TY - JOUR
T1 - Polygenic risk, familial liability and stress reactivity in psychosis
T2 - an experience sampling study
AU - Schick, Anita
AU - van Winkel, Ruud
AU - Lin, Bochao D.
AU - Luykx, Jurjen J.
AU - de Zwarte, Sonja M.C.
AU - van Eijk, Kristel R.
AU - Reininghaus, Ulrich
AU - Myin-Germeys, Inez
AU - Reininghaus, Ulrich
N1 - Funding Information:
Ulrich Reininghaus was supported by a Heisenberg professorship (no. 389624707) funded by the German Research Foundation (DFG). Inez Myin-Germeys was supported by an FWO Odysseus grant (G0F8416N). Ruud van Winkel is supported by Research Foundation Flanders (FWO) (grant number G063518N, Senior Clinical Fellowship 1803616N) and the King Baudoin Foundation (Chair of Transition Psychiatry). The infrastructure for the GROUP study was funded by the Geestkracht programme of the Dutch Health Research Council (ZON-MW, 10-000-1002) and funds from participating universities and mental health care organizations (Amsterdam: Academic Psychiatric Centre of the Academic Medical Center and the mental health institutions: GGZ Ingeest; Arkin, Dijk en Duin; GGZ Rivierduinen; Erasmus Medical Centre and GGZ Noord Holland Noord. Groningen: University Medical Center Groningen and the mental health institutions: Lentis, GGZ Friesland; GGZ Drenthe; Dimence; Mediant; GGNet Warnsveld; Yulius Dordrecht and Parnassia psycho-medical center The Hague. Maastricht: Maastricht University Medical Centre and the mental health institutions: GGZ Eindhoven en De Kempen; GGZ Breburg; GGZ Oost-Brabant; Vincent van Gogh voor Geestelijke Gezondheid; Mondriaan; Virenze riagg; Zuyderland GGZ; MET ggz; Universitair Centrum Sint-Jozef Kortenberg; CAPRI University of Antwerp; PC Ziekeren Sint-Truiden; PZ Sancta Maria Sint-Truiden; GGZ Overpelt and OPZ Rekem. Utrecht: University Medical Center Utrecht and the mental health institutions: Altrecht; GGZ Centraal and Delta).
Publisher Copyright:
Copyright © The Author(s), 2022. Published by Cambridge University Press
PY - 2023/5/7
Y1 - 2023/5/7
N2 - Background There is evidence for a polygenic contribution to psychosis. One targetable mechanism through which polygenic variation may impact on individuals and interact with the social environment is stress sensitization, characterized by elevated reactivity to minor stressors in daily life. The current study aimed to investigate whether stress reactivity is modified by polygenic risk score for schizophrenia (PRS) in cases with enduring non-affective psychotic disorder, first-degree relatives of cases, and controls. Methods We used the experience sampling method to assess minor stressors, negative affect, positive affect and psychotic experiences in 96 cases, 79 first-degree relatives, i.e. siblings, and 73 controls at wave 3 of the Dutch Genetic Risk and Outcome of Psychosis (GROUP) study. Genome-wide data were collected at baseline to calculate PRS. Results We found that associations of momentary stress with psychotic experiences, but not with negative and positive affect, were modified by PRS and group (all pFWE<0.001). In contrast to our hypotheses, siblings with high PRS reported less intense psychotic experiences in response to momentary stress compared to siblings with low PRS. No differences in magnitude of these associations were observed in cases with high v. low level of PRS. By contrast, controls with high PRS showed more intense psychotic experiences in response to stress compared to those with low PRS. Conclusions This tentatively suggests that polygenic risk may operate in different ways than previously assumed and amplify reactivity to stress in unaffected individuals but operate as a resilience factor in relatives by attenuating their stress reactivity.
AB - Background There is evidence for a polygenic contribution to psychosis. One targetable mechanism through which polygenic variation may impact on individuals and interact with the social environment is stress sensitization, characterized by elevated reactivity to minor stressors in daily life. The current study aimed to investigate whether stress reactivity is modified by polygenic risk score for schizophrenia (PRS) in cases with enduring non-affective psychotic disorder, first-degree relatives of cases, and controls. Methods We used the experience sampling method to assess minor stressors, negative affect, positive affect and psychotic experiences in 96 cases, 79 first-degree relatives, i.e. siblings, and 73 controls at wave 3 of the Dutch Genetic Risk and Outcome of Psychosis (GROUP) study. Genome-wide data were collected at baseline to calculate PRS. Results We found that associations of momentary stress with psychotic experiences, but not with negative and positive affect, were modified by PRS and group (all pFWE<0.001). In contrast to our hypotheses, siblings with high PRS reported less intense psychotic experiences in response to momentary stress compared to siblings with low PRS. No differences in magnitude of these associations were observed in cases with high v. low level of PRS. By contrast, controls with high PRS showed more intense psychotic experiences in response to stress compared to those with low PRS. Conclusions This tentatively suggests that polygenic risk may operate in different ways than previously assumed and amplify reactivity to stress in unaffected individuals but operate as a resilience factor in relatives by attenuating their stress reactivity.
KW - Digital phenotyping
KW - ecological momentary assessment
KW - gene–environment interaction
KW - polygenic risk
KW - stress sensitivity
KW - gene-environment interaction
UR - http://www.scopus.com/inward/record.url?scp=85122611709&partnerID=8YFLogxK
U2 - 10.1017/S0033291721004761
DO - 10.1017/S0033291721004761
M3 - Article
C2 - 34991751
AN - SCOPUS:85122611709
SN - 0033-2917
VL - 53
SP - 2798
EP - 2807
JO - Psychological medicine
JF - Psychological medicine
IS - 7
ER -