Evidence map›Paper›PMID 30563176›Full record

ArticleBiomolecules2018

Association of Genetic Variation at

Anna L Westermair, Matthias Munz, Anja Schaich, Stefan Nitsche, Bastian Willenborg, Loreto M Muñoz Venegas, Christina Willenborg, Heribert Schunkert, Ulrich Schweiger, Jeanette Erdmann

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Adenosine AJournal of neurochemistry · 2026
    Article
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  7. dbAQP-SNP: a database of missense single-nucleotide polymorphisms in human aquaporins.Database : the journal of biological databases and curation · 2023
    Article
  8. Review
  9. Review
  10. Article
  11. Pathomechanisms of Vascular Depression in Older Adults.International journal of molecular sciences · 2021
    Review
  12. Review
  13. Article
  14. 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

10 authors at 2 institutions in 1 country.

Anna L WestermairDepartment of Psychiatry and Psychotherapy, University Medical Center Schleswig-Holstein-Campus Lübeck, 23562 Lübeck, Germany. anna.westermair@uksh.de.ORCID 0000-0002-3673-4589
Matthias MunzInstitute for Cardiogenetics, University of Lübeck, 23562 Lübeck, Germany. m.munz@uni-luebeck.de.ORCID 0000-0002-4728-3357
Anja SchaichDepartment of Psychiatry and Psychotherapy, University Medical Center Schleswig-Holstein-Campus Lübeck, 23562 Lübeck, Germany. anja.schaich@uksh.de.
Stefan NitscheInstitute for Cardiogenetics, University of Lübeck, 23562 Lübeck, Germany. stefan.nitsche.gloy@gmx.de.
Bastian WillenborgDepartment of Psychiatry and Psychotherapy, University Medical Center Schleswig-Holstein-Campus Lübeck, 23562 Lübeck, Germany. bastian.willenborg@me.com.
Loreto M Muñoz VenegasInstitute for Cardiogenetics, University of Lübeck, 23562 Lübeck, Germany. maria.munozvenegas@uni-luebeck.de.ORCID 0000-0003-2308-4158
Christina WillenborgInstitute for Cardiogenetics, University of Lübeck, 23562 Lübeck, Germany. christina.willenborg@web.de.
Heribert SchunkertGerman Heart Center Munich, Technical University Munich, 80636 Munich, Germany. siebe@dhm.mhn.de.
Ulrich SchweigerDepartment of Psychiatry and Psychotherapy, University Medical Center Schleswig-Holstein-Campus Lübeck, 23562 Lübeck, Germany. ulrich.schweiger@uksh.de.ORCID 0000-0001-9807-0979
Jeanette ErdmannInstitute for Cardiogenetics, University of Lübeck, 23562 Lübeck, Germany. jeanette.erdmann@uni-luebeck.de.
German Centre for Cardiovascular Research · DEHumboldt-Universität zu Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite its substantial clinical importance, specific genetic variants associated with depression have not yet been identified. We sought to identify genetic variants associated with depression by (a) focusing on a more homogenous subsample (vascular depression) and (b) applying a three-stage approach. First, we contacted 730 participants with a confirmed atherosclerotic disease (coronary artery disease) from a population-based study population (German Myocardial Infarction Family Study IV) for psychiatric assessment with the Mini International Neuropsychiatric Interview. Second, we genotyped these patients using genome-wide single nucleotide polymorphism (SNP) arrays. Third, we characterized the SNP via in-silico analysis. The final sample consisted of 342 patients (78.3% male, age = 63.2 ± 9.9 years), 22.8% with a severe depressive disorder. Variant rs528732638 on chromosome 18q11.2 was a genome-wide significant variant and was associated with 3.6-fold increase in the odds of lifetime depression. The locus belongs to a linkage disequilibrium block showing expression quantitative trait loci effects on three putative

Indexed as

Genetic Association StudiesAquaporin 4DepressionFemaleGenetic Predisposition to DiseaseGenotypeHumansLinkage DisequilibriumMaleMiddle AgedPolymorphism, Single NucleotideQuantitative Trait LociVascular DiseasesAQP4 protein, humanAquaporin 4AQP4aquaporinchromosome 18q11.2coronary artery diseasegenome-wide association studylate-onset depressionvascular depression

Identifiers

PMID30563176
PMCPMC6316852
OpenAlexW2903436002

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.