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Dementia-related psychosis and the potential role for pimavanserin

Published online by Cambridge University Press:  19 August 2020

Jeffery L. Cummings ,
D. P. Devanand  and
Stephen M. Stahl
Jeffery L. Cummings*
Affiliation:
Chambers-Grundy Center for Transformative Neuroscience, Department of Brain Health, School of Integrated Health Sciences, University of Nevada at Las Vegas (UNLV) and Cleveland Clinic, Lou Ruvo Center for Brain Health, Las Vegas, Nevada, USA
D. P. Devanand
Affiliation:
Department of Psychiatry, Columbia University Medical Center, New York, New York, USA
Stephen M. Stahl
Affiliation:
Department of Psychiatry, University of California, San Diego, La Jolla, California, USA
*
*Author for correspondence: Jeffery L. Cummings, Email: [email protected]
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Abstract

Dementia-related psychosis (DRP) is prevalent across dementias and typically manifests as delusions and/or hallucinations. The mechanisms underlying psychosis in dementia are unknown; however, neurobiological and pharmacological evidence has implicated multiple signaling pathways and brain regions. Despite differences in dementia pathology, the neurobiology underlying psychosis appears to involve dysregulation of a cortical and limbic pathway involving serotonergic, gamma-aminobutyric acid ergic, glutamatergic, and dopaminergic signaling. Thus, an imbalance in cortical and mesolimbic excitatory tone may drive symptoms of psychosis. Delusions and hallucinations may result from (1) hyperactivation of pyramidal neurons within the visual cortex, causing visual hallucinations and (2) hyperactivation of the mesolimbic pathway, causing both delusions and hallucinations. Modulation of the 5-HT2A receptor may mitigate hyperactivity at both psychosis-associated pathways. Pimavanserin, an atypical antipsychotic, is a selective serotonin inverse agonist/antagonist at 5-HT2A receptors. Pimavanserin may prove beneficial in treating the hallucinations and delusions of DRP without worsening cognitive or motor function.

Keywords

Alzheimer’sParkinson’sVascularFrontotemporalLewy
Type
Perspective
Information
CNS Spectrums , Volume 27 , Issue 1 , February 2022 , pp. 7 - 15
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
© The Author(s), 2020. Published by Cambridge University Press

Introduction

No pharmacological agents are approved by the U.S. Food and Drug Administration (FDA) to treat dementia-related psychosis (DRP). Pimavanserin, an atypical antipsychotic that acts as a selective serotonin inverse agonist/antagonist at 5-HT2A receptors (and to a lesser extent, at 5-HT2c receptors), is the only FDA-approved treatment for hallucinations and delusions associated with Parkinson’s disease (PD) psychosis.1, Reference Cummings, Isaacson and Mills2 A phase 2 study of pimavanserin in Alzheimer’s disease (AD) psychosis met its primary end point at week 6 (mean change in the Neuropsychiatric Inventory-Nursing Home version psychosis score of −3.76 points [SE 0.65] for pimavanserin and −1.93 points [SE 0.63] for placebo; P =0 .045) with an acceptable tolerability profile and no worsening of cognition or motor function.Reference Ballard, Banister and Khan3 Pimavanserin is being investigated (NCT03325556 and 2017-002227-13) for treating hallucinations and delusions associated with DRP across five common neurodegenerative dementias: AD dementia, PD dementia, dementia with Lewy bodies (DLB), frontotemporal dementia (FTD), and vascular dementia (VaD).4-6 This article discusses the emerging understanding of the neurobiology of psychosis, the current state of knowledge about the neurobiology of psychotic symptoms in dementia syndromes, and the hypothesized role of pimavanserin in treating DRP.

