ELECTRICAL IMPEDANCE MYOGRAPHY IN INDIVIDUALS WITH COLLAGEN 6 AND LAMININ α-2 CONGENITAL MUSCULAR DYSTROPHY: A CROSS-SECTIONAL AND 2-YEAR ANALYSIS

被引:11
|
作者
Nichols, Carmel [1 ,2 ]
Jain, Minal S. [1 ]
Meilleur, Katherine G. [3 ]
Wu, Tianxia [4 ]
Collins, James [5 ]
Waite, Melissa R. [1 ]
Dastgir, Jahannaz [6 ]
Salman, Anam [7 ,8 ]
Donkervoort, Sandra [9 ]
Duong, Tina [10 ]
Keller, Katherine [11 ]
Leach, Meganne E. [9 ]
Lott, Donovan J. [12 ]
Mcguire, Michelle N. [13 ]
Nelson, Leslie [14 ]
Rutkowski, Anne [15 ]
Vuillerot, Carole [16 ,17 ]
Bonnemann, Carsten G. [9 ]
Lehky, Tanya J. [7 ]
机构
[1] NIH, Mark O Hatfield Clin Res Ctr, Bldg 10, Bethesda, MD 20892 USA
[2] Univ Chicago, Sch Med, Chicago, IL 60637 USA
[3] NINR, Tissue Injury Branch, NIH, Bethesda, MD 20892 USA
[4] NINDS, Clin Trials Unit, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA
[5] Mercy Clin Pediat Neurol, Springfield, MO USA
[6] Columbia Univ, New York, NY USA
[7] NINDS, EMG Sect, NIH, Bldg 10,Room 7-5680, Bethesda, MD 20892 USA
[8] Mercy Hosp, Baltimore, MD USA
[9] NINDS, Neuromuscular & Neurogenet Disorders Childhood Se, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA
[10] Stanford Childrens Hlth, Stanford, CA USA
[11] Rady Childrens Hosp, San Diego, CA USA
[12] Univ Florida, Gainesville, FL USA
[13] Cincinnati Childrens Hosp, Cincinnati, OH USA
[14] Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USA
[15] Kaiser Permanente SCPMG Cure CMD, Los Angeles, CA USA
[16] Hosp Civils Lyon, Hop Femme Mere Enfant, Bron, France
[17] Univ Lyon, Lyon, France
关键词
COL6 related dystrophies; congenital muscular dystrophy; electrical impedance myography; LAMA2 related dystrophies; neuromuscular disorders; WHOLE VASTUS LATERALIS; DIFFERENT FIBER TYPES; MYOFIBER HYPERTROPHY; MYONUCLEAR ADDITION; SKELETAL-MUSCLE; MOTOR UNITS; OLDER MEN; NUMBER; YOUNG; MECHANISMS;
D O I
10.1002/mus.25629
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Electrical impedance myography (EIM) is a noninvasive electrophysiological technique that characterizes muscle properties through bioimpedance. We compared EIM measurements to function, strength, and disease severity in a population with congenital muscular dystrophy (CMD). Methods: Forty-one patients with CMD, either collagen 6 related disorders (COL6-RD; n=21) or laminin a-2-related disorders (LAMA2-RD; n=20), and 21 healthy pediatric controls underwent 2 yearly EIM exams. In the CMD cohorts, EIM was compared with functional and strength measurements. Results: Both CMD cohorts exhibited change over time and had correlation with disease severity. The 50-kHZ phase correlated well with function and strength in the COL6-RD cohort but not in the LAMA2-RD cohort. Discussion: EIM is a potentially useful measure in clinical studies with CMD because of its sensitivity to change over a 1-year period and correlation with disease severity. For COL6-RD, there were also functional and strength correlations.
引用
收藏
页码:54 / 60
页数:7
相关论文
共 50 条
  • [1] Cross-sectional Evaluation of Electrical Impedance Myography and Quantitative Ultrasound for the Assessment of Duchenne Muscular Dystrophy in a Clinical Trial Setting
    Rutkove, Seward B.
    Geisbush, Tom R.
    Mijailovic, Aleksandar
    Shklyar, Irina
    Pasternak, Amy
    Visyak, Nicole
    Wu, Jim S.
    Zaidman, Craig
    Darras, Basil T.
    PEDIATRIC NEUROLOGY, 2014, 51 (01) : 88 - 92
  • [2] Clinical outcome measures in Collagen 6 (COL6) and Laminin α2(LAMA2) related congenital muscular dystrophy
    Meilleur, K. G.
