Gait analysis may distinguish progressive supranuclear palsy and Parkinson disease since the earliest stages

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作者
Marianna Amboni
Carlo Ricciardi
Marina Picillo
Chiara De Santis
Gianluca Ricciardelli
Filomena Abate
Maria Francesca Tepedino
Giovanni D’Addio
Giuseppe Cesarelli
Giampiero Volpe
Maria Consiglia Calabrese
Mario Cesarelli
Paolo Barone
机构
[1] University of Salerno,Center for Neurodegenerative Diseases (CEMAND), Department of Medicine, Surgery and Dentistry “Scuola Medica Salernitana”
[2] IDC Hermitage-Capodimonte,Department of Advanced Biomedical Sciences
[3] University of Naples “Federico II”,Department of Chemical, Materials and Production Engineering
[4] Istituti Clinici Scientifici Maugeri IRCCS,Department of Electrical Engineering and Information Technology
[5] Azienda Ospedaliera Universitaria OO. RR. San Giovanni di Dio e Ruggi d’Aragona,undefined
[6] University of Naples “Federico II”,undefined
[7] University of Naples “Federico II”,undefined
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摘要
Progressive supranuclear palsy (PSP) is a rare and rapidly progressing atypical parkinsonism. Albeit existing clinical criteria for PSP have good specificity and sensitivity, there is a need for biomarkers able to capture early objective disease-specific abnormalities. This study aimed to identify gait patterns specifically associated with early PSP. The study population comprised 104 consecutively enrolled participants (83 PD and 21 PSP patients). Gait was investigated using a gait analysis system during normal gait and a cognitive dual task. Univariate statistical analysis and binary logistic regression were used to compare all PD patients and all PSP patients, as well as newly diagnosed PD and early PSP patients. Gait pattern was poorer in PSP patients than in PD patients, even from early stages. PSP patients exhibited reduced velocity and increased measures of dynamic instability when compared to PD patients. Application of predictive models to gait data revealed that PD gait pattern was typified by increased cadence and longer cycle length, whereas a longer stance phase characterized PSP patients in both mid and early disease stages. The present study demonstrates that quantitative gait evaluation clearly distinguishes PSP patients from PD patients since the earliest stages of disease. First, this might candidate gait analysis as a reliable biomarker in both clinical and research setting. Furthermore, our results may offer speculative clues for conceiving early disease-specific rehabilitation strategies.
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