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 ]7Fs$y.  
Page 1 of 7 vm'5s]kdh  
(page number not for citation purposes) = 0- $W5E  
BMC Ophthalmology Z--@.IYoJ  
Research article Open Access z`6fotL  
Comparison of age-specific cataract prevalence in two $o+5/c?|  
population-based surveys 6 years apart zd_HxYrN  
Ava Grace Tan†, Jie Jin Wang*†, Elena Rochtchina† and Paul Mitchell† v?c 0[+?  
Address: Centre for Vision Research, Westmead Millennium Institute, Department of Ophthalmology, University of Sydney, Westmead Hospital, A!vCb 8(TX  
Westmead, NSW, Australia O,<IGO  
Email: Ava Grace Tan - ava_tan@wmi.usyd.edu.au; Jie Jin Wang* - jiejin_wang@wmi.usyd.edu.au; \]9.zlB  
Elena Rochtchina - elena_rochtchina@wmi.usyd.edu.au; Paul Mitchell - paul_mitchell@wmi.usyd.edu.au W- $a Y2  
* Corresponding author †Equal contributors 1shBY@mlq  
Abstract }YOL"<,:o  
Background: In this study, we aimed to compare age-specific cortical, nuclear and posterior hCYQGx0  
subcapsular (PSC) cataract prevalence in two surveys 6 years apart. y{9~&r  
Methods: The Blue Mountains Eye Study examined 3654 participants (82.4% of those eligible) in 6r"u$i` o  
cross-section I (1992–4) and 3509 participants (75.1% of survivors and 85.2% of newly eligible) in +uWYK9  
cross-section II (1997–2000, 66.5% overlap with cross-section I). Cataract was assessed from lens ^2o dr \  
photographs following the Wisconsin Cataract Grading System. Cortical cataract was defined if q4UA]+-*  
cortical opacity comprised ≥ 5% of lens area. Nuclear cataract was defined if nuclear opacity ≥ 39 Y(!q  
Wisconsin standard 4. PSC was defined if any present. Any cataract was defined to include persons Lz DI0a.  
who had previous cataract surgery. Weighted kappa for inter-grader reliability was 0.82, 0.55 and rC_*sx r^  
0.82 for cortical, nuclear and PSC cataract, respectively. We assessed age-specific prevalence using )R_E|@"  
an interval of 5 years, so that participants within each age group were independent between the xw<OLWW  
two surveys. qP!P +'B  
Results: Age and gender distributions were similar between the two populations. The age-specific sP'0Sl~NU  
prevalence of cortical (23.8% in 1st, 23.7% in 2nd) and PSC cataract (6.3%, 6.0%) was similar. The d {2  
prevalence of nuclear cataract increased slightly from 18.7% to 23.9%. After age standardization, 7:NmCpgL!  
the similar prevalence of cortical (23.8%, 23.5%) and PSC cataract (6.3%, 5.9%), and the increased v=I|O%  
prevalence of nuclear cataract (18.7%, 24.2%) remained. #kkY@k$4  
Conclusion: In two surveys of two population-based samples with similar age and gender (IbW; bV  
distributions, we found a relatively stable cortical and PSC cataract prevalence over a 6-year period. qJR!$?  
The increased prevalence of nuclear cataract deserves further study. 5wC* ?>/  
Background iF+ RnWX\  
Age-related cataract is the leading cause of reversible visual >i,iOx|E-  
impairment in older persons [1-6]. In Australia, it is mT*{-n_Zs  
estimated that by the year 2021, the number of people 1+y"i<3)  
affected by cataract will increase by 63%, due to population 7yI @"c#O  
aging [7]. Surgical intervention is an effective treatment 4YU/uQm  
for cataract and normal vision (> 20/40) can usually o=fgin/E\  
be restored with intraocular lens (IOL) implantation. h7_)%U<J2  
Cataract surgery with IOL implantation is currently the TB aVW  
most commonly performed, and is, arguably, the most |f2A89  
cost effective surgical procedure worldwide. Performance `BZ&~vJ_  
Published: 20 April 2006 a?cn9i)#  
BMC Ophthalmology 2006, 6:17 doi:10.1186/1471-2415-6-17 VFD%h }  
Received: 14 December 2005 y@ek=fT%4  
Accepted: 20 April 2006 q$ghLGz  
This article is available from: http://www.biomedcentral.com/1471-2415/6/17 e5v`;(^M  
© 2006 Tan et al; licensee BioMed Central Ltd. &;q<M_<  
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), ySN V^+  
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. FJM;X-UOY  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 Il~01|3+m  
Page 2 of 7 q{4|Kpx@  
(page number not for citation purposes) {0jIY  
of this surgical procedure has been continuously increasing dXu{p  
in the last two decades. Data from the Australian u"VS* hSH  
Health Insurance Commission has shown a steady 4B O %{  
increase in Medicare claims for cataract surgery [8]. A 2.6- +/'<z  
fold increase in the total number of cataract procedures /r$&]C:Fi  
from 1985 to 1994 has been documented in Australia [9]. : 1)}Epo,  
The rate of cataract surgery per thousand persons aged 65 9fVj 8G  
years or older has doubled in the last 20 years [8,9]. In the Q^h5">P  
Blue Mountains Eye Study population, we observed a onethird bcJ@-i0V  
increase in cataract surgery prevalence over a mean nX x=1*X  
6-year interval, from 6% to nearly 8% in two cross-sectional 2)LX^?7 R  
population-based samples with a similar age range EnCU4CU`  
[10]. Further increases in cataract surgery performance LdTIR]  
would be expected as a result of improved surgical skills 6Dzs?P  
and technique, together with extending cataract surgical pzEABA   
benefits to a greater number of older people and an kO3 `54  
increased number of persons with surgery performed on Ggd lVi 2  
both eyes. X ]s"5ju|t  
Both the prevalence and incidence of age-related cataract i,OKf Xp  
link directly to the demand for, and the outcome of, cataract 6VR18Y!y  
surgery and eye health care provision. This report d^aNR Lv  
aimed to assess temporal changes in the prevalence of cortical bXl 8v  
and nuclear cataract and posterior subcapsular cataract BMjfqX  
(PSC) in two cross-sectional population-based |BJqy/  
surveys 6 years apart. /+P5)q TKL  
Methods GN%<"I.  