    Jain, M.
    Kim, E.
    Hynan, L.
    Shieh, C. Y.
    Waite, M.
    Duong, T.
    Glanzman, A.
    Main, M.
    Rose, K.
    McGuire, M.
    Bendixen, R.
    Foley, R.
    Donkervoort, S.
    Schindler, A.
    Kokkinis, A.
    Hartnett, E. J.
    Leach, M.
    Dastgir, J.
    North, K.
    Muntoni, F.
    Rutkowski, A.
    Bonnemann, C. G.
    NEUROMUSCULAR DISORDERS, 2012, 22 (9-10) : 893 - 893
  • [3] Protein and DNA analysis for the prenatal diagnosis of α2-laminin-deficient congenital muscular dystrophy
    Yamamoto, LU
    Gollop, TR
    Naccache, NF
    Pavanello, RCM
    Zanoteli, E
    Zatz, M
    Vainzof, M
    DIAGNOSTIC MOLECULAR PATHOLOGY, 2004, 13 (03) : 167 - 171
  • [4] Genotype/phenotype analysis in Chinese laminin-α2 deficient congenital muscular dystrophy patients
    Xiong, H.
    Tan, D. D.
    Wang, S.
    Chang, X. Z.
    Yuan, Y.
    Wu, X. R.
    NEUROMUSCULAR DISORDERS, 2013, 23 (9-10) : 781 - 781
  • [5] Genotype/phenotype analysis in Chinese laminin-α2 deficient congenital muscular dystrophy patients
    Xiong, H.
    Tan, D.
    Wang, S.
    Song, S.
    Yang, H.
    Gao, K.
    Liu, A.
    Jiao, H.
    Mao, B.
    Ding, J.
    Chang, X.
    Wang, J.
    Wu, Y.
    Yuan, Y.
    Jiang, Y.
    Zhang, F.
    Wu, H.
    Wu, X.
    CLINICAL GENETICS, 2015, 87 (03) : 233 - 243
  • [6] Estimating myofiber cross-sectional area and connective tissue deposition with electrical impedance myography: A study in D2-mdx mice
    Pandeya, Sarbesh R.
    Nagy, Janice A.
    Riveros, Daniela
    Semple, Carson
    Taylor, Rebecca S.
    Mortreux, Marie
    Sanchez, Benjamin
    Kapur, Kush
    Rutkove, Seward B.
    MUSCLE & NERVE, 2021, 63 (06) : 941 - 950
  • [7] Electrical Impedance Myography Correlates with Functional Measures of Disease Progression in D2-mdx Mice and Boys with Duchenne Muscular Dystrophy
    Chrzanowski, Stephen M.
    Nagy, Janice A.
    Pandeya, Sarbesh
    Rutkove, Seward B.
    JOURNAL OF NEUROMUSCULAR DISEASES, 2023, 10 (01) : 81 - 90
  • [8] A Multicenter Cross-Sectional Study of the Swiss Cohort of LAMA2-Related Muscular Dystrophy
    Enzmann, Cornelia
    Steiner, Leonie
    Pospieszny, Katarzyna
    Zweier, Christiane
    Plattner, Kevin
    Baumann, Dominique
    Henzi, Bettina
    Galiart, Elea
    Fink, Mirjam
    Jacquier, David
    Stettner, Georg M.
    Ripellino, Paolo
    Fluss, Joel
    Klein, Andrea
    JOURNAL OF NEUROMUSCULAR DISEASES, 2024, 11 (05) : 1021 - 1033
  • [9] Incidence of Greenlandic stroke-survivors in Greenland: A 2-year cross-sectional study
    Bjorn-Mortensen, Karen
    Lynggaard, Folmer
    Pedersen, Michael Lynge
    INTERNATIONAL JOURNAL OF CIRCUMPOLAR HEALTH, 2013, 72
  • [10] Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2
    HelblingLeclerc, A
    Topaloglu, H
    Tome, FMS
    Sewry, C
    Gyapay, G
    Noam, I
    Muntoni, F
    Dubowitz, V
    Barois, A
    Estournet, B
    Urtizberea, JA
    Weissenbach, J
    Schwartz, K
    Fardeau, M
    Guicheney, P
    COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE III-SCIENCES DE LA VIE-LIFE SCIENCES, 1995, 318 (12): : 1245 - 1252