Questioning the role of palmitoylethanolamide in psychosis: a systematic review of clinical and preclinical evidence

Riccardo Bortoletto, Fabiana Piscitelli, Anna Candolo, Sagnik Bhattacharyya, Matteo Balestrieri, Marco Colizzi, Riccardo Bortoletto, Fabiana Piscitelli, Anna Candolo, Sagnik Bhattacharyya, Matteo Balestrieri, Marco Colizzi

Abstract

Introduction: The endocannabinoid (eCB) system disruption has been suggested to underpin the development of psychosis, fueling the search for novel, better-tolerated antipsychotic agents that target the eCB system. Among these, palmitoylethanolamide (PEA), an N-acylethanolamine (AE) with neuroprotective, anti-inflammatory, and analgesic properties, has drawn attention for its antipsychotic potential.

Methods: This Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020-compliant systematic review aimed at reappraising all clinical and preclinical studies investigating the biobehavioral role of PEA in psychosis.

Results: Overall, 13 studies were eligible for data extraction (11 human, 2 animal). Observational studies investigating PEA tone in psychosis patients converged on the evidence for increased PEA plasma (6 human) and central nervous system (CNS; 1 human) levels, as a potential early compensatory response to illness and its severity, that seems to be lost in the longer-term (CNS; 1 human), opening to the possibility of exogenously supplementing it to sustain control of the disorder. Consistently, PEA oral supplementation reduced negative psychotic and manic symptoms among psychosis patients, with no serious adverse events (3 human). No PEA changes emerged in either preclinical psychosis model (2 animal) studied.

Discussion: Evidence supports PEA signaling as a potential psychosis biomarker, also indicating a therapeutic role of its supplementation in the disorder.

Systematic review registration: https://doi.org/10.17605/OSF.IO/AFMTK.

Keywords: Schizophrenia; antipsychotics; bipolar disorder; cannabidiol; major depressive disorder; nutraceuticals.

Conflict of interest statement

MC has been a consultant/advisor to GW Pharma Limited, F. Hoffmann-La Roche Limited, and GW Pharma Italy SRL, outside of this work. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Copyright © 2023 Bortoletto, Piscitelli, Candolo, Bhattacharyya, Balestrieri and Colizzi.

Figures

Figure 1
Figure 1
PRISMA flowchart of search strategy for systematic review.

