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A longitudinal approach to biological psychiatric research: The PsyCourse study
Author(s) -
Budde Monika,
AndersonSchmidt Heike,
Gade Katrin,
ReichErkelenz Daniela,
Adorjan Kristina,
Kalman Janos L.,
Senner Fanny,
Papiol Sergi,
Andlauer Till F. M.,
Comes Ashley L.,
Schulte Eva C.,
KlöhnSaghatolislam Farah,
Gryaznova Anna,
Hake Maria,
Bartholdi Kim,
Flatau Laura,
Reitt Markus,
Quast Silke,
Stegmaier Sophia,
Meyers Milena,
Emons Barbara,
Haußleiter Ida Sybille,
Juckel Georg,
Nieratschker Vanessa,
Dannlowski Udo,
Schaupp Sabrina K.,
Schmauß Max,
Zimmermann Jörg,
Reimer Jens,
Schulz Sybille,
Wiltfang Jens,
Reininghaus Eva,
Anghelescu IonGeorge,
Arolt Volker,
Baune Bernhard T.,
Konrad Carsten,
Thiel Andreas,
Fallgatter Andreas J.,
Figge Christian,
von Hagen Martin,
Koller Manfred,
Lang Fabian U.,
Wigand Moritz E.,
Becker Thomas,
Jäger Markus,
Dietrich Detlef E.,
Stierl Sebastian,
Scherk Harald,
Spitzer Carsten,
Folkerts Here,
Witt Stephanie H.,
Degenhardt Franziska,
Forstner Andreas J.,
Rietschel Marcella,
Nöthen Markus M.,
Falkai Peter,
Schulze Thomas G.,
Heilbronner Urs
Publication year - 2019
Publication title -
american journal of medical genetics part b: neuropsychiatric genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.393
H-Index - 126
eISSN - 1552-485X
pISSN - 1552-4841
DOI - 10.1002/ajmg.b.32639
Subject(s) - psychopathology , schizophrenia (object oriented programming) , bipolar disorder , categorical variable , psychology , clinical psychology , research diagnostic criteria , research domain criteria , major depressive disorder , longitudinal study , psychosis , psychiatry , medicine , mood , pathology , machine learning , computer science
In current diagnostic systems, schizophrenia and bipolar disorder are still conceptualized as distinct categorical entities. Recently, both clinical and genomic evidence have challenged this Kraepelinian dichotomy. There are only few longitudinal studies addressing potential overlaps between these conditions. Here, we present design and first results of the PsyCourse study ( N  = 891 individuals at baseline), an ongoing transdiagnostic study of the affective‐to‐psychotic continuum that combines longitudinal deep phenotyping and dimensional assessment of psychopathology with an extensive collection of biomaterial. To provide an initial characterization of the PsyCourse study sample, we compare two broad diagnostic groups defined by the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM‐IV) classification system, that is, predominantly affective ( n  = 367 individuals) versus predominantly psychotic disorders ( n  = 524 individuals). Depressive, manic, and psychotic symptoms as well as global functioning over time were contrasted using linear mixed models. Furthermore, we explored the effects of polygenic risk scores for schizophrenia on diagnostic group membership and addressed their effects on nonparticipation in follow‐up visits. While phenotypic results confirmed expected differences in current psychotic symptoms and global functioning, both manic and depressive symptoms did not vary between both groups after correction for multiple testing. Polygenic risk scores for schizophrenia significantly explained part of the variability of diagnostic group. The PsyCourse study presents a unique resource to research the complex relationships of psychopathology and biology in severe mental disorders not confined to traditional diagnostic boundaries and is open for collaborations.

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