Nonlinear dynamic analysis of oscillatory repetitive movements in Parkinson's disease and essential tremor

Uncertainty exists on whether Parkinson's disease (PD) and essential tremor (ET) patients have similar degree of impairment during motor tasks. We investigated this problem by analyzing nonlinear dynamics of repetitive movements in 21 control subjects, 33 mild‐moderate PD patients, and 18 ET pa...

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Published inMovement disorders Vol. 25; no. 15; pp. 2577 - 2586
Main Authors Costa, João, González, Hernán A., Valldeoriola, Francesc, Gaig, Carles, Tolosa, Eduardo, Valls-Solé, Josep
Format Journal Article Publication
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 15.11.2010
Wiley
Wiley Subscription Services, Inc
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ISSN0885-3185
1531-8257
1531-8257
DOI10.1002/mds.23334

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Abstract Uncertainty exists on whether Parkinson's disease (PD) and essential tremor (ET) patients have similar degree of impairment during motor tasks. We investigated this problem by analyzing nonlinear dynamics of repetitive movements in 21 control subjects, 33 mild‐moderate PD patients, and 18 ET patients. Accelerometer signals were recorded during finger tapping and unbounded forearm movements between two points, and processed with moving average filtering to generate a new signal consisting of the temporal distance between consecutive cycles. We calculated: mean interpeak interval (slowness), interpeak interval variability (irregularity), and beat decay (BD) of the auto mutual information (AMI) value, which estimates signal predictability by measuring the loss of signal information over a timescale. Both PD and ET had longer interpeak interval (except for finger tapping), higher interpeak interval variability, and higher BD‐AMI values than controls (P ≤ 0.007, all comparisons). ET patients had higher BD‐AMI values than PD (P = 0.003). BD‐AMI was the parameter that discriminated better between subjects (diagnosis accuracies about 80%). No differences existed between PD patients with and without tremor or between PD or ET patients with different disease stages, for any parameter. Evaluation of nonlinear dynamics of oscillatory repetitive movements is a feasible and promising tool for studying movement physiology. Movement performance is more predictable in PD and ET than in controls, even in early disease stages. Slowness and irregularity of movement in PD and ET cannot be fully explained by tremor. Some common pathogenic mechanisms leading to bradykinesia may contribute to this impairment. © 2010 Movement Disorder Society
AbstractList Peer Reviewed
Uncertainty exists on whether Parkinson's disease (PD) and essential tremor (ET) patients have similar degree of impairment during motor tasks. We investigated this problem by analyzing nonlinear dynamics of repetitive movements in 21 control subjects, 33 mild‐moderate PD patients, and 18 ET patients. Accelerometer signals were recorded during finger tapping and unbounded forearm movements between two points, and processed with moving average filtering to generate a new signal consisting of the temporal distance between consecutive cycles. We calculated: mean interpeak interval (slowness), interpeak interval variability (irregularity), and beat decay (BD) of the auto mutual information (AMI) value, which estimates signal predictability by measuring the loss of signal information over a timescale. Both PD and ET had longer interpeak interval (except for finger tapping), higher interpeak interval variability, and higher BD‐AMI values than controls ( P ≤ 0.007, all comparisons). ET patients had higher BD‐AMI values than PD ( P = 0.003). BD‐AMI was the parameter that discriminated better between subjects (diagnosis accuracies about 80%). No differences existed between PD patients with and without tremor or between PD or ET patients with different disease stages, for any parameter. Evaluation of nonlinear dynamics of oscillatory repetitive movements is a feasible and promising tool for studying movement physiology. Movement performance is more predictable in PD and ET than in controls, even in early disease stages. Slowness and irregularity of movement in PD and ET cannot be fully explained by tremor. Some common pathogenic mechanisms leading to bradykinesia may contribute to this impairment. © 2010 Movement Disorder Society