The Blue Mountains Eye Study (BMES) is a populationbased E4m:1=Nd~]  
cohort study of common eye diseases and other ]PVt o\B=  
health outcomes. The study involved eligible permanent $ 'u \B  
residents aged 49 years and older, living in two postcode nt`<y0ta  
areas in the Blue Mountains, west of Sydney, Australia. rIPl6,w~  
Participants were identified through a census and were ~h|m&XK+Q  
invited to participate. The study was approved at each k!c7a\">{  
stage of the data collection by the Human Ethics Committees thQ J(w  
of the University of Sydney and the Western Sydney kpT>G$s~gy  
Area Health Service and adhered to the recommendations f-]><z  
of the Declaration of Helsinki. Written informed consent ]W|RtdF3.N  
was obtained from each participant. p\ok_*b  
Details of the methods used in this study have been u7 ~mn l  
described previously [11]. The baseline examinations UhA_1A'B  
(BMES cross-section I) were conducted during 1992– @:IL/o*  
1994 and included 3654 (82.4%) of 4433 eligible residents. Bpas[2gYC  
Follow-up examinations (BMES IIA) were conducted @|]G0&gn&?  
during 1997–1999, with 2335 (75.0% of BMES U[Nosh)hu\  
cross section I survivors) participating. A repeat census of tKX}Ok:V%  
the same area was performed in 1999 and identified 1378 BWohMT  
newly eligible residents who moved into the area or the |87W*  
eligible age group. During 1999–2000, 1174 (85.2%) of Q.>/*8R;  
this group participated in an extension study (BMES IIB). )ZeLaaP  
BMES cross-section II thus includes BMES IIA (66.5%) h/{8bC@bi  
and BMES IIB (33.5%) participants (n = 3509). @%%bRY  
Similar procedures were used for all stages of data collection <\Vi,,  
at both surveys. A questionnaire was administered *H?t;,\  
including demographic, family and medical history. A [}@n*D$  
detailed eye examination included subjective refraction, c0SX]4} G  
slit-lamp (Topcon SL-7e camera, Topcon Optical Co, tz3]le|ml  
Tokyo, Japan) and retroillumination (Neitz CT-R camera, ^ }tL nF  
Neitz Instrument Co, Tokyo, Japan) photography of the <qr^Nyo4  
lens. Grading of lens photographs in the BMES has been `fLfT'  
previously described [12]. Briefly, masked grading was !4_!J (q%  
performed on the lens photographs using the Wisconsin hO%Y{Gg  
Cataract Grading System [13]. Cortical cataract and PSC )'=V!H#U*  
were assessed from the retroillumination photographs by va@XbUC  
estimating the percentage of the circular grid involved. 4YBf ~Pp  
Cortical cataract was defined when cortical opacity .:T9pplq  
involved at least 5% of the total lens area. PSC was defined J&'>IA  
when opacity comprised at least 1% of the total lens area. zv`zsqDJ  
Slit-lamp photographs were used to assess nuclear cataract wXP_]-  
using the Wisconsin standard set of four lens photographs 3g^IXm:K$  
[13]. Nuclear cataract was defined when nuclear opacity _dJp 3D  
was at least as great as the standard 4 photograph. Any cataract rtcJ=`)0`  
was defined to include persons who had previous m\l51 }xz  
cataract surgery as well as those with any of three cataract +yt6.L  
types. Inter-grader reliability was high, with weighted fmtuFr^a1  
kappa 0.82 for cortical cataract, 0.55 (simple kappa 0.75) |&9 tU  
for nuclear cataract and 0.82 for PSC grading. The intragrader sYl&Q.\q  
reliability for nuclear cataract was assessed with hT\p)w  
simple kappa 0.83 for the senior grader who graded "$# $f  
nuclear cataract at both surveys. All PSC cases were confirmed GOUY_&}tL  
by an ophthalmologist (PM). Hf;RIl2F  
In cross-section I, 219 persons (6.0%) had missing or (MZ A  
ungradable Neitz photographs, leaving 3435 with photographs -$xKv4  
available for cortical cataract and PSC assessment, 2=i+L z^  
while 1153 (31.6%) had randomly missing or ungradable ]kyle3#-~  
Topcon photographs due to a camera malfunction, leaving ^H f+du  
2501 with photographs available for nuclear cataract ?psOj%  
assessment. Comparison of characteristics between participants FRb&@ (;  
with and without Neitz or Topcon photographs in Wh#os,U $  
cross-section I showed no statistically significant differences KteZK.+#:  
between the two groups, as reported previously &f (sfM_n  
[12]. In cross-section II, 441 persons (12.5%) had missing :_W 0Af09  
or ungradable Neitz photographs, leaving 3068 for cortical XHU<4l:kl  
cataract and PSC assessment, and 648 (18.5%) had fx8y`8}_  
missing or ungradable Topcon photographs, leaving 2860 s^{{@O.  
