TY - JOUR
T1 - The effect of polygenic risk score and childhood adversity on transdiagnostic symptom dimensions at first-episode psychosis
T2 - evidence for an affective pathway to psychosis
AU - Alameda, Luis
AU - Rodriguez, Victoria
AU - Di Forti, Marta
AU - Spinazzola, Edoardo
AU - Trotta, Giulia
AU - Arango, Celso
AU - Arrojo, Manuel
AU - Bernardo, Miguel
AU - Bobes, Julio
AU - de Haan, Lieuwe
AU - Del-Ben, Cristina Marta
AU - Gayer-Anderson, Charlotte
AU - Sideli, Lucia
AU - Jones, Peter B
AU - Kirkbride, James B
AU - La Cascia, Caterina
AU - Tripoli, Giada
AU - Ferraro, Laura
AU - La Barbera, Daniele
AU - Lasalvia, Antonio
AU - Tosato, Sarah
AU - Llorca, Pierre-Michel
AU - Menezes, Paulo Rossi
AU - van Os, Jim
AU - Rutten, Bart P
AU - Santos, Jose Luis
AU - Sanjuán, Julio
AU - Selten, Jean-Paul
AU - Szöke, Andrei
AU - Tarricone, Ilaria
AU - Tortelli, Andrea
AU - Velthorst, Eva
AU - Jongsma, Hannah E
AU - Vassos, Evangelos
AU - Quattrone, Diego
AU - Murray, Robin M
AU - Aas, Monica
PY - 2024/12
Y1 - 2024/12
N2 - Childhood adversity is associated with various clinical dimensions in psychosis; however, how genetic vulnerability shapes the adversity-associated psychopathological signature is yet to be studied. We studied data of 583 First Episode Psychosis (FEP) cases from the EU-GEI FEP case-control study, including Polygenic risk scores for major depressive disorder (MDD-PRS), bipolar disorder (BD-PRS) and schizophrenia (SZ-PRS); childhood adversity measured with the total score of the Childhood Trauma Questionnaire (CTQ); and positive, negative, depressive and manic psychopathological domains from a factor model of transdiagnostic dimensions. Genes and environment interactions were explored as a departure from a multiplicative effect of PRSs and total CTQ on each dimension. Analyses were adjusted for age, sex, 10 PCA, site of recruitment and for medication. A childhood adversity and PRS multiplicative interaction was observed between A) the CTQ and MDD-PRS on the predominance of positive (β = 0.42, 95% CI = [0.155, 0.682], p = 0.004); and depressive (β = 0.33, 95% CI = [0.071, 0.591], p = 0.013) dimensions; B) between the CTQ and BD-PRS on the positive dimension (β = 0.45, 95% CI = [0.106, 0.798], p = 0.010), and C) with the CTQ and SZ-PRS on the positive dimension (β = −0.34, 95% CI = [−0.660, −0.015], p = 0.040). Bonferroni corrected p-value of significance was set at 0.0125. In conclusion, despite being underpowered, this study suggests that genetic liability for MDD and BD may have a moderating effect on the sensibility of childhood adversity on depressive and positive psychotic dimensions. This supports the hypothesis of an affective pathway to psychosis in those exposed to childhood adversity.
AB - Childhood adversity is associated with various clinical dimensions in psychosis; however, how genetic vulnerability shapes the adversity-associated psychopathological signature is yet to be studied. We studied data of 583 First Episode Psychosis (FEP) cases from the EU-GEI FEP case-control study, including Polygenic risk scores for major depressive disorder (MDD-PRS), bipolar disorder (BD-PRS) and schizophrenia (SZ-PRS); childhood adversity measured with the total score of the Childhood Trauma Questionnaire (CTQ); and positive, negative, depressive and manic psychopathological domains from a factor model of transdiagnostic dimensions. Genes and environment interactions were explored as a departure from a multiplicative effect of PRSs and total CTQ on each dimension. Analyses were adjusted for age, sex, 10 PCA, site of recruitment and for medication. A childhood adversity and PRS multiplicative interaction was observed between A) the CTQ and MDD-PRS on the predominance of positive (β = 0.42, 95% CI = [0.155, 0.682], p = 0.004); and depressive (β = 0.33, 95% CI = [0.071, 0.591], p = 0.013) dimensions; B) between the CTQ and BD-PRS on the positive dimension (β = 0.45, 95% CI = [0.106, 0.798], p = 0.010), and C) with the CTQ and SZ-PRS on the positive dimension (β = −0.34, 95% CI = [−0.660, −0.015], p = 0.040). Bonferroni corrected p-value of significance was set at 0.0125. In conclusion, despite being underpowered, this study suggests that genetic liability for MDD and BD may have a moderating effect on the sensibility of childhood adversity on depressive and positive psychotic dimensions. This supports the hypothesis of an affective pathway to psychosis in those exposed to childhood adversity.
KW - Humans
KW - Female
KW - Male
KW - Multifactorial Inheritance
KW - Psychotic Disorders/genetics psychology
KW - Adverse Childhood Experiences/psychology
KW - Adult
KW - Bipolar Disorder/genetics psychology
KW - Depressive Disorder, Major/genetics
KW - Case-Control Studies
KW - Schizophrenia/genetics
KW - Genetic Predisposition to Disease
KW - Young Adult
KW - Gene-Environment Interaction
KW - Adolescent
KW - Risk Factors
KW - Middle Aged
KW - Genetic Risk Score
U2 - 10.1038/s41398-024-03149-7
DO - 10.1038/s41398-024-03149-7
M3 - Article
SN - 2158-3188
VL - 14
JO - Translational Psychiatry
JF - Translational Psychiatry
IS - 1
M1 - 454
ER -