Uncertainty exists on whether Parkinson's disease (PD) and essential tremor (ET) patients have similar degree of impairment during motor tasks. We investigated this problem by analyzing nonlinear dynamics of repetitive movements in 21 control subjects, 33 mild-moderate PD patients, and 18 ET patients. Accelerometer signals were recorded during finger tapping and unbounded forearm movements between two points, and processed with moving average filtering to generate a new signal consisting of the temporal distance between consecutive cycles. We calculated: mean interpeak interval (slowness), interpeak interval variability (irregularity), and beat decay (BD) of the auto mutual information (AMI) value, which estimates signal predictability by measuring the loss of signal information over a timescale. Both PD and ET had longer interpeak interval (except for finger tapping), higher interpeak interval variability, and higher BD-AMI values than controls (P ≤ 0.007, all comparisons). ET patients had higher BD-AMI values than PD (P = 0.003). BD-AMI was the parameter that discriminated better between subjects (diagnosis accuracies about 80%). No differences existed between PD patients with and without tremor or between PD or ET patients with different disease stages, for any parameter. Evaluation of nonlinear dynamics of oscillatory repetitive movements is a feasible and promising tool for studying movement physiology. Movement performance is more predictable in PD and ET than in controls, even in early disease stages. Slowness and irregularity of movement in PD and ET cannot be fully explained by tremor. Some common pathogenic mechanisms leading to bradykinesia may contribute to this impairment.Uncertainty exists on whether Parkinson's disease (PD) and essential tremor (ET) patients have similar degree of impairment during motor tasks. We investigated this problem by analyzing nonlinear dynamics of repetitive movements in 21 control subjects, 33 mild-moderate PD patients, and 18 ET patients. Accelerometer signals were recorded during finger tapping and unbounded forearm movements between two points, and processed with moving average filtering to generate a new signal consisting of the temporal distance between consecutive cycles. We calculated: mean interpeak interval (slowness), interpeak interval variability (irregularity), and beat decay (BD) of the auto mutual information (AMI) value, which estimates signal predictability by measuring the loss of signal information over a timescale. Both PD and ET had longer interpeak interval (except for finger tapping), higher interpeak interval variability, and higher BD-AMI values than controls (P ≤ 0.007, all comparisons). ET patients had higher BD-AMI values than PD (P = 0.003). BD-AMI was the parameter that discriminated better between subjects (diagnosis accuracies about 80%). No differences existed between PD patients with and without tremor or between PD or ET patients with different disease stages, for any parameter. Evaluation of nonlinear dynamics of oscillatory repetitive movements is a feasible and promising tool for studying movement physiology. Movement performance is more predictable in PD and ET than in controls, even in early disease stages. Slowness and irregularity of movement in PD and ET cannot be fully explained by tremor. Some common pathogenic mechanisms leading to bradykinesia may contribute to this impairment.
Uncertainty exists on whether Parkinson's disease (PD) and essential tremor (ET) patients have similar degree of impairment during motor tasks. We investigated this problem by analyzing nonlinear dynamics of repetitive movements in 21 control subjects, 33 mild-moderate PD patients, and 18 ET patients. Accelerometer signals were recorded during finger tapping and unbounded forearm movements between two points, and processed with moving average filtering to generate a new signal consisting of the temporal distance between consecutive cycles. We calculated: mean interpeak interval (slowness), interpeak interval variability (irregularity), and beat decay (BD) of the auto mutual information (AMI) value, which estimates signal predictability by measuring the loss of signal information over a timescale. Both PD and ET had longer interpeak interval (except for finger tapping), higher interpeak interval variability, and higher BD-AMI values than controls (P less than or equal to 0.007, all comparisons). ET patients had higher BD-AMI values than PD (P = 0.003). BD-AMI was the parameter that discriminated better between subjects (diagnosis accuracies about 80%). No differences existed between PD patients with and without tremor or between PD or ET patients with different disease stages, for any parameter. Evaluation of nonlinear dynamics of oscillatory repetitive movements is a feasible and promising tool for studying movement physiology. Movement performance is more predictable in PD and ET than in controls, even in early disease stages. Slowness and irregularity of movement in PD and ET cannot be fully explained by tremor. Some common pathogenic mechanisms leading to bradykinesia may contribute to this impairment. copyright 2010 Movement Disorder Society
