Levodopa treatment does improve Parkinson's disease (PD) dysgraphia, but previous research is not in agreement about which aspects are most responsive. This study investigated the effect of levodopa on the kinematics of writing. Twenty-four patients with PD of less than 10years duration and 25 age-matched controls were recruited. A practically defined off state method was used to assess the levodopa motor response, measured on the Unified Parkinson's Disease Rating Scale PartIII. The kinematic features for six handwriting tasks involving different levels of complexity were recorded from PD patients in off and on states and from the control group. Levodopa is effective for simple writing activities involving repetition of letters, denoting improved fine motor control. But the same benefit was not seen for copying a sentence and a written category fluency test, tasks that carry memory and cognitive loads. We also found significant differences in kinematic features between control participants and PD patients, for all tasks and in both on and off states. Serial testing of handwriting in patients known to be at risk for developing PD might prove to be an effective biomarker for cell loss in the substantia nigra and the associated dopamine deficiency. We recommend using a panel of writing tasks including sentence copying and memory dependence. Dual-task effects may make these activities more sensitive to early motor deficits, while their weaker levodopa responsiveness would cause them to be more stable indicators of motor progression once symptomatic treatment has been commenced.
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Univ Massachusetts, Dept Publ Hlth, Lowell, MA 01545 USA
Edith Nourse Rogers Mem Vet Hosp, ENRM VA Hosp, Dept Vet Affairs, Bedford, MA 01730 USA
Harvard TH Chan Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USAUniv Massachusetts, Dept Publ Hlth, Lowell, MA 01545 USA
Palacios, Natalia
Hannoun, Anas
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Geisel Sch Med Dartmouth, Dept Neurol, Manchester, NH USAUniv Massachusetts, Dept Publ Hlth, Lowell, MA 01545 USA
Hannoun, Anas
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Flahive, Julie
Ward, Doyle
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Univ Massachusetts, Med Sch, Dept Microbiol & Physiol Syst, Worcester, MA 01605 USA
Univ Massachusetts, Dept UMass, Ctr Microbiome Res, Med Sch, Worcester, MA 01605 USAUniv Massachusetts, Dept Publ Hlth, Lowell, MA 01545 USA
Ward, Doyle
Goostrey, Kelsey
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Univ Massachusetts, Med Sch, Dept Neurol, Worcester, MA 01545 USAUniv Massachusetts, Dept Publ Hlth, Lowell, MA 01545 USA
Goostrey, Kelsey
Deb, Anindita
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Univ Massachusetts, Med Sch, Dept Neurol, Worcester, MA 01545 USAUniv Massachusetts, Dept Publ Hlth, Lowell, MA 01545 USA
Deb, Anindita
Smith, Kara M.
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Univ Massachusetts, Med Sch, Dept Neurol, Worcester, MA 01545 USAUniv Massachusetts, Dept Publ Hlth, Lowell, MA 01545 USA
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UCL, Dept Clin Neurosci, Inst Neurol, Natl Hosp Neurol & Neurosurg, London NW3 2PF, England
Royal Free Hosp, London NW3 2PF, EnglandUCL, Dept Clin Neurosci, Inst Neurol, Natl Hosp Neurol & Neurosurg, London NW3 2PF, England
Schapira, A. H. V.
Emre, M.
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Norol ABD, Istanbul Tip Fak, Istanbul Med Sch, Capa, TurkeyUCL, Dept Clin Neurosci, Inst Neurol, Natl Hosp Neurol & Neurosurg, London NW3 2PF, England
Emre, M.
Jenner, P.
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Kings Coll London, Neurodegenerat Dis Res Ctr, Sch Hlth & Biomed Sci, London WC2R 2LS, EnglandUCL, Dept Clin Neurosci, Inst Neurol, Natl Hosp Neurol & Neurosurg, London NW3 2PF, England