Evidence map›Paper›PMID 27103936›Full record

ArticleJournal of circadian rhythms2016

A PER3 Polymorphism Interacts with Sleep Duration to Influence Transient Mood States in Women.

Tatiana D Viena, Christina M Gobin, Ana I Fins, Travis J A Craddock, Aurélien Tartar, Jaime L Tartar

Open access · goldAbstract read
In one paragraph

Article in Journal of circadian rhythms, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Chronotype and Mental Health: Recent Advances.Current psychiatry reports · 2018
    Review
  7. Article
  8. Daytime Sleep Disturbance in Night Shift Work and the Role ofJournal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2018
    Article
  9. Human genetics and sleep behavior.Current opinion in neurobiology · 2017
    Review
  10. Article
  11. 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

6 authors at 1 institution in 1 country.

Tatiana D VienaDepartment of Psychology and Neuroscience, Nova Southeastern University, Ft. Lauderdale, FL USA.
Christina M GobinDepartment of Psychology and Neuroscience, Nova Southeastern University, Ft. Lauderdale, FL USA.
Ana I FinsDepartment of Clinical Psychology, Nova Southeastern University, Ft. Lauderdale, FL USA.
Travis J A CraddockDepartment of Psychology and Neuroscience, Nova Southeastern University, Ft. Lauderdale, FL USA; Clinical Systems Biology Group, Institute for Neuro-Immune Medicine, Nova Southeastern University, Ft. Lauderdale, FL USA; Department of Computer Science, Nova Southeastern University, Ft. Lauderdale, FL USA; Department of Clinical Immunology, Nova Southeastern University, Ft. Lauderdale, FL USA.
Aurélien TartarDepartment of Biological Sciences, Nova Southeastern University, Ft. Lauderdale, FL USA.
Jaime L TartarDepartment of Psychology and Neuroscience, Nova Southeastern University, Ft. Lauderdale, FL USA.
Nova Southeastern University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExpression of the clock family of genes in the suprachiasmatic nuclei (SCN) regulates the molecular control of circadian timing. Increasing evidence also implicates clock gene activity in the development of mood disorders. In particular, variation in the PER3 clock gene has been shown to influence diurnal preference and sleep homeostasis. However, there is not currently a clear association between PER3 polymorphisms and mood. This is possibly because the PER3 gene has been shown to influence homeostatic sleep drive, rather than circadian timing, and the PER3 gene may be behaviorally relevant only under chronic sleep loss conditions.

methodsTo test the association between PER3 allele status and impaired mood, a total of 205 healthy women were genotyped for PER3 allele status and responded to previously-validated psychological questionnaires surveying self-reported sleep habits (MEQ, PSQI) and mood. Our mood measures included two measures of short-term, transient mood (state anxiety and mood disturbance) and two measures of longer term, ongoing mood (trait anxiety and depressive symptomology).

resultsThe PER3 genotype distribution was 88 (42.9%) for PER3(4/4), 98 (47.8%) for PER3(4/5), and 19 (9.3%) for PER3(5/5). Our sleep duration x genotype interaction analyses showed that, relative to longer allele carriers, PER3(4/4) genotypes were at greater risk for transient psychological effects (mood and state anxiety) when they reported reduced sleep durations.

conclusionSleep duration plays a critical role in understanding the extent to which PER3 allele status relates to mood states.

Indexed as

AnxietyDepressionMoodPER3Sleep

Identifiers

PMID27103936
PMCPMC4834748
OpenAlexW2296078884

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.