Original Article
Missense Variations in the Fibulin 5 Gene and Age-Related Macular Degeneration
N Engl J Med 2004; 351:346-353July 22, 2004
- Abstract
Background
Age-related macular degeneration (AMD) is the most common cause of irreversible vision loss in the developed world. The study of a rare mendelian form of macular degeneration implicated fibulin genes in the pathogenesis of more common forms of this disease. We evaluated five fibulin genes in a large series of patients with AMD.
Methods
We studied 402 patients with AMD and 429 control subjects from the same clinic population. Patients were examined by means of indirect ophthalmoscopy, slit-lamp microscopy, and fundus photography to establish the presence and phenotypic pattern of AMD. DNA samples were screened for sequence variations in five members of the fibulin gene family.
Results
Amino acid–altering sequence variations were found in all five fibulin genes, many of which were observed only in patients with AMD. Several of the altered residues have been conserved during evolution. Seven of the 402 patients with AMD had amino acid–altering sequence variations in the fibulin 5 gene, whereas none were observed among 429 control subjects (P<0.01). In addition, these seven patients all had small, circular drusen, which are commonly referred to as basal laminar or cuticular drusen.
Conclusions
Missense mutations in the fibulin 5 gene were found in 1.7 percent of patients with AMD. Many variations in other fibulin genes were also found in these patients, and the evolutionary conservation of the affected residues suggests that several of these variations may also be involved in AMD.
Media in This Article
Figure 1
Locations of Amino Acid–Altering Sequence Variations in the Six Members of the Fibulin Gene Family.Figure 2
Ophthalmoscopic and Angiographic Findings in a 64-Year-Old Woman with an Arg71Gln Variation in the Fibulin 5 Gene.Article Activity
- Article
Age-related macular degeneration (AMD) is the most common cause of irreversible vision loss in the developed world.1-3 In most patients, the disease is manifest as ophthalmoscopically visible yellowish accumulations of protein and lipid (known as drusen) that lie beneath the retinal pigment epithelium and within an elastin-containing structure known as Bruch's membrane. In the United States alone, more than 7 million people have drusen of sufficient size and number that they are at substantial risk for severe visual loss.4 AMD is likely to be a mechanistically heterogeneous group of disorders, and the specific disease mechanisms that underlie the vast majority of cases are currently unknown. However, a number of studies have suggested that both genetic and environmental factors are likely to play a role.5-7 On the basis of the study of other inherited retinal disorders, AMD is likely to display extensive genetic heterogeneity, involving functional sequence variations in numerous genes, sometimes singly and sometimes in combination. Because AMD is a late-onset disorder, many of these variations are likely to have subtle effects on the proteins they encode and will therefore have variable expressivity and incomplete penetrance.
In the past decade, many groups used positional cloning to try to identify genes that cause early-onset heritable macular diseases in the hope that identification of these genes would provide insight into the late-onset forms of disease. Several genes were identified with the use of this approach,8-14 but none have convincingly been demonstrated to be involved in a clinically significant fraction of late-onset macular degeneration.15,16 The mendelian macular disease that is arguably most similar to “typical” AMD is variably known as malattia leventinese, Doyne's honeycomb retinal dystrophy, and radial drusen17 and is caused by a single mutation (Arg345Trp) in the fibulin 3 gene (also known as EFEMP1).
Marmorstein et al.18 examined the eyes of an 86-year-old patient with malattia leventinese and discovered that fibulin 3 accumulates within and beneath the retinal pigment epithelium but not within the drusen themselves. These authors also showed that in patients with typical AMD, fibulin 3 accumulates between the retinal pigment epithelium and drusen, but not elsewhere. Furthermore, while investigating the potential pathophysiological mechanism of the single disease-causing missense mutation, they discovered that the mutant fibulin 3 protein was not secreted from transfected RPE-J cells at the same rate as the wild-type protein and appeared to be misfolded.
Despite the clinical and histopathological similarities between malattia leventinese and typical AMD, variations in the coding sequence of fibulin 3 have not been found in patients with AMD.13 In this study, we tested the hypothesis that variations in other members of the fibulin gene family are involved in the pathogenesis of macular degeneration by examining the coding sequences of the genes for fibulin 1, 2, 4, 5, and 6 in more than 400 patients with AMD.
