Frontotemporal dementia (FTD) is the second most common type of presenile dementia. Three clinical prototypes have been defined; behavioral variant FTD, semantic dementia, and progressive nonfluent aphasia. Progressive supranuclear palsy, corticobasal degeneration, and motor neuron disease may possess clinical and pathological characteristics that overlap with FTD, and it is possible that they may all belong to the same clinicopathological spectrum. Frontotemporal lobar degeneration (FTLD) is a clinicopathological syndrome that encompasses a heterogenous group of neurodegenerative disorders. Owing to the advancement in the field of molecular genetics, diagnostic imaging, and pathology, FTLD has been the focus of great interest. Nevertheless, parkinsonism in FTLD has received relatively less attention. Parkinsonism is found in approximately 20–30% of patients in FTLD. Furthermore, parkinsonism can be seen in all FTLD subtypes, and some patients with familial and sporadic FTLD can present with prominent parkinsonism. Therefore, there is a need to understand parkinsonism in FTLD in order to obtain a better understanding of the disease. With regard to the clinical characteristics, the akinetic rigid type of parkinsonism has predominantly been described. Parkinsonism is frequently observed in familial FTD, more specifically, in FTD with parkinsonism linked to chromosome 17q (FTDP-17). The genes associated with parkinsonism are microtubule associated protein tau (MAPT), progranulin (GRN or PGRN), and chromosome 9 open reading frame 72 (C9ORF72) repeat expansion. The neural substrate of parkinsonism remains to be unveiled. Dopamine transporter (DAT) imaging revealed decreased uptake of DAT, and imaging findings indicated atrophic changes of the basal ganglia. Parkinsonism can be an important feature in FTLD and, therefore, increased attention is needed on the subject.

