Cited by 228Retinal Diseases and TreatmentsComplement system in diseasesRetinal Imaging and Analysis

The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index; 3 of the 49 sources its claims cite were checked for support.

CFH Y402H Confers Similar Risk of Soft Drusen and Both Forms of Advanced AMD

Open access
Magnusson, Kristinn P, Duan, Shan, Sigurdsson, Haraldur, Petursson, Hjorvar, Yang, Zhenglin, Zhao, Yu, Bernstein, Paul S, Ge, Jian, Jonasson, Fridbert, Stefansson, Einar, Helgadottir, Gudleif, Zabriskie, Norman A, Jonsson, Thorlakur, Björnsson, Asgeir, Thorlacius, Theodora, Jonsson, Palmi V, Thorleifsson, Gudmar, Kong, Augustine, Stefansson, Hreinn, Zhang, Kang, Stefansson, Kari, Gulcher, Jeffrey R·2005·PLoS Medicine

Abstract

BACKGROUND: Age-related macular degeneration (AMD) is the most common cause of irreversible visual impairment in the developed world. The two forms of advanced AMD, geographic atrophy and neovascular AMD, represent different pathological processes in the macula that lead to loss of central vision. Soft drusen, characterized by deposits in the macula without visual loss, are considered to be a precursor of advanced AMD. Recently, it has been proposed that a common missense variant, Y402H, in the Complement Factor H (CFH) gene increases the risk for advanced AMD. However, its impact on soft drusen, GA, or neovascular AMD--or the relationship between them--is unclear. METHODS AND FINDINGS: We genotyped 581 Icelandic patients with advanced AMD (278 neovascular AMD, 203 GA, and 100 with mixed neovascular AMD/GA), and 435 with early AMD (of whom 220 had soft drusen). A second cohort of 431 US patients from Utah, 322 with advanced AMD (244 neovascular AMD and 78 GA) and 109 early-AMD cases with soft drusen, were analyzed. We confirmed that the CFH Y402H variant shows significant association to advanced AMD, with odds ratio of 2.39 in Icelandic patients (p = 5.9 x 10(-12)) and odds ratio of 2.14 in US patients from Utah (p = 2.0 x 10(-9)) with advanced AMD. Furthermore, we show that the Y402H variant confers similar risk of soft drusen and both forms of advanced AMD (GA or neovascular AMD). CONCLUSION: Soft drusen occur prior to progression to advanced AMD and represent a histological feature shared by neovascular AMD and GA. Our results suggest that CFH is a major risk factor of soft drusen, and additional genetic factors and/or environmental factors may be required for progression to advanced AMD.

Overview

AI snapshot

Written from the paper’s full text.

TL;DR

The CFH Y402H variant is associated with advanced AMD in Icelandic and Utah cohorts, and it confers similar risk for soft drusen and both advanced subtypes (geographic atrophy and neovascular AMD). The authors conclude CFH mainly increases risk of soft drusen, with additional genetic and/or environmental factors needed for progression to advanced AMD.

Key findings

  • Advanced AMD association was confirmed: Icelandic OR 2.39 (p = 5.9 × 10−12) and Utah OR 2.14 (p = 2.0 × 10−9) in the abstract; subtype ORs were neovascular 2.32, GA 2.27, and mixed GA/neovascular 2.92 in Iceland, and neovascular 2.17 and GA 2.05 in Utah.
  • Y402H conferred similar risk of soft drusen and advanced AMD: soft drusen OR 2.52 in Iceland and 2.10 in Utah; no significant association with pigmentary changes; hard drusen showed significant association in Iceland (p = 0.01, OR 1.57) but not Utah, and soft versus hard drusen differed in Iceland (p = 0.011).
  • HapMap allele frequencies for CFH Y402H were 39% in Caucasians, 30.7% in Africans, 8.1% in Japanese, and 6.8% in Chinese.

Methods

  • Genotyped Icelandic cohort: 581 advanced AMD patients (278 neovascular, 203 GA, 100 mixed) and 435 early AMD patients (220 with soft drusen), compared with 891 population controls or 171 longevous controls; Utah cohort: 322 advanced AMD patients (244 neovascular, 78 GA) and 109 early AMD patients with soft drusen, compared with 203 age-matched controls.
  • TaqMan assay for the Icelandic cohort and direct DNA sequencing for the Utah cohort; single-marker association for rs1061170 used Fisher’s exact test (one-sided p for the at-risk allele), with variance adjustment for familial relatedness; ORs and population-attributable risk were calculated under a multiplicative model.

