Evidence map›Paper›PMID 25290268›Full record

ArticleTranslational psychiatry2014

CACNA1C risk variant affects reward responsiveness in healthy individuals.

T M Lancaster, E A Heerey, K Mantripragada, D E J Linden

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.1field-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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Contribution of D1R-expressing neurons of the dorsal dentate gyrus and CaNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
    Article
  7. Review
  8. Article
  9. The Emerging Neurobiology of Bipolar Disorder.Trends in neurosciences · 2018
    Review
  10. From Gene to Behavior: L-Type Calcium Channel Mechanisms Underlying Neuropsychiatric Symptoms.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2017
    Review
  11. Article
  12. L-type CaThe Journal of physiology · 2016
    Review
  13. CACNA1C risk variant is associated with increased amygdala volume.European archives of psychiatry and clinical neuroscience · 2016
    Article
  14. Article
  15. Review
  16. 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

4 authors at 2 institutions in 1 country.

T M Lancaster1] Neuroscienceand Mental Health Research Institute and MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK [2] School of Psychology, Cardiff University, Cardiff, UK.
E A HeereySchool of Psychology, Bangor University, Bangor, UK.
K MantripragadaNeuroscienceand Mental Health Research Institute and MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK.
D E J Linden1] Neuroscienceand Mental Health Research Institute and MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK [2] School of Psychology, Cardiff University, Cardiff, UK.
Cardiff University · GBBangor University · GB

Funding

Medical Research Council MR/L010305/1Wellcome Trust 100202Wellcome Trust 503147
6 · The paper itself

Abstract

The variant at rs1006737 in the L-type voltage-gated calcium channel (alpha 1c subunit) CACNA1C gene is reliably associated with both bipolar disorder and schizophrenia. We investigated whether this risk variant affects reward responsiveness because reward processing is one of the central cognitive-motivational domains implicated in both disorders. In a sample of 164 young, healthy individuals, we show a dose-dependent response, where the rs1006737 risk genotype was associated with blunted reward responsiveness, whereas discriminability did not significantly differ between genotype groups. This finding suggests that the CACNA1C risk locus may have a role in neural pathways that facilitate value representation for rewarding stimuli. Impaired reward processing may be a transdiagnostic phenotype of variation in CACNA1C that could contribute to anhedonia and other clinical features common to both affective and psychotic disorders.

Indexed as

RewardAdultBrainBrain MappingCalcium Channels, L-TypeFemaleHumansMagnetic Resonance ImagingMalePolymorphism, Single NucleotideReference ValuesRiskYoung AdultCACNA1C protein, humanCalcium Channels, L-Type

Identifiers

PMID25290268
PMCPMC4350510
OpenAlexW2064261566

What OpenQuestion holds

Textmetadata
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.