MAJOR REVIEW - Keratoconus

1 297 MAJOR REVIEW SURVEY OF OPHTHALMOLOGY VOLUME 42 NUMBER 4 JANUARY FEBRUARY 1998 1998 by Elsevier Science $ rights S0039-6257(97)00119-7 Keratoconus YARON S. RABINOWITZ, MD Cornea-Genetic Eye Medical Clinic, Burns and Allen Research Institute, Cedars-Sinai Medical Center and the Department of Ophthalmology, UCLA School of Medicine, Los Angeles, California, USA Abstract. Keratoconus is a bilateral noninflammatory corneal ectasia with an incidence of approxi-mately 1 per 2,000 in the general population. It has well-described clinical signs, but early forms of thedisease may go undetected unless the anterior corneal topography is studied.

2 Early disease is now bestdetected with videokeratography. Classic histopathologic features include stromal thinning, iron depo-sition in the epithelial basement membrane, and breaks in Bowman s layer. Keratoconus is most com-monly an isolated disorder, although several reports describe an association with Down syndrome,Leber s congenital amaurosis, and mitral valve prolapse. The differential diagnosis of keratoconusincludes keratoglobus, pellucid marginal degeneration and Terrien s marginal degeneration. Contactlenses are the most common treatment modality. When contact lenses fail, corneal transplant is the bestand most successful surgical option.

3 Despite intensive clinical and laboratory investigation, the etiologyof Keratoconus remains unclear. Clinical studies provide strong indications of a MAJOR role for genes inits etiology. Videokeratography is playing an increasing role in defining the genetics of Keratoconus ,since early forms of the disease can be more accurately detected and potentially quantified in a repro-ducible manner. Laboratory studies suggest a role for degradative enzymes and proteinase inhibitorsand a possible role for the interleukin-1 system in its pathogenesis, but these roles need to be moreclearly defined.

4 Genes suggested by these studies, as well as collagen genes and their regulatory prod-ucts, could potentially be used as candidate genes to study patients with familial Keratoconus . Such stud-ies may provide the clues needed to enable us to better understand the underlying mechanisms thatcause the corneal thinning in this disorder. ( Surv Ophthalmol 42 :297 319, 1998. 1998 by ElsevierScience Inc. All rights reserved.) Key words. collagen genes contact lenses corneal thinning disorder genetics Keratoconus penetrating keratoplasty segregation analysis videokeratography In 1984 a REVIEW on Keratoconus and related non-inflammatory corneal thinning disorders by Krach- mer et al 66 was published in this journal.

5 It remainsone of the most comprehensive and complete clini-cal descriptions on this subject. In the past 14 years,computer technology and biotechnology have had amajor impact in improving our understanding ofkeratoconus and may ultimately allow us to devise amedical therapy to retard its progression. Computer-assisted videokeratoscopes are now used in clinicalpractice, and videokeratography has enhanced ourability to detect early Keratoconus in a quantifiableand reproducible manner. This will allow us to accu-rately construct family pedigrees with the familialforms of Keratoconus . Biotechnology may allow usto identify a gene or genes that play a MAJOR role inthe pathogenesis of this disorder.

6 This REVIEW fo-cuses on these advances as they relate to our under-standing of Keratoconus and provides an update onbiochemical and clinical research studies and man-agement options developed since the last majorclinical REVIEW . 66 298 Surv Ophthalmol 42 (4) January February 1998 RABINOWITZ I. Epidemiology Keratoconus , classically, has its onset at pubertyand is progressive until the third to fourth decade oflife, when it usually arrests. It may, however, com-mence later in life and progress or arrest at any it may be congenital. 134 It is most commonly anisolated condition, despite multiple singular reportsof coexistence with other disorders (Table 1).

7 Com-monly recognized associations include Down syn-drome, Leber s congenital amaurosis, and connectivetissue disorders. For example, patients with advancedkeratoconus have been reported to have a high inci-dence of mitral valve prolapse (58%). 66,129 Atopy , eyerubbing, and hard contact lenses have also been re-ported to be highly associated with this disorder, and6 8% of reported cases have a positive family historyor show evidence of familial transmission (Table 2). 50,66 The reported incidence of Keratoconus varies,with most estimates being between 50 and 230 per100,000 in the general population (approximately 1per 2,000).

8 Prevalence is per 100,000. 27,35,55 , 60,66 The variability in the reported incidence reflects thesubjective criteria often used to establish the diagno-sis, allowing subtle forms to be often occurs in all ethnic groups with nomale or female preponderance. II. Clinical Features Keratoconus is a condition in which the cornea as-sumes a conical shape as a result of noninflamma-tory thinning of the corneal stroma. The cornealthinning induces irregular astigmatism, myopia, andprotrusion, leading to mild to marked impairmentin the quality of vision. 66 It is a progressive disorder TABLE 1 Diseases Reported in Association With Keratoconus Multisystem DisordersOcular Disorders (Noncorneal)

9 Alagille s syndrome 116 Aniridia 63 Albers-Schonberg disease 40 Anetoderma and bilateral subcapsular cataracts 13 Angleman syndrome 75 Ankyloblepharon 15 Apert s syndrome 44 Bilateral macular coloboma 39 Autographism 57 Blue sclerae 49 Anetoderma 13 Congenital cataracts 64 Bardet-Biedl syndrome 37 Ectodermal and mesodermal anomalies 68 Crouzon s syndrome 95,160 Floppy eyelid syndrome 87 Down syndrome 24 Gyrate atrophy 64 Ehlers-Danlos syndrome 69 Iridoschisis 29 Goltz-Gorlin syndrome 162 Lebers congenital amaurosis 30 Hyperornithemia 63 Persistent pupillary membrane 63 Icthyosis 35 Posterior lenticonus 16 Kurz syndrome 164 Retinitis pigmentosa 35 Laurence-Moon-Bardet-Biedl syndrome 149 Retinal disinsection syndrome 127 Marfan s syndrome 6 Retrolental fibroplasia 74 Mulvihil-Smith syndrome 114 Vernal conjunctivitis 48 Nail patella syndrome 49 Corneal DisordersNeurocutaneous angiomatosis 38 Atopic keratoconjunctivitis 48 Neurofibromatosis 149 Axenfeld s anomaly 135 Noonan s

10 Syndrome 125 Avellino s dystrophy 121 Osteogenesis imperfecta 8 Chandler s syndrome 43 Oculodentodigital syndrome 49 Corneal amyloidosis 63 Pseudoxanthoma elasticum 149 Deep filiform corneal dystrophy 63 Rieger s syndrome 49 Essential iris atrophy 11 Rothmund s syndrome 62 Fleck corneal dystrophy 63 Tourette s disease 32 Fuchs corneal dystrophy 73 Turner s syndrome 91 Iridocorneal dysgenesis 5 Xeroderma pigmentosa 12 Lattice dystrophy 54 Other Systemic DisordersMicrocornea 63 Congenital hip dysplasia 90 Pellucid marginal degeneration 59 False chordae tendinae of left ventricle 64 Posterior polymorphous dystrophy 26 Joint hypermobility 117 Terriens marginal degeneration 63 Mitral valve prolapse 129 Measles retinopathy 94 Ocular hypertension 10 Thalesselis syndrome 138 Reference numbers in superscript.