Electrical impedance myography as a biomarker to assess ALS progression

被引:112
作者
Rutkove, Seward B. [1 ]
Caress, James B. [2 ]
Cartwright, Michael S. [2 ]
Burns, Ted M. [3 ]
Warder, Judy [3 ]
David, William S. [4 ]
Goyal, Namita [4 ]
Maragakis, Nicholas J. [5 ]
Clawson, Lora [5 ]
Benatar, Michael [6 ]
Usher, Sharon [7 ]
Sharma, Khema R. [6 ]
Gautam, Shiva [8 ]
Narayanaswami, Pushpa [1 ]
Raynor, Elizabeth M. [1 ]
Watson, Mary Lou [9 ]
Shefner, Jeremy M. [9 ]
机构
[1] Beth Israel Deaconess Med Ctr, Div Neuromuscular Dis, Boston, MA 02215 USA
[2] Wake Forest Sch Med, Dept Neurol, Winston Salem, NC USA
[3] Univ Virginia, Dept Neurol, Charlottesville, VA USA
[4] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
[5] Johns Hopkins Med Ctr, Dept Neurol, Baltimore, MD 21218 USA
[6] Univ Miami, Dept Neurol, Miami, FL USA
[7] Univ S Florida, Tampa, FL USA
[8] Beth Israel Deaconess Med Ctr, Gen Clin Res Ctr, Boston, MA 02215 USA
[9] Upstate Med Ctr, Dept Neurol, Syracuse, NY USA
来源
AMYOTROPHIC LATERAL SCLEROSIS | 2012年 / 13卷 / 05期
关键词
Clinical trials; amyotrophic lateral sclerosis; electrical impedance myography; AMYOTROPHIC-LATERAL-SCLEROSIS; CLINICAL-TRIALS; DEGENERATION; ATROPHY;
D O I
10.3109/17482968.2012.688837
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Electrical impedance myography (EIM), a non-invasive, electrophysiological technique, has preliminarily shown value as an ALS biomarker. Here we perform a multicenter study to further assess EIM's potential for tracking ALS. ALS patients were enrolled across eight sites. Each subject underwent EIM, handheld dynamometry (HHD), and the ALS Functional Rating Scale-revised (ALSFRS-R) regularly. Techniques were compared by assessing the coefficient of variation (CoV) in the rate of decline and each technique's correlation to survival. Results showed that in the 60 patients followed for one year, EIM phase measured from the most rapidly progressing muscle in each patient had a CoV in the rate of decline of 0.62, compared to HHD (0.82) and the ALSFRS-R (0.74). Restricting the measurements to the first six months gave a CoV of 0.55 for EIM, 0.93 for HHD, and 0.84 for ALSFRS-R. For both time-periods, all three measures correlated with survival. Based on these data, a six-month clinical trial designed to detect a 20% treatment effect with 80% power using EIM would require only 95 patients/arm compared to the ALSFRS-R, which would require 220 subjects/arm. In conclusion, EIM can serve as a useful ALS biomarker that offers the prospect of greatly accelerating phase 2 clinical trials.
引用
收藏
页码:439 / 445
页数:7
相关论文
共 26 条
[1]   Safety and efficacy of lithium in combination with riluzole for treatment of amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial [J].
Aggarwal, Swati P. ;
Zinman, Lorne ;
Simpson, Elizabeth ;
McKinley, Jane ;
Jackson, Katherine E. ;
Pinto, Hanika ;
Kaufman, Petra ;
Conwit, Robin A. ;
Schoenfeld, David ;
Shefner, Jeremy ;
Cudkowicz, Merit .
LANCET NEUROLOGY, 2010, 9 (05) :481-488
[2]   El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis [J].
Brooks, BR ;
Miller, RG ;
Swash, M ;
Munsat, TL .
AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS, 2000, 1 (05) :293-299
[3]   The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function [J].
