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Pharmacotherapy for behavioural manifestations in frontotemporal dementia: An expert consensus from the European Reference Network for Rare Neurological Diseases (ERN‐RND)

Background and Purpose Frontotemporal dementia (FTD) is a neurodegenerative disorder characterized by pervasive personality and behavioural disturbances with severe impact on patients and caregivers. In current clinical practice, treatment is based on nonpharmacological and pharmacological approache...

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Published in:European journal of neurology 2024-12, Vol.31 (12), p.e16446-n/a
Main Authors: Wittebrood, Casper, Boban, Marina, Cagnin, Annchiara, Capellari, Sabina, De Winter, François‐Laurent, Djamshidian, Atbin, González, Manuel Menéndez, Hjermind, Lena E., Krajcovicova, Lenka, Krüger, Johanna, Levin, Johannes, Reetz, Kathrin, Rodriguez, Eloy Rodriguez, Rohrer, Jonathan, Van Langenhove, Tim, Reinhard, Carola, Graessner, Holm, Rusina, Robert, Saracino, Dario, Houot, Marion, Seelar, Harro, Vandenberghe, Rik
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container_title European journal of neurology
container_volume 31
creator Wittebrood, Casper
Boban, Marina
Cagnin, Annchiara
Capellari, Sabina
De Winter, François‐Laurent
Djamshidian, Atbin
González, Manuel Menéndez
Hjermind, Lena E.
Krajcovicova, Lenka
Krüger, Johanna
Levin, Johannes
Reetz, Kathrin
Rodriguez, Eloy Rodriguez
Rohrer, Jonathan
Van Langenhove, Tim
Reinhard, Carola
Graessner, Holm
Rusina, Robert
Saracino, Dario
Houot, Marion
Seelar, Harro
Vandenberghe, Rik
description Background and Purpose Frontotemporal dementia (FTD) is a neurodegenerative disorder characterized by pervasive personality and behavioural disturbances with severe impact on patients and caregivers. In current clinical practice, treatment is based on nonpharmacological and pharmacological approaches. Unfortunately, trial‐based evidence supporting symptomatic pharmacological treatment for the behavioural disturbances in FTD is scarce despite the significant burden this poses on the patients and caregivers. Method The study examined drug management decisions for several behavioural disturbances in patients with FTD by 21 experts across European expert centres affiliated with the European Reference Network for Rare Neurological Diseases (ERN‐RND). Results The study revealed the highest consensus on drug treatments for physical and verbal aggression, impulsivity and obsessive delusions. Antipsychotics (primarily quetiapine) were recommended for behaviours posing safety risks to both patients and caregivers (aggression, self‐injury and self‐harm) and nightly unrest. Selective serotonin reuptake inhibitors were recommended for perseverative somatic complaints, rigidity of thought, hyperphagia, loss of empathy and for impulsivity. Trazodone was specifically recommended for motor unrest, mirtazapine for nightly unrest, and bupropion and methylphenidate for apathy. Additionally, bupropion was strongly advised against in 10 out of the 14 behavioural symptoms, emphasizing a clear recommendation against its use in the majority of cases. Conclusions The survey data can provide expert guidance that is helpful for healthcare professionals involved in the treatment of behavioural symptoms. Additionally, they offer insights that may inform prioritization and design of therapeutic studies, particularly for existing drugs targeting behavioural disturbances in FTD.