Approximately 7.9 million people in the United States have dementia, with this number projected to rise as the elderly population grows.7-9 Although AD dementia is most common in the United States (60%-80% of cases), other forms of dementia include PD dementia, DLB, FTD, and VaD. While distinctive features characterize each form of dementia, broad symptom overlap is observed.10

Dementia is a syndrome characterized by a decline in one or more cognitive domains (eg, memory, language, executive function, problem-solving, attention, and social cognition) sufficiently severe to compromise daily function.11 Besides the well-recognized cognitive deficits characteristic of dementia, noncognitive symptoms (often referred to as behavioral and psychological symptoms of dementia or neuropsychiatric symptoms [NPS]) are estimated to occur in up to 90% of individuals during the course of dementia. NPS include behavioral symptoms (such as agitation, aggression, disinhibition, elation, and irritability), aberrant motor behavior, anxiety, apathy, appetite changes, depression, sleep disturbances, and symptoms of psychosis.Reference Cerejeira, Lagarto and Mukaetova-Ladinska12

Although some dementia patients display no or only a few noncognitive symptoms, multiple NPS commonly occur simultaneously.Reference Cerejeira, Lagarto and Mukaetova-Ladinska12 The Agitation Definition Work Group of the International Psychogeriatric Association defines agitation as occurring in patients with a cognitive impairment or dementia syndrome; exhibiting behavior consistent with emotional distress; manifesting excessive motor activity, verbal aggression, or physical aggression; and evidencing behaviors that cause excess disability and are not solely attributable to another disorder.Reference Cummings, Mintzer and Brodaty13 In contrast, DRP is defined by delusions or hallucinations occurring after the onset of cognitive decline, persisting for at least 1 month, and not better explained by delirium or some other mental illness.11 Both hallucinations and delusions are associated with behavioral symptoms such as physical and verbal aggression in patients with dementia.14–Reference Lopez, Becker and Sweet16

Prevalence estimates for psychosis range from 10% for FTD to 75% for DLB (Table 1).16–Reference Mourik, Rosso and Niermeijer30 In the United States, an estimated 2.34 million people suffer from DRP.16–Reference Mourik, Rosso and Niermeijer30 Visual hallucinations occur in all forms of dementia and are commonly observed in PD dementia and DLB.Reference Fenelon, Soulas, Zenasni and Cleret de Langavant31, Reference McKeith, Boeve and Dickson32 Delusions are also observed in all forms of dementia, most commonly paranoid delusions (eg, theft or spousal infidelity) and misidentifications, though the latter is sometimes considered a type of memory deficit rather than psychosis.Reference Fenelon, Soulas, Zenasni and Cleret de Langavant31, Reference Devanand, Jacobs and Tang33 DRP varies within and across patients in the psychotic symptoms manifested and in the severity of symptoms during the course of illness.Reference Devanand, Jacobs and Tang33 DRP is more frequently observed in patients with more advanced dementia. DRP has consistently been associated with greater caregiver burden and more rapid progression to severe dementia, institutionalization, and death.34–Reference Scarmeas, Brandt and Albert38

Table 1. Prevalence ranges for psychosis, delusions, and hallucinations in AD dementia, VaD, DLB, PD Dementia, and FTD

Many forms of dementia, aside from VaD, result from neurodegenerative disease and are associated with various proteinopathies characterized by protein misfolding and aggregation. Aberrant aggregated proteins in AD produce β-amyloid plaques and neurofibrillary tangles (hyperphosphorylated tau aggregates).Reference Rovelet-Lecrux, Hannequin and Raux39, Reference Hyman, Phelps and Beach40 In DLB and PD dementia, Lewy bodies and Lewy neurites, composed primarily of phosphorylated α-synuclein aggregates, accumulate preferentially in limbic brain regions.41–Reference Hamilton43 FTD may be associated with either aggregated tau protein or aggregated trans-activator regulatory DNA-binding 43 (TDP-43) protein.Reference Nelson, Dickson and Trojanowski44

Post-mortem analyses have revealed most dementia patients exhibit mixed pathology comprising abnormal protein aggregates plus vascular changes.Reference Brenowitz, Keene and Hawes45, Reference Schneider, Arvanitakis, Bang and Bennett46 In one study of community-dwelling adults, 56% of dementia patients were diagnosed with multiple underlying pathologies (AD in combination with either PD/DLB, infarctions representing vascular brain injury, or both).Reference Schneider, Arvanitakis, Bang and Bennett46 After adjusting for age, individuals with multiple diagnoses were deemed to be nearly three times more likely to develop dementia as those with a single underlying pathology.Reference Schneider, Arvanitakis, Bang and Bennett46 In a separate study, database analyses revealed that 59% to 68% of patients with AD neuropathology also displayed Lewy body pathology or vascular brain injury.Reference Brenowitz, Keene and Hawes45

