Abstract
OBJECTIVE—To investigate whether micrographia in patients with Parkinson's disease is lessened either by giving visual targets or by continually reminding them that they should write with a normal amplitude. METHODS—Eleven patients with Parkinson's disease (mean age 65.4 years) were compared with 14 control subjects (mean age 67.1 years). The subjects wrote with a stylus on a graphics tablet. There were three conditions: free writing, writing with dots to indicate the required size, and writing with continuous verbal reminders ("big"). Each condition was performed twice. RESULTS—The patients wrote with a more normal amplitude when given either the visual cues or the auditory reminders. This improvement persisted when, shortly afterwards, the patients wrote freely without external cues. The increase in amplitude was achieved mainly by an increase in movement time rather than in peak velocity. CONCLUSION—Whereas the visual cues directly specified the required amplitude the auditory reminders did not. One effect of external cues is that they draw attention to the goal, and thus encourage the patients to write less automatically.
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- Crawford T. J., Henderson L., Kennard C. Abnormalities of nonvisually-guided eye movements in Parkinson's disease. Brain. 1989 Dec;112(Pt 6):1573–1586. doi: 10.1093/brain/112.6.1573. [DOI] [PubMed] [Google Scholar]
- Crawford T., Goodrich S., Henderson L., Kennard C. Predictive responses in Parkinson's disease: manual keypresses and saccadic eye movements to regular stimulus events. J Neurol Neurosurg Psychiatry. 1989 Sep;52(9):1033–1042. doi: 10.1136/jnnp.52.9.1033. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Flowers K. A. Visual "closed-loop" and "open-loop" characteristics of voluntary movement in patients with Parkinsonism and intention tremor. Brain. 1976 Jun;99(2):269–310. doi: 10.1093/brain/99.2.269. [DOI] [PubMed] [Google Scholar]
- Flowers K. Ballistic and corrective movements on an aiming task. Intention tremor and parkinsonian movement disorders compared. Neurology. 1975 May;25(5):413–421. doi: 10.1212/wnl.25.5.413. [DOI] [PubMed] [Google Scholar]
- Georgiou N., Iansek R., Bradshaw J. L., Phillips J. G., Mattingley J. B., Bradshaw J. A. An evaluation of the role of internal cues in the pathogenesis of parkinsonian hypokinesia. Brain. 1993 Dec;116(Pt 6):1575–1587. doi: 10.1093/brain/116.6.1575. [DOI] [PubMed] [Google Scholar]
- Hallett M., Khoshbin S. A physiological mechanism of bradykinesia. Brain. 1980 Jun;103(2):301–314. doi: 10.1093/brain/103.2.301. [DOI] [PubMed] [Google Scholar]
- Hoehn M. M., Yahr M. D. Parkinsonism: onset, progression and mortality. Neurology. 1967 May;17(5):427–442. doi: 10.1212/wnl.17.5.427. [DOI] [PubMed] [Google Scholar]
- Jackson S. R., Jackson G. M., Harrison J., Henderson L., Kennard C. The internal control of action and Parkinson's disease: a kinematic analysis of visually-guided and memory-guided prehension movements. Exp Brain Res. 1995;105(1):147–162. doi: 10.1007/BF00242190. [DOI] [PubMed] [Google Scholar]
- Jahanshahi M., Jenkins I. H., Brown R. G., Marsden C. D., Passingham R. E., Brooks D. J. Self-initiated versus externally triggered movements. I. An investigation using measurement of regional cerebral blood flow with PET and movement-related potentials in normal and Parkinson's disease subjects. Brain. 1995 Aug;118(Pt 4):913–933. doi: 10.1093/brain/118.4.913. [DOI] [PubMed] [Google Scholar]