doi_str_mv 10.1111/ene.16446
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In current clinical practice, treatment is based on nonpharmacological and pharmacological approaches. Unfortunately, trial‐based evidence supporting symptomatic pharmacological treatment for the behavioural disturbances in FTD is scarce despite the significant burden this poses on the patients and caregivers. Method The study examined drug management decisions for several behavioural disturbances in patients with FTD by 21 experts across European expert centres affiliated with the European Reference Network for Rare Neurological Diseases (ERN‐RND). Results The study revealed the highest consensus on drug treatments for physical and verbal aggression, impulsivity and obsessive delusions. Antipsychotics (primarily quetiapine) were recommended for behaviours posing safety risks to both patients and caregivers (aggression, self‐injury and self‐harm) and nightly unrest. Selective serotonin reuptake inhibitors were recommended for perseverative somatic complaints, rigidity of thought, hyperphagia, loss of empathy and for impulsivity. Trazodone was specifically recommended for motor unrest, mirtazapine for nightly unrest, and bupropion and methylphenidate for apathy. Additionally, bupropion was strongly advised against in 10 out of the 14 behavioural symptoms, emphasizing a clear recommendation against its use in the majority of cases. Conclusions The survey data can provide expert guidance that is helpful for healthcare professionals involved in the treatment of behavioural symptoms. Additionally, they offer insights that may inform prioritization and design of therapeutic studies, particularly for existing drugs targeting behavioural disturbances in FTD.</description><identifier>ISSN: 1351-5101</identifier><identifier>ISSN: 1468-1331</identifier><identifier>EISSN: 1468-1331</identifier><identifier>DOI: 10.1111/ene.16446</identifier><identifier>PMID: 39447217</identifier><language>eng</language><publisher>England: John Wiley &amp; Sons, Inc</publisher><subject>Aggression ; Aggression - drug effects ; ALS and frontotemporal dementia ; Antipsychotic Agents - therapeutic use ; Antipsychotics ; Bupropion ; Caregivers ; Consensus ; Dementia ; Dementia disorders ; Disturbances ; Drug delivery ; Drug development ; Drug therapy ; Emotional behavior ; Europe ; expert testimony ; Frontotemporal dementia ; Frontotemporal Dementia - drug therapy ; Health services ; Humans ; Hyperphagia ; Impulsive behavior ; Impulsive Behavior - drug effects ; Impulsivity ; Medical treatment ; Methylphenidate ; neurobehavioural manifestations ; Neurodegenerative diseases ; Neurological complications ; Neurological diseases ; Original ; Patients ; Pharmacology ; Quetiapine ; Rare diseases ; Rare Diseases - drug therapy ; Rigidity ; Risk taking ; Selective Serotonin Reuptake Inhibitors - therapeutic use ; Serotonin ; Serotonin uptake inhibitors ; Signs and symptoms</subject><ispartof>European journal of neurology, 2024-12, Vol.31 (12), p.e16446-n/a</ispartof><rights>2024 The Author(s). published by John Wiley &amp; Sons Ltd on behalf of European Academy of Neurology.</rights><rights>2024 The Author(s). 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In current clinical practice, treatment is based on nonpharmacological and pharmacological approaches. Unfortunately, trial‐based evidence supporting symptomatic pharmacological treatment for the behavioural disturbances in FTD is scarce despite the significant burden this poses on the patients and caregivers. Method The study examined drug management decisions for several behavioural disturbances in patients with FTD by 21 experts across European expert centres affiliated with the European Reference Network for Rare Neurological Diseases (ERN‐RND). Results The study revealed the highest consensus on drug treatments for physical and verbal aggression, impulsivity and obsessive delusions. Antipsychotics (primarily quetiapine) were recommended for behaviours posing safety risks to both patients and caregivers (aggression, self‐injury and self‐harm) and nightly unrest. Selective serotonin reuptake inhibitors were recommended for perseverative somatic complaints, rigidity of thought, hyperphagia, loss of empathy and for impulsivity. Trazodone was specifically recommended for motor unrest, mirtazapine for nightly unrest, and bupropion and methylphenidate for apathy. Additionally, bupropion was strongly advised against in 10 out of the 14 behavioural symptoms, emphasizing a clear recommendation against its use in the majority of cases. Conclusions The survey data can provide expert guidance that is helpful for healthcare professionals involved in the treatment of behavioural symptoms. Additionally, they offer insights that may inform prioritization and design of therapeutic studies, particularly for existing drugs targeting behavioural disturbances in FTD.