Evidence map›Paper›PMID 20337192›Full record

ArticleSleep2010

Association between a serotonin transporter length polymorphism and primary insomnia.

Michael Deuschle, Michael Schredl, Claudia Schilling, Stefan Wüst, Josef Frank, Stephanie H Witt, Marcella Rietschel, Magdalena Buckert, Andreas Meyer-Lindenberg, Thomas G Schulze

Open access · bronzeAbstract read
In one paragraph

Article in Sleep, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
7.0field-weighted citation impact, top 3% 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

29 citing papers in PubMed, 108 citations in OpenAlex.

  1. Trial
  2. Insomnia disorder.Nature reviews. Disease primers · 2026
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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

10 authors at 1 institution in 1 country.

Michael DeuschleCentral Institute of Mental Health, Department of Psychiatry and Psychotherapy, Mannheim, Germany. michael.deuschle@zi-mannheim.de
Michael Schredl
Claudia Schilling
Stefan Wüst
Josef Frank
Stephanie H Witt
Marcella Rietschel
Magdalena Buckert
Andreas Meyer-Lindenberg
Thomas G Schulze
Central Institute of Mental Health · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

STUDY

objectiveTo test the hypothesis that a 44-base-pair insertion/deletion polymorphism in the 5' regulatory region of the serotonin transporter gene (5-HTTLPR) is associated with primary insomnia.

designAssociation study.

settingSleep laboratory at the Central Institute of Mental Health, Mannheim, Germany. PATIENTS: 157 patients with primary insomnia and 827 healthy controls.

interventionsN/A. MEASUREMENT AND

resultsWe found the short (s-) allele of the 5-HTTLPR to be significantly more frequent in patients suffering from insomnia than in control individuals (47.1% vs. 39.9%: OR = 1.34).

conclusionsThis finding contributes to the understanding of the pathophysiology of primary insomnia and suggests a biological basis between the prevalent comorbidity of primary insomnia and other psychiatric disorders.

Indexed as

AllelesAdultAgedBase PairingDNA Mutational AnalysisFemaleGenetic Predisposition to DiseaseGenotypeHumansINDEL MutationMaleMiddle AgedPolymorphism, GeneticPolysomnographySerotonin Plasma Membrane Transport ProteinsSleep Initiation and Maintenance DisordersSerotonin Plasma Membrane Transport ProteinsSLC6A4 protein, human

Identifiers

PMID20337192
PMCPMC2831428
OpenAlexW62675235

What OpenQuestion holds

Textmetadata
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.