Body composition and myokines in a cohort of patients with Becker muscular dystrophy

被引:4
作者
Barp, Andrea [1 ]
Carraro, Elena [1 ]
Goggi, Giovanni [2 ,3 ]
Lizio, Andrea [1 ]
Zanolini, Alice [1 ]
Messina, Carmelo [4 ]
Perego, Silvia [5 ]
Verdelli, Chiara [6 ]
Lombardi, Giovanni [5 ,7 ]
Sansone, Valeria Ada [1 ]
Corbetta, Sabrina [2 ,8 ]
机构
[1] Univ Milan, NeMO Clin Ctr, Neurorehabil Unit, Piazza Osped Maggiore 3, I-20162 Milan, Italy
[2] IRCCS Ist Ortoped Galeazzi, Endocrinol & Diabetol Serv, Milan, Italy
[3] Univ Milan, Dept Biotechnol & Translat Med, Milan, Italy
[4] IRCCS Ist Ortoped Galeazzi, Milan, Italy
[5] IRCCS Ist Ortoped Galeazzi, Lab Expt Biochem & Mol Biol, Milan, Italy
[6] IRCCS Ist Ortoped Galeazzi, Lab Expt Endocrinol, Milan, Italy
[7] Poznan Univ Phys Educ, Dept Athlet Strength & Conditioning, Poznan, Poland
[8] Univ Milan, Dept Biomed Surg & Dent Sci, Milan, Italy
关键词
Becker muscular dystrophy; bone mineral density; Duchenne muscular dystrophy; DXA; Irisin; X-RAY ABSORPTIOMETRY; BONE-MINERAL DENSITY; SKELETAL-MUSCLE; OSTEOPOROTIC FRACTURES; DIAGNOSTIC-CRITERIA; MASS; SARCOPENIA; IRISIN; PROTEIN; QUANTIFICATION;
D O I
10.1002/mus.27565
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction/Aims Becker muscular dystrophy (BMD) is an X-linked disease leading to muscle wasting and weakness. The decrease in lean body mass (LBM) in Duchenne muscular dystrophy, has shown correlation with loss of muscle function and bone density (BD). Myokines (including irisin) are hormones secreted by skeletal muscle that allow crosstalk between muscle and bone. The present study analyzed body composition and circulating myokine levels in a cohort of BMD patients; moreover, the association between dual energy X-ray absorptiometry (DXA) parameters, functional motor assessments, and myokine levels was investigated. Methods All patients underwent DXA, blood samples for myokine assays, and functional motor assessments. A group of healthy controls (HCs) was also included. Results Thirty BMD patients, median age at evaluation 36.0 y [26.0-41.0], were included. Twenty-nine patients underwent whole-body DXA. Median value of total body Z-score was -0.70. The prevalence of low skeletal muscle mass defined as appendicular skeletal muscle mass index (ASMMI) < 7.59 kg/m(2) was 83%. Irisin levels were significantly lower in BMD compared to HCs (p = .03). All DXA parameters showed significant correlation with the functional motor assessments, in particular the h(2)-standardized lean mass lower limb index (p = .0006); h(2)-standardized total fat mass showed negative correlations with North Star Ambulatory Assessment and 6 min walk test (p = .03). Discussion DXA is a useful tool to evaluate body composition in BMD patients; the decrease in BD and LBM is associated with a reduction of motor function in BMD.
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收藏
页码:63 / 70
页数:8
相关论文
共 40 条
[1]   Relationships of thigh muscle contractile and non-contractile tissue with function, strength, and age in boys with Duchenne muscular dystrophy [J].
Akima, Hiroshi ;
Lott, Donovan ;
Senesac, Claudia ;
Deol, Jasjit ;
Germain, Sean ;
Arpan, Ishu ;
Bendixen, Roxanna ;
Sweeney, H. Lee ;
Walter, Glenn ;
Vandenborne, Krista .
NEUROMUSCULAR DISORDERS, 2012, 22 (01) :16-25
[2]   Circulating irisin is associated with osteoporotic fractures in postmenopausal women with low bone mass but is not affected by either teriparatide or denosumab treatment for 3 months [J].