Neurobiology of Psychosis

The underlying mechanisms behind psychosis in dementia are unknown. The neurobiology of psychosis has primarily been examined in studies of patients with schizophrenia and animals investigated in pharmacological probe paradigms.Reference Gründer and Cumming47 Taken together, the evidence suggests alterations in multiple signaling pathways—including dopaminergic, gamma-aminobutyric acid (GABA)ergic, glutamatergic, and serotonergic neurotransmission—may contribute to psychosis.Reference Hirvonen and Hietala48 Excess dopamine signaling in the mesolimbic pathway, which projects from the ventral tegmental area (VTA) to the nucleus accumbens, has been demonstrated to promote positive symptoms, primarily delusions and hallucinations.Reference Watanabe, Morimoto, Nakamura and Suwaki49 Under basal conditions, GABAergic interneurons provide inhibitory regulation of the activity of cortical pyramidal neurons. Inhibition of N-methyl-d-aspartate (NMDA) receptors reduces the inhibitory activity of GABAergic interneurons, resulting in glutamatergic hyperfunction. In rodent models, NMDA receptor antagonism or cortical and hippocampal NMDA receptor deletion results in psychotic-like behaviors.Reference Zhou, Zhang and Li50, Reference Nakazawa, Zsiros and Jiang51 Similarly, ketamine-induced NMDA antagonism significantly increases positive symptoms in haloperidol-treated patients diagnosed with schizophrenia.Reference Lahti, Koffel, LaPorte and Tamminga52 Glutamatergic projections from the prefrontal cortex provide tonic control of dopaminergic neurons in the VTA. Microdialysis and electrical stimulation rodent models reveal that glutamatergic hyperfunction increases burst firing of dopaminergic neurons in the VTA, stimulating the mesolimbic pathway.Reference Almodovar-Fabregas, Segarra and Colon53, Reference Karreman and Moghaddam54

These findings are supported by basic pharmacological intervention studies showing that multiple signaling pathways contribute to psychosis. These observations include dopamine D2 receptor activation via psychostimulants, glutamate NMDA receptor inhibition via dissociative anesthetics, and serotonin 5-HT2A receptor activation via psychedelics, all of which have been reported to precipitate psychotic symptoms.Reference Rolland, Jardri and Amad55 Methamphetamine, which is a substrate for the dopamine transporter (DAT), increases the firing rate of cultured rat dopamine neurons, triggering an excitatory response at dopamine concentrations lower than those required for D2 autoreceptor activation.Reference Ingram, Prasad and Amara56 Both methamphetamine and the DAT inhibitor cocaine, which increases extracellular dopamine levels via uptake inhibition, induce paranoid delusions as well as auditory and tactile hallucinations in stimulant-dependent individuals.Reference Mahoney, Kalechstein, De La Garza and Newton57, Reference McKetin, Baker, Dawe, Voce and Lubman58 Ketamine, a noncompetitive NMDA receptor antagonist, significantly increases hallucinations and delusions in schizophrenic patients following administration of subanesthetic doses and increases regional cerebral blood flow to the anterior cingulate cortex, while decreasing blood flow to the hippocampus and primary visual cortex.Reference Lahti, Holcomb, Medoff and Tamminga59, Reference Krystal, Karper and Seibyl60 In addition, subanesthetic doses of ketamine induces acute auditory verbal hallucinations and paranoid delusions in control subjects without psychosis in a reduced-stimulation environment.Reference Powers, Gancsos, Finn, Morgan and Corlett61 Administration of the serotonin 5-HT2A receptor agonist lysergic acid diethylamide (LSD) to healthy volunteers results in increased cerebral blood flow and enhanced resting-state functional connectivity in the visual cortex, which strongly correlates with visual hallucinations.Reference Carhart-Harris, Muthukumaraswamy and Roseman62 Administration of the 5-HT2A receptor agonist psilocybin to hallucinogen-naïve adults precipitates mystical delusions that persist at 14-month follow-up in 60% of subjects.Reference Griffiths, Richards, Johnson, McCann and Jesse63 In a separate study in healthy human volunteers, psychotic symptoms that closely mimicked those observed in first-episode schizophrenic patients (including sensory misperceptions and thought-process disruption) occur within 20 to 30 minutes of psilocybin administration. Pretreatment with the 5-HT2A receptor antagonist ketanserin inhibits psilocybin-induced psychosis in a dose-dependent manner, while pretreatment with the D2 receptor antagonist haloperidol does not affect psilocybin-induced hallucinations, further supporting the idea that certain symptoms of hallucinogen-induced psychosis (such as visual hallucinations) result from 5-HT2A agonism, while others (such as auditory hallucinations) are more strongly linked to the D2 receptor.Reference Vollenweider, Vollenweider-Scherpenhuyzen, Babler, Vogel and Hell64 Additional support for multifactorial signaling stems from the observation that conventional antipsychotics exert their effects primarily via D2 receptor inhibition, while atypical antipsychotics act as serotonin–dopamine antagonists, inhibiting both D2 and 5-HT2A receptors.Reference Stahl65