</description><subject>Aggression</subject><subject>Aggression - drug effects</subject><subject>ALS and frontotemporal dementia</subject><subject>Antipsychotic Agents - therapeutic use</subject><subject>Antipsychotics</subject><subject>Bupropion</subject><subject>Caregivers</subject><subject>Consensus</subject><subject>Dementia</subject><subject>Dementia disorders</subject><subject>Disturbances</subject><subject>Drug delivery</subject><subject>Drug development</subject><subject>Drug therapy</subject><subject>Emotional behavior</subject><subject>Europe</subject><subject>expert testimony</subject><subject>Frontotemporal dementia</subject><subject>Frontotemporal Dementia - drug therapy</subject><subject>Health services</subject><subject>Humans</subject><subject>Hyperphagia</subject><subject>Impulsive behavior</subject><subject>Impulsive Behavior - drug effects</subject><subject>Impulsivity</subject><subject>Medical treatment</subject><subject>Methylphenidate</subject><subject>neurobehavioural manifestations</subject><subject>Neurodegenerative diseases</subject><subject>Neurological complications</subject><subject>Neurological diseases</subject><subject>Original</subject><subject>Patients</subject><subject>Pharmacology</subject><subject>Quetiapine</subject><subject>Rare diseases</subject><subject>Rare Diseases - drug therapy</subject><subject>Rigidity</subject><subject>Risk taking</subject><subject>Selective Serotonin Reuptake Inhibitors - therapeutic use</subject><subject>Serotonin</subject><subject>Serotonin uptake inhibitors</subject><subject>Signs and symptoms</subject><issn>1351-5101</issn><issn>1468-1331</issn><issn>1468-1331</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNp1kk1u1DAUgCMEoqWw4ALIEpt2kdaO7STDBlVtCkjVgEawtl6cl45LYqd20jI7jtCLcClOgtMpFSDhjS370-f3lyQvGT1kcR2hxUOWC5E_SnaZyMuUcc4exzOXLJWMsp3kWQiXlNKsyOjTZIcvhCgyVuwmPz6twfeg3bhGD8OGtM6TGtdwbdzkoSM9WNNiGGE0zgZiLGm9s6MbsR_cDDTYox0NvCHHluC3Af1IdETRhinMcE-im1STdwOCJSts0aPVSJY43jj_9e7LFfj5IkKduzA6ek9NQAgYyH61Wv78frtanh48T5600AV8cb_vJV_Oqs8n79Pzj-8-nByfp5pzkaesAKBy0SyKumjbJm-E0CXIMgfG61iEDEsBTCMvZM6ZpDmHhme1xLKWjLWa7yVvt95hqntsdEwwpqoGb3rwG-XAqL9frFmrC3etGJNSUiqjYf_e4N3VFOunehM0dh1YdFNQnGUxQrHIaERf_4NextLbmN9M5WUWu5hF6mBLae9C8Ng-RMOomqdAxSlQd1MQ2Vd_hv9A_m57BI62wI3pcPN_k6qW1Vb5C4PmwFA</recordid><startdate>202412</startdate><enddate>202412</enddate><creator>Wittebrood, Casper</creator><creator>Boban, Marina</creator><creator>Cagnin, Annchiara</creator><creator>Capellari, Sabina</creator><creator>De Winter, François‐Laurent</creator><creator>Djamshidian, Atbin</creator><creator>González, Manuel Menéndez</creator><creator>Hjermind, Lena E.</creator><creator>Krajcovicova, Lenka</creator><creator>Krüger, Johanna</creator><creator>Levin, Johannes</creator><creator>Reetz, Kathrin</creator><creator>Rodriguez, Eloy Rodriguez</creator><creator>Rohrer, Jonathan</creator><creator>Van Langenhove, Tim</creator><creator>Reinhard, Carola</creator><creator>Graessner, Holm</creator><creator>Rusina, Robert</creator><creator>Saracino, Dario</creator><creator>Houot, Marion</creator><creator>Seelar, Harro</creator><creator>Vandenberghe, Rik</creator><general>John Wiley &amp; 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Krajcovicova, Lenka ; Krüger, Johanna ; Levin, Johannes ; Reetz, Kathrin ; Rodriguez, Eloy Rodriguez ; Rohrer, Jonathan ; Van Langenhove, Tim ; Reinhard, Carola ; Graessner, Holm ; Rusina, Robert ; Saracino, Dario ; Houot, Marion ; Seelar, Harro ; Vandenberghe, Rik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3346-17aa059d97b7ffd6d44c8a586a13b0022e84a1ce3756315063ad32b5e8b511fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aggression</topic><topic>Aggression - drug effects</topic><topic>ALS and frontotemporal dementia</topic><topic>Antipsychotic Agents - therapeutic use</topic><topic>Antipsychotics</topic><topic>Bupropion</topic><topic>Caregivers</topic><topic>Consensus</topic><topic>Dementia</topic><topic>Dementia disorders</topic><topic>Disturbances</topic><topic>Drug delivery</topic><topic>Drug development</topic><topic>Drug therapy</topic><topic>Emotional behavior</topic><topic>Europe</topic><topic>expert testimony</topic><topic>Frontotemporal dementia</topic><topic>Frontotemporal Dementia - drug therapy</topic><topic>Health services</topic><topic>Humans</topic><topic>Hyperphagia</topic><topic>Impulsive behavior</topic><topic>Impulsive Behavior - drug effects</topic><topic>Impulsivity</topic><topic>Medical treatment</topic><topic>Methylphenidate</topic><topic>neurobehavioural manifestations</topic><topic>Neurodegenerative diseases</topic><topic>Neurological complications</topic><topic>Neurological diseases</topic><topic>Original</topic><topic>Patients</topic><topic>Pharmacology</topic><topic>Quetiapine</topic><topic>Rare