A prospective natural history study of inclusion body myositis: Implications for clinical trials

被引:52
作者
Rose, MR [1 ]
McDermott, MP
Thornton, CA
Palenski, C
Martens, WB
Griggs, RC
机构
[1] Kings Coll London Hosp, Kings Neurosci Ctr, Dept Neurol, London SE5 9RS, England
[2] Univ Rochester, Med Ctr, Dept Neurol, Rochester, NY 14642 USA
关键词
D O I
10.1212/WNL.57.3.548
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Eleven patients with untreated inclusion body myositis (IBM) were prospectively studied during a 6-month period that included muscle strength, lean body mass, and muscle mass measurements. There was an overall quantifiable mean decline in percent of predicted normal muscle strength of 4% from baseline in a 6-month period, but one third of patients showed no change or slight improvements in strength. Short-term treatment trials in IBM will require large numbers of patients to detect slowing, arrest, or even slight improvement in muscle strength.
引用
收藏
页码:548 / 550
页数:3
相关论文
共 10 条
[1]   ESTIMATION OF TOTAL BODY FAT FROM POTASSIUM-40 CONTENT [J].
FORBES, GB ;
GALLUP, J ;
HURSH, JB .
SCIENCE, 1961, 133 (344) :101-&
[2]   INCLUSION-BODY MYOSITIS AND MYOPATHIES [J].
GRIGGS, RC ;
ASKANAS, V ;
DIMAURO, S ;
ENGEL, A ;
KARPATI, G ;
MENDELL, JR ;
ROWLAND, LP .
ANNALS OF NEUROLOGY, 1995, 38 (05) :705-713
[3]   THE ASSESSMENT OF MUSCLE MASS IN PROGRESSIVE NEUROMUSCULAR DISEASE [J].
GRIGGS, RC ;
FORBES, G ;
MOXLEY, RT ;
HERR, BE .
NEUROLOGY, 1983, 33 (02) :158-165
[4]  
GRIGGS RC, 1998, INCLUSION BODY MYOS
[5]   THE TREATMENT OF INCLUSION-BODY MYOSITIS - A RETROSPECTIVE REVIEW AND A RANDOMIZED, PROSPECTIVE TRIAL OF IMMUNOSUPPRESSIVE THERAPY [J].
LEFF, RL ;
MILLER, FW ;
HICKS, J ;
FRASER, DD ;
PLOTZ, PH .
MEDICINE, 1993, 72 (04) :225-235
[6]  
LINDBERG C, 1994, ACTA NEUROL SCAND, V89, P123
[7]   INCLUSION BODY MYOSITIS - OBSERVATIONS IN 40 PATIENTS [J].
LOTZ, BP ;
ENGEL, AG ;
NISHINO, H ;
STEVENS, JC ;
LITCHY, WJ .
BRAIN, 1989, 112 :727-747
[8]   Disease progression in sporadic inclusion body myositis: Observations in 78 patients [J].
Peng, A ;
Koffman, BM ;
Malley, JD ;
Dalakas, MC .
NEUROLOGY, 2000, 55 (02) :296-298
[9]   FACIOSCAPULOHUMERAL DYSTROPHY NATURAL-HISTORY STUDY - STANDARDIZATION OF TESTING PROCEDURES AND RELIABILITY OF MEASUREMENTS [J].
PERSONIUS, KE ;
PANDYA, S ;
KING, WM ;
TAWIL, R ;
MCDERMOTT, MP .
PHYSICAL THERAPY, 1994, 74 (03) :253-263
[10]   A prospective, quantitative study of the natural history of facioscapulohumeral muscular dystrophy (FSHD): Implications for therapeutic trials [J].
Tawil, R ;
Griggs, RC ;
McDermott, MP ;
Cos, L ;
Personius, KE ;
Langsam, A ;
Pandya, S ;
Maronian, A ;
Sass, A ;
McCoy, K ;
Brower, CA ;
Plumb, S ;
Martens, W ;
Herr, BE ;
Forrester, J ;
Figlewicz, D ;
Mendell, JR ;
Kissel, J ;
Rainey, F ;
Downing, K ;
King, WM .
NEUROLOGY, 1997, 48 (01) :38-46