Impaired motor development in children with familial high risk of schizophrenia or bipolar disorder and the association with psychotic experiences: a 4-year Danish observational follow-up study

Motor abnormalities have clinical relevance as a component of psychotic illness; they are not only a proxy of altered neurodevelopment, but also intimately related to psychotic risk. We aimed to assess motor development and its association with psychotic experiences in children with familial high ri...

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Veröffentlicht in:The Lancet. Psychiatry 2023-02, Vol.10 (2), p.108-118
Hauptverfasser: Burton, Birgitte Klee, Krantz, Mette Falkenberg, Skovgaard, Lene Theil, Brandt, Julie Marie, Gregersen, Maja, Søndergaard, Anne, Knudsen, Christina Bruun, Andreassen, Anna Krogh, Veddum, Lotte, Rohd, Sinnika Birkehøj, Wilms, Martin, Tjott, Camilla, Hjorthøj, Carsten, Ohland, Jessica, Greve, Aja, Hemager, Nicoline, Bliksted, Vibeke Fuglsang, Mors, Ole, Plessen, Kerstin Jessica, Thorup, Anne Amalie Elgaard, Nordentoft, Merete
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Sprache:eng
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Zusammenfassung:Motor abnormalities have clinical relevance as a component of psychotic illness; they are not only a proxy of altered neurodevelopment, but also intimately related to psychotic risk. We aimed to assess motor development and its association with psychotic experiences in children with familial high risk (FHR) of schizophrenia or bipolar disorder compared with controls. The Danish High Risk and Resilience Study is a prospective longitudinal cohort study, for which participants were extracted from Danish registers. Children born in Denmark between Sept 1, 2004, and Aug 31, 2009, with no, one, or two parents born in Denmark with schizophrenia or bipolar disorder, could be included in the study. No ethnicity data were collected. Children with no biological parent diagnosed with schizophrenia spectrum disorder or bipolar disorder were matched to children with FHR of schizophrenia (one or two parents with schizophrenia spectrum disorder) on the basis of sex, age, and municipality. Children with FHR of bipolar disorder (one or two parents with bipolar disorder) were included as a non-matched group. We assessed motor function in children with FHR of schizophrenia, children with FHR of bipolar disorder, and children in the control group at approximately age 8 years (baseline; 2013–16) and age 12 years (follow-up; 2017–20) using the Movement Assessment Battery for Children—Second Edition (Movement ABC-2). Psychotic experiences were assessed using the psychosis section of the Kiddie Schedule for Affective Disorders and Schizophrenia for School-Age Children—Present and Lifetime Version. Raters were masked regarding familial risk status. Motor development from baseline to follow-up in the different groups was assessed using a linear mixed model. Logistic regression examined the relationship between definite motor problems (≤5th percentile on Movement ABC-2) and psychotic experiences. Between March 1, 2017, and June 30, 2020, we studied 437 children (234 [54%] boys, 203 [46%] girls; mean age 11·99 years [SD 0·26, range 11·08–12·86]). Children with FHR of schizophrenia showed stable motor developmental deficits in manual dexterity (difference in intercept –1·62 [95% CI –2·39 to –0·85], p
ISSN:2215-0366
2215-0374
DOI:10.1016/S2215-0366(22)00402-3