Taken together, neurobiological and pharmacological evidence points to a common, interconnected cortical–limbic psychosis pathway (Figure 1). Both the occurrence of hallucinogen 5-HT2A receptor effects in the prefrontal and visual cortices, and the observation that loss of serotonin nerve terminals in the prefrontal and visual cortices of patients with PD psychosis leads to upregulation of 5-HT2A receptors in the cortex support this hypothesis. A possible convergence of many of these pathways into 5-HT2A-modulated systems is suggested by the observation that the 5-HT2A receptor is affected by essentially all atypical antipsychotics, which led to the development of pimavanserin, a 5-HT2A-selective inverse agonist/antagonist.Reference Hacksell, Burstein, McFarland, Mills and Williams66 In preclinical rodent studies, pimavanserin reduced both amphetamine- and NMDA receptor antagonist-induced hyperactivity when combined with haloperidol or haloperidol and risperidone, respectively.Reference Gardell, Vanover and Pounds67 Additionally, pimavanserin was shown to reverse psychosis-like behaviors in rodent models of PD psychosis without impairing motor performance or interfering with the efficacy of PD medications.Reference McFarland, Price and Bonhaus68 Finally, pimavanserin increased dopamine release in the medial prefrontal cortex but not in the nucleus accumbens, suggesting pimavanserin may be beneficial for cognitive, negative, and psychotic symptoms.Reference Li, Ichikawa and Huang69

Figure 1. Hypothesized cortical–limbic psychosis pathway and proposed mechanism of disease for DRP. Neurobiological and pharmacological evidence suggests that hallucinations and delusions are precipitated by overactivation of the mesolimbic pathway, while visual hallucinations are mediated via overactivation of the visual cortex. Dissociative anesthetic-induced (ie, PCP, ketamine) glutamate NMDA receptor antagonism, psychedelic-induced (ie, LSD, psilocybin) serotonin 5-HT2A receptor agonism, and psychostimulant-induced (ie, amphetamine, cocaine) dopamine D2 receptor agonism/DAT antagonism have all been reported to precipitate hallucinations and delusions. In contrast, antipsychotic-mediated D2 and 5-HT2A antagonism treat both hallucinations and delusions. GABAergic interneuron or NMDA receptor dysfunction, and excess serotonin or 5-HT2A receptor upregulation in the cerebral cortex can result in sustained activation of pyramidal neurons and may lead to hyperactive glutamatergic signaling to the VTA, resulting in excess dopamine or D2 receptor upregulation in the ventral striatum, triggering hallucinations and delusions in DRP.Reference Rolland, Jardri and Amad55–Reference Ingram, Prasad and Amara56, Reference Kometer, Schmidt, Jancke and Vollenweider70–Reference Braak and Braak87

Changes in Dementia that may Result in Psychosis Pathway Dysfunction

The cortical–limbic psychosis pathway provides numerous points where dysfunction could trigger delusions and/or hallucinations. The pathology and dysfunction across the dementias leading to delusions and/or hallucinations may be different in specific dementias but each is positioned to affect the function of the cortical–limbic system thought to mediate psychosis. The evidence for dysfunction which could disrupt the cortical–limbic psychosis pathway in each dementia is described below.

