Longitudinal study of keratoconus progression

被引:90
作者
Li, Xiaohui
Yang, Huiying
Rabinowitz, Yaron S.
机构
[1] Cedars Sinai Med Ctr, Cornea Genet Eye Inst, Los Angeles, CA 90048 USA
[2] Cedars Sinai Med Ctr, Cedars Sinai Eye Res Inst, Los Angeles, CA 90048 USA
[3] Cedars Sinai Med Ctr, Inst Med Genet, Los Angeles, CA 90048 USA
关键词
keratoconus; progression; videokeratography;
D O I
10.1016/j.exer.2007.06.016
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
To determine if differences in topographic progression between unaffected keratoconus relatives and normal controls can predict factors associated with the development of keratoconus in a longitudinal study. We recruited 369 unaffected keratoconus relatives and 119 normal controls in Los Angeles. Both eyes of subjects were examined at baseline clinically and by quantitative videokeratography and at a period ranging from I year to 8 years. Progression to keratoconus was evaluated by quantitative videokeratography variables. Unaffected relatives had higher Central K (CK), T-S and KISA values and were younger than normal controls (CK: 44.70 vs 44.01, P < 0.01; I-S: 0.76 vs 0.58, P < 0.01, KISA: 29.97 vs 23.89, P = 0.02; age: 34.8 vs 41.0, P < 0.01) at baseline. All three indices significantly increased with age, and CK and KISA values were associated with a positive family history for keratoconus (P < 0.001 for CK and P = 0.05 for KISA), however, the two groups were not statistically different in progression of keratoconus. After grouping unaffected relatives as high risk (age <= 30 or Central K >= 47.2 and I-S >= 1.2 or KISA >= 60) and low risk (age > 30 and Central K < 47.2 and I-S < 1.2 and KISA >= 60), relatives in the high risk group had a greater increase in CK and T-S values than those in the low risk group (CK: P = 0.009; I-S: P < 0.001), which indicated that there were significantly different rates of progression between two groups. Unaffected relatives had higher videokeratography indices than normal controls, but overall they did not progress to keratoconus quicker than normal controls. However, relatives in the high risk group may have a greater risk of progression to keratoconus. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:502 / 507
页数:6
相关论文
共 27 条
[1]   A locus for autosomal dominant keratoconus maps to human chromosome 3p14-q13 [J].
Brancati, F ;
Valente, EM ;
Sarkozy, A ;
Fehèr, J ;
Castori, M ;
Del Duca, P ;
Mingarelli, R ;
Pizzuti, A ;
Dallapiccola, B .
JOURNAL OF MEDICAL GENETICS, 2004, 41 (03) :188-192
[2]   The genetics of keratoconus [J].
Edwards, M ;
McGhee, CNJ ;
Dean, S .
CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2001, 29 (06) :345-351
[3]  
FALLS HF, 1969, J GENET HUM, V17, P317
[4]   Unilateral keratoconus - Incidence and quantitative topographic analysis [J].
Holland, DR ;
Maeda, N ;
Hannush, SB ;
Riveroll, LH ;
Green, MT ;
Klyce, SD ;
Wilson, SE .
OPHTHALMOLOGY, 1997, 104 (09) :1409-1413
[5]   Identification of a new locus for isolated familial keratoconus at 2p24 [J].
Hutchings, H ;
Ginisty, H ;
Le Gallo, M ;
Levy, D ;
Stoësser, F ;
Rouland, JF ;
Arné, JL ;
Lalaux, MH ;
Calvas, P ;
Roth, MP ;
Hovnanian, A ;
Malecaze, F .
JOURNAL OF MEDICAL GENETICS, 2005, 42 (01) :88-94
[6]  
KLYCE SD, 1984, INVEST OPHTH VIS SCI, V25, P1426
[7]   Longitudinal study of the normal eyes in unilateral keratoconus patients [J].
Li, XH ;
Rabinowitz, YS ;
Rasheed, K ;
Yang, HY .
OPHTHALMOLOGY, 2004, 111 (03) :440-446
[8]   Two-stage genome-wide linkage scan in keratoconus sib pair families [J].
Li, Xiaohui ;
Rabinowitz, Yaron S. ;
Tang, Yongming G. ;
Picornell, Yoana ;
Taylor, Kent D. ;
Hu, Mingshu ;
Yang, Huiying .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2006, 47 (09) :3791-3795
[9]  
Littell RC, 1996, SAS SYSTEM MIXED MOD, P1
[10]  
Liu E, 1997, CORNEA, V16, P414