Evidence map›Paper›PMID 21831326›Full record

ArticleJournal of neuroinflammation2011

CRP gene variation affects early development of Alzheimer's disease-related plaques.

Eloise Helena Kok, Mervi Alanne-Kinnunen, Karita Isotalo, Teemu Luoto, Satu Haikonen, Sirkka Goebeler, Markus Perola, Mikko A Hurme, Hannu Haapasalo, Pekka J Karhunen

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Vascular Lesions, APOE ε4, and Tau Pathology in Alzheimer Disease.Journal of neuropathology and experimental neurology · 2021
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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 5 institutions in 1 country.

Eloise Helena KokSchool of Medicine, University of Tampere and Centre for Laboratory Medicine, Tampere University Hospital, Tampere, Finland. Eloise.kok@uta.fi
Mervi Alanne-Kinnunen
Karita Isotalo
Teemu Luoto
Satu Haikonen
Sirkka Goebeler
Markus Perola
Mikko A Hurme
Hannu Haapasalo
Pekka J Karhunen
Tampere University · FITampere University Hospital · FIFinnish Institute for Health and Welfare · FIUniversity of Helsinki · FIWihuri Research Institute · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWe used the Tampere Autopsy Study (TASTY) series (n = 603, age 0-97 yrs), representing an unselected population outside institutions, to investigate the pathogenic involvement of inflammation in Alzheimer's disease-related lesions.

methodsWe studied senile plaque (SP), neurofibrillary tangles (NFT) and SP phenotype associations with 6 reported haplotype tagging single nucleotide polymorphisms (SNPs) in the CRP gene. CRP and Aβ immunohistochemistry was assessed using brain tissue microarrays.

resultsIn multivariate analyses (age- and APOE-adjusted), non-neuritic SP were associated with the high-CRP TA-genotype (3.0% prevalence) of rs3091244 and CA-genotype (10.8%) of rs3093075 compared to common genotypes. Conversely, the low-CRP C allele (39.3%) of rs2794521 reduced the risk of harbouring early non-neuritic SP, compared to the TT genotype. CRP haplotype TAGCC (high) associated with non-neuritic SP, whereas haplotype CCGCC offered protection. TT genotypes (high) of rs3091244 and rs1130864 were associated with CRP staining. There were no associations between SNPs or haplotypes and NFT. CRP staining of the hippocampal CA1/2 region correlated with Aβ staining.

conclusionsCRP gene variation affects early SP development in prodromal Alzheimer's disease, independent of APOE genotype.

Indexed as

Polymorphism, Single NucleotideAdolescentAdultAgedAged, 80 and overAlzheimer DiseaseAnimalsApolipoprotein E4AutopsyChildChild, PreschoolC-Reactive ProteinGenotypeHumansInfantMaleApolipoprotein E4C-Reactive Protein

Identifiers

PMID21831326
PMCPMC3168418
OpenAlexW2036216712

What OpenQuestion holds

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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.