References

    1. Kraepelin E. Die Erscheinungsformen des Irreseins: (The manifestations of insanity). Hist Psychiatry. (1992) 3:509–29. 10.1177/0957154X9200301208
    1. Potash JB, Bienvenu OJ. Neuropsychiatric disorders: Shared genetics of bipolar disorder and schizophrenia. Nat Rev Neurol. (2009) 5:299–300. 10.1038/nrneurol.2009.71
    1. Craddock N, O'Donovan MC, Owen MJ. Psychosis genetics: modeling the relationship between schizophrenia, bipolar disorder, and mixed (or “schizoaffective”) psychoses. Schizophr Bull. (2009) 35:482–90. 10.1093/schbul/sbp020
    1. Craddock N, Owen MJ. The Kraepelinian dichotomy - going, going but still not gone. Br J Psychiatry. (2010) 196:92–5. 10.1192/bjp.bp.109.073429
    1. Ivleva EI, Morris DW, Moates AF, Suppes T, Thaker GK, Tamminga CA. Genetics and intermediate phenotypes of the schizophrenia–bipolar disorder boundary. Neurosci Biobehav Rev. (2010) 34:897–921. 10.1016/j.neubiorev.2009.11.022
    1. Fusar-Poli L, Aguglia A, Albert U. Editorial: Early identification of affective and non-affective psychoses: from psychopathology to biomarkers. Front Psychiatry. (2023) 14:1144943. 10.3389/fpsyt.2023.1144943
    1. Perala J, Suvisaari J, Saarni SI, Kuoppasalmi K, Isometsa E, Pirkola S, et al. . Lifetime prevalence of psychotic and bipolar I disorders in a general population. Arch Gen Psychiatry. (2007) 64:19–28. 10.1001/archpsyc.64.1.19
    1. Whiteford HA, Degenhardt L, Rehm J, Baxter AJ, Ferrari AJ, Erskine HE, et al. . Global burden of disease attributable to mental and substance use disorders: findings from the Global Burden of Disease Study 2010. Lancet. (2013) 382:1575–86. 10.1016/S0140-6736(13)61611-6
    1. Vargas TG, Mittal VA. The critical roles of early development, stress, and environment in the course of psychosis. Annu Rev Dev Psychol. (2022) 4:423–45. 10.1146/annurev-devpsych-121020-032354
    1. Howes OD, Kambeitz J, Kim E, Stahl D, Slifstein M, Abi-Dargham A, et al. . The nature of dopamine dysfunction in schizophrenia and what this means for treatment. Arch Gen Psychiatry. (2012) 69:776–86. 10.1001/archgenpsychiatry.2012.169
    1. Howes OD, Murray RM. Schizophrenia: an integrated sociodevelopmental-cognitive model. Lancet. (2014) 383:1677–87. 10.1016/S0140-6736(13)62036-X
    1. Howes O, McCutcheon R, Stone J. Glutamate and dopamine in schizophrenia: an update for the 21st century. J Psychopharmacol. (2015) 29:97–115. 10.1177/0269881114563634
    1. Howes OD, McCutcheon R, Owen MJ, Murray RM. The role of genes, stress, and dopamine in the development of schizophrenia. Biol Psychiatry. (2017) 81:9–20. 10.1016/j.biopsych.2016.07.014
    1. Andrews G, Sanderson K, Corry J, Issakidis C, Lapsley H. Cost-effectiveness of current and optimal treatment for schizophrenia. Br J Psychiatry. (2003) 183:427–35. 10.1192/bjp.183.5.427
    1. Obradovic M, Mrhar A, Kos M. Cost-effectiveness of antipsychotics for outpatients with chronic schizophrenia. Int J Clin Pract. (2007) 61:1979–88. 10.1111/j.1742-1241.2007.01431.x
    1. Giuffrida A, Leweke FM, Gerth CW, Schreiber D, Koethe D, Faulhaber J, et al. . Cerebrospinal anandamide levels are elevated in acute schizophrenia and are inversely correlated with psychotic symptoms. Neuropsychopharmacology. (2004) 29:2108–14. 10.1038/sj.npp.1300558
    1. Koethe D, Hoyer C, Leweke FM. The endocannabinoid system as a target for modelling psychosis. Psychopharmacology. (2009) 206:551–61. 10.1007/s00213-009-1591-7
