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Published in: Journal of Neurology 9/2016

Open Access 01-09-2016 | Original Communication

Variables associated with upper extremity function in patients with Duchenne muscular dystrophy

Authors: Mariska M. H. P. Janssen, Jan C. M. Hendriks, Alexander C. H. Geurts, Imelda J. M. de Groot

Published in: Journal of Neurology | Issue 9/2016

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Abstract

Preserving upper extremity (UE) function in patients with Duchenne muscular dystrophy (DMD) is extremely important as it is related to independence and quality of life. For clinical decision making, knowledge of variables associated with UE function is necessary. This knowledge is, however, limited. Therefore, this study aims to gain more insight into the variables associated with UE function in DMD. Data from an international web-based questionnaire on UE function, obtained from 213 DMD patients, were used. Six dependent variables regarding UE function were used in multivariable linear regression analyses. In addition, 26 independent variables regarding patient characteristics, medication, therapy, supportive aids, pain, stiffness and participation were used. Twelve independent variables showed a significant relation to UE function. Variables with a negative relation to UE function were: later disease stage, occurrence of scoliosis, higher age, use of UE splints, more frequent stiffness complaints, more limitations due to stiffness, more frequent elbow pain, and having physical therapy. A positive relation with UE function was seen for going to school or work, use of corticosteroids, higher BMI, and higher age at diagnosis. These variables explained 56–81 % of the variation of the different measures of UE function. Knowledge of variables associated with UE function is very important in the clinical management of DMD patients. The results of this study suggest that corticosteroid use and participation in school and work related activities are positively related to UE function in DMD patients, as well as reducing pain and stiffness and preventing scoliosis.
Literature
1.
go back to reference Balaban B, Matthews DJ, Clayton GH, Carry T (2005) Corticosteroid treatment and functional improvement in Duchenne muscular dystrophy: long-term effect. Am J Phys Med Rehabil 84:843–850CrossRefPubMed Balaban B, Matthews DJ, Clayton GH, Carry T (2005) Corticosteroid treatment and functional improvement in Duchenne muscular dystrophy: long-term effect. Am J Phys Med Rehabil 84:843–850CrossRefPubMed
2.
go back to reference Brooke MH, Griggs RC, Mendell JR, Fenichel GM, Shumate JB, Pellegrino RJ (1981) Clinical trial in Duchenne dystrophy. I. The design of the protocol. Muscle Nerve 4:186–197CrossRefPubMed Brooke MH, Griggs RC, Mendell JR, Fenichel GM, Shumate JB, Pellegrino RJ (1981) Clinical trial in Duchenne dystrophy. I. The design of the protocol. Muscle Nerve 4:186–197CrossRefPubMed
3.
go back to reference Bushby K, Finkel R, Birnkrant DJ, Case LE, Clemens PR, Cripe L, Kaul A, Kinnett K, McDonald C, Pandya S, Poysky J, Shapiro F, Tomezsko J, Constantin C (2010) Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management. Lancet Neurol 9:77–93CrossRefPubMed Bushby K, Finkel R, Birnkrant DJ, Case LE, Clemens PR, Cripe L, Kaul A, Kinnett K, McDonald C, Pandya S, Poysky J, Shapiro F, Tomezsko J, Constantin C (2010) Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management. Lancet Neurol 9:77–93CrossRefPubMed
4.
go back to reference Bushby K, Finkel R, Birnkrant DJ, Case LE, Clemens PR, Cripe L, Kaul A, Kinnett K, McDonald C, Pandya S, Poysky J, Shapiro F, Tomezsko J, Constantin C (2010) Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care. Lancet Neurol 9:177–189CrossRefPubMed Bushby K, Finkel R, Birnkrant DJ, Case LE, Clemens PR, Cripe L, Kaul A, Kinnett K, McDonald C, Pandya S, Poysky J, Shapiro F, Tomezsko J, Constantin C (2010) Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care. Lancet Neurol 9:177–189CrossRefPubMed
5.
