Hostname: page-component-78c5997874-4rdpn Total loading time: 0 Render date: 2024-11-11T02:19:19.876Z Has data issue: false hasContentIssue false

Prevalence, incidence and risk factors of paratonia in patients with dementia: a one-year follow-up study

Published online by Cambridge University Press:  27 January 2011

Johannes S. M. Hobbelen*
Affiliation:
Dutch Institute of Allied Health Care, Amersfoort, The Netherlands Maastricht University, Research School CAPHRI, Maastricht, The Netherlands The Maastricht Institute of Mental Health and Neurosciences/Alzheimer Center Limburg, Maastricht University, Maastricht, The Netherlands Department of Epidemiology, Maastricht University, Maastricht, The Netherlands Institute for Human Movement Studies, Department of Physiotherapy, University of Applied Sciences Utrecht, The Netherlands
Frans E. S. Tan
Affiliation:
Maastricht University, Research School CAPHRI, Maastricht, The Netherlands Department of Methodology and Statistics, Maastricht University, The Netherlands
Frans R. J. Verhey
Affiliation:
The Maastricht Institute of Mental Health and Neurosciences/Alzheimer Center Limburg, Maastricht University, Maastricht, The Netherlands Maastricht University Hospital / Alzheimer Center, Limburg, The Netherlands
Raymond T. C. M. Koopmans
Affiliation:
Department of Primary and Community Care. Center for Family Medicine, Geriatric Care and Public Health, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands
Rob A. de Bie
Affiliation:
Maastricht University, Research School CAPHRI, Maastricht, The Netherlands Department of Epidemiology, Maastricht University, Maastricht, The Netherlands
*
Correspondence should be addressed to: Hans Hobbelen, PhD, PT, PO Box 616, 6200 MD Maastricht, The Netherlands. Phone: +31-43-3882366; Fax: +31-43-3884128. Email: Hans.Hobbelen@EPID.unimaas.nl and hhobbelen@iae.nl.

Abstract

Background: Paratonia is a progressive motor problem that is observed in individuals with dementia and is not a well-known phenomenon. This study explores the development and risk factors of paratonia in moderate stage dementia patients.

Methods: A multi-center, longitudinal, one-year follow-up cohort study was performed. Patients with an established diagnosis of dementia, with a score of 6 or lower on the Global Deterioration Scale (GDS) were included. The participants were assessed using the Paratonia Assessment Instrument (PAI), the Timed Up and GO test, the Qualidem, the Global Deterioration Scale (Reisberg et al., 1982) and the Mini-mental State Examination. Information about each patient's diagnosis of dementia, comorbidities and use of medication were obtained from the participant's medical file. The PAI was assessed every three months, the other variables at baseline and after 12 months. Cross-tabulation χ2 and logistic regression tests were used for the statistical analyses.

Results: Baseline measures were assessed in the 204 participants – 111 (54%) female and 93 (46%) male, with a mean age of 79.8 years (56–97). Seventy-one patients (34.8%) were diagnosed with paratonia at baseline, and 51 patients developed paratonia over one year. The highest hazard ratio (3.1) for developing paratonia within one year was observed in the vascular dementia group. The logistic regression analysis revealed that the presence of diabetes mellitus (OR = 10.7) was significantly related to the development of paratonia (Wald χ2 p-value < 0.01).

Conclusions: Diabetes mellitus and likely vascular damage are risk factors for the development of paratonia.

Type
Research Article
Copyright
Copyright © International Psychogeriatric Association 2011

