Geroin, C;
Petracca, M;
Di Tella, S;
Marcuzzo, E;
Erro, R;
Cuoco, S;
Ceravolo, R;
Mazzucchi, S;
Pilotto, A;
Padovani, A;
et al.
Geroin, C; Petracca, M; Di Tella, S; Marcuzzo, E; Erro, R; Cuoco, S; Ceravolo, R; Mazzucchi, S; Pilotto, A; Padovani, A; Romito, LM; Eleopra, R; Zappia, M; Nicoletti, A; Dallocchio, C; Arbasino, C; Bono, F; Laterza, V; Demartini, B; Gambini, O; Modugno, N; Olivola, E; Bonanni, L; Albanese, A; Ferrazzano, G; Tessitore, A; Lopiano, L; Calandra-Buonaura, G; Morgante, F; Esposito, M; Pisani, A; Manganotti, P; Tesolin, L; Teatini, F; Camozzi, S; Ercoli, T; Stocchi, F; Moja, MC; Defazio, G; Tinazzi, M
(2024)
Elderly Onset of Functional Motor Disorders: Clinical Correlates from the Italian Registry.
MOVEMENT DISORDERS CLINICAL PRACTICE, 11 (1).
pp. 38-44.
ISSN 2330-1619
https://doi.org/10.1002/mdc3.13916
SGUL Authors: Morgante, Francesca
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Abstract
Background Functional motor disorders (FMD) are a frequent neurological condition affecting patients with movement disorders. Commonly described in younger adults, their manifestation can be also associated to an elderly onset. Objective To assess the prevalence and describe the clinical manifestations of FMD with elderly and younger onset and their relationship with demographical and clinical variables. Methods We recruited patients with a “clinically definite” diagnosis of FMD from the Italian Registry of FMD. Patients underwent extensive clinical assessments. For elderly onset, we set a chronological cut-off at 65 years or older according to WHO definition. Multivariate regression models were implemented to estimate adjusted odds ratio of elderly FMD onset related to clinical characteristics. Results Among the 410 patients, 34 (8.2%) experienced elderly-onset FMD, with a mean age at onset of 70.9 years. The most common phenotype was tremor (47.1%), followed by gait disorders, weakness, and dystonia (29.4%, 23.5%, 14.7%, respectively). Eleven elderly patients had a combined phenomenology: 9 exhibited two phenotypes, 2 had three phenotypes. Weakness was isolated in 3/8 patients and combined with another phenotype in 5/8, manifesting as paraplegia (n = 4); upper limb diplegia (n = 2), hemiparesis/hemiplegia (n = 1), and tetraparesis/tetraplegia (n= 1). Non-motor and other functional neurological disorders occurred more frequently in the younger group (89.1%) than the elderly (73.5%). Neurological and non-neurological comorbidities were more prevalent in the elderly group (82.4%) as opposed to the younger (32.7%). In a multivariate regression analysis, elderly-onset FMD was significantly associated with neurological comorbidities, including parkinsonism (OR 6.73) and cerebrovascular diseases (OR 5.48). Conclusions These results highlight the importance of achieving an accurate diagnosis of FMD in the elderly, as it is crucial for effectively managing FMD symptoms and addressing neurological comorbidities.
Item Type: | Article | ||||||||
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Additional Information: | © 2023 The Authors. Movement Disorders Clinical Practice published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. | ||||||||
Keywords: | functional motor disorders, elderly onset, functional neurological disorders, functional parkinsonism, neurological comorbidities | ||||||||
SGUL Research Institute / Research Centre: | Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) | ||||||||
Journal or Publication Title: | MOVEMENT DISORDERS CLINICAL PRACTICE | ||||||||
ISSN: | 2330-1619 | ||||||||
Dates: |
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Publisher License: | Creative Commons: Attribution-Noncommercial-No Derivative Works 4.0 | ||||||||
Web of Science ID: | WOS:001107809800001 | ||||||||
URI: | https://openaccess.sgul.ac.uk/id/eprint/115899 | ||||||||
Publisher's version: | https://doi.org/10.1002/mdc3.13916 |
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