Understanding Lifelong Factors and Prediction Models of Social Functioning After Psychosis Onset Using the Large-Scale GROUP Cohort Study

Uložené v:
Podrobná bibliografia
Názov: Understanding Lifelong Factors and Prediction Models of Social Functioning After Psychosis Onset Using the Large-Scale GROUP Cohort Study
Autori: Natalia Tiles-Sar, Tesfa Dejenie Habtewold, Edith J Liemburg, Lisette van der Meer, Richard Bruggeman, Behrooz Z Alizadeh, Therese van Amelsvoort, Agna A Bartels-Velthuis, Lieuwe de Haan, Frederike Schirmbeck, Claudia J P Simons, Jim van Os
Prispievatelia: Hart- en Vaatziekten Team A, Genetica, Hersenen-Medisch 1, Brain
Zdroj: Schizophr Bull
Informácie o vydavateľovi: Oxford University Press (OUP), 2023.
Rok vydania: 2023
Predmety: Outcome Assessment, association, mixed-effect model/trajectories, Social Interaction, 3. Good health, schizophrenia, Health Care, Cohort Studies, Psychiatry and Mental health, Psychotic Disorders, Outcome Assessment, Health Care, follow-up, Psychotic Disorders/complications, Humans, Social Adjustment, Regular Articles
Popis: Background and hypothesisCurrent rates of poor social functioning (SF) in people with psychosis history reach 80% worldwide. We aimed to identify a core set of lifelong predictors and build prediction models of SF after psychosis onset.Study designWe utilized data of 1119 patients from the Genetic Risk and Outcome in Psychosis (GROUP) longitudinal Dutch cohort. First, we applied group-based trajectory modeling to identify premorbid adjustment trajectories. We further investigated the association between the premorbid adjustment trajectories, six-year-long cognitive deficits, positive, and negative symptoms trajectories, and SF at 3-year and 6-year follow-ups. Next, we checked associations between demographics, clinical, and environmental factors measured at the baseline and SF at follow-up. Finally, we built and internally validated 2 predictive models of SF.Study resultsWe found all trajectories were significantly associated with SF (P < .01), explaining up to 16% of SF variation (R2 0.15 for 3- and 0.16 for 6-year follow-up). Demographics (sex, ethnicity, age, education), clinical parameters (genetic predisposition, illness duration, psychotic episodes, cannabis use), and environment (childhood trauma, number of moves, marriage, employment, urbanicity, unmet needs of social support) were also significantly associated with SF. After validation, final prediction models explained a variance up to 27% (95% CI: 0.23, 0.30) at 3-year and 26% (95% CI: 0.22, 0.31) at 6-year follow-up.ConclusionsWe found a core set of lifelong predictors of SF. Yet, the performance of our prediction models was moderate.
Druh dokumentu: Article
Other literature type
Popis súboru: application/pdf
Jazyk: English
ISSN: 1745-1701
0586-7614
DOI: 10.1093/schbul/sbad046
Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/37104875
https://research.rug.nl/en/publications/3d0bccd0-11be-4842-9900-3c707b64b759
https://doi.org/10.1093/schbul/sbad046
https://hdl.handle.net/11370/3d0bccd0-11be-4842-9900-3c707b64b759
https://cris.maastrichtuniversity.nl/en/publications/00560b34-a5f4-4516-bc65-f1585110feeb
https://doi.org/10.1093/schbul/sbad046
https://dspace.library.uu.nl/handle/1874/451165
https://pure.amsterdamumc.nl/en/publications/85c52243-7c0f-4611-bc60-f4eb34a288ac
https://doi.org/10.1093/schbul/sbad046
Rights: CC BY
URL: http://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Prístupové číslo: edsair.doi.dedup.....b51d0cdce5749464d5a3746b9cce11b6
Databáza: OpenAIRE
Popis
Abstrakt:Background and hypothesisCurrent rates of poor social functioning (SF) in people with psychosis history reach 80% worldwide. We aimed to identify a core set of lifelong predictors and build prediction models of SF after psychosis onset.Study designWe utilized data of 1119 patients from the Genetic Risk and Outcome in Psychosis (GROUP) longitudinal Dutch cohort. First, we applied group-based trajectory modeling to identify premorbid adjustment trajectories. We further investigated the association between the premorbid adjustment trajectories, six-year-long cognitive deficits, positive, and negative symptoms trajectories, and SF at 3-year and 6-year follow-ups. Next, we checked associations between demographics, clinical, and environmental factors measured at the baseline and SF at follow-up. Finally, we built and internally validated 2 predictive models of SF.Study resultsWe found all trajectories were significantly associated with SF (P < .01), explaining up to 16% of SF variation (R2 0.15 for 3- and 0.16 for 6-year follow-up). Demographics (sex, ethnicity, age, education), clinical parameters (genetic predisposition, illness duration, psychotic episodes, cannabis use), and environment (childhood trauma, number of moves, marriage, employment, urbanicity, unmet needs of social support) were also significantly associated with SF. After validation, final prediction models explained a variance up to 27% (95% CI: 0.23, 0.30) at 3-year and 26% (95% CI: 0.22, 0.31) at 6-year follow-up.ConclusionsWe found a core set of lifelong predictors of SF. Yet, the performance of our prediction models was moderate.
ISSN:17451701
05867614
DOI:10.1093/schbul/sbad046