Obsessive-compulsive symptoms in psychotic disorders: longitudinal associations of symptom clusters on between- and within-subject levels
Obsessive-compulsive symptoms (OCS) are frequently reported in patients with schizophrenia and have been associated with subjective distress and higher impairment. Recent studies suggest fluctuation in co-occurring OCS and associations with the course of psychotic symptoms. Current evidence is limit...
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| Hauptverfasser: | , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
8 March 2018
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| In: |
European archives of psychiatry and clinical neuroscience
Year: 2018, Jahrgang: 269, Heft: 2, Pages: 245-255 |
| ISSN: | 1433-8491 |
| DOI: | 10.1007/s00406-018-0884-4 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1007/s00406-018-0884-4
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| Verfasserangaben: | Frederike Schirmbeck, Max Konijn, Vera Hoetjes, Mathias Zink, Lieuwe de Haan, For Genetic Risk and Outcome of Psychosis (GROUP) |
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| 245 | 1 | 0 | |a Obsessive-compulsive symptoms in psychotic disorders |b longitudinal associations of symptom clusters on between- and within-subject levels |c Frederike Schirmbeck, Max Konijn, Vera Hoetjes, Mathias Zink, Lieuwe de Haan, For Genetic Risk and Outcome of Psychosis (GROUP) |
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| 520 | |a Obsessive-compulsive symptoms (OCS) are frequently reported in patients with schizophrenia and have been associated with subjective distress and higher impairment. Recent studies suggest fluctuation in co-occurring OCS and associations with the course of psychotic symptoms. Current evidence is limited by few studies with long assessments intervals and a sole focus on between-subject comparisons. The aim of this study was to specifically investigate co-variation of symptom domains over time within individuals. Patients with a psychotic disorder (n = 56) and un-affected siblings (n = 49) completed monthly assessments of clinical and subclinical symptoms over 6 months. Mixed-model multilevel analyses examined the variability and relationship between OCS and positive, negative, and depressive symptoms on the between- and within-subject level. Symptom domains were associated across subjects and assessment times, in patients and siblings, with the strongest association between OCS and (subclinical) positive symptoms. Within-subjects, substantial variability and co-variation of all symptom domains was found. Particularly, between-subject differences in positive symptoms and within-subject change in depressive symptoms predicted subsequent OCS in patients 1 months later. This is the first prospective study disaggregating between and within-subject associations between co-occurring OCS and symptom cluster of psychosis. Differences on these two levels suggest different underlying mechanisms. The association between depressive symptoms and subsequent increase/decrease of OCS within patients may have important treatment implications. | ||
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