Ethnic variation in AMD-associated complement factor H polymorphism p.Tyr402His

Michael A. Grassi, John H. Fingert, Todd E. Scheetz, Benjamin R. Roos, Robert Ritch, Sheila K West, Kazuhide Kawase, Abdirashid M. Shire, Robert F. Mullins, Edwin M. Stone

Research output: Contribution to journalArticle

Abstract

Age-related macular degeneration (AMD) is the most common cause of irreversible visual loss in the developed world. Previous studies have demonstrated that the c.1204T>C, p.Tyr402His allelic variant in the complement factor H (CFH) gene is associated with an approximately three-fold increased risk for AMD in Caucasians of predominantly European descent. Both the prevalence as well as the phenotypic spectrum of AMD varies widely among persons of different ethnicities. We hypothesized that populations with a lower prevalence of AMD might also have a lower prevalence of the CFH risk allele. In this study we sought to determine the frequency of this sequence variant in control populations of Caucasians, African Americans, Hispanics, Somalis, and Japanese. Normal control populations were assembled for each ethnic group: Caucasian (n = 148), Somali (n = 128), African American (n = 75), Hispanic (n = 81), and Japanese (n = 82). Individuals were genotyped using a restriction digest assay and the frequency of the C allele at nucleotide position 1204 of the CFH gene was determined. A bioinformatic approach was used to identify SNPs in linkage disequilibrium with rs 1061170 (c. 1204T > C, p.Tyr402His) from the human haplotype map project database (HapMap) in order to validate the findings. We found widely discordant frequencies of the risk allele between some of the different ethnic groups: Japanese 0.07±0.02, Hispanics 0.17±0.03, African-Americans 0.35±0.04, Caucasians 0.34±0.03, and Somalis 0.34±0.03. Allele frequencies generated by analysis of the HapMap database were consistent with these findings. This study suggests that there are other yet unidentified genetic factors important in the pathogenesis of AMD that may mitigate the effects of c.1204T>C, p.Tyr402His variant.

Original languageEnglish (US)
Pages (from-to)921-925
Number of pages5
JournalHuman Mutation
Volume27
Issue number9
DOIs
StatePublished - Sep 2006

Fingerprint

Complement Factor H
Macular Degeneration
Hispanic Americans
Gene Frequency
African Americans
Databases
Ethnic Groups
HapMap Project
Population
Linkage Disequilibrium
Computational Biology
Haplotypes
Genes
Single Nucleotide Polymorphism
Nucleotides
Alleles

Keywords

  • Age-related macular degeneration
  • AMD
  • CFH
  • Complement factor H
  • Ethnic variation

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Grassi, M. A., Fingert, J. H., Scheetz, T. E., Roos, B. R., Ritch, R., West, S. K., ... Stone, E. M. (2006). Ethnic variation in AMD-associated complement factor H polymorphism p.Tyr402His. Human Mutation, 27(9), 921-925. https://doi.org/10.1002/humu.20359

Ethnic variation in AMD-associated complement factor H polymorphism p.Tyr402His. / Grassi, Michael A.; Fingert, John H.; Scheetz, Todd E.; Roos, Benjamin R.; Ritch, Robert; West, Sheila K; Kawase, Kazuhide; Shire, Abdirashid M.; Mullins, Robert F.; Stone, Edwin M.

In: Human Mutation, Vol. 27, No. 9, 09.2006, p. 921-925.

Research output: Contribution to journalArticle

Grassi, MA, Fingert, JH, Scheetz, TE, Roos, BR, Ritch, R, West, SK, Kawase, K, Shire, AM, Mullins, RF & Stone, EM 2006, 'Ethnic variation in AMD-associated complement factor H polymorphism p.Tyr402His', Human Mutation, vol. 27, no. 9, pp. 921-925. https://doi.org/10.1002/humu.20359
Grassi, Michael A. ; Fingert, John H. ; Scheetz, Todd E. ; Roos, Benjamin R. ; Ritch, Robert ; West, Sheila K ; Kawase, Kazuhide ; Shire, Abdirashid M. ; Mullins, Robert F. ; Stone, Edwin M. / Ethnic variation in AMD-associated complement factor H polymorphism p.Tyr402His. In: Human Mutation. 2006 ; Vol. 27, No. 9. pp. 921-925.
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abstract = "Age-related macular degeneration (AMD) is the most common cause of irreversible visual loss in the developed world. Previous studies have demonstrated that the c.1204T>C, p.Tyr402His allelic variant in the complement factor H (CFH) gene is associated with an approximately three-fold increased risk for AMD in Caucasians of predominantly European descent. Both the prevalence as well as the phenotypic spectrum of AMD varies widely among persons of different ethnicities. We hypothesized that populations with a lower prevalence of AMD might also have a lower prevalence of the CFH risk allele. In this study we sought to determine the frequency of this sequence variant in control populations of Caucasians, African Americans, Hispanics, Somalis, and Japanese. Normal control populations were assembled for each ethnic group: Caucasian (n = 148), Somali (n = 128), African American (n = 75), Hispanic (n = 81), and Japanese (n = 82). Individuals were genotyped using a restriction digest assay and the frequency of the C allele at nucleotide position 1204 of the CFH gene was determined. A bioinformatic approach was used to identify SNPs in linkage disequilibrium with rs 1061170 (c. 1204T > C, p.Tyr402His) from the human haplotype map project database (HapMap) in order to validate the findings. We found widely discordant frequencies of the risk allele between some of the different ethnic groups: Japanese 0.07±0.02, Hispanics 0.17±0.03, African-Americans 0.35±0.04, Caucasians 0.34±0.03, and Somalis 0.34±0.03. Allele frequencies generated by analysis of the HapMap database were consistent with these findings. This study suggests that there are other yet unidentified genetic factors important in the pathogenesis of AMD that may mitigate the effects of c.1204T>C, p.Tyr402His variant.",
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