Limitations

  • The paper does not present a formal limitations section; it notes that additional genetic and/or environmental factors may be required for progression from soft drusen to advanced AMD, and that other genes remain to be found.
  • The discussion states that genotype–phenotype correlation studies are needed in non-Caucasian populations, and the analyzed cohorts were Icelandic and Utah Caucasian populations, limiting generalization.
  • Evident from the text: the design is cross-sectional genotype–phenotype association, so it cannot directly establish progression or causality from soft drusen to advanced AMD; the paper also notes the Icelandic GA/neovascular ratio is an open question possibly due to genetic or environmental factors.

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Integrity signals

Registry

Crossref · 10.1371/journal.pmed.0030005

Cites

40 of 40 references verified0 citation errors · 0 not checkable

Statistics

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Verification

Claims the paper makes

18 Not checked yet · 14 Own result · 11 Own interpretation · 1 Supported so far

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Show all 19 claims

  • Probably not a substantial claim. 14
  • It may state two separate claims as one. 13
25 of 25
  • The paper relies on this without support.

    Soft drusen are usually precursors of both forms of advanced AMD.

    “Soft drusen located between the RPE and Bruch's membrane are usually precursors of both forms of advanced AMD.”
  • The authors state this as an assumption.

    The multiplicative model holds for interpreting the odds ratio as relative risk and for calculating population-attributable risk.

    “In the case of population controls and assuming the multiplicative model, in which the risks of the two alleles of the single-nucleotide polymorphism a person carries multiply [25,26], this corresponds to an estimate of the relative risk of the mutation compared to the wild-type.”
    “On the basis of the frequency of the at-risk allele and the relative risk, we calculate the population-attributable risk or the reduction in the number of disease cases if the at-risk allele was removed from the population, again assuming the multiplicative model.”
  • The authors state this as an assumption.

    Confidence intervals of relative risks and odds ratios are log-normally distributed.

    “Confidence intervals of relative risks and ORs were based on the variance-adjusted tests for association, assuming a log-normal distribution.”
  • The paper relies on this without support.

    The allele frequency of Y402H is less (0.31 versus 0.39) in African Americans than in Caucasians.

    “The allele frequency of the Y402H is less (0.31 versus 0.39) in African Americans than in Caucasians.”
  • The paper relies on this without support.

    Soft drusen and pigmentary abnormalities of the RPE are considered to be an early indication of risk of developing advanced AMD.

    “Soft drusen and pigmentary abnormalities of the RPE are considered to be an early indication of risk of developing advanced AMD.”
5 of 5

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Metadata

Authors
Magnusson, K. P., Duan, S., Sigurdsson, H., Petursson, H., Yang, Z., Zhao, Y., Bernstein, P. S., Ge, J., Jonasson, F., Stefansson, E., Helgadottir, G., Zabriskie, N. A., Jonsson, T., Björnsson, A., Thorlacius, T., Jonsson, P. V., Thorleifsson, G., Kong, A., Stefansson, H., Zhang, K., Stefansson, K., & Gulcher, J. R.
Affiliations
  • University of Utah (US)
  • Zhongshan Ophthalmic Center, Sun Yat-sen University (CN)
  • deCODE Genetics (Iceland) (IS)
Corresponding author
  • Zhang, Kang
  • Gulcher, Jeffrey R
Venue
PLoS Medicine
Published
2005-11-29
Volume
3
Issue
1
Pages
e5
ISSN
  • 1549-1277 (ISSN-L)
  • 1549-1676
OpenAlex
W2091742941
Cited by
226
References
40
Citations by year
2026: 1 · 2025: 2 · 2024: 6 · 2023: 1 · 2022: 2 · 2021: 4 · 2020: 3 · 2019: 4 · 2018: 8 · 2017: 3 · 2016: 7 · 2015: 9 · 2014: 10 · 2013: 9 · 2012: 18
FWCI
25.98
Type
journal article
Language
en
Open access
Locations
  • PLoS Medicine (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • Hirsla (Landspítali University Hospital) (submittedVersion)
Funders
  • American Health Assistance Foundation
  • Ronald McDonald House Charities
  • Deutsches Krebsforschungszentrum
  • National Institutes of Health (R01EY14428, M01-RR00064)
  • National Eye Institute (R01EY014448, R01EY014428, R01EY14428, R01EY14448, P30EY014800)
  • National Center for Research Resources (M01-RR 00064, M01RR000064)
Topics
  • Health Sciences › Medicine › Ophthalmology › Retinal Diseases and Treatments
  • Life Sciences › Immunology and Microbiology › Immunology › Complement system in diseases
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Retinal Imaging and Analysis
Keywords
age-related macular degeneration, complement factor H, soft drusen, geographic atrophy, neovascular AMD, genetic risk factors, disease progression, early AMD
MeSH terms
Humans, Iceland, Macular Degeneration, Mutation, Risk Factors, Utah, Retinal Drusen, Odds Ratio, Complement Factor H, Genetic Predisposition to Disease

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