Evidence map›Paper›PMID 36200864›Full record

ArticleSchizophrenia bulletin2023

Neurocognitive Subgroups in Children at Familial High-risk of Schizophrenia or Bipolar disorder: Subgroup Membership Stability or Change From Age 7 to 11-The Danish High Risk and Resilience Study.

Christina Bruun Knudsen, Aja Neergaard Greve, Jens Richardt Møllegaard Jepsen, Rikke Lambek, Anna Krogh Andreassen, Lotte Veddum, Julie Marie Brandt, Maja Gregersen, Mette Falkenberg Krantz, Anne Søndergaard and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Schizophrenia bulletin, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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

19 authors at 4 institutions in 1 country.

Christina Bruun KnudsenPsychosis Research Unit, Aarhus University Hospital - Psychiatry, Aarhus, Denmark.
Aja Neergaard GrevePsychosis Research Unit, Aarhus University Hospital - Psychiatry, Aarhus, Denmark.ORCID 0000-0002-1369-6639
Jens Richardt Møllegaard JepsenThe Lundbeck Foundation Initiative for Integrative Psychiatric Research - iPSYCH, Aarhus, Denmark.
Rikke LambekDepartment of Psychology and Behavioral Sciences, Aarhus University, Aarhus, Denmark.
Anna Krogh AndreassenPsychosis Research Unit, Aarhus University Hospital - Psychiatry, Aarhus, Denmark.
Lotte VeddumPsychosis Research Unit, Aarhus University Hospital - Psychiatry, Aarhus, Denmark.
Julie Marie BrandtThe Lundbeck Foundation Initiative for Integrative Psychiatric Research - iPSYCH, Aarhus, Denmark.
Maja GregersenThe Lundbeck Foundation Initiative for Integrative Psychiatric Research - iPSYCH, Aarhus, Denmark.ORCID 0000-0002-6510-1449
Mette Falkenberg KrantzThe Lundbeck Foundation Initiative for Integrative Psychiatric Research - iPSYCH, Aarhus, Denmark.
Anne SøndergaardThe Lundbeck Foundation Initiative for Integrative Psychiatric Research - iPSYCH, Aarhus, Denmark.
Anders Helles CarlsenDepartment of Clinical Medicine, Faculty of Health and Medical Sciences, Aarhus University, Aarhus, Denmark.
Nanna Lawaetz SteffensenPsychosis Research Unit, Aarhus University Hospital - Psychiatry, Aarhus, Denmark.
Anette Faurskov BundgaardPsychosis Research Unit, Aarhus University Hospital - Psychiatry, Aarhus, Denmark.
Birgitte Klee BurtonChild and Adolescent Mental Health Center, Copenhagen University Hospital - Mental Health Services CPH, Copenhagen, Denmark.
Anne Amalie Elgaard ThorupThe Lundbeck Foundation Initiative for Integrative Psychiatric Research - iPSYCH, Aarhus, Denmark.
Merete NordentoftThe Lundbeck Foundation Initiative for Integrative Psychiatric Research - iPSYCH, Aarhus, Denmark.
Ole MorsPsychosis Research Unit, Aarhus University Hospital - Psychiatry, Aarhus, Denmark.
Vibeke Fuglsang BlikstedPsychosis Research Unit, Aarhus University Hospital - Psychiatry, Aarhus, Denmark.
Nicoline HemagerThe Lundbeck Foundation Initiative for Integrative Psychiatric Research - iPSYCH, Aarhus, Denmark.
Aarhus University · DKUniversity of Copenhagen · DKAarhus University Hospital · DKMental Health Services · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and hypothesisSubgroups with distinct levels of neurocognitive functioning exist in children of parents with schizophrenia or bipolar disorder. However, studies investigating the temporal stability of subgroup membership are currently lacking. We hypothesized that a minority of children at familial high-risk of schizophrenia (FHR-SZ) or bipolar disorder (FHR-BP) would transition to a different neurocognitive subgroup from age 7 to 11 and that most transitions would be to a more impaired subgroup. STUDY

designLatent profile analysis was used to identify subgroups at two assessments (age 7 and 11) based on the performance of 320 children at FHR-SZ or FHR-BP across eight neurocognitive functions. Temporal stability in subgroup membership was evaluated with latent profile transition analysis. Population-based controls (age 7, n = 199; age 11, n = 178) were included as a reference group. Children transitioning to a more impaired subgroup were compared with nontransitioning children on sex, FHR-status, global functioning, and psychopathology. STUDY

resultsAt both assessment points, we identified three subgroups based on neurocognitive performance: a moderately-severely impaired, a mildly impaired, and an above-average subgroup. A total of 12.8% of children transitioned to a different subgroup, of which the majority (85.2%) moved to a more impaired subgroup. Parental diagnosis of schizophrenia, but neither parental diagnosis of bipolar disorder, global functioning at age 7, psychopathology, nor sex significantly differentiated children transitioning to a more impaired subgroup from nontransitioning children.

conclusionsDuring pre-adolescence, neurocognitive developmental lag is associated with being at FHR-SZ. Close attention to these children's neurocognitive development is indicated.

Indexed as

Bipolar DisorderChild of Impaired ParentsSchizophreniaAdolescentChildDenmarkHumansNeuropsychological TestsParentscognitive developmentlatent profile transition analysispre-adolescencesevere mental disorders

Identifiers

PMID36200864
PMCPMC9810011
OpenAlexW4302304661

What OpenQuestion holds

Textmetadata
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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.