for nuclear cataract assessment. l:>qR/|m  
Data analysis was performed using the Statistical Analysis \9&YV;Ct  
System (SAS, SAS Institute, Cary, NC, USA). Age-adjusted BaNU}@  
prevalence was calculated using direct standardization of `kaR@t  
the cross-section II population to the cross-section I population. @vVRF Z  
We assessed age-specific prevalence using an e<ism?WG  
interval of 5 years, so that participants within each age Z&?+&q r^  
group were independent between the two cross-sectional j]cXLY  
surveys. s!nSE  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 i-K"9z| )  
Page 3 of 7 s[vPH8qb  
(page number not for citation purposes) 6Zl.Lh  
Results "(HA9:  
Characteristics of the two survey populations have been y~4SKv $  
previously compared [14] and showed that age and sex dA_V:HP  
distributions were similar. Table 1 compares participant .O @q5G  
characteristics between the two cross-sections. Cross-section O?4vC5x  
II participants generally had higher rates of diabetes, O9Jx%tolF%  
hypertension, myopia and more users of inhaled steroids. x):k#cu[L  
Cataract prevalence rates in cross-sections I and II are =2vMw]  
shown in Figure 1. The overall prevalence of cortical cataract FBwncG$]F*  
was 23.8% and 23.7% in cross-sections I and II, ~t.WwxY+  
respectively (age-sex adjusted P = 0.81). Corresponding [EW$7 se~  
prevalence of PSC was 6.3% and 6.0% for the two crosssections d-#u/{jG)  
(age-sex adjusted P = 0.60). There was an  `lV  
increased prevalence of nuclear cataract, from 18.7% in \h'E5LO  
cross-section I to 23.9% in cross-section II over the 6-year 'o#J>a~!9L  
period (age-sex adjusted P < 0.001). Prevalence of any cataract + 8K1]'t$  
(including persons who had cataract surgery), however, a2 klOX{  
was relatively stable (46.9% and 46.8% in crosssections iz%A0Z+`bg  
I and II, respectively). ftI+#0?[!  
After age-standardization, these prevalence rates remained #)h ~.D{  
stable for cortical cataract (23.8% and 23.5% in the two ,SE$Rh  
surveys) and PSC (6.3% and 5.9%). The slightly increased H-\ {w    
prevalence of nuclear cataract (from 18.7% to 24.2%) was @7[.> I(  
not altered. ,Q /nS$  
Table 2 shows the age-specific prevalence rates for cortical 2dd:5L,  
cataract, PSC and nuclear cataract in cross-sections I and 0@FM^ejA#  
II. A similar trend of increasing cataract prevalence with >$S,>d_k`  
increasing age was evident for all three types of cataract in TXh@  
both surveys. Comparing the age-specific prevalence t+4Y3*WeGF  
between the two surveys, a reduction in PSC prevalence in x 1xj\O  
cross-section II was observed in the older age groups (≥ 75 @y\{<X.F\1  
years). In contrast, increased nuclear cataract prevalence P VkN3J  
in cross-section II was observed in the older age groups (≥ }MavI'  
70 years). Age-specific cortical cataract prevalence was relatively @aV~.!!  
