Evidence map›Paper›PMID 20633049›Full record

ArticleGenes, brain, and behavior2010

Anxiety and depression in children and adults: influence of serotonergic and neurotrophic genes?

C M Middeldorp, M C T Slof-Op 't Landt, S E Medland, C E M van Beijsterveldt, M Bartels, G Willemsen, J-J Hottenga, E J C de Geus, H E D Suchiman, C V Dolan and 3 more

Abstract readTwin Study
In one paragraph

Article in Genes, brain, and behavior, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

20 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. The Influence of HLA Alleles on the Affective Distress Profile.International journal of environmental research and public health · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Brain-derived neurotrophic factor serum levels and genotype: association with depression during interferon-α treatment.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2013
    Article
  12. Neurobiology of anxious depression: a review.Depression and anxiety · 2013
    Review
  13. Catechol-O-methyltransferase gene val158met polymorphism and depressive symptoms during early childhood.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2013
    Article
  14. Excessive daytime sleepiness in sleep disorders.Journal of thoracic disease · 2012
    Article
  15. Bringing a developmental perspective to anxiety genetics.Development and psychopathology · 2012
    Review
  16. Fluoxetine pharmacogenetics in child and adult populations.European child & adolescent psychiatry · 2012
    Review
  17. Article
  18. A functional Tph2 C1473G polymorphism causes an anxiety phenotype via compensatory changes in the serotonergic system.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2012
    Article
  19. Article
  20. 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

13 authors.

C M MiddeldorpDepartment of Biological Psychology, VU University Amsterdam, Amsterdam, The Netherlands. cm.middeldorp@psy.vu.nl
M C T Slof-Op 't Landt
S E Medland
C E M van Beijsterveldt
M Bartels
G Willemsen
J-J Hottenga
E J C de Geus
H E D Suchiman
C V Dolan
M C Neale
P E Slagboom
D I Boomsma

Funding

Psychometric and Genetic Assessments of Substance UseR37DA018673 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI NEALE, MICHAEL CHURTON · 2005 to 2014
$3.7M
Psychometric and Genetic Assessments of Substance UseR01DA018673 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI NEALE, MICHAEL CHURTON · 2004 to 2019
$2.3M
GENE MAPPING FOR QUANTITATIVE TRAITSR01HL055976 · NHLBI · PENNSYLVANIA STATE UNIVERSITY-UNIV PARK · PI VOGLER, GEORGE P · 1995 to 1998
–
NHLBI NIH HHS R01 HL055976NHLBI NIH HHS R01 HL55976NIDA NIH HHS DA-18673NIDA NIH HHS R01 DA018673NIDA NIH HHS R37 DA018673
6 · The paper itself

Abstract

There are two major hypotheses regarding the etiology of anxiety and depression: the mono-amine hypothesis and the hypothesis of an abnormal stress response acting partly via reduced neurogenesis. Association studies have focused on genes involved in these processes, but with inconclusive results. This study investigated the effect of 45 single nucleotide polymorphisms (SNPs) in genes encoding for serotonin receptors 1A, 1D, 2A, catechol-O-methyltransferase (COMT), tryptophane hydroxylase type 2 (TPH2), brain derived neurotrophic factor (BDNF), PlexinA2 and regulators of G-protein-coupled signaling (RGS) 2, 4, 16. Anxious depression (A/D) symptoms were assessed five times in 11 years in over 11 000 adults with 1504 subjects genotyped and at age 7, 10, 12 and during adolescence in over 20 000 twins with 1078 subjects genotyped. In both cohorts, a longitudinal model with one latent factor loading on all A/D measures over time was analysed. The genetic association effect modeled at the level of this latent factor was 60% and 70% heritable in the children and adults, respectively, and explained around 50% of the total phenotypic variance. Power analyses showed that the samples contained 80% power to detect an effect explaining between 1.4% and 3.6% of the variance. However, no SNP showed a consistent effect on A/D. To conclude, this longitudinal study in children and adults found no association of SNPs in the serotonergic system or core regulators of neurogenesis with A/D. Overall, there has been no convincing evidence, so far, for a role of genetic variation in these pathways in the development of anxiety and depression.

Indexed as

AdolescentAdultAgedAnxietyChildDepressive DisorderDNAFactor Analysis, StatisticalFemaleGenome-Wide Association StudyGenotypeHumansLongitudinal StudiesMaleMiddle AgedModels, GeneticDNANerve Growth FactorsSerotonin

Identifiers

PMID20633049
PMCPMC3151552

What OpenQuestion holds

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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.