Complement factor H variant increases the risk of age-related macular degeneration.

Article Details

Citation

Haines JL, Hauser MA, Schmidt S, Scott WK, Olson LM, Gallins P, Spencer KL, Kwan SY, Noureddine M, Gilbert JR, Schnetz-Boutaud N, Agarwal A, Postel EA, Pericak-Vance MA

Complement factor H variant increases the risk of age-related macular degeneration.

Science. 2005 Apr 15;308(5720):419-21. Epub 2005 Mar 10.

PubMed ID
15761120 [ View in PubMed
]
Abstract

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. We used single-nucleotide polymorphisms to interrogate this region and identified a strongly associated haplotype in two independent data sets. DNA resequencing of the complement factor H gene within this haplotype revealed a common coding variant, Y402H, that significantly increases the risk for AMD with odds ratios between 2.45 and 5.57. This common variant likely explains approximately 43% of AMD in older adults.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Complement factor HP08603Details