Evidence map›Paper›PMID 31119307›Full record

ArticleSocial psychiatry and psychiatric epidemiology2020

Adult mood problems in children with neurodevelopmental problems: evidence from a prospective birth cohort followed to age 50.

Alishia Addicoat, Ajay K Thapar, Lucy Riglin, Anita Thapar, Stephan Collishaw

Open access · hybridAbstract read
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In one paragraph

Article in Social psychiatry and psychiatric epidemiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Alishia AddicoatDivision of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Child and Adolescent Psychiatry, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, Wales, UK.
Ajay K ThaparDivision of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Child and Adolescent Psychiatry, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, Wales, UK.
Lucy RiglinDivision of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Child and Adolescent Psychiatry, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, Wales, UK.
Anita ThaparDivision of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Child and Adolescent Psychiatry, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, Wales, UK.
Stephan CollishawDivision of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Child and Adolescent Psychiatry, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, Wales, UK. collishaws@cardiff.ac.uk.ORCID http://orcid.org/0000-0002-4296-820X
Cardiff University · GB

Funding

Medical Research Council MR/L010305/1Wellcome Trust 204895/Z/16/Z
6 · The paper itself

Abstract

purposeSpecific child neurodevelopmental (ND) disorders such as ADHD and learning problems are associated with concurrent and future (up to early adulthood) mood problems. However, it is unclear whether findings generalise to population traits as well as diagnoses, to general as well as specific neurodevelopmental domains, and whether risk associations extend to later adulthood or diminish with age.

methodsWe used data from a UK cohort of children born in 1958, the National Child Development Study (NCDS). ND problems were assessed at ages 7 and 11 years with parent- and teacher ratings of restlessness, hyperactivity and motor co-ordination difficulties, and by individual tests of reading, arithmetic and general cognitive ability. Mood (depression/anxiety) problems were assessed using the Malaise symptom screen at 23, 33, 42, and 50 years. Factor analyses were conducted to assess whether the specific neurodevelopmental domains could be aggregated into a general "ND" latent factor as well as specific factors. Associations with mood outcomes were then tested.

resultsA bi-factor model with a general "ND" latent factor and specific "motor" and "cognition" factors fits the data well. The specific cognition and motor factor scores were associated with mood problems in early adulthood only. The "ND" factor demonstrated associations with mood problems at each adult follow-up (men - age 23 years: β = 0.17; age 33: β = 0.16; age 42: β = 0.14; age 50: β = 0.16; women - 23 years: β = 0.25; 33 years: β = 0.26; 42 years: β = 0.14; 50 years: β = 0.16; all ps < 0.01). Interactions by sex indicated that the association between this general factor and mood problems was more pronounced for women than men at ages 23 years (β = 0.09, p = 0.005) and 33 years (β = 0.10, p = 0.003), but not at 42 or 50 years (ps > 0.8).

conclusionsOur results suggest that, in a population-based cohort, a general, childhood neurodevelopmental difficulty factor is stably associated with mood problems in adult life.

Indexed as

AffectAnxietyDepressionAdultChildChild, PreschoolCognitionCohort StudiesFemaleHumansMaleMiddle AgedProspective StudiesYoung AdultAdult depressionBi-factorChildhoodLongitudinalNeurodevelopmental

Identifiers

PMID31119307
OpenAlexW2945257216

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.