PD dementia

While dopamine depletion in the dorsal striatum due to loss of nigrostriatal neurons results in the characteristic motor symptoms of PD, serotonin dysfunction is thought to be the underlying cause of PD psychosis. Post-mortem analyses indicate Lewy body and Lewy neurite deposition in the raphe nucleus magnus, obscurus, and pallidus, and the gigantocellular nucleus of the medullary lateral reticular formation nuclei (which comprise the serotonergic caudal brainstem complex) precedes deposition in dopaminergic midbrain neurons.Reference Braak, Del Tredici and Rub88 In addition, significant decreases in serotonin, the serotonin transporter (SERT), and the serotonin metabolite 5-hydroxyindoleacetic acid (5-HIAA) are observed in the caudate in post-mortem analyses of PD patients.Reference Kish, Tong and Hornykiewicz72 During the early stages of PD, SERT expression is diminished in the forebrain, but preserved in the caudate, and increased serotonergic uptake is observed in the thalamus and raphe nuclei, indicating a shift toward mesolimbic and mesocortical dysfunction.Reference Albin, Koeppe and Bohnen73, Reference Joutsa, Johansson, Seppanen, Noponen and Kaasinen74 As PD progresses, SERT expression in the caudate decreases and is correlated with disease stage.Reference Kerenyi, Ricaurte and Schretlen75 In PD patients with visual hallucinations, upregulation of 5-HT2A receptors has been observed using positron emission tomography in the inferolateral temporal cortex—in complex visual processing—as well as other portions of the ventral visual pathway, including the bilateral inferior occipital gyrus and right fusiform gyrus.Reference Ballanger, Strafella and van Eimeren76, Reference Huot, Johnston and Darr77 5-HT2A receptor upregulation may represent a compensatory mechanism by which the brain attempts to counteract reductions in serotonin levels.Reference Huot, Johnston and Darr77 In a double-blind, randomized, placebo-controlled phase 3 study of the efficacy of pimavanserin in the treatment of hallucinations and delusions associated with PD psychosis, a post-hoc subgroup analysis revealed patients with cognitive impairment (Mini-Mental State Examination scores 21-24) demonstrate a significantly greater improvement in Scale for the Assessment of Positive Symptoms-PD scores from baseline to week 6 with pimavanserin as compared to placebo-treated patients (P =0.002), suggesting pimavanserin may exhibit a more robust effect in cognitively impaired patients.Reference Cummings, Ballard and Tariot89

Imaging studies demonstrate that PD dementia is associated with more widespread cortical cholinergic depletion than that observed in patients with PD who do not exhibit dementia.Reference Bohnen, Kaufer and Ivanco90, Reference Kuhl, Minoshima and Fessler91 Modulation of cholinergic activity has been reported to decrease hallucinations and delusions in PD dementia patients. Treatment with the acetylcholinesterase inhibitor donepezil significantly reduces hallucinations and paranoid ideation, as well as overall rating scale scores for PD psychosis.Reference Fabbrini, Barbanti and Aurilia92 At present, the underlying mechanism for these effects is unknown. Serotonin has been reported to inhibit acetylcholine release from cortical cholinergic nerve terminalsReference Lanctôt, Herrmann and Mazzotta93 and 5-HT receptor inverse agonism/antagonism may represent another therapeutic strategy to modulate cortical cholinergic activity.

Dementia with Lewy bodies

In DLB, the density of Lewy bodies in limbic areas (highest density in the amygdala) is significantly higher than in neocortical areas.Reference Rezaie, Cairns, Chadwick and Lantos94 As in PD, serotonin dysfunction is thought to be the underlying cause of psychosis in DLB. Cortical 5-HT2 binding differs between patients with DLB with and without hallucinations. Significant deficits in 5-HT2 binding are observed in cortical layers III and V (deep cortical layers that contain pyramidal neurons) in patients who did not experience hallucinations, whereas a 5-HT2 binding deficit was observed only in one upper cortical layer in patients who did experience hallucinations, suggesting 5-HT2 receptor preservation in the temporal cortex may contribute to hallucinations in this population.Reference Cheng, Ferrier and Morris78 This hypothesis is further supported by the observation that serotonergic receptor binding and 5-HIAA levels were significantly decreased in nonhallucinating vs hallucinating patients with DLB in a neurochemical analysis of the temporal cortex. In the same study, downregulation of choline acetyltransferase activity was observed in the temporal and parietal cortices, particularly in those experiencing hallucinations.Reference Perry, Marshall and Kerwin79 Treatment with the cholinesterase inhibitor rivastigmine decreased delusions and hallucinations in patients with DLB compared to placebo.Reference McKeith, Del Ser and Spano95 The mechanism underlying the efficacy of cholinesterase inhibition in the treatment of DLB remains unresolved. However, hallucinations in patients with DLB have been proposed to result from imbalances between the serotonergic and cholinergic inputs to the cortex, suggesting restoration of the balance between the two inputs may account for this effect.Reference Perry, Marshall and Thompson96

