The Relationship Between Serotonin‐2A Receptor and Cognitive Functions in Nondemented Parkinson's Disease Patients with Visual Hallucinations. Issue 5 (23rd January 2017)

• Record Type: Journal Article
• Authors: Cho, Sang Soo; Strafella, Antonio P.; Duff‐Canning, Sarah; Zurowski, Mateusz; Vijverman, Anne‐Catherine; Bruno, Veronica; Aquino, Camila C.; Criaud, Marion; Rusjan, Pablo M.; Houle, Sylvain; Fox, Susan H.
• Is Part Of: Movement disorders clinical practice. Volume 4:Issue 5(2017)
• Page Start: 698
• Page End: 709
• Publication Date: 2017-01-23
• Subjects: cognitive decline -- Parkinson's disease -- positron emission tomography (PET) -- serotonin 2A (5‐HT2A) receptor -- visual hallucinations; Movement Disorders; Movement disorders -- Periodicals; Movement disorders; Periodicals; Periodicals; 616
• DOI: 10.1002/mdc3.12466
• Languages: English
• ISSNs: 2330-1619

Abstract

Abstract: Background: There is growing evidence that the serotonergic system, in particular serotonin 2A receptors, is involved in neuropsychiatric symptoms in Parkinson's disease (PD), including cognitive processing and visual hallucinations. However, the relationship between serotonin 2A receptor availability, visual hallucinations, and cognitive profile is unknown. The objective of this study was to investigate the level of serotonin 2A receptor availability in brain regions affected by visual hallucinations and to test the association with cognitive/behavioral changes in patients who have PD with visual hallucinations. Methods: Nondemented patients who had PD with (n = 11) and without (n = 8) visual hallucinations and age‐matched controls (n = 10) were recruited. All participants completed neuropsychological testing, which consisted of visuoperceptual, executive, memory, language, and frontal‐behavioral function. Positron emission tomography scans using [ 18 F]setoperone, a serotonin 2A antagonist radioligand, were acquired in patients with PD, and a parametric binding potential map of [ 18 F]setoperone was calculated with the simplified reference tissue model using the cerebellum as a reference. Results: Patients who had PD with visual hallucinations exhibited significantly lower scores on measures of executive and visuoperceptual functions compared with age‐matched controls. These changes were paralleled by decreased [ 18 F]setoperone binding in the right insula, bilateral dorsolateral prefrontal cortex, right orbitofrontal cortex, right middle temporal gyrus, and right fusiform gyrus. The psychometric correlation analysis revealed significant relationships among tests associated with visuoperceptual function, memory and learning, and serotonin 2A binding in different prefrontal and ventral visual stream regions. There was also reduced serotonin 2A receptor binding in patients who had PD with depression. Conclusions: These findings support a complex interaction between serotonin 2A receptor function and cognitive processing in patients who have PD with visual hallucinations.