diseases</topic><topic>Rare Diseases - drug therapy</topic><topic>Rigidity</topic><topic>Risk taking</topic><topic>Selective Serotonin Reuptake Inhibitors - therapeutic use</topic><topic>Serotonin</topic><topic>Serotonin uptake inhibitors</topic><topic>Signs and symptoms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wittebrood, Casper</creatorcontrib><creatorcontrib>Boban, Marina</creatorcontrib><creatorcontrib>Cagnin, Annchiara</creatorcontrib><creatorcontrib>Capellari, Sabina</creatorcontrib><creatorcontrib>De Winter, François‐Laurent</creatorcontrib><creatorcontrib>Djamshidian, Atbin</creatorcontrib><creatorcontrib>González, Manuel Menéndez</creatorcontrib><creatorcontrib>Hjermind, Lena E.</creatorcontrib><creatorcontrib>Krajcovicova, Lenka</creatorcontrib><creatorcontrib>Krüger, Johanna</creatorcontrib><creatorcontrib>Levin, Johannes</creatorcontrib><creatorcontrib>Reetz, Kathrin</creatorcontrib><creatorcontrib>Rodriguez, Eloy Rodriguez</creatorcontrib><creatorcontrib>Rohrer, Jonathan</creatorcontrib><creatorcontrib>Van Langenhove, Tim</creatorcontrib><creatorcontrib>Reinhard, Carola</creatorcontrib><creatorcontrib>Graessner, Holm</creatorcontrib><creatorcontrib>Rusina, Robert</creatorcontrib><creatorcontrib>Saracino, Dario</creatorcontrib><creatorcontrib>Houot, Marion</creatorcontrib><creatorcontrib>Seelar, Harro</creatorcontrib><creatorcontrib>Vandenberghe, Rik</creatorcontrib><collection>Wiley Open Access</collection><collection>Wiley Online Library Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest Health &amp; 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In current clinical practice, treatment is based on nonpharmacological and pharmacological approaches. Unfortunately, trial‐based evidence supporting symptomatic pharmacological treatment for the behavioural disturbances in FTD is scarce despite the significant burden this poses on the patients and caregivers. Method The study examined drug management decisions for several behavioural disturbances in patients with FTD by 21 experts across European expert centres affiliated with the European Reference Network for Rare Neurological Diseases (ERN‐RND). Results The study revealed the highest consensus on drug treatments for physical and verbal aggression, impulsivity and obsessive delusions. Antipsychotics (primarily quetiapine) were recommended for behaviours posing safety risks to both patients and caregivers (aggression, self‐injury and self‐harm) and nightly unrest. Selective serotonin reuptake inhibitors were recommended for perseverative somatic complaints, rigidity of thought, hyperphagia, loss of empathy and for impulsivity. Trazodone was specifically recommended for motor unrest, mirtazapine for nightly unrest, and bupropion and methylphenidate for apathy. Additionally, bupropion was strongly advised against in 10 out of the 14 behavioural symptoms, emphasizing a clear recommendation against its use in the majority of cases. Conclusions The survey data can provide expert guidance that is helpful for healthcare professionals involved in the treatment of behavioural symptoms. Additionally, they offer insights that may inform prioritization and design of therapeutic studies, particularly for existing drugs targeting behavioural disturbances in FTD.</abstract><cop>England</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>39447217</pmid><doi>10.1111/ene.16446</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-0635-4884</orcidid><orcidid>https://orcid.org/0000-0003-1631-1439</orcidid><orcidid>https://orcid.org/0009-0004-2600-4736</orcidid><orcidid>https://orcid.org/0000-0002-9730-9228</orcidid><oa>free_for_read</oa></addata></record>
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source Wiley Open Access; PubMed Central
subjects Aggression
Aggression - drug effects
ALS and frontotemporal dementia
Antipsychotic Agents - therapeutic use
Antipsychotics
Bupropion
Caregivers
Consensus
Dementia
Dementia disorders
Disturbances
Drug delivery
Drug development
Drug therapy
Emotional behavior
Europe
expert testimony
Frontotemporal dementia
Frontotemporal Dementia - drug therapy
Health services
Humans
Hyperphagia
Impulsive behavior
Impulsive Behavior - drug effects
Impulsivity
Medical treatment
Methylphenidate
neurobehavioural manifestations
Neurodegenerative diseases
Neurological complications
Neurological diseases
Original
Patients
Pharmacology
Quetiapine
Rare diseases
Rare Diseases - drug therapy
Rigidity
Risk taking
Selective Serotonin Reuptake Inhibitors - therapeutic use
Serotonin
Serotonin uptake inhibitors
Signs and symptoms
title Pharmacotherapy for behavioural manifestations in frontotemporal dementia: An expert consensus from the European Reference Network for Rare Neurological Diseases (ERN‐RND)
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