Genetic variants increase the risk of age-related macular degeneration
View Patent ↗Age-related macular degeneration (AMD) is a leading cause of visual impairment and blindness in the elderly whose etiology remains largely unknown. Previous studies identified chromosome 1q32 as harboring a susceptibility locus for AMD, but it was not identified. We identified a strongly associated haplotype in two independent data sets. DNA sequencing of the complement factor II gene (CFII) within this haplotype revealed a coding variant, Y402II, that significantly increases the risk for AMD with odds ratios between 2.45 and 5.57. This identifies Complement factor II as involved in pathogenesis of AMD. This single variant alone is so common that it likely explains 43 percent of AMD in older adults. In addition, we have replicated and refined previous reports implicating a coding change in LOC387715 as the second major AMD susceptibility allele. The effect of rs10490924 appears to be completely independent of the Y402H variant in the CFH gene. The joint effect of these two susceptibility genes is consistent with a multiplicative model, and together, they may explain as much as 65% of the PAR of AMD. In contrast, the effect of rs10490924 appears to be strongly modified by cigarette smoking. Smoking and LOC387715 together may explain as much as 34% of AMD. Our data indicate that variant genotypes at rs10490924 confer a substantially larger AMD risk to cigarette smokers than non-smokers. This observation is supported by traditional case-control modeling, by ordered subset linkage analysis (OSA) incorporating pack-years of cigarette smoking as a covariate, and by family-based association analysis using a more homogeneous set of families as defined by OSA.
1. A method to assess risk of AMD in a patient comprising:
determining whether the patient has a T allele at rs10490924;
determining whether the patient is a cigarette smoker; and
identifying the patient as:
being at high risk of AMD if the patient has the T allele and is a cigarette smoker,
being at lower risk of AMD if the patient has the T allele but is not a cigarette smoker or is a cigarette smoker but does not have the T allele, and
being at lowest risk if the patient does not have the T allele and is not a cigarette smoker.
2. A method to assess risk of and treat AMD in a patient comprising:
determining whether the patient has a T allele at rs10490924;
determining whether the patient is a cigarette smoker; and
providing the patient with a behavioral therapy to encourage smoking cessation if the patient has the T allele at rs10490924 and is a cigarette smoker.
3. A method to assess risk of and treat AMD in a patient comprising:
determining whether the patient has a T allele at rs10490924;
determining whether the patient is a cigarette smoker; and
providing the patient with smokeless nicotine to encourage smoking cessation if the patient as the T allele and is a cigarette smoker.
4. The method of claim 2 wherein the step of providing comprises prescribing the behavioral therapy.
5. The method of claim 2 wherein the behavioral therapy is counseling.
6. The method of claim 2 wherein the behavioral therapy is a class.
7. The method of claim 2 wherein the behavioral therapy is information.
8. The method of claim 2 wherein the information is printed matter.
9. The method of claim 2 wherein the information is on a data storage medium.
10. The method of claim 2 wherein the information is on an audio tape.
11. The method of claim 2 wherein the information is on a video tape.
12. The method of claim 3 wherein the smokeless nicotine is nicotine gum.
13. The method of claim 3 wherein the smokeless nicotine is in a transdermal patch.
14. The method of claim 3 wherein the smokeless nicotine is in a nasal spray.
15. The method of claim 3 wherein the smokeless nicotine is in an inhaler.
16. The method of claim 3 wherein the step of providing comprises prescribing or recommending a form of smokeless nicotine.
17. The method of claim 1 further comprising determining if the patient has a variant of Complement Factor H protein or coding sequence.
18. The method of claim 17 wherein a variant protein is determined.
19. The method of claim 17 wherein a variant coding sequence is determined.