    1. Appiah-Kusi E, Leyden E, Parmar S, Mondelli V, McGuire P, Bhattacharyya S. Abnormalities in neuroendocrine stress response in psychosis: the role of endocannabinoids. Psychol Med. (2016) 46:27–45. 10.1017/S0033291715001786
    1. Colizzi M, McGuire P, Pertwee RG, Bhattacharyya S. Effect of cannabis on glutamate signalling in the brain: a systematic review of human and animal evidence. Neurosci Biobehav Rev. (2016) 64:359–81. 10.1016/j.neubiorev.2016.03.010
    1. Schubart CD, Sommer IE, Fusar-Poli P, de Witte L, Kahn RS, Boks MP. Cannabidiol as a potential treatment for psychosis. Eur Neuropsychopharmacol. (2014) 24:51–64. 10.1016/j.euroneuro.2013.11.002
    1. McGuire P, Robson P, Cubala WJ, Vasile D, Morrison PD, Barron R, et al. . Cannabidiol (CBD) as an adjunctive therapy in schizophrenia: a multicenter randomized controlled trial. Am J Psychiatry. (2018) 175:225–31. 10.1176/appi.ajp.2017.17030325
    1. Bhattacharyya S, Wilson R, Appiah-Kusi E, O'Neill A, Brammer M, Perez J, et al. . Effect of cannabidiol on medial temporal, midbrain, and striatal dysfunction in people at clinical high risk of psychosis: a randomized clinical trial. JAMA Psychiatry. (2018) 75:1107–17. 10.1001/jamapsychiatry.2018.2309
    1. Appiah-Kusi E, Petros N, Wilson R, Colizzi M, Bossong MG, Valmaggia L, et al. . Effects of short-term cannabidiol treatment on response to social stress in subjects at clinical high risk of developing psychosis. Psychopharmacology (Berl). (2020) 237:1121–30. 10.1007/s00213-019-05442-6
    1. Kelly JR, Minuto C, Cryan JF, Clarke G, Dinan TG. The role of the gut microbiome in the development of schizophrenia. Schizophr Res. (2021) 234:4–23. 10.1016/j.schres.2020.02.010
    1. Minichino A, Jackson MA, Francesconi M, Steves CJ, Menni C, Burnet PWJ, et al. . Endocannabinoid system mediates the association between gut-microbial diversity and anhedonia/amotivation in a general population cohort. Mol Psychiatry. (2021) 26:6269–76. 10.1038/s41380-021-01147-5
    1. Khandaker GM, Cousins L, Deakin J, Lennox BR, Yolken R, Jones PB. Inflammation and immunity in schizophrenia: implications for pathophysiology and treatment. Lancet Psychiatry. (2015) 2:258–70. 10.1016/S2215-0366(14)00122-9
    1. Fraguas D, Diaz-Caneja CM, Ayora M, Hernandez-Alvarez F, Rodriguez-Quiroga A, Recio S, et al. . Oxidative stress and inflammation in first-episode psychosis: a systematic review and meta-analysis. Schizophr Bull. (2019) 45:742–51. 10.1093/schbul/sby125
    1. Petrosino S, Di Marzo V. The pharmacology of palmitoylethanolamide and first data on the therapeutic efficacy of some of its new formulations. Br J Pharmacol. (2017) 174:1349–65. 10.1111/bph.13580
    1. Petrosino S, Schiano Moriello A. Palmitoylethanolamide: a nutritional approach to keep neuroinflammation within physiological boundaries: a systematic review. Int J Mol Sci. (2020) 21:526. 10.3390/ijms21249526
    1. Skaper SD, Facci L. Mast cell-glia axis in neuroinflammation and therapeutic potential of the anandamide congener palmitoylethanolamide. Philos Trans R Soc Lond B Biol Sci. (2012) 367:3312–25. 10.1098/rstb.2011.0391
    1. Skaper SD, Facci L, Giusti P. Glia and mast cells as targets for palmitoylethanolamide, an anti-inflammatory and neuroprotective lipid mediator. Mol Neurobiol. (2013) 48:340–52. 10.1007/s12035-013-8487-6
