Evidence map›Paper›PMID 23253771›Full record

ArticleThe international journal of neuropsychopharmacology2013

Age-modulated association between prefrontal NAA and the BDNF gene.

Basira Salehi, Nora Preuss, Jan Willem van der Veen, Jun Shen, Alexander Neumeister, Wayne C Drevets, Colin Hodgkinson, David Goldman, Jens R Wendland, Andrew Singleton and 3 more

Abstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 48% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. 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

13 authors at 7 institutions in 2 countries.

Basira SalehiPsychiatric University Hospital, University of Bern, Bern, Switzerland.
Nora Preuss
Jan Willem van der Veen
Jun Shen
Alexander Neumeister
Wayne C Drevets
Colin Hodgkinson
David Goldman
Jens R Wendland
Andrew Singleton
Jesse R Gibbs
Mark R Cookson
Gregor Hasler
National Institute of Mental Health · USNational Institute on Aging · USNational Institute on Alcohol Abuse and Alcoholism · USUniversity Hospital of Bern · CHNew York University · USUniversity of Bern · CHUniversity of Oklahoma · US

Funding

Integrative genetics of behavior with high throughput technologiesZIAAA000301 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI GOLDMAN, DAVID · 2009 to 2025
$68.6M
Magnetic Resonance Spectroscopy and Imaging Studies of Brain FunctionsZIAMH002803 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI SHEN, JUN · 2009 to 2025
$24.9M
Magnetic Resonance Spectroscopy Core FacilityZICMH002894 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI SHEN, JUN · 2009 to 2024
$13.5M
Gene expression in the human brainZIAAG000947 · NIA · NATIONAL INSTITUTE ON AGING · PI COOKSON, MARK · 2009 to 2025
$7.2M
Intramural NIH HHS Z99 MH999999Intramural NIH HHS ZIA AG000947
6 · The paper itself

Abstract

Brain-derived neurotrophic factor (BDNF) has been implicated in the pathophysiology of psychiatric and neurological disorders and in the mechanisms of antidepressant pharmacotherapy. Psychiatric and neurological conditions have also been associated with reduced brain levels of N-acetyl-aspartate (NAA), which has been used as a putative marker of neural integrity. However, few studies have explored the relationship between BDNF polymorphisms and NAA levels directly. Here, we present data from a single-voxel proton magnetic resonance spectroscopy study of 64 individuals and explore the relationship between BDNF polymorphisms and prefrontal NAA level. Our results indicate an association between a single nucleotide polymorphism (SNP) within BDNF, known as rs1519480, and reduced NAA level (p = 0.023). NAA levels were further predicted by age and Asian ancestry. There was a significant rs1519480 × age interaction on NAA level (p = 0.031). Specifically, the effect of rs1519480 on NAA level became significant at age ⩾34.17 yr. NAA level decreased with advancing age for genotype TT (p = 0.001) but not for genotype CT (p = 0.82) or CC (p = 0.34). Additional in silico analysis of 142 post-mortem brain samples revealed an association between the same SNP and reduced BDNF mRNA expression in the prefrontal cortex. The rs1519480 SNP influences BDNF mRNA expression and has an impact on prefrontal NAA level over time. This genetic mechanism may contribute to inter-individual variation in cognitive performance seen during normal ageing, as well as contributing to the risk for developing psychiatric and neurological conditions.

Indexed as

AdolescentAdultAgingAspartic AcidBrain-Derived Neurotrophic FactorDepressionFemaleGenetic Association StudiesGenotypeHumansLinear ModelsMagnetic Resonance ImagingMagnetic Resonance SpectroscopyMajor Depressive DisorderMaleMiddle AgedAspartic AcidBrain-Derived Neurotrophic FactorN-acetylaspartateRNA, Messenger

Identifiers

PMID23253771
PMCPMC4025926
OpenAlexW2154979488

What OpenQuestion holds

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LicenceTDM
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.