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
    FORBES, GB
    GALLUP, J
    HURSH, JB
    [J]. SCIENCE, 1961, 133 (344) : 101 - &
  • [2] INCLUSION-BODY MYOSITIS AND MYOPATHIES
    GRIGGS, RC
    ASKANAS, V
    DIMAURO, S
    ENGEL, A
    KARPATI, G
    MENDELL, JR
    ROWLAND, LP
    [J]. ANNALS OF NEUROLOGY, 1995, 38 (05) : 705 - 713
  • [3] THE ASSESSMENT OF MUSCLE MASS IN PROGRESSIVE NEUROMUSCULAR DISEASE
    GRIGGS, RC
    FORBES, G
    MOXLEY, RT
    HERR, BE
    [J]. 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
    LEFF, RL
    MILLER, FW
    HICKS, J
    FRASER, DD
    PLOTZ, PH
    [J]. MEDICINE, 1993, 72 (04) : 225 - 235
  • [6] LINDBERG C, 1994, ACTA NEUROL SCAND, V89, P123
  • [7] INCLUSION BODY MYOSITIS - OBSERVATIONS IN 40 PATIENTS
    LOTZ, BP
    ENGEL, AG
    NISHINO, H
    STEVENS, JC
    LITCHY, WJ
    [J]. BRAIN, 1989, 112 : 727 - 747
  • [8] Disease progression in sporadic inclusion body myositis: Observations in 78 patients
    Peng, A
    Koffman, BM
    Malley, JD
    Dalakas, MC
    [J]. NEUROLOGY, 2000, 55 (02) : 296 - 298
  • [9] FACIOSCAPULOHUMERAL DYSTROPHY NATURAL-HISTORY STUDY - STANDARDIZATION OF TESTING PROCEDURES AND RELIABILITY OF MEASUREMENTS
    PERSONIUS, KE
    PANDYA, S
    KING, WM
    TAWIL, R
    MCDERMOTT, MP
    [J]. 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
    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
    [J]. NEUROLOGY, 1997, 48 (01) : 38 - 46