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

American Psychiatric Association (1994). Diagnostic and Statistical Manual of Mental Disorders (DSM-IV). Washington, DC: American Psychiatric Association.Google Scholar
Araki, A. and Ito, H. (2009). Diabetes mellitus and geriatric syndromes.Geriatrics and Gerontology International, 9, 105114.Google Scholar
Arvanitakis, Z., Wilson, R. S., Schneider, J. A., Bienias, J. L., Evans, D. A. and Bennett, D. A. (2004). Diabetes mellitus and progression of rigidity and gait disturbance in older persons. Neurology, 63, 9961001.Google Scholar
Arvanitakis, Z., Wilson, R. S., Bienias, J. L. and Bennett, D. A. (2007). Diabetes and parkinsonian signs in older persons. Alzheimer Disease and Associated Disorders, 21, 144149.Google Scholar
Beversdorf, D. Q. and Heilman, K. M. (1998). Facilitory paratonia and frontal lobe functioning. Neurology, 51, 968971.Google Scholar
Chodzko-Zajko, W. J. et al. (2009). American College of Sports Medicine position stand: exercise and physical activity for older adults. Medicine and Science in Sports and Exercise, 41, 15101530.Google Scholar
Ettema, T. P., Droes, R. M., de Lange, J., Mellenbergh, G. J. and Ribbe, M. W. (2007). QUALIDEM: development and evaluation of a dementia specific quality of life instrument – validation. International Journal of Geriatric Psychiatry, 22, 424430.Google Scholar
Folstein, M. F., Folstein, S. E. and McHugh, P. R. (1975). “Mini-mental state”: a practical method for grading the cognitive state of patients for the clinician. Journal of Psychiatry Research, 12, 189198.Google Scholar
Franssen, E. H., Kluger, A., Torossian, C. L. and Reisberg, B. (1993). The neurologic syndrome of severe Alzheimer's disease: relationship to functional decline. Archives of Neurology, 50, 10291039.Google Scholar
Hobbelen, J., de Bie, R. and van Rossum, E. (2003). Effect of passive movement on severity of paratonia: a partially blinded, randomized clinical trial. Nederlands Tijdschrift voor Fysiotherapie, 113, 132137.Google Scholar
Hobbelen, J. S., Koopmans, R. T., Verhey, F. R., van Peppen, R. P. and de Bie, R. A. (2006). Paratonia: a delphi procedure for consensus definition. Journal of Geriatric Physical Therapy, 29, 5056.Google Scholar
Hobbelen, J. S., Koopmans, R. T., Verhey, F. R., Habraken, K. M. and de Bie, R. A. (2008). Diagnosing paratonia in the demented elderly: reliability and validity of the Paratonia Assessment Instrument (PAI). International Psychogeriatrics, 20, 840852.Google Scholar
Kurlan, R., Richard, I. H., Papka, M. and Marshall, F. (2000). Movement disorders in Alzheimer's disease: more rigidity of definitions is needed. Movement Disorders, 15, 2429.Google Scholar
McKeith, I. G. et al. (1996). Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB): report of the consortium on DLB international workshop. Neurology, 47, 11131124.Google Scholar
McKhann, G., Drachman, D., Folstein, M., Katzman, R., Price, D. and Stadlan, E. M. (1984). Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease. Neurology, 34, 939944.Google Scholar
Mourey, F., Manckoundia, P., Martin-Arveux, I., Tavernier-Vidal, B. and Pfitzenmeyer, P. (2004). Psychomotor disadaptation syndrome: a new clinical entity in geriatric patients. Geriatrics, 59, 2024.Google Scholar
O'Keeffe, S. T., Kazeem, H., Philpott, R. M., Playfer, J. R., Gosney, M. and Lye, M. (1996). Gait disturbance in Alzheimer's disease: a clinical study. Age and Ageing, 25, 313316.Google Scholar
Podsiadlo, D. and Richardson, S. (1991). The timed “Up & Go”: a test of basic functional mobility for frail elderly persons. Journal of the American Geriatrics Society, 39, 142148.Google Scholar
Prehogan, A. and Cohen, C. I. (2004). Motor dysfunction in dementias. Geriatrics, 59, 5360.Google Scholar
Reisberg, B., Ferris, S. H., de Leon, M. J. and Crook, T. (1982). The Global Deterioration Scale for assessment of primary degenerative dementia. American Journal of psychiatry, 139, 11361139.Google Scholar
Ries, J. D., Echternach, J. L., Nof, L. and Gagnon Blodgett, M. (2009). Test-retest reliability and minimal detectable change scores for the timed “up & go” test, the six-minute walk test, and gait speed in people with Alzheimer disease. Physical Therapy, 89, 569579.Google Scholar
Risse, S. C. et al. (1990). Myoclonus, seizures, and paratonia in Alzheimer disease. Alzheimer Disease and Associated Disorders, 4, 217225.Google Scholar
Román, G. C. et al. (1993). Vascular dementia: diagnostic criteria for research studies. Report of the NINDS-AIREN International Workshop. Neurology, 43, 250260.Google Scholar
Sigal, R. J., Kenny, G. P., Wasserman, D. H., Castaneda-Sceppa, C. and White, R. D. (2006). Physical activity/exercise and type 2 diabetes: a consensus statement from the American Diabetes Association. Diabetes Care, 29, 14331438.Google Scholar
Skrbo, A., Begović, B. and Skrbo, S. (2004). [Classification of drugs using the ATC system and the latest changes]. Medicinski Arhive, 58 (Suppl. 2), 138141.Google Scholar
Soininen, H., Laulumaa, V., Helkala, E. L., Hartikainen, P. and Riekkinen, P. J. (1992). Extrapyramidal signs in Alzheimer's disease: a 3-year follow-up study. Journal of Neural Transmission, 4, 107119.Google Scholar
Sonnen, J. A. et al. (2009). Different patterns of cerebral injury in dementia with or without diabetes. Archives of Neurology, 66, 315322.Google Scholar
Souren, L. E., Franssen, E. H. and Reisberg, B. (1997). Neuromotor changes in Alzheimer's disease: implications for patient care. Journal of Geriatric Psychiatry and Neurology, 10, 9398.Google Scholar
Stevens, T., Livingston, G., Kitchen, G., Manela, M., Walker, Z. and Katona, C. (2002). Islington study of dementia subtypes in the community. British Journal of Psychiatry, 180, 270276.Google Scholar
Tyrrell, P. J. et al. (1990). Clinical and positron emission tomographic studies in the “extrapyramidal syndrome” of dementia of the Alzheimer type. Archives of Neurology, 47, 13181323.Google Scholar
Ulrich, P. and Cerami, A. (2001). Protein glycation, diabetes, and aging. Recent Progress in Hormone Research, 56, 121.Google Scholar
Vahia, I., Cohen, C. I., Prehogan, A. and Memon, Z. (2007). Prevalence and impact of paratonia in Alzheimer disease in a multiracial sample. American Journal of Geriatric Psychiatry, 15, 351353.Google Scholar