Evidence map›Paper›PMID 32321835›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

A genome-wide association study identifies key modulators of complement factor H binding to malondialdehyde-epitopes.

Lejla Alic, Nikolina Papac-Milicevic, Darina Czamara, Ramona B Rudnick, Maria Ozsvar-Kozma, Andrea Hartmann, Michael Gurbisz, Gregor Hoermann, Stefanie Haslinger-Hutter, Peter F Zipfel and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 38 citations in OpenAlex.

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  12. The human factor H protein family - an update.Frontiers in immunology · 2024
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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

13 authors at 6 institutions in 3 countries.

Lejla AlicDepartment of Laboratory Medicine, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0003-0197-0837
Nikolina Papac-MilicevicDepartment of Laboratory Medicine, Medical University of Vienna, 1090 Vienna, Austria; nikolina.papac@meduniwien.ac.at christoph.binder@meduniwien.ac.at.
Darina CzamaraDepartment of Translational Research in Psychiatry, Max Planck Institute of Psychiatry, 80804 Munich, Germany.
Ramona B RudnickDepartment of Infection Biology, Leibniz Institute for Natural Product Research and Infection Biology, 07745 Jena, Germany.
Maria Ozsvar-KozmaDepartment of Laboratory Medicine, Medical University of Vienna, 1090 Vienna, Austria.
Andrea HartmannDepartment of Infection Biology, Leibniz Institute for Natural Product Research and Infection Biology, 07745 Jena, Germany.
Michael GurbiszDepartment of Laboratory Medicine, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-7773-8228
Gregor HoermannDepartment of Laboratory Medicine, Medical University of Vienna, 1090 Vienna, Austria.
Stefanie Haslinger-HutterDepartment of Laboratory Medicine, Medical University of Vienna, 1090 Vienna, Austria.
Peter F ZipfelDepartment of Infection Biology, Leibniz Institute for Natural Product Research and Infection Biology, 07745 Jena, Germany.
Christine SkerkaDepartment of Infection Biology, Leibniz Institute for Natural Product Research and Infection Biology, 07745 Jena, Germany.ORCID 0000-0003-2374-6473
Elisabeth B BinderDepartment of Translational Research in Psychiatry, Max Planck Institute of Psychiatry, 80804 Munich, Germany.ORCID 0000-0001-7088-6618
Christoph J BinderDepartment of Laboratory Medicine, Medical University of Vienna, 1090 Vienna, Austria; nikolina.papac@meduniwien.ac.at christoph.binder@meduniwien.ac.at.
Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI) · DEAustrian Academy of Sciences · ATMax Planck Institute of Psychiatry · DEMedical University of Vienna · ATUniversity Hospital Innsbruck · ATUniversity of Sarajevo · BA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic variants within complement factor H (CFH), a major alternative complement pathway regulator, are associated with the development of age-related macular degeneration (AMD) and other complementopathies. This is explained with the reduced binding of CFH or its splice variant factor H-like protein 1 (FHL-1) to self-ligands or altered self-ligands (e.g., malondialdehyde [MDA]-modified molecules) involved in homeostasis, thereby causing impaired complement regulation. Considering the critical role of CFH in inhibiting alternative pathway activation on MDA-modified surfaces, we performed an unbiased genome-wide search for genetic variants that modify the ability of plasma CFH to bind MDA in 1,830 individuals and characterized the mechanistic basis and the functional consequences of this. In a cohort of healthy individuals, we identified rs1061170 in

Indexed as

AgedBlood ProteinsComplement C3b Inactivator ProteinsComplement Factor HEpitopesFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMacular DegenerationMaleMalondialdehydeMiddle AgedPolymorphism, Single NucleotideProtein BindingBlood ProteinsCFH protein, humanCFHR1 protein, humanCFHR3 protein, humanComplement C3b Inactivator ProteinsComplement Factor HEpitopesMalondialdehydecomplement factor Hcomplement factor H-related protein 1complement factor H-related protein 3genome-wide association studymalondialdehyde

Identifiers

PMID32321835
PMCPMC7211993
OpenAlexW3017496971

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.