Literature DB >> 27385750

Quantitative strength testing in ALS clinical trials.

Jeremy M Shefner1, Dawei Liu2, Melanie L Leitner2, David Schoenfeld2, Donald R Johns2, Toby Ferguson2, Merit Cudkowicz2.   

Abstract

OBJECTIVE: To study the attributes of quantitative strength testing using hand-held dynamometry (HHD) as an efficacy measure in 2 large phase 3 amyotrophic lateral sclerosis (ALS) trials.
METHODS: In the phase 3 trials of ceftriaxone and dexpramipexole, 513 and 943 patients, respectively, were enrolled in double-blind, randomized, placebo-controlled trials with planned follow-up of at least 1 year. Patients were studied every 3 months in the ceftriaxone study and every 2 months in the dexpramipexole study. Evaluators of HHD were trained and had to show evidence of adequate performance of strength testing; the testing paradigm involved testing 9 muscle groups in the upper and lower extremity bilaterally. Neither drug significantly affected any outcome measure. Strength measurements were evaluated by individual muscle and by megascores, which averaged scaled strength measures to produce an overall measure of muscle strength.
RESULTS: A measure combining rate of decline with both within- and between-patient variabilities of measurement, the coefficient of variation for rate of change, was calculated, and showed that HHD overall performed slightly less well than Amyotrophic Lateral Sclerosis Functional Rating Scale-revised (ALSFRS-R) but better than vital capacity. Individual muscles were highly correlated to the identical muscles on the contralateral side, as well as to other muscles in the same body region. Strength decline was correlated both with ALSFRS-R and vital capacity.
CONCLUSION: Quantitative strength testing using HHD is a reliable and reproducible measure of decline in ALS.
© 2016 American Academy of Neurology.

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Year:  2016        PMID: 27385750      PMCID: PMC4977369          DOI: 10.1212/WNL.0000000000002941

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  16 in total

1.  A comparison of muscle strength testing techniques in amyotrophic lateral sclerosis.

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Journal:  Neurology       Date:  2003-12-09       Impact factor: 9.910

2.  Functional outcome measures as clinical trial endpoints in ALS.

Authors:  B J Traynor; H Zhang; J M Shefner; D Schoenfeld; M E Cudkowicz
Journal:  Neurology       Date:  2004-11-23       Impact factor: 9.910

3.  Multipoint incremental motor unit number estimation as an outcome measure in ALS.

Authors:  J M Shefner; M L Watson; L Simionescu; J B Caress; T M Burns; N J Maragakis; M Benatar; W S David; K R Sharma; S B Rutkove
Journal:  Neurology       Date:  2011-06-15       Impact factor: 9.910

4.  Safety and efficacy of lithium in combination with riluzole for treatment of amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial.

Authors:  Swati P Aggarwal; Lorne Zinman; Elizabeth Simpson; Jane McKinley; Katherine E Jackson; Hanika Pinto; Petra Kaufman; Robin A Conwit; David Schoenfeld; Jeremy Shefner; Merit Cudkowicz
Journal:  Lancet Neurol       Date:  2010-04-01       Impact factor: 44.182

5.  Quality of life in ALS is maintained as physical function declines.

Authors:  R A Robbins; Z Simmons; B A Bremer; S M Walsh; S Fischer
Journal:  Neurology       Date:  2001-02-27       Impact factor: 9.910

6.  Safety and efficacy of ceftriaxone for amyotrophic lateral sclerosis: a multi-stage, randomised, double-blind, placebo-controlled trial.

Authors:  Merit E Cudkowicz; Sarah Titus; Marianne Kearney; Hong Yu; Alexander Sherman; David Schoenfeld; Douglas Hayden; Amy Shui; Benjamin Brooks; Robin Conwit; Donna Felsenstein; David J Greenblatt; Myles Keroack; John T Kissel; Robert Miller; Jeffrey Rosenfeld; Jeffrey D Rothstein; Ericka Simpson; Nina Tolkoff-Rubin; Lorne Zinman; Jeremy M Shefner
Journal:  Lancet Neurol       Date:  2014-10-05       Impact factor: 44.182

7.  Glatiramer acetate has no impact on disease progression in ALS at 40 mg/day: a double- blind, randomized, multicentre, placebo-controlled trial.

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Journal:  Amyotroph Lateral Scler       Date:  2009 Oct-Dec

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  18 in total

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Review 2.  Strength Testing in Motor Neuron Diseases.

Authors:  Jeremy M Shefner
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Review 5.  Considerations for Amyotrophic Lateral Sclerosis (ALS) Clinical Trial Design.

Authors:  Christina N Fournier
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Review 6.  Assessment of Motor Units in Neuromuscular Disease.

Authors:  Robert D Henderson; Pamela A McCombe
Journal:  Neurotherapeutics       Date:  2017-01       Impact factor: 7.620

7.  Patients with ALS show highly correlated progression rates in left and right limb muscles.

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8.  Reliability of Handheld Dynamometry to Measure Focal Muscle Weakness in Neurofibromatosis Types 1 and 2.

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Journal:  Neurology       Date:  2021-07-06       Impact factor: 11.800

9.  Progressive arm muscle weakness in ALS follows the same sequence regardless of onset site: use of TOMS, a novel analytic method to track limb strength.

Authors:  Nimish J Thakore; Brian J Drawert; Brittany R Lapin; Erik P Pioro
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10.  Muscle contractility dysfunction precedes loss of motor unit connectivity in SOD1(G93A) mice.

Authors:  Christopher G Wier; Alexander E Crum; Anthony B Reynolds; Chitra C Iyer; Deepti Chugh; Marilly S Palettas; Patrick L Heilman; David M Kline; W David Arnold; Stephen J Kolb
Journal:  Muscle Nerve       Date:  2018-12-21       Impact factor: 3.217

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