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Preclinical drug trials in the mdx mouse: Assessment of reliable and sensitive outcome measures

  • Christopher F. Spurney
  • , Heather Gordish-Dressman
  • , Alfredo D. Guerron
  • , Arpana Sali
  • , Gouri S. Pandey
  • , Rashmi Rawat
  • , Jack H. Van Der Meulen
  • , Hee Jae Cha
  • , Emidio E. Pistilli
  • , Terence A. Partridge
  • , Eric P. Hoffman
  • , Kanneboyina Nagaraju

Research output: Contribution to journalArticlepeer-review

136 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)591-602
Number of pages12
JournalMuscle and Nerve
Volume39
Issue number5
DOIs
StatePublished - May 2009

Keywords

  • Duchenne muscular dystrophy
  • Echocardiography
  • Exercise
  • Muscle function tests
  • Phenotyping
  • Preclinical trials
  • Statistical analysis
  • mdx mouse

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