consistent between the two surveys, except for a I\uB"Z{9  
reduction in prevalence observed in the 80–84 age group h3d\MYO)B  
and an increasing prevalence in the older age groups (≥ 85 # !d^3iB2  
years). EAd:`X,Y  
Similar gender differences in cataract prevalence were tj^:SW.0  
observed in both surveys (Table 3). Higher prevalence of sQw`U{JG  
cortical and nuclear cataract in women than men was evident h^_taAdS`  
but the difference was only significant for cortical $@qs(Xwr  
cataract (age-adjusted odds ratio, OR, for women 1.3, `)C`_g3Ew  
95% confidence intervals, CI, 1.1–1.5 in cross-section I } Ved  
and OR 1.4, 95% CI 1.1–1.6 in cross-section II). In con- .kKwdqO+zB  
Table 1: Participant characteristics. g\{! 21M  
Characteristics Cross-section I Cross-section II ;7n*PBUJJ  
n % n % BfE-s<  
Age (mean) (66.2) (66.7) \;:@=9`  
50–54 485 13.3 350 10.0 7@cvy? v{  
55–59 534 14.6 580 16.5 -b>O4_N  
60–64 638 17.5 600 17.1 /e?ux~f|  
65–69 671 18.4 639 18.2 i`nw"8  
70–74 538 14.7 572 16.3 :9 iOuu  
75–79 422 11.6 407 11.6 ?M-8Fp3 +  
80–84 230 6.3 226 6.4 JX0_UU  
85–89 100 2.7 110 3.1 [O+^eE6h  
90+ 36 1.0 24 0.7 ODvpMt:+  
Female 2072 56.7 1998 57.0 "gikX/Co=  
Ever Smokers 1784 51.2 1789 51.2 Qp{-!*  
Use of inhaled steroids 370 10.94 478 13.8^ cTa D{!zm5  
History of: s1\BjSzk  
Diabetes 284 7.8 347 9.9^ 9c %  Tv  
Hypertension 1669 46.0 1825 52.2^ bl>b/u7/6  
Emmetropia* 1558 42.9 1478 42.2 :;WDPRx  
Myopia* 442 12.2 495 14.1^ yW(+?7U  
Hyperopia* 1633 45.0 1532 43.7 A^@<+?  
n = number of persons affected )$4DH:WN  
* best spherical equivalent refraction correction ; GT)sI   
^ P < 0.01 :Q L p`s  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 LbbQ3$@ WD  
Page 4 of 7 OLup`~  
(page number not for citation purposes) 9x{prCr  
t ({nSs5)$  
rast, men had slightly higher PSC prevalence than women DMN H?6  
in both cross-sections but the difference was not significant _1c_TMh}9  
(OR 1.1, 95% CI 0.8–1.4 for men in cross-section I tRBK1h  
and OR 1.2, 95% 0.9–1.6 in cross-section II). P}QbxkS 8  
Discussion Byj~\QMD|  
Findings from two surveys of BMES cross-sectional populations 5@%-=87S  
with similar age and gender distribution showed 32P]0&_O  
that the prevalence of cortical cataract and PSC remained j$oZIV7  
stable, while the prevalence of nuclear cataract appeared +##I4vP  
to have increased. Comparison of age-specific prevalence, J\D3fh97-  
with totally independent samples within each age group, m e{SVG{  
confirmed the robustness of our findings from the two I'b]s~u  
survey samples. Although lens photographs taken from 'k Z1&_{  
the two surveys were graded for nuclear cataract by the 6|cl`}g_j  
same graders, who documented a high inter- and intragrader Wj=ex3K3u.  
reliability, we cannot exclude the possibility that l8Qi^<i/  
variations in photography, performed by different photographers, qJt gnk|  
may have contributed to the observed difference @\}36y  
in nuclear cataract prevalence. However, the overall zL8A?G)= M  
Table 2: Age-specific prevalence of cataract types in cross sections I and II. tgA |Vwwk  
Cataract type Age (years) Cross-section I Cross-section II Hvo27THLo  
n % (95% CL)* n % (95% CL)* &~f_1<  
Cortical 50–54 473 4.4 (2.6–6.3) 338 7.4 (4.6–10.2) Lta\AN!c  
55–59 522 9.2 (6.7–11.7) 542 9.0 (6.6–11.5) 9'h^59  
60–64 615 16.4 (13.5–19.4) 556 16.7 (13.6–19.8) ved Qwzh  
65–69 653 26.2 (22.8–29.6) 581 23.6 (20.1–27.0) <U pjAuG8  
70–74 516 31.2 (27.2–35.2) 514 35.4 (31.3–39.6) AI;=k  