Cedarbaum, JM ;
Stambler, N ;
Malta, E ;
Fuller, C ;
Hilt, D ;
Thurmond, B ;
Nakanishi, A .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1999, 169 (1-2) :13-21
[4]   ALS clinical trials Do enrolled patients accurately represent the ALS population? [J].
Chio, A. ;
Canosa, A. ;
Gallo, S. ;
Cammarosano, S. ;
Moglia, C. ;
Fuda, G. ;
Calvo, A. ;
Mora, G. .
NEUROLOGY, 2011, 77 (15) :1432-1437
[5]   A randomized, placebo-controlled trial of topiramate in amyotrophic lateral sclerosis [J].
Cudkowicz, ME ;
Shefner, JM ;
Schoenfeld, DA ;
Brown, RH ;
Johnson, H ;
Qureshi, M ;
Jacobs, M ;
Rothstein, JD ;
Appel, SH ;
Pascuzzi, RM ;
Heiman-Patterson, TD ;
Donofrio, PD ;
David, WS ;
Russell, JA ;
Tandan, R ;
Pioro, EP ;
Felice, KJ ;
Rosenfeld, J ;
Mandler, RN ;
Sachs, GM ;
Bradley, WG ;
Raynor, EM ;
Baquis, GD ;
Belsh, JM ;
Novella, S ;
Goldstein, J ;
Hulihan, J .
NEUROLOGY, 2003, 61 (04) :456-464
[6]   Trial of celecoxib in amyotrophic lateral sclerosis [J].
Cudkowicz, Merit E. ;
Shefner, Jeremy M. ;
Schoenfeld, David A. ;
Zhang, Hui ;
Andreasson, Katrin I. ;
Rothstein, Jeffrey D. ;
Drachman, Daniel B. .
ANNALS OF NEUROLOGY, 2006, 60 (01) :22-31
[7]   Toward more efficient clinical trials for amyotrophic lateral sclerosis [J].
Cudkowicz, Merit E. ;
Katz, Jon ;
Moore, Dan H. ;
O'neill, Gilmore ;
Glass, Jonathan D. ;
Mitsumoto, Hiroshi ;
Appel, Stanley ;
Ravina, Bernard ;
Kieburtz, Karl ;
Shoulson, Ira ;
Kaufmann, Petra ;
Khan, Jaffar ;
Simpson, Ericka ;
Shefner, Jeremy ;
Levin, Bruce ;
Cwik, Valerie ;
Schoenfeld, David ;
Aggarwal, Swati ;
McDermott, Michael P. ;
Miller, Robert G. .
AMYOTROPHIC LATERAL SCLEROSIS, 2010, 11 (03) :259-265
[8]   Phase angle is a prognostic factor for survival in amyotrophic lateral sclerosis [J].
Desport, Jean-Claude ;
Marin, Benoit ;
Funalot, Benoiet ;
Preux, Pierre-Marie ;
Couratier, Philippe .
AMYOTROPHIC LATERAL SCLEROSIS, 2008, 9 (05) :273-278
[9]   Efficacy of minocycline in patients with amyotrophic lateral sclerosis: a phase III randomised trial [J].
Gordon, Paul H. ;
Moore, Dan H. ;
Miller, Robert G. ;
Florence, Julaine M. ;
Verheijde, Joseph L. ;
Doorish, Carolyn ;
Hilton, Joan F. ;
Spitalny, G. Mark ;
MacArthur, Robert B. ;
Mitsumoto, Hiroshi ;
Neville, Hans E. ;
Boylan, Kevin ;
Mozaffar, Tahseen ;
Belsh, Jerry M. ;
Ravits, John ;
Bedlack, Richard S. ;
Graves, Michael C. ;
McCluskey, Leo F. ;
Barohn, Richard J. ;
Tandan, Rup .
LANCET NEUROLOGY, 2007, 6 (12) :1045-1053
[10]   Body composition determination by bioimpedance: an update [J].
Jaffrin, Michel Y. .
CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE, 2009, 12 (05) :482-486