AD dementia

Although serotonergic signaling is altered in AD, it may not be the primary dysfunction contributing to psychosis. When compared to healthy controls, significant reductions in 5-HT2 receptor binding and expression have been observed in the frontal, temporal, and cingulate cortices, as well as the amygdala and hippocampus, in patients with AD.97–Reference Jansen, Faull, Dragunow and Synek101 In a study of psychopathology in late-onset AD patients, the 5-HT2A receptor polymorphism 102-T/C was significantly associated with visual and auditory hallucinations, and the 5-HT2C receptor polymorphism Cys23Ser was significantly associated with visual hallucinations, implicating neurodegeneration in the biology of the psychotic symptoms of individuals expressing these genetic variations. However, the 5-HT2A 102-T/C polymorphism reduces 5-HT2A receptor expression while the 5-HT2C Cys23Ser polymorphism leads to functional downregulation of the 5-HT2C receptor.102–Reference Okada, Northup and Ozaki104

Concomitant serotonergic and cholinergic deficits have been observed in the frontal and temporal cortices in AD patients as compared to healthy controls, and the ratio of serotonin to acetylcholinesterase in the temporal cortex is correlated with psychosis in female patients.Reference Garcia-Alloza, Gil-Bea and Diez-Ariza105 Cholinesterase inhibitors used in the treatment of AD may improve hallucinations and delusions in some patients.Reference Cummings, McRae and Zhang106

There is evidence of GABAergic and glutamatergic dysfunction in AD which might disrupt the cortical–limbic psychosis pathway. Significant reductions in GABA concentrations in numerous cortical areas, including the temporal, frontal (orbitofrontal and premotor cortex), parietal, and occipital cortices, are observed in biopsy and autopsy specimens obtained from AD patients.107-111 Alterations in NMDA-mediated glutamatergic signaling appears to vary throughout the course of AD. Under normal circumstances, glutamate regulates the inhibitory tone of these GABA neurons; amyloid appears to increase the sensitivity of these receptors to glutamate, leading to glutamatergic hyperactivation and GABAergic neuronal degeneration. During the later stages of disease progression, excessive GABAergic neuronal degeneration results in NMDA receptor hypofunction.Reference Olney, Wozniak and Farber80 Evidence of GABAergic or glutamatergic dysfunction has yet to be directly associated with psychosis in AD. Treatment of AD patients with the NMDA receptor antagonist memantine, which was shown to inhibit the excitotoxic effects of NMDA glutamate receptors, has occasionally been reported to worsen or induce new visual hallucinations in AD patients.Reference Monastero, Camarda, Pipia and Camarda81

Frontotemporal dementia

Deficiencies in the serotonergic system have been reported in imaging studies, post-mortem tissue analyses, and cerebrospinal fluid studies of patients with FTD. Decreased 5-HT2A receptor expression has been observed in the orbitofrontal, frontal medial, and cingulate cortices of such patients.Reference Huey, Putnam and Grafman82 Data regarding how GABAergic and glutamatergic signaling are affected in FTD are incomplete; however, loss of glutamatergic pyramidal cells and GABAergic neurons in the upper layers of the frontal and temporal cortices has been reported.Reference Ferrer83 MRI studies have revealed widespread limbic atrophy in FTD,Reference Meyer, Mueller and Stuke112, Reference Boccardi, Sabattoli and Laakso113 suggesting disruption of the cortical–limbic psychosis pathway may occur. However, data regarding dysfunction specific to psychosis in this population are not yet reported, possibly because psychosis is less common in FTD.