75–79 366 40.2 (35.1–45.2) 332 39.8 (34.5–45.1) mP[u[|]  
80–84 194 58.8 (51.8–65.8) 163 42.9 (35.3–50.6) ,0~TvJS  
85–89 74 52.7 (41.1–64.4) 73 54.8 (43.1–66.5) <5~>.DuE  
90+ 22 68.2 (47.0–89.3) 14 78.6 (54.0–103.2) 1Di&vpn0u  
PSC 50–54 474 2.7 (1.3–4.2) 338 2.4 (0.7–4.0) 'Sh5W%NM  
55–59 522 2.9 (1.4–4.3) 541 2.6 (1.3–3.9) BG=_i#V  
60–64 616 4.6 (2.9–6.2) 548 5.7 (3.7–7.6) 'v  X"l  
65–69 655 6.3 (4.4–8.1) 573 4.5 (2.8–6.3) ]]3D` F}  
70–74 517 6.8 (4.6–8.9) 505 9.7 (7.1–12.3) 3vU (4}@  
75–79 367 11.4 (8.2–14.7) 327 9.5 (6.3–12.7) C ,hsr  
80–84 196 12.2 (7.6–16.9) 155 10.3 (5.5–15.2) {hz :[  
85–89 74 18.9 (9.8–28.1) 69 11.6 (3.9–19.4) ;xwQzu%M>5  
90+ 23 21.7 (3.5–40.0) 11 0.0 #mYxO  
Nuclear 50–54 323 1.6 (0.2–2.9) 331 0.9 (–0.2–1.9) Shz;)0To  
55–59 386 2.3 (0.8–3.8) 507 3.6 (1.9–5.2) F9W5x=EK\  
60–64 453 5.3 (3.2–7.4) 501 11.6 (8.8–14.4) j83 V$ Le  
65–69 478 17.2 (13.8–20.1) 534 18.5 (15.2–21.9) "g-NUl`'  
70–74 392 27.6 (23.1–32.0) 453 36.0 (31.6–40.4) :TI1tJS~*  
75–79 255 45.1 (39.0–51.3) 302 55.6 (50.0–61.3) Dzr5qP?#  
80–84 146 54.1 (45.9–62.3) 147 73.5 (66.3–80.7) y{JkY\g  
85–89 50 64.0 (50.2–77.8) 70 80.0 (70.4–89.6) 7l3q~dQ  
90+ 18 72.2 (49.3–95.1) 15 73.3 (48.0–98.7) n TG| Isa  
n = number of persons 2l?J9c}Wo  
* 95% Confidence Limits .~J^`/o  
Cataract FMioguunrtea i1n ps rEeyvea lSetnucdey in cross-sections I and II of the Blue NY x4& *le  
Cataract prevalence in cross-sections I and II of the Blue bAp`lmFI  
Mountains Eye Study. p~IvkW>ln)  
0 kx[8#+P  
10 uE(w$2Wi  
20 ?*,q#ZkA9W  
30 :%{7Q$Xv<  
40 l<0V0R(  
50 DxHeZQ"LL  
cortical PSC nuclear any nj mE>2  
cataract Ry C7  
Cataract type STe;Sr&p  
% P6Ei!t,>  
Cross-section I Rs wR DLl  
Cross-section II G1rgp>m  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 #LiC@>  
Page 5 of 7 F/8y p<_r  
(page number not for citation purposes) =E}/Z  
prevalence of any cataract (including cataract surgery) was I$$!YMm.N  
relatively stable over the 6-year period. lgl/| ^ Uw  
Although different population-based studies used different # V +e  
grading systems to assess cataract [15], the overall Ax ^9J)C  
prevalence of the three cataract types were similar across PyYe>a;.  
different study populations [12,16-23]. Most studies have C}CX n X  
suggested that nuclear cataract is the most prevalent type Oaui@q  
of cataract, followed by cortical cataract [16-20]. Ours and T~la,>p|}  
other studies reported that cortical cataract was the most Ap/WgVw;  
prevalent type [12,21-23]. @ o]F~x  
Our age-specific prevalence data show a reduction of ~c4Y*]J  
15.9% in cortical cataract prevalence for the 80–84 year 3jeR;N]x  
age group, concordant with an increase in cataract surgery 95}"AIi  
prevalence by 9% in those aged 80+ years observed in the a`}-^;}SW  
same study population [10]. Although cortical cataract is V%))%?3x_  
thought to be the least likely cataract type leading to a cataract H_9~gi  
surgery, this may not be the case in all older persons. F)C8LH  
A relatively stable cortical cataract and PSC prevalence 1z)+P1nH]  
over the 6-year period is expected. We cannot offer a di"*K*~y  
definitive explanation for the increase in nuclear cataract fYwumx`J  
prevalence. A possible explanation could be that a moderate s:%>H|-  
level of nuclear cataract causes less visual disturbance %BL+'&q  
than the other two types of cataract, thus for the oldest age GFvOrRlP\  
groups, persons with nuclear cataract could have been less x[]n \\a?  