Uncertainty exists on whether Parkinson's disease (PD) and essential tremor (ET) patients have similar degree of impairment during motor tasks. We investigated this problem by analyzing nonlinear dynamics of repetitive movements in 21 control subjects, 33 mild-moderate PD patients, and 18 ET patients. Accelerometer signals were recorded during finger tapping and unbounded forearm movements between two points, and processed with moving average filtering to generate a new signal consisting of the temporal distance between consecutive cycles. We calculated: mean interpeak interval (slowness), interpeak interval variability (irregularity), and beat decay (BD) of the auto mutual information (AMI) value, which estimates signal predictability by measuring the loss of signal information over a timescale. Both PD and ET had longer interpeak interval (except for finger tapping), higher interpeak interval variability, and higher BD-AMI values than controls (P ≤ 0.007, all comparisons). ET patients had higher BD-AMI values than PD (P = 0.003). BD-AMI was the parameter that discriminated better between subjects (diagnosis accuracies about 80%). No differences existed between PD patients with and without tremor or between PD or ET patients with different disease stages, for any parameter. Evaluation of nonlinear dynamics of oscillatory repetitive movements is a feasible and promising tool for studying movement physiology. Movement performance is more predictable in PD and ET than in controls, even in early disease stages. Slowness and irregularity of movement in PD and ET cannot be fully explained by tremor. Some common pathogenic mechanisms leading to bradykinesia may contribute to this impairment.
Uncertainty exists on whether Parkinson's disease (PD) and essential tremor (ET) patients have similar degree of impairment during motor tasks. We investigated this problem by analyzing nonlinear dynamics of repetitive movements in 21 control subjects, 33 mild-moderate PD patients, and 18 ET patients. Accelerometer signals were recorded during finger tapping and unbounded forearm movements between two points, and processed with moving average filtering to generate a new signal consisting of the temporal distance between consecutive cycles. We calculated: mean interpeak interval (slowness), interpeak interval variability (irregularity), and beat decay (BD) of the auto mutual information (AMI) value, which estimates signal predictability by measuring the loss of signal information over a timescale. Both PD and ET had longer interpeak interval (except for finger tapping), higher interpeak interval variability, and higher BD-AMI values than controls (P ≤ 0.007, all comparisons). ET patients had higher BD-AMI values than PD (P = 0.003). BD-AMI was the parameter that discriminated better between subjects (diagnosis accuracies about 80%). No differences existed between PD patients with and without tremor or between PD or ET patients with different disease stages, for any parameter. Evaluation of nonlinear dynamics of oscillatory repetitive movements is a feasible and promising tool for studying movement physiology. Movement performance is more predictable in PD and ET than in controls, even in early disease stages. Slowness and irregularity of movement in PD and ET cannot be fully explained by tremor. Some common pathogenic mechanisms leading to bradykinesia may contribute to this impairment. © 2010 Movement Disorder Society [PUBLICATION ABSTRACT]
Author Costa, João
Valldeoriola, Francesc
Gaig, Carles
Tolosa, Eduardo
González, Hernán A.
Valls-Solé, Josep
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Issue 15
Keywords Nervous system diseases
Parkinson's disease
Tremor
Parkinson disease
Involuntary movement
Cerebral disorder
Neurophysiology
Central nervous system disease
Signal processing
Nonlinearity
essential tremor
Degenerative disease
Neurological disorder
nonlinear dynamics
Extrapyramidal syndrome
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
CC BY 4.0
2010 Movement Disorder Society.
cc-by-nc-nd
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Notes Aircraft Medical (former Morpheus Medical)
Potential conflict of interest: Nothing to report.
