Evidence map›Paper›PMID 22669473›Full record

ArticleMolecular medicine (Cambridge, Mass.)2012

Common variants of the genes encoding erythropoietin and its receptor modulate cognitive performance in schizophrenia.

Anne Kästner, Sabrina Grube, Ahmed El-Kordi, Beata Stepniak, Heidi Friedrichs, Derya Sargin, Judith Schwitulla, Martin Begemann, Ina Giegling, Kamilla W Miskowiak and 8 more

Open access · goldAbstract read
In one paragraph

Article in Molecular medicine (Cambridge, Mass.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Recombinant human erythropoietin for treating treatment-resistant depression: a double-blind, randomized, placebo-controlled phase 2 trial.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2014
    Trial
  3. Review
  4. Article
  5. Article
  6. Review
  7. The ErythropoetinGenes · 2020
    Article
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  11. Review
  12. Article
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  14. Review
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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

18 authors at 6 institutions in 2 countries.

Anne KästnerDivision of Clinical Neuroscience, Max Planck Institute of Experimental Medicine, Göttingen, Germany.
Sabrina Grube
Ahmed El-Kordi
Beata Stepniak
Heidi Friedrichs
Derya Sargin
Judith Schwitulla
Martin Begemann
Ina Giegling
Kamilla W Miskowiak
Swetlana Sperling
Kathrin Hannke
Anna Ramin
Ralf Heinrich
Olaf Gefeller
Klaus-Armin Nave
Dan Rujescu
Hannelore Ehrenreich
Max Planck Institute of Experimental Medicine · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DELudwig-Maximilians-Universität München · DECopenhagen University Hospital · DKNanoscale Microscopy and Molecular Physiology of the Brain Cluster of Excellence 171 — DFG Research Center 103 · DEUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Erythropoietin (EPO) improves cognitive performance in clinical studies and rodent experiments. We hypothesized that an intrinsic role of EPO for cognition exists, with particular relevance in situations of cognitive decline, which is reflected by associations of EPO and EPO receptor (EPOR) genotypes with cognitive functions. To prove this hypothesis, schizophrenic patients (N > 1000) were genotyped for 5' upstream-located gene variants, EPO SNP rs1617640 (T/G) and EPORSTR(GA)(n). Associations of these variants were obtained for cognitive processing speed, fine motor skills and short-term memory readouts, with one particular combination of genotypes superior to all others (p < 0.0001). In an independent healthy control sample (N > 800), these associations were confirmed. A matching preclinical study with mice demonstrated cognitive processing speed and memory enhanced upon transgenic expression of constitutively active EPOR in pyramidal neurons of cortex and hippocampus. We thus predicted that the human genotypes associated with better cognition would reflect gain-of-function effects. Indeed, reporter gene assays and quantitative transcriptional analysis of peripheral blood mononuclear cells showed genotype-dependent EPO/EPOR expression differences. Together, these findings reveal a role of endogenous EPO/EPOR for cognition, at least in schizophrenic patients.

Indexed as

CognitionGenetic Predisposition to DiseasePolymorphism, GeneticAdolescentAdultAgedAnimalsCase-Control StudiesCerebral CortexDemographyErythropoietinFemaleGenetic Association StudiesHippocampusHumansMaleErythropoietinReceptors, Erythropoietin

Identifiers

PMID22669473
PMCPMC3459483
OpenAlexW1707428129

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.