  
Aust N Z J Ophthalmol 1996, 24:313-317. . ;ea]_Z  
10. Tan AG, Wang JJ, Rochtchina E, Jakobsen K, Mitchell P: Increase in 4MF}FS2)  
cataract surgery prevalence from 1992–1994 to 1997–2000: wTMHoU*>  
Analysis of two population cross-sections. Clin Experiment Ophthalmol Ae{4AZ  
2004, 32:284-288. yOn2}Z  
11. Mitchell P, Smith W, Attebo K, Wang JJ: Prevalence of age-related J:mu%N`  
maculopathy in Australia. The Blue Mountains Eye Study. 4f*Ua`E_  
Ophthalmology 1995, 102:1450-1460. i6g[E 4nk  
12. Mitchell P, Cumming RG, Attebo K, Panchapakesan J: Prevalence of 2t`9_zqLw  
cataract in Australia: the Blue Mountains eye study. Ophthalmology |>/&EElD  
1997, 104:581-588. Y4 ~wNs6  
13. Klein BEK, Magli YL, Neider MW, Klein R: Wisconsin system for classification sKG~<8M}  
of cataracts from photographs (protocol) Madison, WI; 1990. oN6*WN tJ  
14. Foran S, Wang JJ, Mitchell P: Causes of visual impairment in two Qdx`c^4m  
older population cross-sections: the Blue Mountains Eye W1vAK  
Study. Ophthalmic Epidemiol 2003, 10:215-225. D-+)M8bt  
15. Congdon N, Vingerling JR, Klein BE, West S, Friedman DS, Kempen J, C+#;L+$Gi  
O'Colmain B, Wu SY, Taylor HR: Prevalence of cataract and o|*|   
pseudophakia/aphakia among adults in the United States. LG@c)H74  
Arch Ophthalmol 2004, 122:487-494. 6<Pg>Bg  
16. Sperduto RD, Hiller R: The prevalence of nuclear, cortical, and }$k`[ivBx(  
posterior subcapsular lens opacities in a general population ,, H$>r_;  
sample. Ophthalmology 1984, 91:815-818. 8.3_Wb(c  
17. Adamsons I, Munoz B, Enger C, Taylor HR: Prevalence of lens ?D^,K`wY=B  
opacities in surgical and general populations. Arch Ophthalmol a^}P_hg}-  
1991, 109:993-997. C=_-p"O#  
18. Klein BE, Klein R, Linton KL: Prevalence of age-related lens $8T|r+<  
opacities in a population. The Beaver Dam Eye Study. Ophthalmology DEwtP   
1992, 99:546-552. (#l_YI -  
19. West SK, Munoz B, Schein OD, Duncan DD, Rubin GS: Racial differences eN?P) ,  
in lens opacities: the Salisbury Eye Evaluation (SEE) kcz#8K]~  
project. Am J Epidemiol 1998, 148:1033-1039. ZYD88kQ  
20. Congdon N, West SK, Buhrmann RR, Kouzis A, Munoz B, Mkocha H: SnF[mN'  
Prevalence of the different types of age-related cataract in *I1W+W`G  
an African population. Invest Ophthalmol Vis Sci 2001, tDLk ZCP  
42:2478-2482. \NQ)Po@z  
21. Livingston PM, Guest CS, Stanislavsky Y, Lee S, Bayley S, Walker C, a&c#* 9t{  
McKean C, Taylor HR: A population-based estimate of cataract }: D~yEP  
prevalence: the Melbourne Visual Impairment Project experience. ;@Hi*d[  
Dev Ophthalmol 1994, 26:1-6. g*c\'~f;  
22. Leske MC, Connell AM, Wu SY, Hyman L, Schachat A: Prevalence WKJL< D ]:  
of lens opacities in the Barbados Eye Study. Arch Ophthalmol "oXAIfU#T  
1997, 115:105-111. published erratum appears in Arch Ophthalmol 898wZ{9  
1997 Jul;115(7):931  aC }1]7  
23. Seah SK, Wong TY, Foster PJ, Ng TP, Johnson GJ: Prevalence of .&}4  
lens opacity in Chinese residents of Singapore: the tanjong C<@1H>S4_  
pagar survey. Ophthalmology 2002, 109:2058-2064. <J }9.k  
24. Stifter E, Sacu S, Weghaupt H, Konig F, Richter-Muksch S, Thaler A, iE gM ~  
Velikay-Parel M, Radner W: Reading performance depending on m"7R 4O  
the type of cataract and its predictability on the visual outcome. %s :  
J Cataract Refract Surg 2004, 30:1259-1267. ;AB,:*  
25. Stifter E, Sacu S, Weghaupt H: Functional vision with cataracts of }_/h~D9-T#  
different morphologies: comparative study. J Cataract Refract q[+: t   
Surg 2004, 30:1883-1891. WJ8 vHPSM  
26. Leske MC, Chylack LT Jr, Wu SY: The Lens Opacities Case-Control la{uJ9Iw@}  
Study. Risk factors for cataract. Arch Ophthalmol 1991, Hg_ XD,  
109:244-251. .:!x*v  
27. Leske MC, Wu SY, Hyman L, Sperduto R, Underwood B, Chylack LT, AbI*/ |sY  
Milton RC, Srivastava S, Ansari N: Biochemical factors in the lens `/ReJj&~  
opacities. Case-control study. The Lens Opacities Case-Control V+~{a:8[pq  
Study Group. Arch Ophthalmol 1995, 113:1113-1119. ZV4' |q  
28. Yip R, Johnson C, Dallman PR: Age-related changes in laboratory zp-~'kIJ  
values used in the diagnosis of anemia and iron deficiency. xWb?i6)z&  
Am J Clin Nutr 1984, 39:427-436. RW[<e   
29. Mitchell P, Smith W, Wang JJ, Cumming RG, Leeder SR, Burnett L: poFjhq /#(  
Diabetes in an older Australian population. Diabetes Res Clin :BxYaAVt^  
Pract 1998, 41:177-184. &:f'{>3 z  
Pre-publication history '?GZ"C2  
The pre-publication history for this paper can be accessed 6@ ^`-N;  
here: @wJa33QT  
Publish with BioMed Central and every aMg f6veM  
scientist can read your work free of charge [m[~A|S  
"BioMed Central will be the most significant development for x)Kh _ G  
disseminating the results of biomedical research in our lifetime." y/VmjsN}  
Sir Paul Nurse, Cancer Research UK xm, yqM!0A  
Your research papers will be: f|1FqL+T]  
available free of charge to the entire biomedical community NfN6KDd]2L  
peer reviewed and published immediately upon acceptance pFRnPOv  
cited in PubMed and archived on PubMed Central '6J$X-  
yours — you keep the copyright %-po6Vf  
Submit your manuscript here: zb,`K*Z{  
http://www.biomedcentral.com/info/publishing_adv.asp Y,}43a0A  
BioMedcentral _!1c.[ \T  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 [N+ruc?)  
Page 7 of 7 BTtYlpN6  
(page number not for citation purposes) T7_rnEOO   
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:
免费考博论坛网址是什么? 正确答案:freekaobo.com
按"Ctrl+Enter"直接提交