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PublicationCentury 2000
PublicationDate 15 November 2010
PublicationDateYYYYMMDD 2010-11-15
PublicationDate_xml – month: 11
  year: 2010
  text: 15 November 2010
  day: 15
PublicationDecade 2010
PublicationPlace Hoboken
PublicationPlace_xml – name: Hoboken
– name: Hoboken, NJ
– name: United States
PublicationTitle Movement disorders
PublicationTitleAlternate Mov. Disord
PublicationYear 2010
Publisher Wiley Subscription Services, Inc., A Wiley Company
Wiley
Wiley Subscription Services, Inc
Publisher_xml – name: Wiley Subscription Services, Inc., A Wiley Company
– name: Wiley
– name: Wiley Subscription Services, Inc
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Hughes AJ,Daniel SE,Kilford L,Lees AJ. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinicopathologicalstudy of 100 cases. J Neurol Neurosurg Psychiatry 1992; 55: 181-184.
Bonett DG,Price RM. Statistical inference for a linear function of medians: confidence intervals, hypothesis testing, and sample size requirements. Psychol Methods 2002; 7: 370-383.
Louis ED,Levy G,Cote LJ,Mejia H,Fahn S,Marder K. Clinical correlates of action tremor in Parkinson disease. Arch Neurol 2001; 58: 1630-1634.
Elble RJ,Higgins C,Hughes L. Essential tremor entrains rapid voluntary movements. Exp Neurol 1994; 126: 138-143.
Farkas Z,Szirmai I,Kamondi A. Impaired rhythm generation in essential tremor. Mov Disord 2006; 21: 1196-1199.
Jankovic J. Parkinson's disease: clinical features and diagnosis. JNeurol Neurosurg Psychiatry 2008; 79: 368-376.
Yang M,Zhang H,Zheng H,Wang H,Lin Q. Mutual information-based approach to the analysis of dynamic electrocardiograms. Technol Health Care 2008; 16: 367-375.
Breit S,Spieker S,Schulz JB,Gasser T. Long-term EMG recordings differentiate between parkinsonian and essential tremor. J Neurol 2008; 255: 103-111.
Jiménez-Jiménez FJ,Rubio L,Alonso-Navarro H et al. Impairment of rapid repetitive finger movements and visual reaction time in patients with essential tremor. Eur J Neurol 2010; 17: 152-159.
Gómez C,Hornero R,Fernández A,Abasolo D,Escudero J,López M. Magnetoencephalogram background activity analysis in Alzheimer's disease patients using auto mutual information. Conf Proc IEEE Eng Med Biol Soc 2006; 1: 6181-6184.
Montgomery EB,Jr,Baker KB,Lyons K,Koller WC. Motor initiation and execution in essential tremor and Parkinson's disease. Mov Disord 2000; 15: 511-515.
Deuschl G. Neurophysiological tests for the assessments of tremors. Adv Neurol 1999; 80: 57-65
Nakamura R,Nagasaki H,Narabayashi H. Disturbances of rhythm formation in patients with Parkinson's disease. I. Characteristics of tapping response to the periodic signals. Percept Mot Skills 1978; 46: 63-75.
Novellino F,Arabia G,Bagnato A, et al. Combined use of DAT-SPECT and cardiac MIBG scintigraphy in mixed tremors. Mov Disord 2009; 24: 2242-2248.
Hedera P,Fang JY,Phibbs F,Cooper MK,Charles PD,Davis TL. Positive family history of essential tremor influences the motor phenotype of Parkinson's disease. Mov Disord 2009; 24: 2285-2288.
Lauk M,Timmer J,Guschlbauer B,Hellwig B,Lücking CH. Variability of frequency and phase between antagonistic muscle pairs in pathological human tremors. Muscle Nerve 2001; 24: 1365-1370.
Pereda E,Quiroga RQ,Bhattacharya J. Non-linear multivariate analysis of neurophysiological signals. Prog Neurobiol 2005; 77: 1-37.
Burne JA,Hayes MW,Fung VS,Yiannikas C,Boljevac D. The contribution of tremor studies to diagnosis of parkinsonian and essential tremor: a statistical evaluation. J Clin Neurosci 2002; 9: 237-242.
Héroux ME,Parisi SL,Larocerie-Salgado J,Norman KE. Upper-extremity disability in essential tremor. Arch Phys Med Rehabil 2006; 87: 661-670.
