Evidence map›Paper›PMID 25325458›Full record

ArticleSleep2015

The heritability of insomnia progression during childhood/adolescence: results from a longitudinal twin study.

Nicola L Barclay, Philip R Gehrman, Alice M Gregory, Lindon J Eaves, Judy L Silberg

Open access · bronzeAbstract readTwin Study
In one paragraph

Article in Sleep, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 3 pooled it
3.3field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 3 syntheses or guidelines pooled it, 53 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Article
  7. Child Eveningness as a Predictor of Parental Sleep.Children (Basel, Switzerland) · 2022
    Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. The Different Faces of Insomnia.Frontiers in psychiatry · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Mean Blood Pressure Difference among Adolescents Based on Dyssomnia Types.Open access Macedonian journal of medical sciences · 2018
    Article
  20. Genetic Pathways to Insomnia.Brain sciences · 2016
    Review
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

5 authors at 4 institutions in 2 countries.

Nicola L BarclayNorthumbria Centre for Sleep Research, Department of Psychology, Northumbria University, UK.
Philip R GehrmanDepartment of Psychiatry and Penn Sleep Centre, University of Pennsylvania, Philadelphia, PA.
Alice M GregoryDepartment of Psychology, Goldsmiths, University of London, UK.
Lindon J EavesVirginia Institute for Psychiatric and Behavioral Genetics, Richmond, VA.
Judy L SilbergVirginia Commonwealth University School of Medicine, Richmond, VA.
Goldsmiths University of London · GBNorthumbria University · GBPenn Center for AIDS Research · USVirginia Commonwealth University · US

Funding

Center for Clinical and Translational ResearchUL1TR000058 · NCATS · VIRGINIA COMMONWEALTH UNIVERSITY · PI MOELLER, FREDERICK GERARD · 2012 to 2015
$12.5M
NCATS NIH HHS UL1TR000058
6 · The paper itself

Abstract

STUDY

objectivesTo determine prevalence and heritability of insomnia during middle/late childhood and adolescence; examine longitudinal associations in insomnia over time; and assess the extent to which genetic and environmental factors on insomnia remain stable, or whether new factors come into play, across this developmental period.

designLongitudinal twin study.

settingAcademic medical center. PATIENTS OR

participantsThere were 739 complete monozygotic twin pairs (52%) and 672 complete dizygotic twin pairs (48%) initially enrolled and were followed up at three additional time points (waves). Mode ages at each wave were 8, 10, 14, and 15 y (ages ranged from 8-18 y).

interventionsNone. MEASUREMENTS AND

resultsClinical ratings of insomnia symptoms were assessed using the Child and Adolescent Psychiatric Assessment (CAPA) by trained clinicians, and rated according to Diagnostic and Statistical Manual of Mental Disorders (DSM)-III-R criteria for presence of 'clinically significant insomnia', over four sequential waves. Insomnia symptoms were prevalent but significantly decreased across the four waves (ranging from 16.6% to 31.2%). 'Clinically significant insomnia' was moderately heritable at all waves (h² range = 14% to 38%), and the remaining source of variance was the nonshared environment. Multivariate models indicated that genetic influences at wave 1 contributed to insomnia at all subsequent waves, and that new genetic influences came into play at wave 2, which further contributed to stability of symptoms. Nonshared environmental influences were time-specific.

conclusionInsomnia is prevalent in childhood and adolescence, and is moderately heritable. The progression of insomnia across this developmental time period is influenced by stable as well as new genetic factors that come into play at wave 2 (modal age 10 y). Molecular genetic studies should now identify genes related to insomnia progression during childhood and adolescence.

Indexed as

Disease ProgressionAdolescentAgingChildDiagnostic and Statistical Manual of Mental DisordersEnvironmentFemaleHumansLongitudinal StudiesMaleModels, GeneticPhenotypePrevalenceSleep Initiation and Maintenance DisordersTime FactorsTwins, Dizygoticgeneticsinsomniasleeptwins

Identifiers

PMID25325458
PMCPMC4262942
OpenAlexW1980430415

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.