    1. Petrosino S, Schiano Moriello A, Verde R, Allara M, Imperatore R, Ligresti A, et al. . Palmitoylethanolamide counteracts substance P-induced mast cell activation in vitro by stimulating diacylglycerol lipase activity. J Neuroinflammation. (2019) 16:274. 10.1186/s12974-019-1671-5
    1. Clayton P, Hill M, Bogoda N, Subah S, Venkatesh R. Palmitoylethanolamide: A Natural Compound for Health Management. Int J Mol Sci. (2021) 22:305. 10.3390/ijms22105305
    1. De Petrocellis L, Davis JB, Di Marzo V. Palmitoylethanolamide enhances anandamide stimulation of human vanilloid VR1 receptors. FEBS Lett. (2001) 506:253–6. 10.1016/S0014-5793(01)02934-9
    1. Petrosino S, Schiano Moriello A, Cerrato S, Fusco M, Puigdemont A, De Petrocellis L, et al. . The anti-inflammatory mediator palmitoylethanolamide enhances the levels of 2-arachidonoyl-glycerol and potentiates its actions at TRPV1 cation channels. Br J Pharmacol. (2016) 173:1154–62. 10.1111/bph.13084
    1. Couch DG, Cook H, Ortori C, Barrett D, Lund JN, O'Sullivan SE. Palmitoylethanolamide and cannabidiol prevent inflammation-induced hyperpermeability of the human gut in vitro and in vivo: a randomized, placebo-controlled, double-blind controlled trial. Inflamm Bowel Dis. (2019) 25:1006–18. 10.1093/ibd/izz017
    1. Clayton P, Subah S, Venkatesh R, Hill M, Bogoda N. Palmitoylethanolamide: a potential alternative to cannabidiol. J Diet Suppl. (2021) 5:1–26. 10.1080/19390211.2021.2005733
    1. Colizzi M, Bortoletto R, Costa R, Zoccante L. Palmitoylethanolamide and its biobehavioral correlates in autism spectrum disorder: a systematic review of human and animal evidence. Nutrients. (2021) 13:1346. 10.3390/nu13041346
    1. Bortoletto R, Balestrieri M, Bhattacharyya S, Colizzi M. Is it time to test the antiseizure potential of palmitoylethanolamide in human studies? A systematic review of preclinical evidence. Brain Sci. (2022) 12:101. 10.3390/brainsci12010101
    1. Colizzi M, Bortoletto R, Colli C, Bonomo E, Pagliaro D, Maso E, et al. . Therapeutic effect of palmitoylethanolamide in cognitive decline: a systematic review and preliminary meta-analysis of preclinical and clinical evidence. Front Psychiatry. (2022) 13:8122. 10.3389/fpsyt.2022.1038122
    1. Parums DV. Editorial: review articles, systematic reviews, meta-analysis, and the updated preferred reporting items for systematic reviews and meta-analyses (PRISMA) 2020 guidelines. Med Sci Monit. (2021) 27:e934475. 10.12659/MSM.934475
    1. West S, King V, Carey TS, Lohr KN, McKoy N, Sutton SF, et al. . Systems to rate the strength of scientific evidence. Evid Rep Technol Assess. (2002) 47:1–11.
    1. Leweke FM, Giuffrida A, Wurster U, Emrich HM, Piomelli D. Elevated endogenous cannabinoids in schizophrenia. Neuroreport. (1999) 10:1665–9. 10.1097/00001756-199906030-00008
    1. Leweke FM, Piomelli D, Pahlisch F, Muhl D, Gerth CW, Hoyer C, et al. . Cannabidiol enhances anandamide signaling and alleviates psychotic symptoms of schizophrenia. Transl Psychiatry. (2012) 2:e94. 10.1038/tp.2012.15
    1. Muguruza C, Lehtonen M, Aaltonen N, Morentin B, Meana JJ, Callado LF. Quantification of endocannabinoids in postmortem brain of schizophrenic subjects. Schizophr Res. (2013) 148:145–50. 10.1016/j.schres.2013.06.013
    1. Koethe D, Pahlisch F, Hellmich M, Rohleder C, Mueller JK, Meyer-Lindenberg A, et al. . Familial abnormalities of endocannabinoid signaling in schizophrenia. World J Biol Psychiatry. (2019) 20:117–25. 10.1080/15622975.2018.1449966