Ozekmekçi S,Kiziltan G,Vural M,Ertan S,Apaydin H,Erginöz E. Assessment of movement time in patients with essential tremor. J Neurol 2005; 252: 964-967.
Catafau AM,Tolosa E. Impact of dopamine transporter SPECT using 123I-Ioflupane on diagnosis and management of patients with clinically uncertain Parkinsonian syndromes. Mov Disord 2004; 19: 1175-1182.
Swets JA. Measuring the accuracy of diagnostic systems. Science 1988; 240: 1285-1293.
Flowers K. Ballistic and corrective movements on an aiming task. Intention tremor and parkinsonian movement disorders compared. Neurology 1975; 25: 413-421.
Tan EK,Lee SS,Fook-Chong S,Lum SY. Evidence of increased odds of essential tremor in Parkinson's disease. Mov Disord 2008; 23: 993-997.
Machowska-Majchrzak A,Pierzchała K,Pietraszek S. Analysis of selected parameters of tremor recorded by a biaxial accelerometer in patients with parkinsonian tremor, essential tremor and cerebellar tremor. Neurol Neurochir Pol 2007; 41: 241-250.
Tolosa E,Wenning G,Poewe W. The diagnosis of Parkinson's disease. Lancet Neurol 2006; 5: 75-86.
Ahlstrom C,Ask P,Rask P, et al. Assessment of suspected aortic stenosis by auto mutual information analysis of murmurs. Conf Proc IEEE Eng Med Biol Soc 2007; 2007: 1945-1948.
Jeong J,Gore JC,Peterson BS. Mutual information analysis of the EEG in patients with Alzheimer's disease. Clin Neurophysiol 2001; 112: 827-835.
Molnar GF,Pilliar A,Lozano AM,Dostrovsky JO. Differences in neuronal firing rates in pallidal and cerebellar receiving areas of thalamus in patients with Parkinson's disease, essential tremor, and pain. J Neurophysiol 2005; 93: 3094-3101.
Na SH,Jin SH,Kim SY,Ham BJ. EEG in schizophrenic patients: mutual information analysis. Clin Neurophysiol 2002; 113: 1954-1960.
Hornero R,Abásolo D,Escudero J,Gómez C. Non-linear analysis of electroencephalogram and magnetoencephalogram recordings in patients with Alzheimer's disease. Philos Transact A Math Phys Eng Sci 2009; 367: 317-336.
Escudero J,Hornero R,Abasolo D,Lopez M. On the application of the auto mutual information rate of decrease to biomedical signals. Conf Proc IEEE Eng Med Biol Soc 2008; 2008: 2137-2140.
Tamás G,Pálvölgyi L,Takáts A,Szirmai I,Kamondi A. Delayed beta synchronization after movement of the more affected hand in essential tremor. Neurosci Lett 2006; 405: 246-251.
Benito-León J,Louis ED. Essential tremor: emerging views of a common disorder. Nat Clin Pract Neurol 2006; 2: 666-678.
Hoyer D,Leder U,Hoyer H,Pompe B,Sommer M,Zwiener U. Mutual information and phase dependencies: measures of reduced non-linear cardiorespiratory interactions after myocardial infarction. Med Eng Phys 2002; 24: 33-43.
Deuschl G,Elble R. Essential tremor-neurodegenerative or nondegenerative disease towards a working definition of ET. Mov Disord 2009; 24: 2033-2041.
Duval C,Sadikot AF,Panisset M. The detection of tremor during slow alternating movements performed by patients with early Parkinson's disease. Exp Brain Res 2004; 154: 395-398.
Pompe B. Measuring statistical dependences in a time series. J Stat Phys 1993; 73: 587-610.
Abásolo D,Escudero J,Hornero R,Gómez C,Espino P. Approximate entropy and auto mutual information analysis of the electroencephalogram in Alzheimer's disease patients. Med Biol Eng Comput 2008; 46: 1019-1028.
Farkas Z,Csillik A,Szirmai I,Kamondi A. Asymmetry of tremor intensity and frequency in Parkinson's disease and essential tremor. Parkinsonism Relat Disord 2006; 12: 49-55.