likely to have surgery unless it is very dense or co-existing m#uutomi0  
with cortical cataract or PSC. Previous studies have shown #N*~Q  
that functional vision and reading performance were high f.!cR3XgV  
in patients undergoing cataract surgery who had nuclear  ST{<G  
cataract only compared to those with mixed type of cataract -50|r;a  
(nuclear and cortical) or PSC [24,25]. In addition, the @rE>D  
overall prevalence of any cataract (including cataract surgery) Zvc{o8^z  
was similar in the two cross-sections, which appears x k#/J]j  
to support our speculation that in the oldest age group, YS/4<QA[  
nuclear cataract may have been less likely to be operated ^s^X nQhE  
than the other two types of cataract. This could have J g@PhN<9  
resulted in an increased nuclear cataract prevalence (due LcQ\ d*  
to less being operated), compensated by the decreased zH.7!jeE  
prevalence of cortical cataract and PSC (due to these being gP`8hNwR  
more likely to be operated), leading to stable overall prevalence nP] ~8ViS  
of any cataract. vFQ'sd]C  
Possible selection bias arising from selective survival hS<+=3 <M  
among persons without cataract could have led to underestimation (R{W Jjj  
of cataract prevalence in both surveys. We J@52<.>6  
assume that such an underestimation occurred equally in [8<)^k  
both surveys, and thus should not have influenced our KATt9ox@  
assessment of temporal changes. O.}{s;  
Measurement error could also have partially contributed gE|_hfm (  
to the observed difference in nuclear cataract prevalence. Po% V%~  
Assessment of nuclear cataract from photographs is a 2-FL&DE  
potentially subjective process that can be influenced by N\rbnr  
variations in photography (light exposure, focus and the P/4]x@{ih  
slit-lamp angle when the photograph was taken) and 0X.pI1jCO  
grading. Although we used the same Topcon slit-lamp 2ACN5lyUS  
camera and the same two graders who graded photos I6~.s Tl  
from both surveys, we are still not able to exclude the possibility LNtBYdB`pK  
of a partial influence from photographic variation Z%k)'%_   
on this result. I!~5.  
A similar gender difference (women having a higher rate $)mK]57  
than men) in cortical cataract prevalence was observed in [?^,,.Dd  
both surveys. Our findings are in keeping with observations ng"R[/)In  
from the Beaver Dam Eye Study [18], the Barbados -r7*C :E  
Eye Study [22] and the Lens Opacities Case-Control xx_]e4  
Group [26]. It has been suggested that the difference /0IvvD!7N  
could be related to hormonal factors [18,22]. A previous ,E <(K8  
study on biochemical factors and cataract showed that a u,I_p[`E  
lower level of iron was associated with an increased risk of ;N#d'E\  
cortical cataract [27]. No interaction between sex and biochemical  R5(<:]  
factors were detected and no gender difference v'mRch)d  
was assessed in this study [27]. The gender difference seen Yj;KKgk  
in cortical cataract could be related to relatively low iron W1fEUVj  
levels and low hemoglobin concentration usually seen in 2r4owB?  
women [28]. Diabetes is a known risk factor for cortical e0Zwhz,  
Table 3: Gender distribution of cataract types in cross-sections I and II. wylbs@  
Cataract type Gender Cross-section I Cross-section II .SzP ig  
n % (95% CL)* n % (95% CL)* -PPH]?],  
Cortical Male 1496 21.1 (19.0–23.1) 1328 20.4 (18.2–22.6) )RG@D\t,  
Female 1939 25.9 (23.9–27.8) 1785 26.2 (24.2–28.3) ji9 (!G  
PSC Male 1500 6.5 (5.2–7.7) 1314 6.4 (5.1–7.7) o`,|{K$H  
Female 1944 6.2 (5.1–7.2) 1753 5.7 (4.6–6.7) 2:3-mWE  
Nuclear Male 1106 17.6 (15.4–19.9) 1225 22.5 (20.1–24.8) >>22:JI`  
Female 1395 19.5 (17.4–21.6) 1635 25.0 (22.9–27.1) dNK Q&TC  
n = number of persons ++1<A& a  
* 95% Confidence Limits 1$mxMXNsJ  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 }ya@*jH  
Page 6 of 7 dp;;20z  
(page number not for citation purposes) jd ]$U_U(  
cataract but in this particular population diabetes is more M uz+j.0  
prevalent in men than women in all age groups [29]. Differential s[<a(  
exposures to cataract risk factors or different dietary [Ume^  
or lifestyle patterns between men and women may gJ;jh7e@  
also be related to these observations and warrant further dAg<BK/  
study. GY% ^!r  
Conclusion bT93R8yp  
In summary, in two population-based surveys 6 years Qg9*mlm`  
apart, we have documented a relatively stable prevalence )\K;Ncp[  
of cortical cataract and PSC over the period. The observed 5~8FZ-x  
overall increased nuclear cataract prevalence by 5% over a (p6$Vgdt  
6-year period needs confirmation by future studies, and cl\Gh  
reasons for such an increase deserve further study. 7 k:w3M  
Competing interests TTGk"2 Q'  
The author(s) declare that they have no competing interests. Xgb ~ED]  
Authors' contributions XHN*'@ 77;  
AGT graded the photographs, performed literature search [l`_2{:  
and wrote the first draft of the manuscript. JJW graded the y"bSn5B[  
photographs, critically reviewed and modified the manuscript. S{uKm1a  
ER performed the statistical analysis and critically fS@V`"O6  
reviewed the manuscript. PM designed and directed the Jy iP3whW  
study, adjudicated cataract cases and critically reviewed o x|K2A  
and modified the manuscript. All authors read and *- S/{ .&  
approved the final manuscript. ]'"aVGqa.  