Methods
A total of 402 unrelated patients with the clinical diagnosis of AMD were enrolled in the study after providing written informed consent. Among these patients, 367 were patients of the Retina Clinic of the University of Iowa, and the remaining 35 were patients of retina specialists elsewhere in the United States. All patients had been examined by fellowship-trained retina specialists and had received a diagnosis of AMD on the basis of the presence of one or more of the following features: drusen, disruption or atrophy of the retinal pigment epithelium, and choroidal neovascularization. Approximately 40 percent of the study patients had choroidal neovascularization.
Two groups of unrelated control subjects from the University of Iowa were studied. The first group consisted of 263 subjects (general-population controls) over the age of 50 years who had no history of macular degeneration. The eyes of these subjects were not examined as part of this study. The second group consisted of 166 subjects over the age of 50 years (average age, 75.5) who had no family history of macular degeneration and who had been examined by an ophthalmologist and found to be free of macular degeneration. The patients and controls from the University of Iowa were all enrolled during the same period by the same clinic. Over 80 percent of both groups described themselves as “caucasian.” Genotype data from previous studies of large subgroups of these groups19,20 have shown that the patient and control groups are closely matched ethnically.
DNA was extracted from peripheral blood according to a previously described protocol.21 Samples from the 402 patients with AMD and the 263 general-population controls were screened for coding-sequence variations in the genes for fibulin 1, 2, 4, 5, and 6 with the use of single-strand conformational polymorphism analysis as previously described.20 With the exception of a single exon each in the genes for fibulin 1 and fibulin 2 (which would not amplify reliably), the entire coding sequences of fibulin 1, 2, 4, and 5 (a total of 67 amplimers) were screened. Twenty-five of 107 exons of fibulin 6 were selected for screening on the basis of the location of known functional domains. An additional 166 controls without AMD were screened for variations in the entire coding sequence of fibulin 5. Samples from all 402 patients with AMD and all 429 controls were screened for the Gln5346Arg change in exon 104 of the fibulin 6 gene reported by Schultz et al.22 with the use of a denaturing high-performance liquid chromatography assay. The three samples found to harbor the Gln5346Arg change were confirmed by means of bidirection-al automated DNA sequencing. Differences in the frequencies of coding-sequence variations between patients with AMD and controls were evaluated by means of Fisher's exact test. To evaluate the evolutionary conservation of residues with sequence variations, we used the nucleotide BLAST program and published expressed sequence tags. Each exon from the human fibulin 5 gene was used to identify homologous expressed sequence tags across multiple species. The expressed sequence tags used for subsequent analysis exhibited a minimum of 80 percent agreement with the human sequence.
For reverse-transcriptase–polymerase-chain-reaction (RT-PCR) analysis of the expression of fibulin 5, total RNA was extracted from the neurosensory retina and the retinal pigment epithelium of an eye from an adult donor with the use of Qiagen RNeasy minipreps. One microgram of DNase-treated RNA was reverse-transcribed in a random primed reaction with SuperScriptIII reverse transcriptase. Then 25-ng aliquots of this material were amplified by means of PCR.
Results
We found 114 different variations in the sequences of the genes for fibulin 1, 2, 4, 5, and 6 (Table 1Table 1
Number of Different Sequence Variations.). Of these, 62 percent would not be expected to alter the structure of the encoded protein, whereas the remainder (38 percent) would alter one or more amino acids. Table 2Table 2
Amino Acid Variants. lists all the amino acid–altering variations we observed as well as their distribution in patients and controls. All but two of these changes were so rare that they were observed only in the heterozygous state. The two common changes — Ser361Gly in fibulin 2 and Ile2419Thr in fibulin 6 — were observed in the homozygous state in some subjects, but the frequencies of homozygosity were the same among patients and controls and were compatible with the presence of Hardy–Weinberg equilibrium. Table 3Table 3
Amino Acid Variants in Patients and Controls. shows the number of patients and controls who had one or more amino acid variants in a given fibulin gene. Only fibulin 5 showed a significant association between amino acid variations and AMD (P<0.01 by Fisher's exact test). Fibulin 2 and fibulin 6 each had a very common amino acid change that was present in equal frequency among patients and controls (Table 2). After the removal of these changes from the analysis, the remaining variations in these genes were still not significantly associated with the AMD phenotype (Table 3).The Gln5346Arg change in fibulin 6 reported by Schultz and coworkers22 was observed in two patients with AMD and one control subject. However, this control had had photographs taken of his eyes in our glaucoma clinic in the past, and careful review of these photographs revealed several small, round drusen near the optic-nerve head that were similar in appearance to those seen in the patients with fibulin 5 changes.
