Abstract | PURPOSE: METHODS: Data from a Central European cohort of 349 patients with early AMD in at least one eye were analyzed for potential associations of the CFB (R32Q/rs641153) polymorphism with phenotypic features of early AMD. Early AMD was classified according to the International Classification and Grading System into predominant drusen size, largest drusen, drusen covered surface, central or ring-like location, peripheral drusen, and pigmentary changes. The potential association with single nucleotide polymorphisms on CFB (R32Q/rs641153) was evaluated for all patients, corrected for age, sex, and the polymorphisms of CFH (Y402H) and ARMS2 (A69S). RESULTS: CFB (R32Q) polymorphisms showed a significant association with smaller drusen size (largest drusen ≤ 250 µm, p = 0.021, predominant drusen ≤ 125 µm, p = 0.016), with smaller surface covered by drusen (≤ 10%; p = 0.02), and with more frequent occurrence of peripheral drusen (p = 0.007). No association was found for pigmentary changes. CONCLUSIONS: The CFB (R32Q) polymorphism was associated with AMD characterized by small drusen only, and appeared to be protective of large drusen (OR 0.48/0.45) and of larger drusen covered area (OR 0.34). Furthermore, peripheral drusen were more frequently found (OR 2.27). This result supports the role of complement components and their polymorphisms in drusen formation and may enable a better understanding of AMD pathogenesis.
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Authors | Irmela Mantel, Aude Ambresin, Leila Moetteli, Ivaine Droz, Raphaël Roduit, Francis L Munier, Daniel F Schorderet |
Journal | Ophthalmic genetics
(Ophthalmic Genet)
Vol. 35
Issue 1
Pg. 12-7
(Mar 2014)
ISSN: 1744-5094 [Electronic] England |
PMID | 23373431
(Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S.)
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Chemical References |
- ARMS2 protein, human
- CFH protein, human
- Proteins
- Complement Factor H
- Complement Factor B
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Topics |
- Aged
- Aged, 80 and over
- Complement Factor B
(genetics)
- Complement Factor H
(genetics)
- Female
- Genetic Association Studies
- Genotyping Techniques
- Humans
- Macular Degeneration
(genetics)
- Male
- Middle Aged
- Polymorphism, Single Nucleotide
- Proteins
(genetics)
- Retinal Drusen
(genetics)
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