Age-related changes in motor unit number estimates in adult patients with Charcot-Marie-Tooth type 1A

被引:14
|
作者
van Dijk, J. P. [1 ]
Verhamme, C. [2 ]
van Schaik, I. N. [2 ]
Schelhaas, H. J. [1 ]
Mans, E. [2 ]
Bour, L. J. [2 ]
Stegeman, D. F. [1 ,3 ]
Zwarts, M. J. [1 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Neurol Clin Neurophysiol, Donders Inst Brain Cognit & Behav, NL-6500 HB Nijmegen, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Neurol & Clin Neurophysiol, NL-1105 AZ Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Fac Human Movement Sci, Res Inst MOVE, Amsterdam, Netherlands
关键词
axonal dysfunction; Charcot-Marie-Tooth disease; CMT1A; compound muscle action potential; hereditary motor and sensory neuropathies; hereditary motor and sensory neuropathy Ia; high-density surface EMG; motor unit number estimation; DISEASE TYPE 1A; HEREDITARY MOTOR; NATURAL-HISTORY; DUPLICATION; CHILDREN; SURFACE; ABNORMALITIES; DYSFUNCTION; SEVERITY; STRENGTH;
D O I
10.1111/j.1468-1331.2010.03027.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Charcot-Marie-Tooth disease type 1A (CMT1A) is known as a demyelinating hereditary neuropathy. Secondary axonal dysfunction is the most important determinant of disease severity. In adult patients, clinical progression may be because of further axonal deterioration as was shown with compound muscle action potential (CMAP) amplitude reductions over time. The motor unit number estimation (MUNE) technique may be more accurate to determine the number of axons as it is not disturbed by the effect of reinnervation. The purpose of this study was to investigate the number and size of motor units in relation to age in patients and controls. Methods: In a cross-sectional design, we assessed arm and hand strength and performed electrophysiological examinations, including CMAP amplitudes and MUNE of the thenar muscles using high-density surface EMG in 69 adult patients with CMT1A and 55 age-matched healthy controls. Results: In patients, lower CMAP amplitudes and MUNE values were related to hand weakness. The CMAP amplitude and MUNE value of the thenar muscles were significantly lower in patients than in controls. CMAP amplitudes declined with age in controls, but not in patients. MUNE values declined with age in both patients and controls. Conclusions: The age-dependent decrease in the number of motor units was not significantly different between patients with CMT1A and controls, indicating that loss of motor units in adult patients is limited.
引用
收藏
页码:1098 / 1104
页数:7
相关论文
共 50 条
  • [21] Neurophysiologic abnormalities in children with Charcot-Marie-Tooth disease type 1A
    Yiu, Eppie M.
    Burns, Joshua
    Ryan, Monique M.
    Ouvrier, Robert A.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2008, 13 (03) : 236 - 241
  • [22] ELECTROMYOGRAPHIC TENDON REFLEX RECORDING: AN ACCURATE AND COMFORTABLE METHOD FOR DIAGNOSIS OF CHARCOT-MARIE-TOOTH DISEASE TYPE 1A
    Garcia, Antonio
    Pelayo-Negro, Ana L.
    Alvarez-Paradelo, Silvia
    Antolin, Francisco M.
    Berciano, Jose
    MUSCLE & NERVE, 2015, 52 (01) : 39 - 44
  • [23] Charcot-Marie-Tooth type 1A disease from patient to laboratory
    Perveen, Shazia
    Mannan, Shazia
    Hussain, Abrar
    Kanwal, Sumaira
    JOURNAL OF THE PAKISTAN MEDICAL ASSOCIATION, 2015, 65 (02) : 206 - 212
  • [24] Hand involvement in children with Charcot-Marie-Tooth disease type 1A
    Burns, Joshua
    Bray, Paula
    Cross, Lauren A.
    North, Kathryn N.
    Ryan, Monique M.
    Ouvrier, Robert A.
    NEUROMUSCULAR DISORDERS, 2008, 18 (12) : 970 - 973
  • [25] Severe vincristine neuropathy in Charcot-Marie-Tooth disease type 1A
    Graf, WD
    Chance, PF
    Lensch, MW
    Eng, LJ
    Lipe, HP
    Thomas, TD
    CANCER, 1996, 77 (07) : 1356 - 1362
  • [26] High-density surface electromyography to assess motor unit firing rate in Charcot-Marie-Tooth disease type 1A patients
    Noto, Yu-ichi
    Watanabe, Kohei
    Holobar, Ales
    Kitaoji, Takamasa
    Tsuji, Yukiko
    Kojima, Yuta
    Kitani-Morii, Fukiko
    Mizuno, Toshiki
    Nakagawa, Masanori
    CLINICAL NEUROPHYSIOLOGY, 2021, 132 (03) : 812 - 818
  • [27] Neuromuscular hip dysplasia in Charcot-Marie-Tooth disease type 1A
    Bamford, Nigel S.
    White, Klane K.
    Robinett, Stephanie A.
    Otto, Randolph K.
    Gospe, Sidney M., Jr.
    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2009, 51 (05) : 408 - 411
  • [28] Preimplantation genetic diagnosis for Charcot-Marie-Tooth disease type 1A
    De Vos, A
    Sermon, K
    De Rijcke, M
    Goossens, V
    Henderix, P
    Van Ranst, N
    Platteau, P
    Lissens, W
    Devroey, P
    Van Steirteghem, A
    Liebaers, I
    MOLECULAR HUMAN REPRODUCTION, 2003, 9 (07) : 429 - 435
  • [29] Phrenic nerve involvement and respiratory muscle weakness in patients with Charcot-Marie-Tooth disease 1A
    Spiesshoefer, Jens
    Henke, Carolin
    Kabitz, Hans-Joachim
    Akova-Oeztuerk, Esra
    Draeger, Bianca
    Herkenrath, Simon
    Randerath, Winfried
    Young, Peter
    Brix, Tobias
    Boentert, Matthias
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2019, 24 (03) : 283 - 293
  • [30] Gait Pattern in Charcot-Marie-Tooth Disease Type 1A According to Disease Severity
    Park, Jihyun
    Joo, So Young
    Choi, Byung-Ok
    Kim, Dae-Hyun
    Park, Jong Bum
    Lee, Jong Weon
    Kim, Deog Young
    JOURNAL OF PERSONALIZED MEDICINE, 2023, 13 (10):