Citations

Citations to this article as recorded by  

• Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
  Chiara Pedicone, Sarah A. Weitzman, Alan E. Renton, Alison M. Goate
  Molecular Neurodegeneration.2024;[Epub]     CrossRef
• Genetic and clinical landscape of Chinese frontotemporal dementia: dominance of TBK1 and OPTN mutations
  Haitian Nan, Yeon-Jeong Kim, Min Chu, Dan Li, Jieying Li, Deming Jiang, Yiming Wu, Toshihisa Ohtsuka, Liyong Wu
  Alzheimer's Research & Therapy.2024;[Epub]     CrossRef
• Treatment of Acquired Deforming Hypertonia with Botulinum Toxin in Older Population: A Retrospective Study
  Pablo Maldonado, Hugo Bessaguet, Cédric Chol, Pascal Giraux, Ludovic Lafaie, Ahmed Adham, Romain David, Thomas Celarier, Etienne Ojardias
  Toxins.2024; 16(8): 365.     CrossRef
• Multitracer PET/CT Findings in a Case of Behavioral Variant Frontotemporal Dementia With Parkinsonism
  Shuai Chen, Chang Fu, Jing-Yu Shao, Jun-Ling Xu, Jie-Wen Zhang
  Clinical Nuclear Medicine.2024;[Epub]     CrossRef
• Antidepressant medications in dementia: evidence and potential mechanisms of treatment-resistance
  Harry Costello, Jonathan P. Roiser, Robert Howard
  Psychological Medicine.2023; 53(3): 654.     CrossRef
• Movement disorders are linked to TDP-43 burden in the substantia nigra of FTLD-TDP brain donors
  Luigi Fiondella, Priya Gami-Patel, Christian A. Blok, Annemieke J. M. Rozemuller, Jeroen J. M. Hoozemans, Yolande A. L. Pijnenburg, Marta Scarioni, Anke A. Dijkstra
  Acta Neuropathologica Communications.2023;[Epub]     CrossRef
• Demencias degenerativas: ¿un dilema de síndromes o de enfermedades?
  A. Robles Bayón
  Neurología.2022; 37(6): 480.     CrossRef
• Degenerative dementias: a question of syndrome or disease?
  A. Robles Bayón
  Neurología (English Edition).2022; 37(6): 480.     CrossRef
• Deficient neurotransmitter systems and synaptic function in frontotemporal lobar degeneration—Insights into disease mechanisms and current therapeutic approaches
  Nadine Huber, Sonja Korhonen, Dorit Hoffmann, Stina Leskelä, Hannah Rostalski, Anne M. Remes, Paavo Honkakoski, Eino Solje, Annakaisa Haapasalo
  Molecular Psychiatry.2022; 27(3): 1300.     CrossRef
• Novel frameshift CTSF mutation causing kufs disease type B mimicking frontotemporal dementia-parkinsonism
  Murat Gultekin, Zeynep Tufekcioglu, Recep Baydemir
  Neurocase.2022; 28(1): 107.     CrossRef
• Dopamine Transporter Imaging for Frontotemporal Lobar Degeneration With Motor Neuron Disease
  Ryota Kobayashi, Shinobu Kawakatsu, Makoto Ohba, Daichi Morioka, Masafumi Kanoto, Koichi Otani
  Frontiers in Neuroscience.2022;[Epub]     CrossRef
• Investigational therapeutics for the treatment of progressive supranuclear palsy
  David G Coughlin, Irene Litvan
  Expert Opinion on Investigational Drugs.2022; 31(8): 813.     CrossRef
• Frequency and Longitudinal Course of Motor Signs in Genetic Frontotemporal Dementia
  Sonja Schönecker, Francisco J. Martinez-Murcia, Boris-Stephan Rauchmann, Nicolai Franzmeier, Catharina Prix, Elisabeth Wlasich, Sandra V. Loosli, Katja Bochmann, Juan-Manuel Gorriz Saez, Robert Laforce, Simon Ducharme, Maria Carmela Tartaglia, Elizabeth F
  Neurology.2022;[Epub]     CrossRef
• Multi-Modal Synergistic 99mTc-TRODAT-1 SPECT and MRI for Evaluation of the Efficacy of Hyperbaric Oxygen Therapy in CO-Induced Delayed Parkinsonian and Non-Parkinsonian Syndromes
  Skye Hsin-Hsien Yeh, Chuang-Hsin Chiu, Hung-Wen Kao, Ching-Po Lin, Yu-Hus Lai, Wen-Sheng Huang
  Antioxidants.2022; 11(11): 2289.     CrossRef
• Defective Lysosomal Lipid Catabolism as a Common Pathogenic Mechanism for Dementia
  Jun Yup Lee, Oana C. Marian, Anthony S. Don
  NeuroMolecular Medicine.2021; 23(1): 1.     CrossRef
• Different miRNA Profiles in Plasma Derived Small and Large Extracellular Vesicles from Patients with Neurodegenerative Diseases
  Daisy Sproviero, Stella Gagliardi, Susanna Zucca, Maddalena Arigoni, Marta Giannini, Maria Garofalo, Martina Olivero, Michela Dell’Orco, Orietta Pansarasa, Stefano Bernuzzi, Micol Avenali, Matteo Cotta Ramusino, Luca Diamanti, Brigida Minafra, Giulia Peri
  International Journal of Molecular Sciences.2021; 22(5): 2737.     CrossRef
• Parkin beyond Parkinson’s Disease—A Functional Meaning of Parkin Downregulation in TDP-43 Proteinopathies
  Katarzyna Gaweda-Walerych, Emilia Jadwiga Sitek, Ewa Narożańska, Emanuele Buratti
  Cells.2021; 10(12): 3389.     CrossRef
• Joint contractures and acquired deforming hypertonia in older people: Which determinants?
  Patrick Dehail, Nathaly Gaudreault, Haodong Zhou, Véronique Cressot, Anne Martineau, Julie Kirouac-Laplante, Guy Trudel
  Annals of Physical and Rehabilitation Medicine.2019; 62(6): 435.     CrossRef
• Review: Clinical, genetic and neuroimaging features of frontotemporal dementia
  R. Convery, S. Mead, J. D. Rohrer
  Neuropathology and Applied Neurobiology.2019; 45(1): 6.     CrossRef
• Granulin in Frontotemporal Lobar Degeneration: Molecular Mechanisms of the Disease
  Zemfira N. Karamysheva, Elena B. Tikhonova, Andrey L. Karamyshev
  Frontiers in Neuroscience.2019;[Epub]     CrossRef
• The Whole Exome Sequencing Clarifies the Genotype- Phenotype Correlations in Patients with Early-Onset Dementia
  Yangqi Xu, Xiaoli Liu, Junyi Shen, Wotu Tian, Rong Fang, Binyin Li, Jianfang Ma, Li Cao, Shengdi Chen, Guanjun Li, Huidong Tang
  Aging and disease.2018; 9(4): 696.     CrossRef
• Mouse models of frontotemporal dementia: A comparison of phenotypes with clinical symptomatology
  Rebekah M. Ahmed, Muireann Irish, Janet van Eersel, Arne Ittner, Yazi D. Ke, Alexander Volkerling, Julia van der Hoven, Kimi Tanaka, Tim Karl, Michael Kassiou, Jillian J. Kril, Olivier Piguet, Jürgen Götz, Matthew C. Kiernan, Glenda M. Halliday, John R. H
  Neuroscience & Biobehavioral Reviews.2017; 74: 126.     CrossRef
• Translocator Protein-18 kDa (TSPO) Positron Emission Tomography (PET) Imaging and Its Clinical Impact in Neurodegenerative Diseases
  Anne-Claire Dupont, Bérenger Largeau, Maria Santiago Ribeiro, Denis Guilloteau, Claire Tronel, Nicolas Arlicot
  International Journal of Molecular Sciences.2017; 18(4): 785.     CrossRef
• Intrinsic functional connectivity alterations in progressive supranuclear palsy: Differential effects in frontal cortex, motor, and midbrain networks
  Johannes Rosskopf, Martin Gorges, Hans‐Peter Müller, Dorothée Lulé, Ingo Uttner, Albert C. Ludolph, Elmar Pinkhardt, Freimut D. Juengling, Jan Kassubek
  Movement Disorders.2017; 32(7): 1006.     CrossRef
• Phenotypic variability related to C9orf72 mutation in a large Sardinian kindred
  Gianluca Floris, Giuseppe Borghero, Francesca Di Stefano, Rosanna Melis, Roberta Puddu, Laura Fadda, Maria R. Murru, Daniela Corongiu, Stefania Cuccu, Stefania Tranquilli, Antonino Cannas, Maria G. Marrosu, Adriano Chiò, Francesco Marrosu
  Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration.2016; 17(3-4): 245.     CrossRef
• Clinical features ofTBK1carriers compared withC9orf72,GRNand non-mutation carriers in a Belgian cohort
  Sara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, Sebastiaan Engelborghs, Anne Sieben, Tim Van Langenhove, Jan De Bleecker, Jonathan Baets, Mathieu Vandenbulcke, Koen Van Laere, Sarah Ceyssens, Marleen Van den Broeck, Karin Peeters, Maria Mattheijs
  Brain.2016; 139(2): 452.     CrossRef
• Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis
  Carmen Gasca-Salas, Mario Masellis, Edwin Khoo, Binit B. Shah, David Fisman, Anthony E. Lang, Galit Kleiner-Fisman, Patrick Lewis
  PLOS ONE.2016; 11(4): e0153852.     CrossRef
• The clinical spectrum of sporadic and familial forms of frontotemporal dementia
  Ione O. C. Woollacott, Jonathan D. Rohrer
  Journal of Neurochemistry.2016; 138(S1): 6.     CrossRef
• Genetics of Progressive Supranuclear Palsy
  Sun Young Im, Young Eun Kim, Yun Joong Kim
  Journal of Movement Disorders.2015; 8(3): 122.     CrossRef