go back to reference Chen CL, Yeung KT, Bih LI, Wang CH, Chen MI, Chien JC (2003) The relationship between sitting stability and functional performance in patients with paraplegia. Arch Phys Med Rehabil 84:1276–1281CrossRefPubMed Chen CL, Yeung KT, Bih LI, Wang CH, Chen MI, Chien JC (2003) The relationship between sitting stability and functional performance in patients with paraplegia. Arch Phys Med Rehabil 84:1276–1281CrossRefPubMed
6.
go back to reference Connolly AM, Schierbecker J, Renna R, Florence J (2002) High dose weekly oral prednisone improves strength in boys with Duchenne muscular dystrophy. Neuromuscul Disord 12:917–925CrossRefPubMed Connolly AM, Schierbecker J, Renna R, Florence J (2002) High dose weekly oral prednisone improves strength in boys with Duchenne muscular dystrophy. Neuromuscul Disord 12:917–925CrossRefPubMed
7.
go back to reference Davidson ZE, Truby H (2009) A review of nutrition in Duchenne muscular dystrophy. J Hum Nutr Diet: Off J Br Diet Assoc 22:383–393CrossRef Davidson ZE, Truby H (2009) A review of nutrition in Duchenne muscular dystrophy. J Hum Nutr Diet: Off J Br Diet Assoc 22:383–393CrossRef
8.
go back to reference Eagle M, Baudouin SV, Chandler C, Giddings DR, Bullock R, Bushby K (2002) Survival in Duchenne muscular dystrophy: improvements in life expectancy since 1967 and the impact of home nocturnal ventilation. Neuromuscul Disord 12:926–929CrossRefPubMed Eagle M, Baudouin SV, Chandler C, Giddings DR, Bullock R, Bushby K (2002) Survival in Duchenne muscular dystrophy: improvements in life expectancy since 1967 and the impact of home nocturnal ventilation. Neuromuscul Disord 12:926–929CrossRefPubMed
9.
go back to reference Emery AE (1997) Diagnostic criteria for neuromuscular disorders. Royal Society of Medicine Press, London Emery AE (1997) Diagnostic criteria for neuromuscular disorders. Royal Society of Medicine Press, London
10.
go back to reference Flatters I, Mushtaq F, Hill LJ, Holt RJ, Wilkie RM, Mon-Williams M (2014) The relationship between a child’s postural stability and manual dexterity. Exp Brain Res 232:2907–2917CrossRefPubMedPubMedCentral Flatters I, Mushtaq F, Hill LJ, Holt RJ, Wilkie RM, Mon-Williams M (2014) The relationship between a child’s postural stability and manual dexterity. Exp Brain Res 232:2907–2917CrossRefPubMedPubMedCentral
11.
go back to reference Flatters I, Mushtaq F, Hill LJ, Rossiter A, Jarrett-Peet K, Culmer P, Holt R, Wilkie RM, Mon-Williams M (2014) Children’s head movements and postural stability as a function of task. Exp Brain Res 232:1953–1970CrossRefPubMed Flatters I, Mushtaq F, Hill LJ, Rossiter A, Jarrett-Peet K, Culmer P, Holt R, Wilkie RM, Mon-Williams M (2014) Children’s head movements and postural stability as a function of task. Exp Brain Res 232:1953–1970CrossRefPubMed
12.
go back to reference Henricson EK, Abresch RT, Cnaan A, Hu F, Duong T, Arrieta A, Han J, Escolar DM, Florence JM, Clemens PR, Hoffman EP, McDonald CM, Investigators C (2013) The cooperative international neuromuscular research group Duchenne natural history study: glucocorticoid treatment preserves clinically meaningful functional milestones and reduces rate of disease progression as measured by manual muscle testing and other commonly used clinical trial outcome measures. Muscle Nerve 48:55–67CrossRefPubMedPubMedCentral Henricson EK, Abresch RT, Cnaan A, Hu F, Duong T, Arrieta A, Han J, Escolar DM, Florence JM, Clemens PR, Hoffman EP, McDonald CM, Investigators C (2013) The cooperative international neuromuscular research group Duchenne natural history study: glucocorticoid treatment preserves clinically meaningful functional milestones and reduces rate of disease progression as measured by manual muscle testing and other commonly used clinical trial outcome measures. Muscle Nerve 48:55–67CrossRefPubMedPubMedCentral
13.
go back to reference Jansen M, van Alfen N, Geurts AC, de Groot IJ (2013) Assisted bicycle training delays functional deterioration in boys with Duchenne muscular dystrophy: the randomized controlled trial “no use is disuse”. Neurorehabil Neural Repair 27:816–827CrossRefPubMed Jansen M, van Alfen N, Geurts AC, de Groot IJ (2013) Assisted bicycle training delays functional deterioration in boys with Duchenne muscular dystrophy: the randomized controlled trial “no use is disuse”. Neurorehabil Neural Repair 27:816–827CrossRefPubMed