Fraser AM,Swinney HL. Independent coordinates for strange attractors from mutual information. Phys Rev A 1986; 33: 1134-1140.
Louis ED. Essential tremors: a family of neurodegenerative disorders? Arch Neurol 2009; 66: 1202-1208.
Louis ED,Ford B,Bismuth B. Reliability between two observers using a protocol for diagnosing essential tremor. Mov Disord 1998; 13: 287-293.
Stelmach GE,Worringham CJ. The preparation and production of isometric force in Parkinson's disease. Neuropsychologia 1988; 26: 93-104.
Stam CJ. Non-linear dynamical analysis of EEG and MEG: review of an emerging field. Clin Neurophysiol 2005; 116: 2266-2301.
Louis ED,Frucht SJ. Prevalence of essential tremor in patients with Parkinson's disease vs. Parkinson-plus syndromes. Mov Disord 2007; 22: 1402-1407.
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2009; 66
2009; 24
2005; 252
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2006; 12
2010; 17
1986; 33
2002; 113
2005; 116
2002; 7
2008; 16
2006; 5
2008; 79
1993
1988; 240
2006; 1
2006; 2
1991
1999; 80
2001; 24
1992; 55
2008; 2008
2004; 154
2001; 112
2006; 405
1994; 126
1993; 73
2000; 15
2004; 19
2006; 21
2006; 87
2007; 2007
1988; 26
2002; 24
2006; 1115
2008; 23
1975; 25
2008; 46
2005; 93
2007; 41
1978; 46
2008; 255
2007; 22
2001; 58
2005; 77
2009; 367
1998; 13
e_1_2_7_5_2
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Yang M (e_1_2_7_42_2) 2008; 16
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Machowska‐Majchrzak A (e_1_2_7_8_2) 2007; 41
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Fahn S (e_1_2_7_30_2) 1993
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Gómez C (e_1_2_7_44_2) 2006; 1
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Ahlstrom C (e_1_2_7_38_2) 2007; 2007
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Escudero J (e_1_2_7_36_2) 2008; 2008
Deuschl G (e_1_2_7_6_2) 1999; 80
References_xml – reference: Hedera P,Fang JY,Phibbs F,Cooper MK,Charles PD,Davis TL. Positive family history of essential tremor influences the motor phenotype of Parkinson's disease. Mov Disord 2009; 24: 2285-2288.
– reference: Deuschl G,Elble R. Essential tremor-neurodegenerative or nondegenerative disease towards a working definition of ET. Mov Disord 2009; 24: 2033-2041.
– reference: Héroux ME,Parisi SL,Larocerie-Salgado J,Norman KE. Upper-extremity disability in essential tremor. Arch Phys Med Rehabil 2006; 87: 661-670.
– reference: Pompe B. Measuring statistical dependences in a time series. J Stat Phys 1993; 73: 587-610.
– reference: Louis ED. Essential tremors: a family of neurodegenerative disorders? Arch Neurol 2009; 66: 1202-1208.
– reference: Gómez C,Hornero R,Fernández A,Abasolo D,Escudero J,López M. Magnetoencephalogram background activity analysis in Alzheimer's disease patients using auto mutual information. Conf Proc IEEE Eng Med Biol Soc 2006; 1: 6181-6184.
– reference: Pereda E,Quiroga RQ,Bhattacharya J. Non-linear multivariate analysis of neurophysiological signals. Prog Neurobiol 2005; 77: 1-37.
– reference: Farkas Z,Szirmai I,Kamondi A. Impaired rhythm generation in essential tremor. Mov Disord 2006; 21: 1196-1199.
– reference: Tan EK,Lee SS,Fook-Chong S,Lum SY. Evidence of increased odds of essential tremor in Parkinson's disease. Mov Disord 2008; 23: 993-997.
– reference: Jeong J,Gore JC,Peterson BS. Mutual information analysis of the EEG in patients with Alzheimer's disease. Clin Neurophysiol 2001; 112: 827-835.
– reference: Swets JA. Measuring the accuracy of diagnostic systems. Science 1988; 240: 1285-1293.