    1. Appiah-Kusi E, Wilson R, Colizzi M, Foglia E, Klamerus E, Caldwell A, et al. . Childhood trauma and being at-risk for psychosis are associated with higher peripheral endocannabinoids. Psychol Med. (2020) 50:1862–71. 10.1017/S0033291719001946
    1. Ibarra-Lecue I, Unzueta-Larrinaga P, Barrena-Barbadillo R, Villate A, Horrillo I, Mendivil B, et al. . Cannabis use selectively modulates circulating biomarkers in the blood of schizophrenia patients. Addict Biol. (2022) 27:3233. 10.1111/adb.13233
    1. Parksepp M, Haring L, Kilk K, Koch K, Uppin K, Kangro R, et al. . The expanded endocannabinoid system contributes to metabolic and body mass shifts in first-episode schizophrenia: a 5-year follow-up study. Biomedicines. (2022) 10:243. 10.3390/biomedicines10020243
    1. Topuz RD, Gorgulu Y, Uluturk MK. Could serum endocannabinoid and N-acylethanolamine levels be important in bipolar disorder? World J Biol Psychiatry. (2022) 24:314–20. 10.1080/15622975.2022.2111713
    1. Brotini S, Schievano C, Guidi L. Ultra-micronized Palmitoylethanolamide: an efficacious adjuvant therapy for Parkinson's disease. CNS Neurol Disord Drug Targets. (2017) 16:705–13. 10.2174/1871527316666170321124949
    1. Salehi A, Namaei P, TaghaviZanjani F, Bagheri S, Moradi K, Khodaei Ardakani MR, et al. . Adjuvant palmitoylethanolamide therapy with risperidone improves negative symptoms in patients with schizophrenia: a randomized, double-blinded, placebo-controlled trial. Psychiatry Res. (2022) 316:114737. 10.1016/j.psychres.2022.114737
    1. Abedini T, Hosseyni R, Ghannadi F, Moghaddam HS, Ardakani MK, Talaei A, et al. . Efficacy and safety of palmitoylethanolamide as an adjunctive treatment for acute mania: a randomized, double-blind, placebo-controlled trial. Psychiatry Clin Neurosci. (2022) 76:505–11. 10.1111/pcn.13441
    1. Stark T, Ruda-Kucerova J, Iannotti FA, D'Addario C, Di Marco R, Pekarik V, et al. . Peripubertal cannabidiol treatment rescues behavioral and neurochemical abnormalities in the MAM model of schizophrenia. Neuropharmacology. (2019) 146:212–21. 10.1016/j.neuropharm.2018.11.035
    1. Di Bartolomeo M, Stark T, Maurel OM, Iannotti FA, Kuchar M, Ruda-Kucerova J, et al. . Crosstalk between the transcriptional regulation of dopamine D2 and cannabinoid CB1 receptors in schizophrenia: analyses in patients and in perinatal Δ9-tetrahydrocannabinol-exposed rats. Pharmacol Res. (2021) 164:105357. 10.1016/j.phrs.2020.105357
    1. Bonaccorso S, Ricciardi A, Zangani C, Chiappini S, Schifano F. Cannabidiol (CBD) use in psychiatric disorders: a systematic review. Neurotoxicology. (2019) 74:282–98. 10.1016/j.neuro.2019.08.002
    1. Ghabrash MF, Coronado-Montoya S, Aoun J, Gagne AA, Mansour F, Ouellet-Plamondon C, et al. . Cannabidiol for the treatment of psychosis among patients with schizophrenia and other primary psychotic disorders: a systematic review with a risk of bias assessment. Psychiatry Res. (2020) 286:112890. 10.1016/j.psychres.2020.112890
    1. Wang Z, Cao Y, Zhu Y, Li K, Jiang X, Zhuo C, et al. . Differences in demographic and clinical characteristics of patients with depressive vs. manic first episode of bipolar disorder. Front Psychiatry. (2021) 12:616415. 10.3389/fpsyt.2021.616415
    1. Perugi G, Micheli C, Akiskal HS, Madaro D, Socci C, Quilici C, et al. . Polarity of the first episode, clinical characteristics, and course of manic depressive illness: a systematic retrospective investigation of 320 bipolar I patients. Compr Psychiatry. (2000) 41:13–8. 10.1016/S0010-440X(00)90125-1

Source: PubMed

3
S'abonner