Evidence map›Paper›PMID 21346737›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2011

Impact of common KIBRA allele on human cognitive functions.

H Wersching, K Guske, S Hasenkamp, C Hagedorn, S Schiwek, S Jansen, V Witte, J Wellmann, H Lohmann, K Duning and 4 more

Abstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. KIBRA T allele influences memory performance and progression of cognitive decline: a 7-year follow-up study in subjective cognitive decline and mild cognitive impairment.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2019
    Article
  5. The role of KIBRA in reconstructive episodic memory.Molecular medicine (Cambridge, Mass.) · 2018
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Age-Modulated Associations betweenFrontiers in aging neuroscience · 2017
    Article
  12. Review
  13. Impact of KIBRA Polymorphism on Memory Function and the Hippocampus in Older Adults.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2016
    Article
  14. Serum KIBRA mRNA and Protein Expression and Cognitive Functions in Depression.Medical science monitor : international medical journal of experimental and clinical research · 2016
    Article
  15. KIBRA: In the brain and beyond.Cellular signalling · 2014
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

14 authors.

H WerschingDepartment of Neurology, University Hospital Münster, Münster, Germany.
K Guske
S Hasenkamp
C Hagedorn
S Schiwek
S Jansen
V Witte
J Wellmann
H Lohmann
K Duning
J Kremerskothen
S Knecht
E Brand
A Floel

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The rs17070145 polymorphism (C → T substitution, intron 9) of the KIBRA gene has recently been associated with episodic memory and cognitive flexibility. These findings were inconsistent across reports though, and largely lacked gene-gene or gene-environment interactions. The aim of the present study was to determine the impact of the rs17070145 polymorphism on clinically relevant cognitive domains and its interaction with the modifiers 'lifestyle' and 'cardiovascular risk factors'. Five-hundred forty-five elderly volunteers (mean age 64 years, ±7 years, 56% women) accomplished a comprehensive cognitive testing. Principal component analysis was used to reveal the internal structure of the data, rendering four composite scores: verbal memory, word fluency, executive function/psychomotor speed, and working memory. Lifestyle was assessed with a detailed questionnaire, age-associated risk factors by clinical interview and examination. There was no main effect of the rs17070145 genotype on any cognitive composite scores. However, we found worse performance in executive functions for T-allele carriers in the presence of arterial hypertension (β=-0.365, p=0.0077 and 0.031 after Bonferroni correction). This association was further modified by gender, showing the strongest association in hypertensive females (β=-0.500, p=0.0072 and 0.029 after Bonferroni correction). The effect of KIBRA on cognitive function seems to be complex and modified by gender and arterial hypertension.

Indexed as

AgedCardiovascular DiseasesCognitionCognition DisordersCohort StudiesComorbidityFemaleGenotypeHumansHypertensionIntracellular Signaling Peptides and ProteinsMaleMiddle AgedPhosphoproteinsIntracellular Signaling Peptides and ProteinsPhosphoproteinsWWC1 protein, human

Identifiers

PMID21346737
PMCPMC3079841

What OpenQuestion holds

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Registered trials

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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.