Vascular dementia

Serotonergic dysfunction is present in VaD, with increased 5-HT1A and 5-HT2A receptor binding observed in the temporal cortex of post-mortem tissue samples from multi-infarct VaD patients.Reference Elliott, Ballard and Kalaria84 The relationship between this increased receptor binding and psychosis is unknown. Data regarding the roles of GABAergic and glutamatergic signaling in VaD is lacking.

Neurotransmission alterations across dementias

While the strength of the evidence varies across these dementias, all have been associated with alterations in neurotransmission which have the potential to impact the cortical–limbic psychosis pathway. Each of these conditions is highly heterogeneous and the likelihood an individual patient will develop psychosis varies greatly. Further research is required to confirm how etiological factors, such as the anatomical locations of neurodegeneration, compensatory mechanisms, and genetic influences contribute to the development of psychosis.

Proposed Mechanism for DRP

The proposed mechanism for DRP is believed to involve a common cortical–limbic psychosis pathway (Figure 1). Cortical GABAergic interneuron or NMDA receptor dysfunction is hypothesized to result in loss of inhibitory tone, leading to hyperactivity of glutamatergic neurons that signal to the VTA. Alternatively, excessive signaling via 5-HT2A receptors on pyramidal glutamate neurons can lead to hyperactive glutamatergic neurons that signal to the VTA. Sustained hyperactive glutamatergic signaling then leads to mesolimbic dopamine pathway hyperactivation, resulting in hallucinations and delusions. Excess signaling via 5-HT2A receptors in the visual cortex may be responsible specifically for visual hallucinations.64–Reference Hacksell, Burstein, McFarland, Mills and Williams66, Reference Kometer, Schmidt, Jancke and Vollenweider70, 72–Reference Braak and Braak87

The cortical–limbic psychosis pathway can be triggered in a variety of different ways across dementias based on which neurons are lost or damaged and which signaling pathways become disordered but appears to be responsive to serotonin modulation. Cortical GABA interneuron dysfunction, excess serotonin, cortical 5-HT2A receptor upregulation, excess striatal dopamine, striatal D2 receptor upregulation, and excess glutamate signaling all have the potential to contribute to pathway dysfunction.

Proposed Mechanism of Action of Pimavanserin

Across the underlying causes of cortical–limbic psychosis pathway hyperactivation, 5-HT2A receptor antagonism represents a common point of regulation and for treatment intervention with antipsychotics.Reference Hacksell, Burstein, McFarland, Mills and Williams66 Pimavanserin is a selective serotonin inverse agonist/antagonist at 5-HT2A receptors, with 40-fold less activity at 5-HT2C receptors and no affinity for dopaminergic, histaminergic, muscarinic, or adrenergic receptors, and is proposed to act as a targeted serotonergic modulator of circuits (Figure 2).Reference Hacksell, Burstein, McFarland, Mills and Williams66 Pimavanserin is thought to reduce the activity of these receptors to below basal levels and regulate the effects of both cortical GABAergic deficits and excess cortical serotonergic signaling. This is posited to decrease visual hallucinations and attenuate glutamate signaling to the VTA and mesolimbic pathway, further decreasing delusions and hallucinations.

Figure 2. Pimavanserin-mediated 5-HT2A receptor inhibition: hypothesized modulation of signaling through a variety of neurotransmitters. Through 5-HT2A antagonism/reverse agonism, pimavanserin is proposed to act as a targeted serotonergic modulator of circuits, mitigating the effects of GABAergic deficits and excess serotonergic signaling, while also reducing hyperactive glutamatergic signaling and mesolimbic pathway activation.

Summary

DRP is a commonly occurring phenomenon across dementias, yet no pharmacological agents are currently approved by the FDA for DRP treatment. Commonly used typical and atypical antipsychotics have an increased risk of death and other treatment-limiting side effects.Reference Schneider, Dagerman and Insel114, 115 While the etiology of DRP is unknown, neurobiological and pharmacological evidence supports a common, interconnected cortical–limbic psychosis pathway mediating DRP, which may be modified via 5-HT2A receptor inverse agonism/antagonism. The only FDA-approved agent to treat hallucinations and delusions associated with PD psychosis, pimavanserin (proposed to act as a targeted serotonergic modulator of circuits), is being investigated to treat DRP in a phase 3 trial completed in 2019.5 The selectivity of pimavanserin presents a potential novel mechanism for the management of hallucinations and delusions associated with DRP.Reference Hacksell, Burstein, McFarland, Mills and Williams66, Reference Cummings, Ballard and Tariot89