Figure 1Figure 1
Locations of Amino Acid–Altering Sequence Variations in the Six Members of the Fibulin Gene Family. shows the placement of the amino acid variations we observed with respect to the repeated domain structure of the fibulin gene family. The insertion of 1 bp in fibulin 2 would be expected to cause a premature truncation of the molecule before the anaphylatoxin and epidermal growth factor (EGF)–like domains. This particular variation was observed in seven of eight affected members of a large family with AMD (data not shown). Similarly, the Gln5346Arg change in fibulin 6 (previously reported by Schultz et al.22) is found in the EGF-like domain that is nearest the carboxy terminal of a cluster of these domains — a position similar to the location of the Arg345Trp mutation in fibulin 3. Figure 1 also shows which of these variations were observed only in patients with AMD and not in controls, since these would be somewhat more likely to be true disease-causing variations than those appearing with equal frequency among patients and controls.The seven patients with amino acid changes in fibulin 5 had all been examined and photographed in the retina clinic at the University of Iowa in the past 12 years. All seven described themselves as “caucasian.” Five had fluorescein angiograms as part of their medical record. Review of the retinal photographs revealed that these seven patients all had clusters of small, round, uniform drusen in association with variable degrees of detachment of retinal pigment epithelium. Figure 2AFigure 2
Ophthalmoscopic and Angiographic Findings in a 64-Year-Old Woman with an Arg71Gln Variation in the Fibulin 5 Gene. shows the color fundus photograph and fluorescein angiogram of the patient with the Arg71Gln change in fibulin 5. The most characteristic lesions are the numerous small, round, yellow lesions visible at the temporal edge of the macula. The larger, less distinct yellow areas nearer the center of the macula represent areas of pigment epithelial detachment. The fluorescein angiogram of this eye (Figure 2B, Figure 2C, and Figure 2D) reveals these small, dot-like lesions to be brightly hyperfluorescent, whereas the areas of pigment epithelial detachment are much less visible. Three of the seven patients with fibulin 5 mutations (43 percent) had evidence of choroidal neovascularization when they were last examined. This rate was nearly identical to the rate of choroidal neovascularization in the group of patients with AMD as a whole (40 percent).Although fibulin genes are known to be widely expressed and expressed sequence tags for fibulin 5 have been found in complementary-DNA libraries derived from eye and brain, we confirmed the expression of fibulin 5 in the retina and the retinal pigment epithelium by means of RT-PCR analysis (data not shown).
Discussion
The fibulins are a relatively recently recognized family of extracellular proteins23 that are widely expressed in the basement membranes of epithelia and blood vessels. Their most recognizable structural feature is the tandem array of four or more calcium-binding EGF-like domains (Figure 1). Fibulin 3, 4, and 5 are the smallest members of the family and are nearly identical in their modular organization. In addition, fibulin 4 and fibulin 5 are over 40 percent identical to fibulin 3 at the amino acid level. All fibulins have binding sites for other basement-membrane proteins, such as fibrillin, fibronectin, proteoglycans, integrins, and tropoelastin. Fibulin 5 appears to be essential for the polymerization of elastin, because in mice and humans without functional copies of the fibulin 5 gene, tropoelastin is synthesized but is not assembled into its mature elastin fibrils.24-26
In 1999, an amino acid variation (Arg345Trp) in fibulin 3 was shown to be responsible for a specific form of drusen that are inherited in an autosomal dominant fashion.13 The drusen caused by this mutation are quite unusual in that they are distributed in streaks and lines that radiate from the center of the fovea. The molecular basis for this radial distribution is unknown, but it may be relevant that fibulin 6, or hemicentin, is capable of organizing cells into linear arrays during development.27 In 2003, Schultz and coworkers22 found that an amino acid variation in fibulin 6 (Gln5346Arg) segregated in a large family with AMD.
Each of the five fibulin genes we examined had at least one amino acid variant in patients with AMD that was not present in control subjects. In all, we observed 27 such changes, and many of these may cause AMD. Fifteen of these 27 changes affect residues that are completely conserved among all species for which expressed sequence tags could be identified with our search strategy. However, four of the fibulin genes also harbor one or more amino acid variations that were present in both patients and controls, and eight of these variants (present in 12 subjects) were present only in controls. Only the variations in fibulin 5 were significantly more numerous among patients than controls.
