Gali H Weissberger1, Rebecca J Melrose2, Theresa A Narvaez3, Dylan Harwood4, Mark A Mandelkern5, David L Sultzer4. 1. Brain Behavior and Aging Research Center, VA Greater Los Angeles Healthcare System, Los Angeles, CA; Geriatric Research Education and Clinical Center, VA Greater Los Angeles Healthcare System, Los Angeles, CA. Electronic address: gweissbe@gmail.com. 2. Brain Behavior and Aging Research Center, VA Greater Los Angeles Healthcare System, Los Angeles, CA; Geriatric Research Education and Clinical Center, VA Greater Los Angeles Healthcare System, Los Angeles, CA; Department of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine at UCLA, Los Angeles, CA. 3. Brain Behavior and Aging Research Center, VA Greater Los Angeles Healthcare System, Los Angeles, CA. 4. Brain Behavior and Aging Research Center, VA Greater Los Angeles Healthcare System, Los Angeles, CA; Department of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine at UCLA, Los Angeles, CA. 5. Imaging Service, VA Greater Los Angeles Healthcare System, Los Angeles, CA.
Abstract
OBJECTIVE: This study aimed to investigate the neurobiologic correlates of two distinct clusters of agitation symptoms to identify the unique biologic substrates underlying agitated behaviors. METHODS: Eighty-eight outpatients with mild to moderate Alzheimer disease (AD) were recruited from the VA Greater Los Angeles Healthcare System Geropsychiatry Outpatient Program. A cross-sectional investigation was conducted of the relationship between cerebral glucose metabolism measured via 18F-fluorodeoxyglucose positron emission tomography and agitated symptoms from the Neuropsychiatric Inventory (NPI) in patients with AD. Two empirically derived clusters of agitation symptoms were investigated: an Agitation factor comprising agitation/aggression and irritability/lability items of the NPI, and a Behavioral Dyscontrol factor comprising elation/euphoria, disinhibition, aberrant motor behavior, sleep, and appetite items of the NPI. Mean cerebral metabolism for patients who scored positively on each of the two factors was compared with mean cerebral metabolism for those who did not. RESULTS: Patients with AD who scored positively on the Agitation factor showed reduced glucose metabolism of the right temporal, right frontal, and bilateral cingulate cortex. In contrast, the Behavioral Dyscontrol factor did not show specific neurobiologic correlates. CONCLUSION: Symptoms encompassed within the Agitation factor have distinct neurobiologic underpinnings. The precipitants, course, and outcomes related to these symptoms may be unique from other neuropsychiatric symptoms characteristic of AD. Special attention to treatment of agitated behaviors involving anger, aggressiveness, hostility, and irritability/emotional lability is warranted, because they appear to reflect a clinically relevant symptom cluster with unique underlying neurobiologic correlates. Published by Elsevier Inc.
OBJECTIVE: This study aimed to investigate the neurobiologic correlates of two distinct clusters of agitation symptoms to identify the unique biologic substrates underlying agitated behaviors. METHODS: Eighty-eight outpatients with mild to moderate Alzheimer disease (AD) were recruited from the VA Greater Los Angeles Healthcare System Geropsychiatry Outpatient Program. A cross-sectional investigation was conducted of the relationship between cerebral glucose metabolism measured via 18F-fluorodeoxyglucose positron emission tomography and agitated symptoms from the Neuropsychiatric Inventory (NPI) in patients with AD. Two empirically derived clusters of agitation symptoms were investigated: an Agitation factor comprising agitation/aggression and irritability/lability items of the NPI, and a Behavioral Dyscontrol factor comprising elation/euphoria, disinhibition, aberrant motor behavior, sleep, and appetite items of the NPI. Mean cerebral metabolism for patients who scored positively on each of the two factors was compared with mean cerebral metabolism for those who did not. RESULTS:Patients with AD who scored positively on the Agitation factor showed reduced glucose metabolism of the right temporal, right frontal, and bilateral cingulate cortex. In contrast, the Behavioral Dyscontrol factor did not show specific neurobiologic correlates. CONCLUSION: Symptoms encompassed within the Agitation factor have distinct neurobiologic underpinnings. The precipitants, course, and outcomes related to these symptoms may be unique from other neuropsychiatric symptoms characteristic of AD. Special attention to treatment of agitated behaviors involving anger, aggressiveness, hostility, and irritability/emotional lability is warranted, because they appear to reflect a clinically relevant symptom cluster with unique underlying neurobiologic correlates. Published by Elsevier Inc.
Authors: Myuri Ruthirakuhan; Nathan Herrmann; Ana C Andreazza; Nicolaas Paul L G Verhoeff; Damien Gallagher; Sandra E Black; Alex Kiss; Krista L Lanctôt Journal: J Alzheimers Dis Date: 2019 Impact factor: 4.472
Authors: Claudia Carrarini; Mirella Russo; Fedele Dono; Filomena Barbone; Marianna G Rispoli; Laura Ferri; Martina Di Pietro; Anna Digiovanni; Paola Ajdinaj; Rino Speranza; Alberto Granzotto; Valerio Frazzini; Astrid Thomas; Andrea Pilotto; Alessandro Padovani; Marco Onofrj; Stefano L Sensi; Laura Bonanni Journal: Front Neurol Date: 2021-04-16 Impact factor: 4.003
Authors: Cécile Tissot; Joseph Therriault; Tharick A Pascoal; Mira Chamoun; Firoza Z Lussier; Melissa Savard; Sulantha S Mathotaarachchi; Andréa L Benedet; Emilie M Thomas; Marlee Parsons; Ziad Nasreddine; Pedro Rosa-Neto; Serge Gauthier Journal: Alzheimers Dement (N Y) Date: 2021-03-31
Authors: Janina Krell-Roesch; Jeremy A Syrjanen; Maria Vassilaki; Val J Lowe; Prashanthi Vemuri; Michelle M Mielke; Mary M Machulda; Gorazd B Stokin; Teresa J Christianson; Walter K Kremers; Clifford R Jack; David S Knopman; Ronald C Petersen; Yonas E Geda Journal: Am J Geriatr Psychiatry Date: 2020-06-17 Impact factor: 4.105
Authors: Nicole S Tommasi; Christopher Gonzalez; Danielle Briggs; Michael J Properzi; Jennifer R Gatchel; Gad A Marshall Journal: Int J Geriatr Psychiatry Date: 2021-03-15 Impact factor: 3.850