14.
go back to reference Janssen MM, Bergsma A, Geurts AC, de Groot IJ (2014) Patterns of decline in upper limb function of boys and men with DMD: an international survey. J Neurol 261:1269–1288CrossRefPubMed Janssen MM, Bergsma A, Geurts AC, de Groot IJ (2014) Patterns of decline in upper limb function of boys and men with DMD: an international survey. J Neurol 261:1269–1288CrossRefPubMed
15.
go back to reference Janssen MM, Geurts AC, Groot IJ (2016) Towards a short questionnaire for stepwise assessment of upper limb function, pain and stiffness in Duchenne muscular dystrophy. Disabil Rehabil (Submitted) Janssen MM, Geurts AC, Groot IJ (2016) Towards a short questionnaire for stepwise assessment of upper limb function, pain and stiffness in Duchenne muscular dystrophy. Disabil Rehabil (Submitted)
16.
go back to reference Kaidar-Person O, Person B, Szomstein S, Rosenthal RJ (2008) Nutritional deficiencies in morbidly obese patients: a new form of malnutrition? Part A: vitamins. Obes Surg 18:870–876CrossRefPubMed Kaidar-Person O, Person B, Szomstein S, Rosenthal RJ (2008) Nutritional deficiencies in morbidly obese patients: a new form of malnutrition? Part A: vitamins. Obes Surg 18:870–876CrossRefPubMed
17.
go back to reference Kaidar-Person O, Person B, Szomstein S, Rosenthal RJ (2008) Nutritional deficiencies in morbidly obese patients: a new form of malnutrition? Part B: minerals. Obes Surg 18:1028–1034CrossRefPubMed Kaidar-Person O, Person B, Szomstein S, Rosenthal RJ (2008) Nutritional deficiencies in morbidly obese patients: a new form of malnutrition? Part B: minerals. Obes Surg 18:1028–1034CrossRefPubMed
18.
go back to reference Kieny P, Chollet S, Delalande P, Le Fort M, Magot A, Pereon Y, Perrouin Verbe B (2013) Evolution of life expectancy of patients with Duchenne muscular dystrophy at AFM Yolaine de Kepper centre between 1981 and 2011. Ann Phys Rehabil Med 56:443–454CrossRefPubMed Kieny P, Chollet S, Delalande P, Le Fort M, Magot A, Pereon Y, Perrouin Verbe B (2013) Evolution of life expectancy of patients with Duchenne muscular dystrophy at AFM Yolaine de Kepper centre between 1981 and 2011. Ann Phys Rehabil Med 56:443–454CrossRefPubMed
19.
go back to reference Kohler M, Clarenbach CF, Bahler C, Brack T, Russi EW, Bloch KE (2009) Disability and survival in Duchenne muscular dystrophy. J Neurol Neurosurg Psychiatry 80:320–325CrossRefPubMed Kohler M, Clarenbach CF, Bahler C, Brack T, Russi EW, Bloch KE (2009) Disability and survival in Duchenne muscular dystrophy. J Neurol Neurosurg Psychiatry 80:320–325CrossRefPubMed
20.
go back to reference Lopes J, Russell DM, Whitwell J, Jeejeebhoy KN (1982) Skeletal muscle function in malnutrition. Am J Clin Nutr 36:602–610PubMed Lopes J, Russell DM, Whitwell J, Jeejeebhoy KN (1982) Skeletal muscle function in malnutrition. Am J Clin Nutr 36:602–610PubMed
21.
go back to reference Marino RJ, Shea JA, Stineman MG (1998) The capabilities of upper extremity instrument: reliability and validity of a measure of functional limitation in tetraplegia. Arch Phys Med Rehabil 79:1512–1521CrossRefPubMed Marino RJ, Shea JA, Stineman MG (1998) The capabilities of upper extremity instrument: reliability and validity of a measure of functional limitation in tetraplegia. Arch Phys Med Rehabil 79:1512–1521CrossRefPubMed
22.
go back to reference McDonald CM (2002) Physical activity, health impairments, and disability in neuromuscular disease. Am J Phys Med Rehabil 81:S108–S120CrossRefPubMed McDonald CM (2002) Physical activity, health impairments, and disability in neuromuscular disease. Am J Phys Med Rehabil 81:S108–S120CrossRefPubMed
23.
go back to reference McDonald CM, Abresch RT, Carter GT, Fowler WM Jr, Johnson ER, Kilmer DD, Sigford BJ (1995) Profiles of neuromuscular diseases. Duchenne muscular dystrophy. Am J Phys Med Rehabil 74:S70–S92CrossRefPubMed McDonald CM, Abresch RT, Carter GT, Fowler WM Jr, Johnson ER, Kilmer DD, Sigford BJ (1995) Profiles of neuromuscular diseases. Duchenne muscular dystrophy. Am J Phys Med Rehabil 74:S70–S92CrossRefPubMed