Citations

Citations to this article as recorded by  

• Outcomes of stereotactic thalamotomy in patients of essential tremor: A systematic review
  Sagun Ghimire, Bibechan Thapa, Durga Neupane, Pashupati Pokharel
  Journal of Clinical Neuroscience.2024; 126: 38.     CrossRef
• Displaced center of pressure on the treated side in individuals with essential tremor after radiofrequency ablation: a longitudinal case–control study
  Atsuya Sato, Takaomi Taira, Kazuya Kitada, Toshiki Ando, Toyohiro Hamaguchi, Michiko Konno, Yoshinori Kitabatake, Toshiyuki Ishioka
  Frontiers in Neurology.2023;[Epub]     CrossRef
• Commentary on: A Network Approach to Understanding the Effects of Focused Ultrasound for Essential Tremor: Insights into Pathophysiology, Treatment, and Imaging Biomarkers
  Prashin Unadkat, David Eidelberg
  Neurotherapeutics.2022; 19(6): 1883.     CrossRef
• Deep Brain Stimulation for Tremor: Update on Long-Term Outcomes, Target Considerations and Future Directions
  Naomi I. Kremer, Rik W. J. Pauwels, Nicolò G. Pozzi, Florian Lange, Jonas Roothans, Jens Volkmann, Martin M. Reich
  Journal of Clinical Medicine.2021; 10(16): 3468.     CrossRef
• Clinical improvement associated with targeted interruption of the cerebellothalamic tract following MR-guided focused ultrasound for essential tremor
  J. Levi Chazen, Harini Sarva, Philip E. Stieg, Robert J. Min, Douglas J. Ballon, Kane O. Pryor, Paul M. Riegelhaupt, Michael G. Kaplitt
  Journal of Neurosurgery.2018; 129(2): 315.     CrossRef
• Innovations in Functional Neurosurgery and Anesthetic Implications
  Lauren K. Dunn, Marcel E. Durieux, W. Jeffrey Elias, Edward C. Nemergut, Bhiken I. Naik
  Journal of Neurosurgical Anesthesiology.2018; 30(1): 18.     CrossRef
• Surgical treatments for essential tremor
  Rodger J. Elble, Ludy Shih, Jeffrey W. Cozzens
  Expert Review of Neurotherapeutics.2018; 18(4): 303.     CrossRef
• The Current Status of Deep Brain Stimulation for the Treatment of Parkinson Disease in the Republic of Korea
  Jung-Il Lee
  Journal of Movement Disorders.2015; 8(3): 115.     CrossRef