Evidence map›Paper›PMID 25034031›Full record

ReviewMolecular immunology2014

Genetic variants in the complement system predisposing to age-related macular degeneration: a review.

Elizabeth C Schramm, Simon J Clark, Michael P Triebwasser, Soumya Raychaudhuri, Johanna Seddon, John P Atkinson

Open access · greenAbstract readReview
In one paragraph

Review in Molecular immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 1 pooled it
14.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

73 citing papers in PubMed, 1 synthesis or guideline pooled it, 117 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
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  5. Article
  6. Rare DysfunctionalOphthalmology science · 2023
    Article
  7. Review
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  10. Review
  11. Review
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  15. Article
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  18. Review
  19. Article
  20. Investigational Agents in Development for the Treatment of Geographic Atrophy Secondary to Age-Related Macular Degeneration.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2021
    Review

13 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

Elizabeth C Schramm *Division of Rheumatology, Department of Medicine, Washington University School of Medicine, Saint Louis, Missouri, USA.
Simon J Clark *Centre for Hearing & Vision Research, Institute of Human Development, University of Manchester, Oxford Road, Manchester M13 9PT, UK.
Michael P TriebwasserDivision of Rheumatology, Department of Medicine, Washington University School of Medicine, Saint Louis, Missouri, USA.
Soumya RaychaudhuriDivisions of Rheumatology and Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Johanna SeddonDepartment of Ophthalmology, Tufts University School of Medicine, Boston, Massachusetts, USA.
John P AtkinsonDivision of Rheumatology, Department of Medicine, Washington University School of Medicine, Saint Louis, Missouri, USA.
Washington University in St. Louis · USMass General Brigham · USTufts Medical Center · USUniversity of Manchester · GB

Funding

ETIOLOGIC STUDIES OF AGE-RELATED MACULAR DEGENERATIONR01EY011309 · NEI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SEDDON, JOHANNA M · 2003 to 2017
$9.3M
Viral Discovery in Rheumatoid ArthritisP30AR048335 · NIAMS · WASHINGTON UNIVERSITY · PI WEIHL, CONRAD C · 2001 to 2015
$8.9M
Translational Research Skills Development CoreU54HL112303 · NHLBI · WASHINGTON UNIVERSITY · PI SADLER, J EVAN · 2012 to 2016
$8.8M
Complement Receptor One (CRI): Structure/FunctionR01AI041592 · NIAID · WASHINGTON UNIVERSITY · PI ATKINSON, JOHN · 1997 to 2013
$3.9M
INTRACELLULAR C3 PROTEINS: SOURCE, COMPOSITION, TRAFFICKING AND FUNCTIONR01GM099111 · NIGMS · WASHINGTON UNIVERSITY · PI ATKINSON, JOHN · 2011 to 2019
$2.7M
Medical Research Council MR/K004441/1Medical Research Council MR/K024418/1NEI NIH HHS R01 EY011309NEI NIH HHS R01-EY11309NHLBI NIH HHS U54 HL112303NIAID NIH HHS R01 AI041592NIAMS NIH HHS P30 AR048335NIAMS NIH HHS P30AR48335NIGMS NIH HHS R01 GM099111
6 · The paper itself

Abstract

Age-related macular degeneration (AMD) is a major cause of visual impairment in the western world. It is characterized by the presence of lipoproteinaceous deposits (drusen) in the inner layers of the retina. Immunohistochemistry studies identified deposition of complement proteins in the drusen as well as in the choroid. In the last decade, genetic studies have linked both common and rare variants in genes of the complement system to increased risk of development of AMD. Here, we review the variants described to date and discuss the functional implications of dysregulation of the alternative pathway of complement in AMD.

Indexed as

Genetic Predisposition to DiseaseGenetic VariationComplement System ProteinsHumansMacular DegenerationComplement System ProteinsAge-related macular degenerationAlternative pathwayComplement systemGenetic variants

Identifiers

PMID25034031
PMCPMC4149817
OpenAlexW1987637624

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.