Multicenter Validation of the Charcot-Marie-Tooth Functional Outcome Measure

被引:3
|
作者
Mandarakas, Melissa R. [1 ,2 ]
Eichinger, Katy J. [3 ]
Bray, Paula [1 ,2 ]
Cornett, Kayla M. D. [1 ,2 ]
Shy, Michael E. [4 ]
Reilly, Mary M. [5 ]
Ramdharry, Gita M. [5 ]
Scherer, Steven S. [6 ]
Pareyson, Davide [7 ]
Estilow, Timothy [8 ,9 ]
McKay, Marnee J. [1 ]
Herrmann, David N. [3 ]
Burns, Joshua [1 ,2 ]
机构
[1] Univ Sydney, Fac Med & Hlth, Sch Hlth Sci, Sydney, Australia
[2] Sydney Childrens Hosp Network Randwick & Westmead, Sydney, NSW, Australia
[3] Univ Rochester, Dept Neurol, Rochester, NY USA
[4] Univ Iowa, Carver Coll Med, Dept Neurol, Iowa City, IA USA
[5] UCL Queen Sq Inst Neurol, Ctr Neuromuscular Dis, Dept Neuromuscular Dis, London, England
[6] Univ Penn, Perelman Sch Med, Dept Neurol, Philadelphia, PA USA
[7] Fdn IRCCS Ist Neurol Carlo Besta, Milan, Italy
[8] Childrens Hosp Philadelphia, Philadelphia, PA USA
[9] Univ Penn, Perelman Sch Med, Philadelphia, PA USA
关键词
REFERENCE VALUES; NATURAL-HISTORY; SCALE;
D O I
10.1212/WNL.0000000000207963
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and ObjectivesCharcot-Marie-Tooth disease type 1A (CMT1A), caused by a duplication of PMP22, is the most common hereditary peripheral neuropathy. For participants with CMT1A, few clinical trials have been performed; however, multiple therapies have reached an advanced stage of preclinical development. In preparation for imminent clinical trials in participants with CMT1A, we have produced a Clinical Outcome Assessment (COA), known as the CMT-Functional Outcome Measure (CMT-FOM), in accordance with the FDA Roadmap to Patient-Focused Outcome Measurement to capture the key clinical end point of function. MethodsParticipants were recruited through CMT clinics in the United States (n = 130), the United Kingdom (n = 52), and Italy (n = 32). To derive the most accurate signal with the fewest items to identify a therapeutic response, a series of validation studies were conducted including item and factor analysis, Rasch model analysis and testing of interrater reliability, discriminative ability, and convergent validity. ResultsA total of 214 participants aged 18-75 years with CMT1A (58% female) were included in this study. Item, factor, and Rasch analysis supported the viability of the 12-item CMT-FOM as a unidimensional interval scale of function in adults with CMT1A. The CMT-FOM covers strength, upper and lower limb function, balance, and mobility. The 0-100 point scoring system showed good overall model fit, no evidence of misfitting items, and no person misfit, and it was well targeted for adults with CMT1A exhibiting high inter-rater reliability across a range of clinical settings and evaluators. The CMT-FOM was significantly correlated with the CMT Examination Score (r = 0.643; p < 0.001) and the Overall Neuropathy Limitation Scale (r = 0.516; p < 0.001). Significantly higher CMT-FOM total scores were observed in participants self-reporting daily trips and falls, unsteady ankles, hand tremor, and hand weakness (p < 0.05). DiscussionThe CMT-FOM is a psychometrically robust multi-item, unidimensional, disease-specific COA covering strength, upper and lower limb function, balance, and mobility to capture how participants with CMT1A function to identify therapeutic efficacy.
引用
收藏
页数:12
相关论文
共 50 条
  • [31] CHARCOT-MARIE-TOOTH DISEASE
    MCLAIN, LW
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1974, 229 (07): : 767 - 767
  • [32] Charcot-Marie-Tooth disease
    Buteica, Elena
    Rosulescu, Eugenia
    Stanoiu, B.