– reference: Louis ED,Frucht SJ. Prevalence of essential tremor in patients with Parkinson's disease vs. Parkinson-plus syndromes. Mov Disord 2007; 22: 1402-1407.
– reference: Catafau AM,Tolosa E. Impact of dopamine transporter SPECT using 123I-Ioflupane on diagnosis and management of patients with clinically uncertain Parkinsonian syndromes. Mov Disord 2004; 19: 1175-1182.
– reference: Hoyer D,Leder U,Hoyer H,Pompe B,Sommer M,Zwiener U. Mutual information and phase dependencies: measures of reduced non-linear cardiorespiratory interactions after myocardial infarction. Med Eng Phys 2002; 24: 33-43.
– reference: Deuschl G. Neurophysiological tests for the assessments of tremors. Adv Neurol 1999; 80: 57-65
– reference: Tolosa E,Wenning G,Poewe W. The diagnosis of Parkinson's disease. Lancet Neurol 2006; 5: 75-86.
– reference: Escudero J,Hornero R,Abasolo D,Lopez M. On the application of the auto mutual information rate of decrease to biomedical signals. Conf Proc IEEE Eng Med Biol Soc 2008; 2008: 2137-2140.
– reference: Tamás G,Pálvölgyi L,Takáts A,Szirmai I,Kamondi A. Delayed beta synchronization after movement of the more affected hand in essential tremor. Neurosci Lett 2006; 405: 246-251.
– reference: Louis ED,Ford B,Bismuth B. Reliability between two observers using a protocol for diagnosing essential tremor. Mov Disord 1998; 13: 287-293.
– reference: Na SH,Jin SH,Kim SY,Ham BJ. EEG in schizophrenic patients: mutual information analysis. Clin Neurophysiol 2002; 113: 1954-1960.
– reference: Benito-León J,Louis ED. Essential tremor: emerging views of a common disorder. Nat Clin Pract Neurol 2006; 2: 666-678.
– reference: Stam CJ. Non-linear dynamical analysis of EEG and MEG: review of an emerging field. Clin Neurophysiol 2005; 116: 2266-2301.
– reference: Jankovic J. Parkinson's disease: clinical features and diagnosis. JNeurol Neurosurg Psychiatry 2008; 79: 368-376.
– reference: Jiménez-Jiménez FJ,Rubio L,Alonso-Navarro H et al. Impairment of rapid repetitive finger movements and visual reaction time in patients with essential tremor. Eur J Neurol 2010; 17: 152-159.
– reference: Louis ED,Levy G,Cote LJ,Mejia H,Fahn S,Marder K. Clinical correlates of action tremor in Parkinson disease. Arch Neurol 2001; 58: 1630-1634.
– reference: Duval C,Sadikot AF,Panisset M. The detection of tremor during slow alternating movements performed by patients with early Parkinson's disease. Exp Brain Res 2004; 154: 395-398.
– reference: Flowers K. Ballistic and corrective movements on an aiming task. Intention tremor and parkinsonian movement disorders compared. Neurology 1975; 25: 413-421.
– reference: Breit S,Spieker S,Schulz JB,Gasser T. Long-term EMG recordings differentiate between parkinsonian and essential tremor. J Neurol 2008; 255: 103-111.
– reference: Hughes AJ,Daniel SE,Kilford L,Lees AJ. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinicopathologicalstudy of 100 cases. J Neurol Neurosurg Psychiatry 1992; 55: 181-184.
– reference: Bonett DG,Price RM. Statistical inference for a linear function of medians: confidence intervals, hypothesis testing, and sample size requirements. Psychol Methods 2002; 7: 370-383.
– reference: Hornero R,Abásolo D,Escudero J,Gómez C. Non-linear analysis of electroencephalogram and magnetoencephalogram recordings in patients with Alzheimer's disease. Philos Transact A Math Phys Eng Sci 2009; 367: 317-336.
– reference: Lauk M,Timmer J,Guschlbauer B,Hellwig B,Lücking CH. Variability of frequency and phase between antagonistic muscle pairs in pathological human tremors. Muscle Nerve 2001; 24: 1365-1370.
