Predictive value of fundus autofluorescence for development of geographic atrophy in age-related macular degeneration.

PURPOSE It has been suggested that lipofuscin accumulation, as measured by increased fundus autofluorescence (FAF), precedes progression or development of junctional zone geographic atrophy (GA) in age-related macular degeneration (AMD). The tools of biomedical image analysis were used to measure the probabilistic relationship of GA progression to increased FAF. METHODS Serial AF images of eight eyes of six patients with AMD with GA were registered on computer. The images were leveled with a 12-zone quadratic polynomial mathematical model to minimize background variability. Semiautomated segmentation of GA was performed on the leveled images. Increased FAF was defined as a gray level greater than 2 standard deviations above the leveled image mean, identified on the initial image with automated segmentation, and measured as a fraction of the 250-microm border zone surrounding the initial GA lesion. Areas of GA lesions were identified on the final image. The positive predictive value (PPV) of increased FAF was determined as the probability that any pixel with increased FAF in the initial image would become part of new GA in the final image. Relative PPV was determined relative to the total quantity of new GA. The NPV (NPV) of increased FAF was calculated as the probability that any pixels without increased FAF would not become atrophic. The relative NPV was determined similarly. A similar analysis was also conducted with a 500-microm border zone to determine the predictive value of proximity to the original GA lesion ("proximity") for GA progression. RESULTS As a fraction of the geographic atrophy border zone, the mean new GA was 0.44+/-0.20, and the mean increased FAF was 0.06+/-0.06. The mean PPV of increased FAF for new GA formation was 0.50+/-0.26. Compared with the relative PPV of chance of 1.0, the mean relative PPV of increased FAF was 1.15+/-0.28. The mean NPV of increased FAF was 0.57+/-0.20. The mean relative NPV of increased FAF was 1.00+/-0.02. In the 500-microm border zone, the mean relative PPV of FAF and of proximity were essentially equal (1.56+/-.70 and 1.52+/-0.26, respectively), whereas the mean relative NPV of proximity was significantly greater than that of FAF (1.26+/-0.19 and 1.01+/-0.01, respectively, P=0.02) CONCLUSIONS The results of digital image analysis suggest that although increased FAF may have a modest PPV for new GA development, the relative PPV is generally no greater than chance. Similarly, the relative NPV demonstrates negligible difference from chance and is also lower than the relative NPV of proximity. This suggests that increased FAF, though a disease manifestation, is not a strong risk factor for development or extension of GA.

[1]  R. Klein,et al.  The Wisconsin age-related maculopathy grading system. , 1991, Ophthalmology.

[2]  P T de Jong,et al.  An international classification and grading system for age-related maculopathy and age-related macular degeneration , 1995 .

[3]  G. Fishman,et al.  Histopathologic findings in Best's vitelliform macular dystrophy. , 1988, Archives of ophthalmology.

[4]  N. Otsu A threshold selection method from gray level histograms , 1979 .

[5]  S. Fine,et al.  A histopathologic study of Best's macular dystrophy. , 1982, Archives of ophthalmology.

[6]  C K Dorey,et al.  In vivo fluorescence of the ocular fundus exhibits retinal pigment epithelium lipofuscin characteristics. , 1995, Investigative ophthalmology & visual science.

[7]  P. Maguire,et al.  Geographic atrophy of the retinal pigment epithelium. , 1986, American journal of ophthalmology.

[8]  Y. Jang,et al.  Mechanisms for the induction of HNE- MDA- and AGE-adducts, RAGE and VEGF in retinal pigment epithelial cells. , 2005, Experimental eye research.

[9]  J S Sunness,et al.  The natural history of geographic atrophy, the advanced atrophic form of age-related macular degeneration. , 1999, Molecular vision.

[10]  R Theodore Smith,et al.  Autofluorescence characteristics of normal foveas and reconstruction of foveal autofluorescence from limited data subsets. , 2005, Investigative ophthalmology & visual science.

[11]  R W Young,et al.  Pathophysiology of age-related macular degeneration. , 1987, Survey of ophthalmology.

[12]  Giovanni Staurenghi,et al.  Classification of fundus autofluorescence patterns in early age-related macular disease. , 2005, Investigative ophthalmology & visual science.

[13]  M. Boulton,et al.  RPE lipofuscin and its role in retinal pathobiology. , 2005, Experimental eye research.

[14]  M. Boulton,et al.  The formation of autofluorescent granules in cultured human RPE. , 1989, Investigative ophthalmology & visual science.

[15]  C K Dorey,et al.  Autofluorescence distribution associated with drusen in age-related macular degeneration. , 2000, Investigative ophthalmology & visual science.

[16]  A Hofman,et al.  Age-specific prevalence and causes of blindness and visual impairment in an older population: the Rotterdam Study. , 1998, Archives of ophthalmology.

[17]  C Bellman,et al.  Fundus autofluorescence and development of geographic atrophy in age-related macular degeneration. , 2001, Investigative ophthalmology & visual science.

[18]  Ian J Constable,et al.  Lipofuscin of the retinal pigment epithelium: A review , 1995, Eye.

[19]  E. Berman,et al.  Lipofuscin of human retinal pigment epithelium. , 1980, American journal of ophthalmology.

[20]  D. Altman,et al.  STATISTICAL METHODS FOR ASSESSING AGREEMENT BETWEEN TWO METHODS OF CLINICAL MEASUREMENT , 1986, The Lancet.

[21]  J. Weiter,et al.  Retinal pigment epithelial lipofuscin and melanin and choroidal melanin in human eyes. , 1986, Investigative ophthalmology & visual science.

[22]  M. Katz,et al.  Formation of lipofuscin-like fluorophores by reaction of retinal with photoreceptor outer segments and liposomes , 1996, Mechanisms of Ageing and Development.

[23]  R. T. Smith,et al.  Automated detection of macular drusen using geometric background leveling and threshold selection. , 2005, Archives of ophthalmology.

[24]  J. Weiter,et al.  Cell loss in the aging retina. Relationship to lipofuscin accumulation and macular degeneration. , 1989, Investigative ophthalmology & visual science.

[25]  M. Killingsworth,et al.  Evolution of geographic atrophy of the retinal pigment epithelium , 1988, Eye.

[26]  K. Nakanishi,et al.  A2E, a byproduct of the visual cycle , 2003, Vision Research.

[27]  F W Fitzke,et al.  Fundus autofluorescence in age-related macular disease imaged with a laser scanning ophthalmoscope. , 1997, Investigative ophthalmology & visual science.

[28]  F. Kruse,et al.  Inhibition of lysosomal degradative functions in RPE cells by a retinoid component of lipofuscin. , 1999, Investigative ophthalmology & visual science.

[29]  R. Klein,et al.  The five-year incidence and progression of age-related maculopathy: the Beaver Dam Eye Study. , 1997, Ophthalmology.

[30]  F W Fitzke,et al.  Distribution of fundus autofluorescence with a scanning laser ophthalmoscope. , 1995, The British journal of ophthalmology.