Acknowledgements /7`fg0A  
This study was supported by the Australian National Health & Medical ?^X e^1(  
Research Council, Canberra, Australia (Grant Nos 974159, 991407). The jIvSjlmI  
abstract was presented at the Association for Research in Vision and Ophthalmology &x mYpQ  
(ARVO) meeting in Fort Lauderdale, Florida, USA, May 2005. U??T>  
References ",O}{z  
1. Congdon N, O'Colmain B, Klaver CC, Klein R, Munoz B, Friedman 7^hwRZJ{  
DS, Kempen J, Taylor HR, Mitchell P: Causes and prevalence of 1s"/R  
visual impairment among adults in the United States. Arch ;$FpxurX  
Ophthalmol 2004, 122(4):477-485. d*cAm$   
2. Rahmani B, Tielsch JM, Katz J, Gottsch J, Quigley H, Javitt J, Sommer !et[Rdbu  
A: The cause-specific prevalence of visual impairment in an +k?0C?/T;  
urban population. The Baltimore Eye Survey. Ophthalmology H)5V \  
1996, 103:1721-1726. Qzh`x-S  
3. Keeffe JE, Konyama K, Taylor HR: Vision impairment in the v:xfGA nP  
Pacific region. Br J Ophthalmol 2002, 86:605-610. %~{G*%:  
4. Reidy A, Minassian DC, Vafidis G, Joseph J, Farrow S, Wu J, Desai P, "TQ3{=j{  
Connolly A: Prevalence of serious eye disease and visual =X24C'!Mpe  
impairment in a north London population: population based, 5h!ZoB)n  
cross sectional study. BMJ 1998, 316:1643-1646. jb'A Os  
5. Resnikoff S, Pascolini D, Etya'ale D, Kocur I, Pararajasegaram R, xlHC?d0}  
Pokharel GP, Mariotti SP: Global data on visual impairment in jn:9Cr,o;g  
the year 2002. Bull World Health Organ 2004, 82:844-851. lDU@Q(V#}<  
6. Pascolini D, Mariotti SP, Pokharel GP, Pararajasegaram R, Etya'ale D, P_y8[Y]?  
Negrel AD, Resnikoff S: 2002 global update of available data on ?z/ )Hkw  
visual impairment: a compilation of population-based prevalence ?E2$  
studies. Ophthalmic Epidemiol 2004, 11:67-115. wVMR&R<t  
7. Rochtchina E, Mukesh BN, Wang JJ, McCarty CA, Taylor HR, Mitchell ),%(A~\  
P: Projected prevalence of age-related cataract and cataract + m+v1(@  
surgery in Australia for the years 2001 and 2021: pooled data b$,~S\\c  
from two population-based surveys. Clin Experiment Ophthalmol m,1Hlp  
2003, 31:233-236. = VFPZ  
8. Medicare Benefits Schedule Statistics [http://www.medicar {g@?\  
eaustralia.gov.au/statistics/dyn_mbs/forms/mbs_tab4.shtml] _ !r]**  
9. Keeffe JE, Taylor HR: Cataract surgery in Australia 1985–94. aZBS!X  
Aust N Z J Ophthalmol 1996, 24:313-317. M7x*LiKc2  
10. Tan AG, Wang JJ, Rochtchina E, Jakobsen K, Mitchell P: Increase in 9%  wVE]  
cataract surgery prevalence from 1992–1994 to 1997–2000: J6s@}@R1  
Analysis of two population cross-sections. Clin Experiment Ophthalmol =IC cN|  
2004, 32:284-288. w /l\p3n  
11. Mitchell P, Smith W, Attebo K, Wang JJ: Prevalence of age-related k  __MYb  
maculopathy in Australia. The Blue Mountains Eye Study. "IE*MmsEz  
Ophthalmology 1995, 102:1450-1460. KO''B or  
12. Mitchell P, Cumming RG, Attebo K, Panchapakesan J: Prevalence of AJWV#J%nB  
cataract in Australia: the Blue Mountains eye study. Ophthalmology R{3vPG  
1997, 104:581-588. `rQDX<?  
13. Klein BEK, Magli YL, Neider MW, Klein R: Wisconsin system for classification /jB 0  
of cataracts from photographs (protocol) Madison, WI; 1990. ^W)h=49 PN  
14. Foran S, Wang JJ, Mitchell P: Causes of visual impairment in two : l&g5  
older population cross-sections: the Blue Mountains Eye q8-*3K  
Study. Ophthalmic Epidemiol 2003, 10:215-225. g6V>_|  
15. Congdon N, Vingerling JR, Klein BE, West S, Friedman DS, Kempen J, 3`%U)gCT5  
O'Colmain B, Wu SY, Taylor HR: Prevalence of cataract and wrJ:jTh  
pseudophakia/aphakia among adults in the United States. Of?3|I3 l  
Arch Ophthalmol 2004, 122:487-494. ;mtv  
16. Sperduto RD, Hiller R: The prevalence of nuclear, cortical, and Aav|N3  
posterior subcapsular lens opacities in a general population QgB%\mO=  
sample. Ophthalmology 1984, 91:815-818. miv)R   
17. Adamsons I, Munoz B, Enger C, Taylor HR: Prevalence of lens WJJwhr  
opacities in surgical and general populations. Arch Ophthalmol %!HBPLk  
1991, 109:993-997. @+EO3-X5  
18. Klein BE, Klein R, Linton KL: Prevalence of age-related lens UL <*z!y  
opacities in a population. The Beaver Dam Eye Study. Ophthalmology iLR^V!  