- Jenkins I. H., Brooks D. J., Nixon P. D., Frackowiak R. S., Passingham R. E. Motor sequence learning: a study with positron emission tomography. J Neurosci. 1994 Jun;14(6):3775–3790. doi: 10.1523/JNEUROSCI.14-06-03775.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jenkins I. H., Fernandez W., Playford E. D., Lees A. J., Frackowiak R. S., Passingham R. E., Brooks D. J. Impaired activation of the supplementary motor area in Parkinson's disease is reversed when akinesia is treated with apomorphine. Ann Neurol. 1992 Dec;32(6):749–757. doi: 10.1002/ana.410320608. [DOI] [PubMed] [Google Scholar]
- Jueptner M., Stephan K. M., Frith C. D., Brooks D. J., Frackowiak R. S., Passingham R. E. Anatomy of motor learning. I. Frontal cortex and attention to action. J Neurophysiol. 1997 Mar;77(3):1313–1324. doi: 10.1152/jn.1997.77.3.1313. [DOI] [PubMed] [Google Scholar]
- Klockgether T., Dichgans J. Visual control of arm movement in Parkinson's disease. Mov Disord. 1994 Jan;9(1):48–56. doi: 10.1002/mds.870090108. [DOI] [PubMed] [Google Scholar]
- Lueck C. J., Crawford T. J., Henderson L., Van Gisbergen J. A., Duysens J., Kennard C. Saccadic eye movements in Parkinson's disease: II. Remembered saccades--towards a unified hypothesis? Q J Exp Psychol A. 1992 Aug;45(2):211–233. doi: 10.1080/14640749208401325. [DOI] [PubMed] [Google Scholar]
- Lueck C. J., Crawford T. J., Henderson L., Van Gisbergen J. A., Duysens J., Kennard C. Saccadic eye movements in Parkinson's disease: II. Remembered saccades--towards a unified hypothesis? Q J Exp Psychol A. 1992 Aug;45(2):211–233. doi: 10.1080/14640749208401325. [DOI] [PubMed] [Google Scholar]
- Lueck C. J., Tanyeri S., Crawford T. J., Henderson L., Kennard C. Antisaccades and remembered saccades in Parkinson's disease. J Neurol Neurosurg Psychiatry. 1990 Apr;53(4):284–288. doi: 10.1136/jnnp.53.4.284. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lynch J. C., Graybiel A. M., Lobeck L. J. The differential projection of two cytoarchitectonic subregions of the inferior parietal lobule of macaque upon the deep layers of the superior colliculus. J Comp Neurol. 1985 May 8;235(2):241–254. doi: 10.1002/cne.902350207. [DOI] [PubMed] [Google Scholar]
- McLennan J. E., Nakano K., Tyler H. R., Schwab R. S. Micrographia in Parkinson's disease. J Neurol Sci. 1972 Feb;15(2):141–152. doi: 10.1016/0022-510x(72)90002-0. [DOI] [PubMed] [Google Scholar]
- Mitz A. R., Godschalk M., Wise S. P. Learning-dependent neuronal activity in the premotor cortex: activity during the acquisition of conditional motor associations. J Neurosci. 1991 Jun;11(6):1855–1872. doi: 10.1523/JNEUROSCI.11-06-01855.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morris M. E., Iansek R., Matyas T. A., Summers J. J. Stride length regulation in Parkinson's disease. Normalization strategies and underlying mechanisms. Brain. 1996 Apr;119(Pt 2):551–568. doi: 10.1093/brain/119.2.551. [DOI] [PubMed] [Google Scholar]
- Pierrot-Deseilligny C., Rivaud S., Gaymard B., Agid Y. Cortical control of reflexive visually-guided saccades. Brain. 1991 Jun;114(Pt 3):1473–1485. doi: 10.1093/brain/114.3.1473. [DOI] [PubMed] [Google Scholar]
- Playford E. D., Jenkins I. H., Passingham R. E., Nutt J., Frackowiak R. S., Brooks D. J. Impaired mesial frontal and putamen activation in Parkinson's disease: a positron emission tomography study. Ann Neurol. 1992 Aug;32(2):151–161. doi: 10.1002/ana.410320206. [DOI] [PubMed] [Google Scholar]
- Rascol O., Sabatini U., Chollet F., Celsis P., Montastruc J. L., Marc-Vergnes J. P., Rascol A. Supplementary and primary sensory motor area activity in Parkinson's disease. Regional cerebral blood flow changes during finger movements and effects of apomorphine. Arch Neurol. 1992 Feb;49(2):144–148. doi: 10.1001/archneur.1992.00530260044017. [DOI] [PubMed] [Google Scholar]
- Webster D. D. Critical analysis of the disability in Parkinson's disease. Mod Treat. 1968 Mar;5(2):257–282. [PubMed] [Google Scholar]