Acknowledgments

The authors received editorial assistance in the preparation of this manuscript from Arbor Scientia, Inc., which was supported by Acadia Pharmaceuticals Inc., San Diego, CA. Dr. Cummings is supported by Keep Memory Alive (KMA), National Institute of General Medical Sciences (NIGMS) grant P20GM109025, National Institute of Neurological Disorders and Stroke (NINDS) grant U01NS093334, and National Institute of Aging (NIA) grant R01AG053798. Dr. Devanand is supported by the NIA.

Disclosures

Dr. Cummings has provided consultation to Acadia, Actinogen, Alkahest, Allergan, Alzheon, Avanir, Axsome, BiOasis, Biogen, Cassava, Cerecin, Cortexyme, Diadem, EIP Pharma, Eisai, Foresight, Genentech, Green Valley, Grifols, Otsuka, Resverlogix, Roche, Samumed, Samus, Signant, Third Rock, Toyama, and United Neuroscience pharmaceutical and assessment companies. Dr. Cummings has stock options in Prana, Neurokos, Adamas, MedAvante-ProPhase, Anovis, and BiOasis.

Dr. Devanand has provided consultation to Acadia, BXcel, Corium, Eisai, Genentech, and Grifols.

Dr. Stahl has served as a consultant to Acadia, Alkermes, Allergan, Arbor Pharmaceuticals, Axovant, Axsome, Celgene, Concert, Clearview, EMD Serono, Eisai Pharmaceuticals, Ferring, Impel NeuroPharma, Intra-Cellular Therapies, Ironshore Pharmaceuticals, Janssen, Lilly, Lundbeck, Merck, Otsuka, Pfizer, Sage Therapeutics, Servier, Shire, Sunovion, Takeda, Taliaz, Teva, Tonix, Tris Pharma, and Vifor Pharma; he is a board member of Genomind; he has served on speakers bureaus for Acadia, Lundbeck, Otsuka, Perrigo, Servier, Sunovion, Takeda and Vertex; and he has received research and/or grant support from Acadia, Avanir, Braeburn Pharmaceuticals, Eli Lilly, Intra-Cellular Therapies, Ironshore Pharmaceuticals, ISSWSH, Neurocrine, Otsuka, Shire, Sunovion, and TMS NeuroHealth Centers.

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Figure 0

Table 1. Prevalence ranges for psychosis, delusions, and hallucinations in AD dementia, VaD, DLB, PD Dementia, and FTD

Figure 1

Figure 1. Hypothesized cortical–limbic psychosis pathway and proposed mechanism of disease for DRP. Neurobiological and pharmacological evidence suggests that hallucinations and delusions are precipitated by overactivation of the mesolimbic pathway, while visual hallucinations are mediated via overactivation of the visual cortex. Dissociative anesthetic-induced (ie, PCP, ketamine) glutamate NMDA receptor antagonism, psychedelic-induced (ie, LSD, psilocybin) serotonin 5-HT2A receptor agonism, and psychostimulant-induced (ie, amphetamine, cocaine) dopamine D2 receptor agonism/DAT antagonism have all been reported to precipitate hallucinations and delusions. In contrast, antipsychotic-mediated D2 and 5-HT2A antagonism treat both hallucinations and delusions. GABAergic interneuron or NMDA receptor dysfunction, and excess serotonin or 5-HT2A receptor upregulation in the cerebral cortex can result in sustained activation of pyramidal neurons and may lead to hyperactive glutamatergic signaling to the VTA, resulting in excess dopamine or D2 receptor upregulation in the ventral striatum, triggering hallucinations and delusions in DRP.55–56,70–87

Figure 2

Figure 2. Pimavanserin-mediated 5-HT2A receptor inhibition: hypothesized modulation of signaling through a variety of neurotransmitters. Through 5-HT2A antagonism/reverse agonism, pimavanserin is proposed to act as a targeted serotonergic modulator of circuits, mitigating the effects of GABAergic deficits and excess serotonergic signaling, while also reducing hyperactive glutamatergic signaling and mesolimbic pathway activation.