A COMPARISON OF DAILY AND ALTERNATE-DAY PREDNISONE THERAPY IN THE TREATMENT OF DUCHENNE MUSCULAR-DYSTROPHY

被引:96
作者
FENICHEL, GM
MENDELL, JR
MOXLEY, RT
GRIGGS, RC
BROOKE, MH
MILLER, JP
PESTRONK, A
ROBISON, J
KING, W
SIGNORE, L
PANDYA, S
FLORENCE, J
SCHIERBECKER, J
WILSON, B
机构
[1] WALTER MCKENZIE CTR HLTH SCI, DEPT NEUROL, EDMONTON, ALBERTA, CANADA
[2] OHIO STATE UNIV, COLL MED, DEPT NEUROL, COLUMBUS, OH 43210 USA
[3] WASHINGTON UNIV, SCH MED, DIV BIOSTAT, ST LOUIS, MO 63110 USA
[4] UNIV ROCHESTER, DEPT NEUROL, ROCHESTER, NY 14627 USA
[5] WASHINGTON UNIV, SCH MED, DEPT NEUROL, ST LOUIS, MO 63110 USA
关键词
D O I
10.1001/archneur.1991.00530180027012
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We previously reported the results of a randomized, double-blind 6-month trial of prednisone therapy in which 102 boys aged 5 to 15 years with Duchenne muscular dystrophy received daily doses of 1.5 and 0.75 mg/kg per day and were compared with those receiving placebo. The strength and function in both prednisone-treated groups improved equally and were significantly better than in the placebo group. To compare alternate-day and daily dosing of prednisone with respect to benefits and adverse side effects, the placebo group was started on alternate-day prednisone therapy, and the treatment group regimens were changed to equivalent doses of alternate-day prednisone without breaking the double-blind nature. At the end of 6 months, the group that was changed from daily to alternate-day therapy had declined in strength back to levels observed 12 months previously, at the start of daily therapy. The group in which alternate-day therapy was started showed a significant improvement in strength at 3 months, similar in magnitude to the response of boys treated with daily therapy. However, their strength declined significantly in the subsequent 3 months compared with boys who received daily therapy. The frequency of side effects was not significantly different for alternate-day therapy compared with daily therapy. We conclude that alternate-day prednisone therapy effectively increases strength but does not sustain the improvement to the same extent as daily therapy or mitigate side effects.
引用
收藏
页码:575 / 579
页数:5
相关论文
共 17 条
[1]  
[Anonymous], 1988, SAS STAT USERS GUIDE
[2]   HYPOXANTHINE AND MCARDLE DISEASE - A CLUE TO METABOLIC STRESS IN THE WORKING FOREARM [J].
BROOKE, MH ;
PATTERSON, VH ;
KAISER, KK .
MUSCLE & NERVE, 1983, 6 (03) :204-206
[3]   CLINICAL-TRIAL IN DUCHENNE DYSTROPHY .1. THE DESIGN OF THE PROTOCOL [J].
BROOKE, MH ;
GRIGGS, RC ;
MENDELL, JR ;
FENICHEL, GM ;
SHUMATE, JB ;
PELLEGRINO, RJ .
MUSCLE & NERVE, 1981, 4 (03) :186-197
[4]  
BURROW K L, 1990, Neurology, V40, P206
[5]   GLUCOCORTICOSTEROID THERAPY - MECHANISMS OF ACTION AND CLINICAL CONSIDERATIONS [J].
FAUCI, AS ;
DALE, DC ;
BALOW, JE .
ANNALS OF INTERNAL MEDICINE, 1976, 84 (03) :304-315
[6]   ALTERNATE-DAY CORTICOSTEROID-THERAPY [J].
FAUCI, AS .
AMERICAN JOURNAL OF MEDICINE, 1978, 64 (05) :729-731
[7]   LONG-TERM BENEFIT FROM PREDNISONE THERAPY IN DUCHENNE MUSCULAR-DYSTROPHY [J].
FENICHEL, GM ;
FLORENCE, JM ;
PESTRONK, A ;
MENDELL, JR ;
MOXLEY, RT ;
GRIGGS, RC ;
BROOKE, MH ;
MILLER, JP ;
ROBISON, J ;
KING, W ;
SIGNORE, L ;
PANDYA, S ;
SCHIERBECKER, J ;
WILSON, B .
NEUROLOGY, 1991, 41 (12) :1874-1877
[8]   URINARY CREATININE EXCRETION AND LEAN BODY-MASS [J].
FORBES, GB ;
BRUINING, GJ .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1976, 29 (12) :1359-1366
[9]   THE ASSESSMENT OF MUSCLE MASS IN PROGRESSIVE NEUROMUSCULAR DISEASE [J].
GRIGGS, RC ;
FORBES, G ;
MOXLEY, RT ;
HERR, BE .
NEUROLOGY, 1983, 33 (02) :158-165
[10]   STUDIES ON AN INTERMITTENT CORTICOSTEROID DOSAGE REGIMEN [J].
HARTER, JG ;
THORN, GW ;
REDDY, WJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1963, 269 (12) :591-&