Evidence map›Paper›PMID 22059990›Full record

SynthesisClinical and experimental immunology2011

The major risk alleles of age-related macular degeneration (AMD) in CFH do not play a major role in rheumatoid arthritis (RA).

L A Trouw, S Böhringer, N A Daha, E A Stahl, S Raychaudhuri, F A Kurreeman, G Stoeken-Rijsbergen, J J Houwing-Duistermaat, T W Huizinga, R E Toes

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In one paragraph

Synthesis in Clinical and experimental immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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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

10 authors at 2 institutions in 2 countries.

L A TrouwDepartment of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands. l.a.trouw@lumc.nl
S Böhringer
N A Daha
E A Stahl
S Raychaudhuri
F A Kurreeman
G Stoeken-Rijsbergen
J J Houwing-Duistermaat
T W Huizinga
R E Toes
Brigham and Women's Hospital · USLeiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Because activation of the alternative pathway (AP) of the complement system is an important aspect of both age-related macular degeneration (AMD) and rheumatoid arthritis (RA), we wished to address the question whether genetic risk factors of the AP inhibitor complement factor H (CFH) for AMD would also be risk factors for RA. For this purpose we genotyped single nucleotide polymorphisms (SNPs) in a Dutch set of RA patients and controls. Similarly, a meta-analysis using a Spanish cohort of RA as well as six large genome-wide association studies (GWAS) studies was performed. For these SNPs we analysed more than 6000 patients and 20,000 controls. The CFH variants, I62V, Y402H, IVS1 and IVS10, known to associate strongly with AMD, did not show a significant association with the risk of developing RA despite a strong statistical power to detect such differences. In conclusion, the major risk alleles of AMD in CFH do not have a similar effect on developing RA.

Indexed as

AgedAged, 80 and overAllelesArthritis, RheumatoidCohort StudiesComplement C3-C5 Convertases, Alternative PathwayComplement Factor HGenome-Wide Association StudyGenotypeHumansMacular DegenerationMiddle AgedPolymorphism, Single NucleotideRisk FactorsCFH protein, humanComplement C3-C5 Convertases, Alternative PathwayComplement Factor H

Identifiers

PMID22059990
PMCPMC3232380
OpenAlexW1499601030

What OpenQuestion holds

Textmetadata
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.