Evidence map›Paper›PMID 26156558›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2016

Impact of KIBRA Polymorphism on Memory Function and the Hippocampus in Older Adults.

A Veronica Witte, Theresa Köbe, Lucia Kerti, Dan Rujescu, Agnes Flöel

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Genes · 2023
    Pooled it
  2. Review
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  11. 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
  12. Article
  13. Article
  14. The role of KIBRA in reconstructive episodic memory.Molecular medicine (Cambridge, Mass.) · 2018
    Article
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  18. 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

5 authors at 2 institutions in 1 country.

A Veronica WitteDepartment of Neurology, Charité-Universitätsmedizin Berlin, CCM, Berlin, Germany.
Theresa KöbeDepartment of Neurology, Charité-Universitätsmedizin Berlin, CCM, Berlin, Germany.
Lucia KertiDepartment of Neurology, Charité-Universitätsmedizin Berlin, CCM, Berlin, Germany.
Dan RujescuKlinik und Poliklinik für Psychiatrie, Psychotherapie und Psychosomatik, Universitätsklinikum Halle (Saale), Halle (Saale), Germany.
Agnes FlöelDepartment of Neurology, Charité-Universitätsmedizin Berlin, CCM, Berlin, Germany.
Charité - Universitätsmedizin Berlin · DEKlinik und Poliklinik für Psychiatrie und Psychotherapie · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The single nucleotide polymorphism rs17070145 within the KIBRA gene (kidney and brain expressed protein) has been associated with variations in memory functions and related brain areas. However, previous studies yielded conflicting results, which might be due to divergent sample characteristics or task-specific effects. Therefore, we aimed to determine the impact of KIBRA genotype on learning and memory formation, and volume, microstructural integrity and functional connectivity (FC) of the hippocampus and its subfields in a well-characterized cohort of healthy older adults. One-hundred and forty subjects (72 women, age 50-80) were KIBRA genotyped and memory was tested using the Auditory Verbal Learning Task. Also, subjects underwent structural and resting-state functional magnetic resonance imaging at 3T. Subfields were delineated using automated segmentation (FreeSurfer software). Microstructural integrity was measured using mean diffusivity (MD) derived from diffusion tensor images. Seed-based analyses were used to assess FC patterns of the hippocampus. KIBRA T-allele carriers showed a trend for better memory performance, and in the hippocampus significantly higher volumes and partly lower MD, indicative for better microstructure, compared with non-T-allele carriers in the cornu ammonis (CA)2/3 and CA4/dentate gyrus subfields (all P⩽0.008, Bonferroni corrected). Also, T-allele carriers exhibited lower FC of the left hippocampus with areas outside the synchronized HC network. In sum, we could show for the first time that older T-allele carriers exhibited larger volumes and better microstructure within those hippocampus subfields that are implicated in long-term potentiation and neurogenesis, key features of memory processes. Moreover, T-allele carriers showed a more selective FC network of the hippocampus.

Indexed as

Memory, EpisodicPolymorphism, Single NucleotideAgedAged, 80 and overCohort StudiesFemaleGenotyping TechniquesHeterozygoteHippocampusHumansIntracellular Signaling Peptides and ProteinsLearningMagnetic Resonance ImagingMaleMiddle AgedNeural PathwaysIntracellular Signaling Peptides and ProteinsPhosphoproteinsWWC1 protein, human

Identifiers

PMID26156558
PMCPMC4707824
OpenAlexW2255450970

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.