TY - JOUR
T1 - Genetic vulnerability to schizophrenia is associated with cannabis use patterns during adolescence
AU - Hiemstra, Marieke
AU - Nelemans, Stefanie A.
AU - Branje, Susan
AU - van Eijk, Kristel R.
AU - Hottenga, Jouke Jan
AU - Vinkers, Christiaan H.
AU - van Lier, Pol
AU - Meeus, Wim
AU - Boks, Marco P.
PY - 2018/9/1
Y1 - 2018/9/1
N2 - Background: Previously reported comorbidity between schizophrenia and substance use may be explained by shared underlying risk factors, such as genetic background. The aim of the present longitudinal study was to investigate how a genetic predisposition to schizophrenia was associated with patterns of substance use (cannabis use, smoking, alcohol use) during adolescence (comparing ages 13–16 with 16–20 years). Method: Using piecewise latent growth curve modelling in a longitudinal adolescent cohort (RADAR-Y study, N = 372), we analyzed the association of polygenic risk scores for schizophrenia (PRS; p-value thresholds (pt) < 5e-8 to pt < 0.5) with increase in substance use over the years, including stratified analyses for gender. Significance thresholds were set to adjust for multiple testing using Bonferroni at p ≤ 0.001. Results: High schizophrenia vulnerability was associated with a stronger increase in cannabis use at age 16–20 (PRS thresholds pt < 5e-5 and pt < 5e-4; pt < 5e-6 was marginally significant), whereas more lenient PRS thresholds (PRS thresholds pt < 5e-3 to pt < 0.5) showed the reverse association. For smoking and alcohol, no clear relations were found. Conclusions: In conclusion, our findings support a relation between genetic risk to schizophrenia and prospective cannabis use patterns during adolescence. In contrast, no relation between alcohol and smoking was established.
AB - Background: Previously reported comorbidity between schizophrenia and substance use may be explained by shared underlying risk factors, such as genetic background. The aim of the present longitudinal study was to investigate how a genetic predisposition to schizophrenia was associated with patterns of substance use (cannabis use, smoking, alcohol use) during adolescence (comparing ages 13–16 with 16–20 years). Method: Using piecewise latent growth curve modelling in a longitudinal adolescent cohort (RADAR-Y study, N = 372), we analyzed the association of polygenic risk scores for schizophrenia (PRS; p-value thresholds (pt) < 5e-8 to pt < 0.5) with increase in substance use over the years, including stratified analyses for gender. Significance thresholds were set to adjust for multiple testing using Bonferroni at p ≤ 0.001. Results: High schizophrenia vulnerability was associated with a stronger increase in cannabis use at age 16–20 (PRS thresholds pt < 5e-5 and pt < 5e-4; pt < 5e-6 was marginally significant), whereas more lenient PRS thresholds (PRS thresholds pt < 5e-3 to pt < 0.5) showed the reverse association. For smoking and alcohol, no clear relations were found. Conclusions: In conclusion, our findings support a relation between genetic risk to schizophrenia and prospective cannabis use patterns during adolescence. In contrast, no relation between alcohol and smoking was established.
KW - Adolescence
KW - Alcohol use
KW - Cannabis use
KW - Genetic
KW - Polygenic risk score
KW - Schizophrenia
KW - Smoking
KW - Substance use
UR - http://www.scopus.com/inward/record.url?scp=85050124067&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85050124067&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.drugalcdep.2018.05.024
DO - https://doi.org/10.1016/j.drugalcdep.2018.05.024
M3 - Article
C2 - 30031300
SN - 0376-8716
VL - 190
SP - 143
EP - 150
JO - Drug and alcohol dependence
JF - Drug and alcohol dependence
ER -