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.
引用
收藏
页码:63 / 70
页数:8
相关论文
共 50 条
  • [31] Creation of Becker muscular dystrophy murine models to predict the efficacy of therapy for patients with Duchenne muscular dystrophy
    Polikarpova, A.
    Galkin, I.
    Korshunova, D.
    Skopenkova, V.
    Dzhenkova, M.
    Tsvirkun, D.
    Shmidt, A.
    Khamatova, A.
    Loginov, V.
    Deikin, A.
    Bardina, M.
    Egorova, T.
    NEUROMUSCULAR DISORDERS, 2021, 31 : S74 - S74
  • [32] Dystrophin levels and clinical severity in Becker muscular dystrophy patients
    van den Bergen, J. C.
    Wokke, B. H.
    Janson, A. A.
    van Duinen, S. G.
    Hulsker, M. A.
    Ginjaar, H. B.
    van Deutekom, J. C.
    Aartsma-Rus, A.
    Kan, H. E.
    Verschuuren, J. J.
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2014, 85 (07): : 747 - 753
  • [33] Effects of Sildenafil on Cerebrovascular Reactivity in Patients with Becker Muscular Dystrophy
    Ulrich Lindberg
    Nanna Witting
    Stine Lundgaard Jørgensen
    John Vissing
    Egill Rostrup
    Henrik Bo Wiberg Larsson
    Christina Kruuse
    Neurotherapeutics, 2017, 14 : 182 - 190
  • [34] Deletion patterns in Argentine patients with Duchenne and Becker muscular dystrophy
    Baranzini, SE
    Giliberto, F
    Herrera, M
    Bernath, V
    Barreiro, C
    Erro, MG
    Grippo, J
    Szijan, I
    NEUROLOGICAL RESEARCH, 1998, 20 (05) : 409 - 414
  • [35] Effects of Sildenafil on Cerebrovascular Reactivity in Patients with Becker Muscular Dystrophy
    Lindberg, Ulrich
    Witting, Nanna
    Jorgensen, Stine Lundgaard
    Vissing, John
    Rostrup, Egill
    Larsson, Henrik Bo Wiberg
    Kruuse, Christina
    NEUROTHERAPEUTICS, 2017, 14 (01) : 182 - 190
  • [36] EFFECT OF SILDENAFIL ON CEREBROVASCULAR REACTIVITY IN PATIENTS WITH BECKER MUSCULAR DYSTROPHY
    Lindberg, U.
    Witting, N.
    Joergensen, S.
    Vissing, J.
    Rostrup, E.
    Larsson, H. B. W.
    Kruuse, C.
    JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2016, 36 : 424 - 425
  • [37] Genotype–phenotype correlation in Becker muscular dystrophy in Chinese patients
    Ruiyi Yuan
    Junfei Yi
    Zhiying Xie
    Yimeng Zheng
    Miao Han
    Yue Hou
    Zhaoxia Wang
    Yun Yuan
    Journal of Human Genetics, 2018, 63 : 1041 - 1048
  • [38] Tadalafil Alleviates Muscle Ischemia in Patients with Becker Muscular Dystrophy
    Martin, Elizabeth A.
    Barresi, Rita
    Byrne, Barry J.
    Tsimerinov, Evgeny I.
    Scott, Bryan L.
    Walker, Ashley E.
    Gurudevan, Swaminatha V.
    Anene, Francine
    Elashoff, Robert M.
    Thomas, Gail D.
    Victor, Ronald G.
    SCIENCE TRANSLATIONAL MEDICINE, 2012, 4 (162)
  • [39] Altered somatosensory neurovascular response in patients with Becker muscular dystrophy
    Lindberg, Ulrich
    Kruuse, Christina
    Witting, Nanna
    Jorgensen, Stine Lundgaard
    Vissing, John
    Rostrup, Egill
    Larsson, Henrik Bo Wiberg
    BRAIN AND BEHAVIOR, 2018, 8 (06):
  • [40] Clinical profile of pediatric patients with Becker Muscular Dystrophy (BMD)
    Shellenbarger, K. C.
    Rybalsky, I.
    Bange, J.
    Wong, B. L.
    NEUROMUSCULAR DISORDERS, 2014, 24 (9-10) : 794 - 795