Evidence map›Paper›PMID 30852114›Full record

ArticleSchizophrenia research2019

Association between developmental milestones and age of schizophrenia onset: Results from the Northern Finland Birth Cohort 1966.

Jan Stochl, Anjalene Whittier, Adam P Wagner, Juha Veijola, Erika Jääskeläinen, Jouko Miettunen, Golam M Khandaker, Peter B Jones

Open access · hybridAbstract read
In one paragraph

Article in Schizophrenia research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 8 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

8 authors at 4 institutions in 3 countries.

Jan StochlDepartment of Psychiatry, University of Cambridge, Cambridge, UK; National Institute for Health Research Collaboration for Leadership in Applied Health Research and Care East of England, Cambridge, UK; Department of Kinanthropology, Charles University, Prague, Czech Republic. Electronic address: js883@cam.ac.uk.
Anjalene WhittierDepartment of Psychiatry, University of Cambridge, Cambridge, UK. Electronic address: abw25@cam.ac.uk.
Adam P WagnerNational Institute for Health Research Collaboration for Leadership in Applied Health Research and Care East of England, Cambridge, UK; Norwich Medical School, University of East Anglia, Norwich, UK. Electronic address: adam.wagner@uea.ac.uk.
Juha VeijolaCenter for Life Course Health Research, University of Oulu, Oulu, Finland; Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland; Department of Psychiatry, Oulu University Hospital, Oulu, Finland; Department of Psychiatry, Research Unit of Clinical Neuroscience, University of Oulu, Oulu, Finland. Electronic address: juha.veijola@oulu.fi.
Erika JääskeläinenCenter for Life Course Health Research, University of Oulu, Oulu, Finland; Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland; Department of Psychiatry, Oulu University Hospital, Oulu, Finland. Electronic address: erika.jaaskelainen@oulu.fi.
Jouko MiettunenCenter for Life Course Health Research, University of Oulu, Oulu, Finland; Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland. Electronic address: jouko.miettunen@oulu.fi.
Golam M KhandakerDepartment of Psychiatry, University of Cambridge, Cambridge, UK; Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, UK. Electronic address: gmk24@medschl.cam.ac.uk.
Peter B JonesDepartment of Psychiatry, University of Cambridge, Cambridge, UK; National Institute for Health Research Collaboration for Leadership in Applied Health Research and Care East of England, Cambridge, UK; Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, UK. Electronic address: pbj21@cam.ac.uk.
Oulu University Hospital · FIUniversity of Cambridge · GBCharles University · CZUniversity of East Anglia · GB

Funding

Medical Research Council MC_PC_17213Wellcome Trust 201486/Z/16/Z
6 · The paper itself

Abstract

We investigated relationships between early developmental milestones, schizophrenia incidence and variability in its age at onset. We hypothesized that the period of risk for schizophrenia would be longer for those with later development. The Northern Finland Birth Cohort 1966 was followed until 47 years of age, and those members diagnosed with schizophrenia or any other non-affective psychoses identified. Latent profile analysis was used to classify people into homogenous classes with respect to developmental milestones, and subsequently survival analysis explored relationship between classes and age of schizophrenia onset. Results suggest that 4-classes (early, regular, late, and extra late developers) can be identified, but due to few cases in one class (n = 93, <0.01% of 10,501), only 3 classes (early, regular, late) could be meaningfully compared. Schizophrenia incidence until 47 years of age differed systematically between classes: late developers had the highest cumulative incidence (2.39%); regular were intermediate (1.25%); and early developers had the lowest incidence (0.99%). However, age at onset and its variability was similar across classes, suggesting that our hypothesis of a wider 'window' for schizophrenia onset in late developers was not supported.

Indexed as

Age of OnsetCohort StudiesDevelopmental DisabilitiesFemaleFinlandHumansIncidenceMaleMiddle AgedSchizophreniaAge at onsetDevelopmental milestonesNon-affective psychosesSchizophrenia

Identifiers

PMID30852114
PMCPMC6551363
OpenAlexW2921983975

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.