24.
go back to reference Mendell JR, Lloyd-Puryear M (2013) Report of MDA muscle disease symposium on newborn screening for Duchenne muscular dystrophy. Muscle Nerve 48:21–26CrossRefPubMed Mendell JR, Lloyd-Puryear M (2013) Report of MDA muscle disease symposium on newborn screening for Duchenne muscular dystrophy. Muscle Nerve 48:21–26CrossRefPubMed
25.
go back to reference Natterlund B, Ahlstrom G (2001) Activities of daily living and quality of life in persons with muscular dystrophy. J Rehabil Med 33:206–211CrossRefPubMed Natterlund B, Ahlstrom G (2001) Activities of daily living and quality of life in persons with muscular dystrophy. J Rehabil Med 33:206–211CrossRefPubMed
26.
go back to reference Pane M, Fanelli L, Mazzone ES et al (2015) Benefits of glucocorticoids in non-ambulant boys/men with Duchenne muscular dystrophy: a multicentric longitudinal study using the performance of upper limb test. Neuromuscul Disord 25:749–753CrossRefPubMedPubMedCentral Pane M, Fanelli L, Mazzone ES et al (2015) Benefits of glucocorticoids in non-ambulant boys/men with Duchenne muscular dystrophy: a multicentric longitudinal study using the performance of upper limb test. Neuromuscul Disord 25:749–753CrossRefPubMedPubMedCentral
27.
go back to reference Salerno DF, Franzblau A, Armstrong TJ, Werner RA, Becker MP (2001) Test-retest reliability of the upper extremity questionnaire among keyboard operators. Am J Ind Med 40:655–666CrossRefPubMed Salerno DF, Franzblau A, Armstrong TJ, Werner RA, Becker MP (2001) Test-retest reliability of the upper extremity questionnaire among keyboard operators. Am J Ind Med 40:655–666CrossRefPubMed
28.
29.
go back to reference Stommen NC, Verbunt JA, Gorter SL, Goossens ME (2012) Physical activity and disability among adolescents and young adults with non-specific musculoskeletal pain. Disabil Rehabil 34:1438–1443CrossRefPubMed Stommen NC, Verbunt JA, Gorter SL, Goossens ME (2012) Physical activity and disability among adolescents and young adults with non-specific musculoskeletal pain. Disabil Rehabil 34:1438–1443CrossRefPubMed
30.
go back to reference van den Engel-Hoek L, Erasmus CE, Hendriks JC, Geurts AC, Klein WM, Pillen S, Sie LT, de Swart BJ, de Groot IJ (2013) Oral muscles are progressively affected in Duchenne muscular dystrophy: implications for dysphagia treatment. J Neurol 260:1295–1303CrossRefPubMed van den Engel-Hoek L, Erasmus CE, Hendriks JC, Geurts AC, Klein WM, Pillen S, Sie LT, de Swart BJ, de Groot IJ (2013) Oral muscles are progressively affected in Duchenne muscular dystrophy: implications for dysphagia treatment. J Neurol 260:1295–1303CrossRefPubMed
31.
go back to reference Vandervelde L, Van den Bergh PY, Penta M, Thonnard JL (2010) Validation of the ABILHAND questionnaire to measure manual ability in children and adults with neuromuscular disorders. J Neurol Neurosurg Psychiatry 81:506–512CrossRefPubMed Vandervelde L, Van den Bergh PY, Penta M, Thonnard JL (2010) Validation of the ABILHAND questionnaire to measure manual ability in children and adults with neuromuscular disorders. J Neurol Neurosurg Psychiatry 81:506–512CrossRefPubMed
32.
go back to reference Wagner KR, Lechtzin N, Judge DP (2007) Current treatment of adult Duchenne muscular dystrophy. Biochim Biophys Acta 1772:229–237CrossRefPubMed Wagner KR, Lechtzin N, Judge DP (2007) Current treatment of adult Duchenne muscular dystrophy. Biochim Biophys Acta 1772:229–237CrossRefPubMed
Metadata
Title
Variables associated with upper extremity function in patients with Duchenne muscular dystrophy
Authors
Mariska M. H. P. Janssen
Jan C. M. Hendriks
Alexander C. H. Geurts
Imelda J. M. de Groot
Publication date
01-09-2016
Publisher
Springer Berlin Heidelberg
Published in
Journal of Neurology / Issue 9/2016
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-016-8193-1

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