Evidence map›Paper›PMID 27015428›Full record

ArticlePloS one2016

The Idea Is Good, but…: Failure to Replicate Associations of Oxytocinergic Polymorphisms with Face-Inversion in the N170.

Aisha J L Munk, Andrea Hermann, Jasmin El Shazly, Phillip Grant, Jürgen Hennig

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  4. 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

5 authors.

Aisha J L MunkJustus Liebig University Giessen, Department of Psychology, Personality and Biological Psychology, Otto-Behaghel-Strasse 10F, 35394 Giessen, Germany.
Andrea HermannJustus Liebig University Giessen, Department of Psychology, Psychotherapy and Systems Neuroscience, Otto-Behaghel-Strasse 10F, 35394 Giessen, Germany.
Jasmin El ShazlyJustus Liebig University Giessen, Faculty of Medicine, Center for Psychiatry and Psychotherapy, Am Steg 28, 35392 Giessen, Germany.
Phillip GrantJustus Liebig University Giessen, Department of Psychology, Personality and Biological Psychology, Otto-Behaghel-Strasse 10F, 35394 Giessen, Germany.
Jürgen HennigJustus Liebig University Giessen, Department of Psychology, Personality and Biological Psychology, Otto-Behaghel-Strasse 10F, 35394 Giessen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn event-related potentials, the N170 manifests itself especially in reaction to faces. In the healthy population, face-inversion leads to stronger negative amplitudes and prolonged latencies of the N170, effects not being present in patients with autism-spectrum-disorder (ASD). ASD has frequently been associated with differences in oxytocinergic neurotransmission. This ERP-study aimed to investigate the face-inversion effect in association with oxytocinergic candidate genes. It was expected that risk-allele-carriers of the oxytocin-receptor-gene-polymorphism (rs53576) and of CD38 (rs379863) responded similar to upright and inverted faces as persons with ASD. Additionally, reactions to different facial emotional expressions were studied. As there have been difficulties with replications of those molecular genetic association studies, we aimed to replicate our findings in a second study.

methodSeventy-two male subjects in the first-, and seventy-eight young male subjects in the replication-study conducted a face-inversion-paradigm, while recording EEG. DNA was extracted from buccal cells.

resultsResults revealed stronger N170-amplitudes and longer latencies in reaction to inverted faces in comparison to upright ones. Furthermore, effects of emotion on N170 were evident. Those effects were present in the first and in the second study. Whereas we found molecular-genetic associations of oxytocinergic polymorphisms with the N170 in the first study, we failed to do so in the replication sample.

conclusionResults indicate that a deeper theoretical understanding of this research-field is needed, in order to generate possible explanations for these findings. Results, furthermore, support the hypotheses that success of reproducibility is correlated with strength of lower original p-values and larger effect sizes in the original study.

Indexed as

EmotionsAdultAutism Spectrum DisorderElectroencephalographyEvoked PotentialsFaceGenetic Association StudiesGenotypeHumansMaleReceptors, OxytocinSerotoninSynaptic TransmissionVisual PerceptionOXTR protein, humanReceptors, OxytocinSerotonin

Identifiers

PMID27015428
PMCPMC4807783

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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.