TY - JOUR
T1 - Genetic Susceptibility to the Environment Moderates the Impact of Childhood Experiences on Psychotic, Depressive, and Anxiety Dimensions
AU - Barrantes-Vidal, Neus
AU - Torrecilla, Pilar
AU - Mas-Bermejo, Patricia
AU - Papiol, Sergi
AU - Bakermans-Kranenburg, Marian J.
AU - van IJzendoorn, Marinus H.
AU - Jolicoeur-Martineau, Alexia
AU - Kwapil, Thomas R.
AU - Rosa, Araceli
N1 - The authors want to express their gratitude to Dr Tamara Sheinbaum for her substantial contribution to the BLISS project. This work was supported by Ministerio de Ciencia e Innovaci\u00F3n (PSI2017-91814-EXP and PID2020-119211RB-I00) and Generalitat de Catalunya (2021SGR01010). The genotyping service was carried out at Centro Nacional de Genotipado (CEGEN-PRB3-ISCIII) supported by grant PT17/0019 of the Plan Estatal I+D+i 2013\u20132016, funded by Instituto de Salud Carlos III (ISCIII) and European Regional Development Fund (ERDF). N.B.V. is supported by the ICREA Academia Award of the Generalitat de Catalunya. P.T. was funded by Ministerio de Ciencia e Innovaci\u00F3n (PRE2018-085299). P.M.B. was funded by Institut de Biomedicina de la Universitat de Barcelona (IBUB) and the PhD scholarship program FI-SDUR (2021-FISDU-00032) from Agencia de Gesti\u00F3n de Ayudas Universitarias y de Investigaci\u00F3n.
This work was supported by Ministerio de Ciencia e Innovaci\u00F3n (PSI2017-91814-EXP and PID2020-119211RB-I00) and Generalitat de Catalunya (2021SGR01010). The genotyping service was carried out at Centro Nacional de Genotipado (CEGEN-PRB3-ISCIII) supported by grant PT17/0019 of the Plan Estatal I+D+i 2013\u20132016, funded by Instituto de Salud Carlos III (ISCIII) and European Regional Development Fund (ERDF). N.B.V. is supported by the ICREA Academia Award of the Generalitat de Catalunya. P.T. was funded by Ministerio de Ciencia e Innovaci\u00F3n (PRE2018-085299). P.M.B. was funded by Institut de Biomedicina de la Universitat de Barcelona (IBUB) and the PhD scholarship program FI-SDUR (2021-FISDU-00032) from Agencia de Gesti\u00F3n de Ayudas Universitarias y de Investigaci\u00F3n.
PY - 2025/3/1
Y1 - 2025/3/1
N2 - Background and Hypothesis: Gene-by-environment (GxE) studies in psychosis have exclusively focused on negative exposures. However, evidence supports the resilience-enhancing effect of positive factors on psychosis outcome. The Differential Susceptibility (DS) model proposes that common genetic variants may confer not only disproportionate responsiveness to negative environments, but also greater sensitivity to positive, resilience-enhancing conditions. This study is the first to apply the DS model to the expression of subclinical psychosis, employing polygenic risk scores of environmental sensitivity (PRS-ES). PRS-ES were hypothesized to moderate, in a DS manner, associations between childhood adversity and psychosis, affective, and anxiety dimensions in young adults. An exploratory goal examined whether PRS for psychotic-like experiences (PRS-PLE) also showed DS patterns. Study Design: PRS, schizotypy, PLE, depression, anxiety, and childhood adversity ratings were obtained for 197 nonclinical young adults. LEGIT software for testing competitive-confirmatory GxE models was employed. Study Results: Results largely supported DS: Individuals high on PRS-ES showed increased subclinical psychosis, depression, and anxiety if they had experienced elevated childhood adversity, and lower symptoms if exposed to low levels of adversity as compared with those with low PRS-ES. Similarly, PRS-PLE moderated the effect of adversity on PLE, positive schizotypy, and depression following the DS model, but only PRS-ES moderation on PLE survived statistical correction. Conclusions: Our results suggest that genetic DS to the environment is relevant to psychosis, depression, and anxiety. Current debates on reconceptualization of genetic “risk” and resilience may benefit from this insight that support optimistic views on preventative efforts for early detection and intervention.
AB - Background and Hypothesis: Gene-by-environment (GxE) studies in psychosis have exclusively focused on negative exposures. However, evidence supports the resilience-enhancing effect of positive factors on psychosis outcome. The Differential Susceptibility (DS) model proposes that common genetic variants may confer not only disproportionate responsiveness to negative environments, but also greater sensitivity to positive, resilience-enhancing conditions. This study is the first to apply the DS model to the expression of subclinical psychosis, employing polygenic risk scores of environmental sensitivity (PRS-ES). PRS-ES were hypothesized to moderate, in a DS manner, associations between childhood adversity and psychosis, affective, and anxiety dimensions in young adults. An exploratory goal examined whether PRS for psychotic-like experiences (PRS-PLE) also showed DS patterns. Study Design: PRS, schizotypy, PLE, depression, anxiety, and childhood adversity ratings were obtained for 197 nonclinical young adults. LEGIT software for testing competitive-confirmatory GxE models was employed. Study Results: Results largely supported DS: Individuals high on PRS-ES showed increased subclinical psychosis, depression, and anxiety if they had experienced elevated childhood adversity, and lower symptoms if exposed to low levels of adversity as compared with those with low PRS-ES. Similarly, PRS-PLE moderated the effect of adversity on PLE, positive schizotypy, and depression following the DS model, but only PRS-ES moderation on PLE survived statistical correction. Conclusions: Our results suggest that genetic DS to the environment is relevant to psychosis, depression, and anxiety. Current debates on reconceptualization of genetic “risk” and resilience may benefit from this insight that support optimistic views on preventative efforts for early detection and intervention.
KW - childhood adversity
KW - gene–environment interaction
KW - psychosis
KW - resilience
KW - risk factors
KW - schizotypy
UR - http://www.scopus.com/inward/record.url?scp=86000597400&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=86000597400&partnerID=8YFLogxK
U2 - 10.1093/schbul/sbad130
DO - 10.1093/schbul/sbad130
M3 - Article
C2 - 40037819
AN - SCOPUS:86000597400
SN - 0586-7614
VL - 51
SP - S95-S106
JO - Schizophrenia Bulletin
JF - Schizophrenia Bulletin
ER -