Walking capacity evaluated by the 6-minute walk test in spinal and bulbar muscular atrophy

被引:56
作者
Takeuchi, Yu [1 ]
Katsuno, Masahisa [1 ,2 ]
Banno, Haruhiko [1 ]
Suzuki, Keisuke [1 ]
Kawashima, Motoshi [1 ]
Atsuta, Naoki [1 ]
Ito, Mizuki [1 ]
Watanabe, Hirohisa [1 ]
Tanaka, Fumiaki [1 ]
Sobue, Gen [1 ]
机构
[1] Nagoya Univ, Sch Med, Dept Neurol, Showa Ku, Nagoya, Aichi 4668550, Japan
[2] Nagoya Univ, Inst Adv Res, Nagoya, Aichi 4668550, Japan
关键词
spinal and bulbar muscular atrophy; 6-minute walk test; biomarker; exercise test; 6-minute walk duration;
D O I
10.1002/mus.21077
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Spinal and bulbar muscular atrophy (SBMA) is an adult-onset motor neuron disease caused by a CAG repeat expansion in the androgen receptor gene. Because the progression of SBMA is slow, it is plausible to identify biomarkers that monitor disease course for therapeutic development. To verify whether the 6-min walk test (6MWT) is a biomarker of SBIVIA, we performed the 6MWT in 35 genetically confirmed patients and in 29 age-matched healthy controls. The walk distance covered within 6 min (6MWD) was significantly less in SBMA than it was in controls (323.3 +/- 143.9 m and 637.6 +/- 94.2 m respectively; P < 0.001). In test-retest analysis, the intraclass correlation coefficient for the 6MWD was high in SBIVIA patients (r = 0.982). In a 1-year follow-up the 6MWD significantly decreased at a rate of 11.3% per year. Our observations suggest that the 6MWT is a biomarker that can be used to monitor progression of motor impairment in SBIVIA.
引用
收藏
页码:964 / 971
页数:8
相关论文
共 36 条
[1]
Widespread nuclear and cytoplasmic accumulation of mutant androgen receptor in SBMA patients [J].
Adachi, H ;
Katsuno, M ;
Minamiyama, M ;
Waza, M ;
Sang, C ;
Nakagomi, Y ;
Kobayashi, Y ;
Tanaka, F ;
Doyu, M ;
Inukai, A ;
Yoshida, M ;
Hashizume, Y ;
Sobue, G .
BRAIN, 2005, 128 :659-670
[2]
Six-minute walk test in adults with cerebral palsy. A study of reliability [J].
Andersson, Christina ;
Asztalos, Lena ;
Mattsson, Eva .
CLINICAL REHABILITATION, 2006, 20 (06) :488-495
[3]
Rethinking genotype and phenotype correlations in polyglutamine expansion disorders [J].
Andrew, SE ;
Goldberg, YP ;
Hayden, MR .
HUMAN MOLECULAR GENETICS, 1997, 6 (12) :2005-2010
[4]
Natural history of spinal and bulbar muscular atrophy (SBMA): a study of 223 Japanese patients [J].
Atsuta, Naoki ;
Watanabe, Hirohisa ;
Ito, Mizuki ;
Banno, Haruhiko ;
Suzuki, Keisuke ;
Katsuno, Masahisa ;
Tanaka, Fumiaki ;
Tamakoshi, Akiko ;
Sobue, Gen .
BRAIN, 2006, 129 :1446-1455
[5]
Mutant androgen receptor accumulation in spinal and bulbar muscular atrophy scrotal skin: A pathogenic marker [J].
Banno, H ;
Adachi, H ;
Katsuno, M ;
Suzuki, K ;
Atsuta, N ;
Watanabe, H ;
Tanaka, F ;
Doyu, M ;
Sobue, G .
ANNALS OF NEUROLOGY, 2006, 59 (03) :520-526
[6]
Comparison of speeds used for the 15.2-meter and 6-minute walks over the year after an incomplete spinal cord injury: The SCILT trial [J].
Barbeau, H. ;
Elashoff, R. ;
Deforge, D. ;
Ditunno, J. ;
Saulino, M. ;
Dobkin, B. H. .
NEUROREHABILITATION AND NEURAL REPAIR, 2007, 21 (04) :302-306
[7]
Walking capacity in mild to moderate Parkinson's disease [J].
Canning, CG ;
Ada, L ;
Johnson, JJ ;
McWhirter, S .
ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION, 2006, 87 (03) :371-375
[8]
ATS statement: Guidelines for the six-minute walk test [J].
Crapo, RO ;
Casaburi, R ;
Coates, AL ;
Enright, PL ;
MacIntyre, NR ;
McKay, RT ;
Johnson, D ;
Wanger, JS ;
Zeballos, RJ ;
Bittner, V ;
Mottram, C .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 166 (01) :111-117
[9]
A randomized controlled trial of functional neuromuscular stimulation in chronic stroke subjects [J].
Daly, JJ ;
Roenigk, K ;
Holcomb, J ;
Rogers, JM ;
Butler, K ;
Gansen, J ;
McCabe, J ;
Fredrickson, E ;
Marsolais, EB ;
Ruff, RL .
STROKE, 2006, 37 (01) :172-178
[10]
SEVERITY OF X-LINKED RECESSIVE BULBOSPINAL NEURONOPATHY CORRELATES WITH SIZE OF THE TANDEM CAG REPEAT IN ANDROGEN RECEPTOR GENE [J].
DOYU, M ;
SOBUE, G ;
MUKAI, E ;
KACHI, T ;
YASUDA, T ;
MITSUMA, T ;
TAKAHASHI, A .
ANNALS OF NEUROLOGY, 1992, 32 (05) :707-710