Evidence map›Paper›PMID 15322730›Full record

ArticlePsychopharmacology2005

Evidence of a role for the 5-HTTLPR genotype in the modulation of motor response to antidepressant treatment.

Albert Putzhammer, Anja Schoeler, Thomas Rohrmeier, Philipp Sand, Goeran Hajak, Peter Eichhammer

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Psychopharmacology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 29 citations in OpenAlex.

  1. Trial
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  4. Review
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  6. Review
  7. Beyond affect: a role for genetic variation of the serotonin transporter in neural activation during a cognitive attention task.Proceedings of the National Academy of Sciences of the United States of America · 2005
    Article
  8. 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.

Albert PutzhammerDepartment of Psychiatry, University of Regensburg, 93042 Regensburg, Germany. albert.putzhammer@medbo.de
Anja Schoeler
Thomas Rohrmeier
Philipp Sand
Goeran Hajak
Peter Eichhammer
University of Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleSerotonergic mechanisms are thought to play an important role in the regulation of mood, motor activity and sleep patterns. Serotonin reuptake is controlled by the serotonin transporter (5-HTT) and by a common functional insertion/deletion polymorphism in the corresponding gene's promoter region (5-HTTLPR). Homozygosity for the long variant may confer a favourable response to treatment with serotonin reuptake inhibitors (SSRIs), and to sleep deprivation.

objectivesThe study assessed the role of the 5-HTTLPR genotype in determining motor side effects of antidepressant medication.

methodsMotor activity patterns of 62 patients with major depression who were being treated with either SSRIs or tricyclic antidepressants (TCAs) were monitored over a 24-h period using a wrist-actograph. Additionally, motor activity was rated in a semi-structured interview using the motor agitation and retardation scale (MARS).

resultsNight-time motor activity was significantly increased in homozygous carriers of the long 5-HTTLPR allele (LL-genotype) who were being treated with SSRIs in comparison to short allele carriers (LS-genotype and SS-genotype), regardless of the type of antidepressant treatment (P<0.001). It was also significantly increased in comparison to patients with the LL-genotype who were being treated with TCAs (P<0.01). Differences in actographic motor activity were most prominent between 11 p.m. and 4 a.m. Clinical ratings of motor activity also showed a trend toward higher agitation scores in patients with the LL-genotype who received SSRI treatment.

conclusionsHomozygosity for the long variant of the 5-HTTLPR may cause a predisposition to increased night-time motor activity in conjunction with SSRI treatment.

Indexed as

PhenotypeAkathisia, Drug-InducedAllelesAntidepressive Agents, TricyclicChromosome DeletionCircadian RhythmFemaleGenetic Carrier ScreeningGenetic Predisposition to DiseaseGenotypeHomozygoteHumansMajor Depressive DisorderMaleMembrane GlycoproteinsMembrane Transport ProteinsAntidepressive Agents, TricyclicMembrane GlycoproteinsMembrane Transport ProteinsNerve Tissue ProteinsSelective Serotonin Reuptake InhibitorsSerotonin Plasma Membrane Transport ProteinsSLC6A4 protein, human

Identifiers

PMID15322730
OpenAlexW2112322821

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.