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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 3.

Cerebrospinal fluid endocannabinoids in psychotic disorders.

Condition & treatment n (cases/controls) AEA PEA OEA Greater symptom severity Reference
Untreated
 First-episode psychosis 47/84 n.s. ↓ AEA Giuffrida et al., 2004
 First-episode psychosis 28/81 - - - Reuter et al., 2017
 First-episode psychosis 47/81 Leweke et al., 2007
(cannabis >20 times) 19/26 n.s. ↓ AEA
(cannabis <5 times) 25/55 - - ↓ AEA
Mixed (treated & untreated)
 First-episode psychosis 10/11 n.s. - Leweke et al., 1999
Treated
 Schizophrenia (atypical AP) 35/84 n.s. - - Giuffrida et al., 2004
 Schizophrenia (typical AP) 37/84 n.s. n.s. - - Giuffrida et al., 2004
Psychosis risk
  Psychosis risk 27/81 - n.s. ↓ AEA Koethe et al., 2009

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

AP: antipsychotics; AEA: anandamide; PEA: N-palmitoylethanolamide; OEA: N-olcoylethanolamide.