– reference: Stelmach GE,Worringham CJ. The preparation and production of isometric force in Parkinson's disease. Neuropsychologia 1988; 26: 93-104.
– reference: Montgomery EB,Jr,Baker KB,Lyons K,Koller WC. Motor initiation and execution in essential tremor and Parkinson's disease. Mov Disord 2000; 15: 511-515.
– reference: Elble RJ,Higgins C,Hughes L. Essential tremor entrains rapid voluntary movements. Exp Neurol 1994; 126: 138-143.
– reference: Machowska-Majchrzak A,Pierzchała K,Pietraszek S. Analysis of selected parameters of tremor recorded by a biaxial accelerometer in patients with parkinsonian tremor, essential tremor and cerebellar tremor. Neurol Neurochir Pol 2007; 41: 241-250.
– reference: Novellino F,Arabia G,Bagnato A, et al. Combined use of DAT-SPECT and cardiac MIBG scintigraphy in mixed tremors. Mov Disord 2009; 24: 2242-2248.
– reference: Ahlstrom C,Ask P,Rask P, et al. Assessment of suspected aortic stenosis by auto mutual information analysis of murmurs. Conf Proc IEEE Eng Med Biol Soc 2007; 2007: 1945-1948.
– reference: Molnar GF,Pilliar A,Lozano AM,Dostrovsky JO. Differences in neuronal firing rates in pallidal and cerebellar receiving areas of thalamus in patients with Parkinson's disease, essential tremor, and pain. J Neurophysiol 2005; 93: 3094-3101.
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– reference: Farkas Z,Csillik A,Szirmai I,Kamondi A. Asymmetry of tremor intensity and frequency in Parkinson's disease and essential tremor. Parkinsonism Relat Disord 2006; 12: 49-55.
– reference: Burne JA,Hayes MW,Fung VS,Yiannikas C,Boljevac D. The contribution of tremor studies to diagnosis of parkinsonian and essential tremor: a statistical evaluation. J Clin Neurosci 2002; 9: 237-242.
– reference: Duval C,Sadikot AF,Panisset M. Bradykinesia in patients with essential tremor. Brain Res 2006; 1115: 213-216.
– reference: Fraser AM,Swinney HL. Independent coordinates for strange attractors from mutual information. Phys Rev A 1986; 33: 1134-1140.
– reference: Nakamura R,Nagasaki H,Narabayashi H. Disturbances of rhythm formation in patients with Parkinson's disease. I. Characteristics of tapping response to the periodic signals. Percept Mot Skills 1978; 46: 63-75.
– reference: Yang M,Zhang H,Zheng H,Wang H,Lin Q. Mutual information-based approach to the analysis of dynamic electrocardiograms. Technol Health Care 2008; 16: 367-375.
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– volume: 79
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  year: 2008
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  article-title: Parkinson's disease: clinical features and diagnosis
  publication-title: JNeurol Neurosurg Psychiatry
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Snippet Uncertainty exists on whether Parkinson's disease (PD) and essential tremor (ET) patients have similar degree of impairment during motor tasks. We investigated...
Peer Reviewed
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StartPage 2577
SubjectTerms Adult
Aged
Aged, 80 and over
Biological and medical sciences
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Enginyeria mecànica
essential tremor
Essential Tremor - physiopathology
Female
Fingers - physiopathology
Forearm - physiopathology
Humans
Male
Mechanical engineering
Medical research
Medical sciences
Middle Aged
Movement disorders
Neurology
neurophysiology
Nonlinear Dynamics
Parkinson Disease - physiopathology
Parkinson's disease
Parkinson, Malaltia de
Psychomotor Performance
signal processing
Signal Processing, Computer-Assisted
Statistics, Nonparametric
Tremor - physiopathology
Àrees temàtiques de la UPC
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Title Nonlinear dynamic analysis of oscillatory repetitive movements in Parkinson's disease and essential tremor
URI https://api.istex.fr/ark:/67375/WNG-80XFZ7BN-W/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fmds.23334
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