1992, 99:546-552. Z7:TPY$b  
19. West SK, Munoz B, Schein OD, Duncan DD, Rubin GS: Racial differences azT@S=,  
in lens opacities: the Salisbury Eye Evaluation (SEE) XkE'k; AEx  
project. Am J Epidemiol 1998, 148:1033-1039. `j1(GQt  
20. Congdon N, West SK, Buhrmann RR, Kouzis A, Munoz B, Mkocha H: T>e4Og"?  
Prevalence of the different types of age-related cataract in aH(B}wh{  
an African population. Invest Ophthalmol Vis Sci 2001, P{tH4V23T  
42:2478-2482. ;VlA~tv  
21. Livingston PM, Guest CS, Stanislavsky Y, Lee S, Bayley S, Walker C, l$mfsm|{:  
McKean C, Taylor HR: A population-based estimate of cataract B33H,e)  
prevalence: the Melbourne Visual Impairment Project experience. %"{jNC?  
Dev Ophthalmol 1994, 26:1-6. Th%2pwvER  
22. Leske MC, Connell AM, Wu SY, Hyman L, Schachat A: Prevalence kntM  
of lens opacities in the Barbados Eye Study. Arch Ophthalmol %g+*.8;"b  
1997, 115:105-111. published erratum appears in Arch Ophthalmol WK)2/$7@  
1997 Jul;115(7):931 ),53(=/hl  
23. Seah SK, Wong TY, Foster PJ, Ng TP, Johnson GJ: Prevalence of ~o?(O1QY  
lens opacity in Chinese residents of Singapore: the tanjong *~H\#N|x  
pagar survey. Ophthalmology 2002, 109:2058-2064. ,4`=gKn  
24. Stifter E, Sacu S, Weghaupt H, Konig F, Richter-Muksch S, Thaler A, OqNtTk+  
Velikay-Parel M, Radner W: Reading performance depending on kH9P(`;Vq  
the type of cataract and its predictability on the visual outcome. )*tV  
J Cataract Refract Surg 2004, 30:1259-1267. #eKg!]4-R  
25. Stifter E, Sacu S, Weghaupt H: Functional vision with cataracts of <1xs ya[e  
different morphologies: comparative study. J Cataract Refract W!.vP~>  
Surg 2004, 30:1883-1891. $lYy`OuC  
26. Leske MC, Chylack LT Jr, Wu SY: The Lens Opacities Case-Control *W&}}iL  
Study. Risk factors for cataract. Arch Ophthalmol 1991, ;5TQH_g  
109:244-251. ay-M.J  
27. Leske MC, Wu SY, Hyman L, Sperduto R, Underwood B, Chylack LT, (|kcSnF0  
Milton RC, Srivastava S, Ansari N: Biochemical factors in the lens ~E J+<[/  
opacities. Case-control study. The Lens Opacities Case-Control h|Z%b_a  
Study Group. Arch Ophthalmol 1995, 113:1113-1119. o:x,zfW  
28. Yip R, Johnson C, Dallman PR: Age-related changes in laboratory }>T$2"pf  
values used in the diagnosis of anemia and iron deficiency. YA,vT[kX  
Am J Clin Nutr 1984, 39:427-436. Rx\.x? &  
29. Mitchell P, Smith W, Wang JJ, Cumming RG, Leeder SR, Burnett L: ecg>_%.>  
Diabetes in an older Australian population. Diabetes Res Clin oMNgyAp^  
Pract 1998, 41:177-184.  |)'6U3  
Pre-publication history 9+!1jTGSkf  
The pre-publication history for this paper can be accessed 45+w)Vf!  
here: ja1W I  
Publish with BioMed Central and every I]dt1iXu_{  
scientist can read your work free of charge -hjGPu  
"BioMed Central will be the most significant development for p#fd+  
disseminating the results of biomedical research in our lifetime." )4@La&  
Sir Paul Nurse, Cancer Research UK V < ;vy&&  
Your research papers will be: %%-hax.x0X  
available free of charge to the entire biomedical community ESQgN+llj  
peer reviewed and published immediately upon acceptance djGzJLH  
cited in PubMed and archived on PubMed Central 6.|Q yk*  
yours — you keep the copyright XX])B%*  
Submit your manuscript here: nGvWlx  
http://www.biomedcentral.com/info/publishing_adv.asp 6L\?+=X  
BioMedcentral $&>z`bAS>  
BMC Ophthalmology 2006, 6:17 http://www.biomedcentral.com/1471-2415/6/17 qwz_.=5E6  
Page 7 of 7 -N4km5  
(page number not for citation purposes) K$K 6,54y  
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:
2+6=? 正确答案:8
按"Ctrl+Enter"直接提交