All seven of the amino acid–altering fibulin variants differed from one another. If we had observed only a single variation, there is a possibility that an unrecognized difference in ancestry might exist between the patients and controls or that the observed variation was in linkage disequilibrium with a true disease-causing variation nearby. However, given that seven different variations were observed, the most plausible explanation is that the variations themselves are actually involved in the disease. Six of these variations were completely conserved among the four to six species for which homology was detected. The expression of fibulin 5 in the retinal pigment epithelium (the tissue beneath which drusen accumulate) and the homology between fibulin 5 and fibulin 3 (a gene known to cause human macular disease) are further evidence that fibulin 5 has a role in the pathogenesis of AMD.
All seven of the patients with amino acid variations in this gene were found to have a phenotype that includes small, round, uniform drusen. First described by Gass in 1977,28 such drusen (when very numerous) are referred to by clinicians as either basal laminar or cuticular drusen. Gass et al. later observed that patients with this phenotype are prone to large detachments of the retinal pigment epithelium.29 This observation suggests that the molecular abnormality that gives rise to this type of drusen might also alter the attachment of the retinal pigment epithelium to Bruch's membrane. The photographs of five of the seven patients in this study with variations in fibulin 5 revealed regions of detachment of retinal pigment epithelium (Figure 2). Cuticular drusen and detachments of retinal pigment epithelium are present in at least 20 percent of patients with AMD. Thus, missense changes in the fibulin 5 gene cannot be the sole cause of this phenotype.
The mechanism by which heterozygous missense mutations in the fibulin 5 gene could cause macular degeneration is not known. The fact that a drusen-causing missense variation in the closely related fibulin 3 gene is associated with misfolding and impaired secretion from retinal pigment epithelial cells18 raises the possibility that a similar mechanism may be operative for at least some of the variations we observed. As noted, fibulin 5 is essential for the polymerization of elastin in humans and mice.24-26 Elastin is a major component of the multilayered structure, known as Bruch's membrane, in which drusen form, and it is possible that reduced amounts of fibulin 5 protein in the extracellular space — or changes in specific residues that are important for the interaction with tropoelastin — alter the normal assembly of elastin within Bruch's membrane. It is also possible that interference with some other function of fibulin 5, such as integrin-mediated cell attachment,25 will prove on further study to be the mechanism involved in fibulin 5–associated AMD. The fact that all of our patients with missense mutations in the fibulin 5 gene had some ophthalmoscopically visible detachment of the retinal pigment epithelium would support such a hypothesis.
In conclusion, we have demonstrated a significant association between sequence variations in a member of the fibulin gene family and typical AMD — the most common cause of irreversible vision loss in the developed world. In addition, we detected a number of other amino acid–altering variations in other fibulin genes in our patients with AMD, and the degree of evolutionary conservation of some of these residues suggests that they, too, may be involved in the pathogenesis of this disease. These findings should intensify interest in the components of Bruch's membrane as important participants in the pathophysiology of AMD and may facilitate the development of a murine model of AMD. Such a model would be useful in the search for drugs and other interventions for this common cause of blindness.
Supported by the Foundation Fighting Blindness, the Carver Endowment for Molecular Ophthalmology, the Grousbeck Family Foundation, the Macula Vision Research Foundation, and Research to Prevent Blindness. Drs. Stone and Sheffield are Investigators of the Howard Hughes Medical Institute.
We are indebted to J. Donald M. Gass, M.D., to whom this article is dedicated; to the patients and their families for their participation in the study; to Dr. Dennis Schultz for providing a DNA sample with the Gln5346Arg change for use as a positive control; to Heidi Haines, Gretel Beck, and Katherine Schrum for technical assistance; to Drs. Michael Grassi, Rod Philp, and Todd Scheetz for their help in preparing the manuscript; and to Linda Koser for administrative assistance.
Source Information
From the Center for Macular Degeneration (E.M.S., T.A.B., S.R.R., M.H.K., P.A.M., C.G.E., T.L.C., V.C.S.) and the Howard Hughes Medical Institute (E.M.S., V.C.S.), University of Iowa, Iowa City; and the Department of Ophthalmology, University of Southampton, Southampton, United Kingdom (A.J.L.).
Address reprint requests to Dr. Stone at the Center for Macular Degeneration, University of Iowa Carver College of Medicine, 200 Hawkins Dr., Iowa City, IA 52242, or at edwin-stone@uiowa.edu.
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