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. Author manuscript; available in PMC: 2022 Mar 2.
Published in final edited form as: Prog Neuropsychopharmacol Biol Psychiatry. 2020 Sep 6;106:110096. doi: 10.1016/j.pnpbp.2020.110096

Table 1.

Peripheral blood endocannabinoids in psychotic disorders.

Condition & treatment n (cases/controls) Type AEA PEA OEA 2-AG Reference
Untreated
First-episode psychosis 47/84 serum n.s. - - - Giuffrida et al., 2004
First-episode psychosis 28/81 serum n.s. - - - Reuter et al., 2017
Schizophrenia 115/88 serum - - Wang et al., 2018
Schizophrenia 12/20 whole blood - - - De Marchi et al., 2003
Treated
Schizophrenia 115/88 serum n.s. - - Wang et al., 2018
Schizophrenia 25/16 plasma n.s. n.s. Koethe et al., 2019
Schizophrenia 12/20 whole blood n.s. - - - De Marchi et al., 2003
Schizophrenia 25/27 plasma n.s. - n.s. - Desfossés et al., 2012
Schizophrenia with substance use disorder 29/17 plasma n.s. Potvin et al., 2008
Psychosis Risk
Unaffected twin of Schizophrenia 25/16 plasma n.s. n.s. Koethe et al., 2019
Clinical high risk 33/58 plasma n.s. n.s. Appiah-Kusi et al., 2019
Psychosis risk 27/81 serum n.s. - n.s. - Koethe et al., 2009

↑: higher; ↓: lower; n.s.: no significant difference from healthy controls; -: no available data;

AEA: anandamide; PEA: N-palmitoylethanolamide; OEA: N-olcoylethanolamide; 2-AG: 2-arachidonoyglycerol.