Endocannabinoid system alterations in Alzheimer’s disease: A systematic review of human studies

•Endocannabinoid system functioning is altered in Alzheimer’s disease.•Expression and activity of CB2R, MAGL and FAAH may be increased in Alzheimer’s disease.•Very few studies included patients with mild cognitive impairment (MCI)•TRPV1 expression appears unaltered in Alzheimer’s disease.•Few studies have investigated correlations between neuropsychiatric symptomatology and endocannabinoid alterations. Studies investigating alterations of the endocannabinoid system (ECS) in Alzheimer’s disease (AD) in humans have reported inconsistent findings so far. We performed a systematic review of studies examining alterations of the ECS specifically within humans with AD or mild cognitive impairment (MCI), including neuroimaging studies, studies of serum and cerebrospinal fluid biomarkers, and post-mortem studies. We attempted to identify reported changes in the expression and activity of: cannabinoid receptors 1 and 2; anandamide (AEA); 2-arachidonoylglycerol (2-AG); monoacylglycerol lipase (MAGL); fatty acid amide hydrolase (FAAH); and transient receptor potential cation channel V1 (TRPV1). Twenty-two studies were identified for inclusion. Mixed findings were reported for most aspects of the ECS in AD, making it difficult to identify a particular profile of ECS alterations characterising AD. The included studies tended to be small, methodologically heterogeneous, and frequently did not control for important potential confounders, such as pathological progression of AD. Eight studies correlated ECS alterations with neuropsychometric performance measures, though studies infrequently examined behavioural and neuropsychiatric correlates. PROSPERO database identifier: CRD42018096249.