Association between age of cannabis initiation and gray matter covariance networks in recent onset psychosis
Penzel Nora; Antonucci Linda A; Betz Linda T; Sanfelici Rachele; Weiske Johanna; Pogarell Oliver; Cumming Paul; Quednow Boris B; Howes Oliver; Falkai Peter; Upthegrove Rachel; Bertolino Alessandro; Borgwardt Stefan; Brambilla Paolo; Lencer Rebekka; Meisenzahl Eva; Rosen Marlene; Haidl Theresa; Kambeitz-Ilankovic Lana; Ruhrmann Stephan; Salokangas Raimo RK; Pantelis Christos; Wood Stephen J; Koutsouleris Nikolaos; Kambeitz Joseph; PRONIA
Association between age of cannabis initiation and gray matter covariance networks in recent onset psychosis
Penzel Nora
Antonucci Linda A
Betz Linda T
Sanfelici Rachele
Weiske Johanna
Pogarell Oliver
Cumming Paul
Quednow Boris B
Howes Oliver
Falkai Peter
Upthegrove Rachel
Bertolino Alessandro
Borgwardt Stefan
Brambilla Paolo
Lencer Rebekka
Meisenzahl Eva
Rosen Marlene
Haidl Theresa
Kambeitz-Ilankovic Lana
Ruhrmann Stephan
Salokangas Raimo RK
Pantelis Christos
Wood Stephen J
Koutsouleris Nikolaos
Kambeitz Joseph
PRONIA
SPRINGERNATURE
Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2021042826999
https://urn.fi/URN:NBN:fi-fe2021042826999
Tiivistelmä
Cannabis use during adolescence is associated with an increased risk of developing psychosis. According to a current hypothesis, this results from detrimental effects of early cannabis use on brain maturation during this vulnerable period. However, studies investigating the interaction between early cannabis use and brain structural alterations hitherto reported inconclusive findings. We investigated effects of age of cannabis initiation on psychosis using data from the multicentric Personalized Prognostic Tools for Early Psychosis Management (PRONIA) and the Cannabis Induced Psychosis (CIP) studies, yielding a total sample of 102 clinically-relevant cannabis users with recent onset psychosis. GM covariance underlies shared maturational processes. Therefore, we performed source-based morphometry analysis with spatial constraints on structural brain networks showing significant alterations in schizophrenia in a previous multisite study, thus testing associations of these networks with the age of cannabis initiation and with confounding factors. Earlier cannabis initiation was associated with more severe positive symptoms in our cohort. Greater gray matter volume (GMV) in the previously identified cerebellar schizophrenia-related network had a significant association with early cannabis use, independent of several possibly confounding factors. Moreover, GMV in the cerebellar network was associated with lower volume in another network previously associated with schizophrenia, comprising the insula, superior temporal, and inferior frontal gyrus. These findings are in line with previous investigations in healthy cannabis users, and suggest that early initiation of cannabis perturbs the developmental trajectory of certain structural brain networks in a manner imparting risk for psychosis later in life.
Kokoelmat
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