Anastasilakis, A. D. ;
Polyzos, S. A. ;
Makras, P. ;
Gkiomisi, A. ;
Bisbinas, I. ;
Katsarou, A. ;
Filippaios, A. ;
Mantzoros, C. S. .
OSTEOPOROSIS INTERNATIONAL, 2014, 25 (05) :1633-1642
[3]   CLINICAL-MOLECULAR CORRELATION IN 104 MILD X-LINKED MUSCULAR-DYSTROPHY PATIENTS - CHARACTERIZATION OF SUBCLINICAL PHENOTYPES [J].
ANGELINI, C ;
FANIN, M ;
PEGORARO, E ;
FREDA, MP ;
CADALDINI, M ;
MARTINELLO, F .
NEUROMUSCULAR DISORDERS, 1994, 4 (04) :349-358
[4]   Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials [J].
Anthony, Karen ;
Cirak, Sebahattin ;
Torelli, Silvia ;
Tasca, Giorgio ;
Feng, Lucy ;
Arechavala-Gomeza, Virginia ;
Armaroli, Annarita ;
Guglieri, Michela ;
Straathof, Chiara S. ;
Verschuuren, Jan J. ;
Aartsma-Rus, Annemieke ;
Helderman-van den Enden, Paula ;
Bushby, Katherine ;
Straub, Volker ;
Sewry, Caroline ;
Ferlini, Alessandra ;
Ricci, Enzo ;
Morgan, Jennifer E. ;
Muntoni, Francesco .
BRAIN, 2011, 134 :3544-3556
[5]  
Barzegar M, 2018, IRAN J CHILD NEUROL, V12, P77
[6]   Epidemiology of sarcopenia among the elderly in New Mexico [J].
Baumgartner, RN ;
Koehler, KM ;
Gallagher, D ;
Romero, L ;
Heymsfield, SB ;
Ross, RR ;
Garry, PJ ;
Lindeman, RD .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1998, 147 (08) :755-763
[7]   Diagnostic criteria for sarcopenia and physical performance [J].
Bijlsma, A. Y. ;
Meskers, C. G. M. ;
van den Eshof, N. ;
Westendorp, R. G. ;
Sipila, S. ;
Stenroth, L. ;
Sillanpaa, E. ;
McPhee, J. S. ;
Jones, D. A. ;
Narici, M. V. ;
Gapeyeva, H. ;
Paeaesuke, M. ;
Voit, T. ;
Barnouin, Y. ;
Hogrel, J. Y. ;
Butler-Browne, G. ;
Maier, A. B. .
AGE, 2014, 36 (01) :275-285
[8]   THE CLINICAL, GENETIC AND DYSTROPHIN CHARACTERISTICS OF BECKER MUSCULAR-DYSTROPHY .2. CORRELATION OF PHENOTYPE WITH GENETIC AND PROTEIN ABNORMALITIES [J].
BUSHBY, KMD ;
GARDNERMEDWIN, D ;
NICHOLSON, LVB ;
JOHNSON, MA ;
HAGGERTY, ID ;
CLEGHORN, NJ ;
HARRIS, JB ;
BHATTACHARYA, SS .
JOURNAL OF NEUROLOGY, 1993, 240 (02) :105-112
[9]   Analysis of dystrophin gene deletions indicates that the hinge III region of the protein correlates with disease severity [J].
Carsana, A ;
Frisso, G ;
Tremolaterra, MR ;
Lanzillo, R ;
Vitale, DF ;
Santoro, L ;
Salvatore, F .
ANNALS OF HUMAN GENETICS, 2005, 69 :253-259
[10]   Circulating irisin levels as a predictive biomarker for sarcopenia: A cross-sectional community-based study [J].
Chang, Jae Seung ;
Kim, Tae Ho ;
Tuyet Thi Nguyen ;
Park, Kyu-Sang ;
Kim, Nahyun ;
Kong, In Deok .
GERIATRICS & GERONTOLOGY INTERNATIONAL, 2017, 17 (11) :2266-2273