PRECLINICAL DRUG TRIALS IN THE mdx MOUSE: ASSESSMENT OF RELIABLE AND SENSITIVE OUTCOME MEASURES

被引:127
作者
Spurney, Christopher F. [1 ]
Gordish-Dressman, Heather [1 ]
Guerron, Alfredo D. [1 ]
Sali, Arpana [1 ]
Pandey, Gouri S. [1 ]
Rawat, Rashmi [1 ]
Van Der Meulen, Jack H. [1 ]
Cha, Hee-Jae [1 ]
Pistilli, Emidio E. [1 ]
Partridge, Terence A. [1 ]
Hoffman, Eric P. [1 ]
Nagaraju, Kanneboyina [1 ]
机构
[1] Childrens Natl Med Ctr, Med Genet Res Ctr, Washington, DC 20010 USA
关键词
Duchenne muscular dystrophy; mdx mouse; preclinical trials; statistical analysis; phenotyping; muscle function tests; exercise; echocardiography; DUCHENNE MUSCULAR-DYSTROPHY; SKELETAL-MUSCLE; DIAPHRAGM MUSCLE; IN-VIVO; VOLUNTARY EXERCISE; MICE LACKING; IMPROVES; MODEL; STRENGTH; GENE;
D O I
10.1002/mus.21211
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The availability of animal models for Duchenne muscular dystrophy has led to extensive preclinical research on potential therapeutics. Few studies have focused on reliability and sensitivity of endpoints for mdx mouse drug trials. Therefore, we sought to compare a wide variety of reported and novel endpoint measures in exercised mdx and normal control mice at 10, 20, and 40 weeks of age. Statistical analysis as well as power calculations for expected effect sizes in mdx preclinical drug trials across different ages showed that body weight, normalized grip strength, horizontal activity, rest time, cardiac function measurements, blood pressure, total central/peripheral nuclei per fiber, and serum creatine kinase are the most effective measurements for detecting drug-induced changes. These data provide an experimental basis upon which standardization of preclinical drug testing can be developed.
引用
收藏
页码:591 / 602
页数:12
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