    Burada, F.
    Stanoiu, Cosmina
    Zavaleanu, Mihaela
    ROMANIAN JOURNAL OF MORPHOLOGY AND EMBRYOLOGY, 2008, 49 (01): : 115 - 119
  • [33] Syndromic Charcot-Marie-Tooth is easily neglected in ordinary diagnostics of Charcot-Marie-Tooth disease
    Braathen, G. J.
    Eek, A. K.
    Hoyer, H.
    Bergsaker, D. K.
    Russell, M. B.
    EUROPEAN JOURNAL OF NEUROLOGY, 2010, 17 : 607 - 607
  • [34] In search of responsive outcome measures in Charcot-Marie-Tooth disease
    Pareyson, D.
    EUROPEAN JOURNAL OF NEUROLOGY, 2017, 24 : 730 - 730
  • [35] Development and validation of the Charcot-Marie-Tooth Disease Infant Scale
    Mandarakas, Melissa R.
    Menezes, Manoj P.
    Rose, Kristy J.
    Shy, Rosemary
    Eichinger, Kate
    Foscan, Maria
    Estilow, Timothy
    Kennedy, Rachel
    Herbert, Karen
    Bray, Paula
    Refshauge, Kathryn
    Ryan, Monique M.
    Yiu, Eppie M.
    Farrar, Michelle
    Sampaio, Hugo
    Moroni, Isabella
    Pagliano, Emanuela
    Pareyson, Davide
    Yum, SabrinaW.
    Herrmann, David N.
    Acsadi, Gyula
    Shy, Michael E.
    Burns, Joshua
    Sanmaneechai, Oranee
    BRAIN, 2018, 141 : 3319 - 3330
  • [36] Clinical Outcome Assessments and Biomarkers in Charcot-Marie-Tooth Disease
    Mccray, Brett A.
    Fridman, Vera
    NEUROLOGY, 2024, 103 (12)
  • [37] Responsiveness of clinical outcome measures in Charcot-Marie-Tooth disease
    Piscosquito, G.
    Reilly, M. M.
    Schenone, A.
    Fabrizi, G. M.
    Cavallaro, T.
    Santoro, L.
    Manganelli, F.
    Vita, G.
    Quattrone, A.
    Padua, L.
    Gemignani, F.
    Visioli, F.
    Laura, M.
    Calabrese, D.
    Hughes, R. A. C.
    Radice, D.
    Solari, A.
    Pareyson, D.
    EUROPEAN JOURNAL OF NEUROLOGY, 2015, 22 (12) : 1556 - 1563
  • [38] Reliability of clinical outcome measures in Charcot-Marie-Tooth disease
    Solari, A.
    Laura, M.
    Salsano, E.
    Radice, D.
    Pareyson, D.
    NEUROMUSCULAR DISORDERS, 2008, 18 (01) : 19 - 26
  • [39] FUNCTIONAL IMPLICATIONS OF HAND IMPAIRMENT IN PEDIATRIC CHARCOT-MARIE-TOOTH
    Estilow, T.
    Glanzman, A. M.
    Burns, J.
    Cornett, K. M. D.
    Menezes, M. P.
    Shy, R.
    Moroni, I
    Foscan, M.
    Pagliano, E.
    Pareyson, D.
    Laura, M.
    Bhandari, T.
    Muntoni, F.
    Reilly, M. M.
    Finkel, R. S.
    Sowden, J.
    Eichinger, K.
    Herrmann, D. N.
    Shy, M. E.
    Yum, S. W.
    Ramchandren, S.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2017, 22 (03) : 279 - 279
  • [40] Diagnosis of Charcot-Marie-Tooth Disease
    Banchs, Isabel
    Casasnovas, Carlos
    Alberti, Antonia
    De Jorge, Laura
    Povedano, Monica
    Montero, Jordi
    Antonio Martinez-Matos, Juan
    Volpini, Victor
    JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2009,