Evidence map›Paper›PMID 37558806›Full record

ArticleScientific reports2023

Associations of the serotonin transporter gene polymorphism, 5-HTTLPR, and adverse life events with late life depression in the elderly Lithuanian population.

Sandrita Simonyte, Ingrida Grabauskyte, Jurate Macijauskiene, Vita Lesauskaite, Vaiva Lesauskaite, Kari Sofie Kvaal, Robert Stewart

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. New Personalized Medicine Model for Medication Management.Journal of personalized medicine · 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

7 authors at 3 institutions in 3 countries.

Sandrita SimonyteInstitute of Cardiology of Medical Academy, Lithuanian University of Health Sciences, Kaunas, Lithuania. sandrita.simonyte@lsmu.lt.
Ingrida GrabauskyteDepartment of Physics, Mathematics and Biophysics of Medical Academy, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Jurate MacijauskieneDepartment of Geriatrics of Medical Academy, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Vita LesauskaiteDepartment of Geriatrics of Medical Academy, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Vaiva LesauskaiteInstitute of Cardiology of Medical Academy, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Kari Sofie KvaalFaculty of Social and Health Sciences, Inland Norway University of Applied Sciences, Lillehammer, Innlandet, Norway.
Robert StewartKing's College London (Institute of Psychiatry, Psychology and Neuroscience), London, UK.
Lithuanian University of Health Sciences · LTInland Norway University of Applied Sciences · NOSouth London and Maudsley NHS Foundation Trust · GB

Funding

Department of HealthMedical Research Council MR/W014386
6 · The paper itself

Abstract

Late-life depression (LLD) is a multifactorial disorder, with susceptibility and vulnerability potentially influenced by gene-environment interaction. The aim of this study was to investigate whether the 5-HTTLPR polymorphism is associated with LLD. The sample of 353 participants aged 65 years and over was randomly selected from the list of Kaunas city inhabitants by Residents' Register Service of Lithuania. Depressive symptoms were ascertained using the EURO-D scale. The List of Threatening Events Questionnaire was used to identify stressful life events that happened over the last 6 months and during lifetime. A 5-HTTLPR and lifetime stressful events interaction was indicated by higher odds of depression in those with s/s genotype who experienced high stress compared to l/l carriers with low or medium stress, while 5-HTTLPR and current stressful events interaction analysis revealed that carriers of either one or two copies of the s allele had increased odds of depressive symptoms associated with stress compared to participants with the l/l genotype not exposed to stressful situations. Although no significant direct association was found between the 5-HTTLPR short allele and depression, our findings demonstrated that lifetime or current stressful life events and their modification by 5-HTTLPR genotype are risk factors for late-life depression.

Indexed as

DepressionSerotonin Plasma Membrane Transport ProteinsAgedAllelesGenotypeHumansLife Change EventsLithuaniaPolymorphism, GeneticSerotonin Plasma Membrane Transport ProteinsSLC6A4 protein, human

Identifiers

PMID37558806
PMCPMC10412533
OpenAlexW4385700402

What OpenQuestion holds

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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.