Body composition analysis as an indirect marker of skeletal muscle mass in Huntington's disease

被引:7
作者
Cubo, Esther [1 ]
Rivadeneyra, Jessica [2 ]
Gil-Polo, Cecilia [1 ]
Armesto, Diana [3 ]
Mateos, Ana [4 ]
Mariscal-Perez, Natividad [1 ]
机构
[1] Hosp Univ Burgos, Dept Neurol, Burgos 09006, Spain
[2] Hosp Univ Burgos, Res Unit, Burgos, Spain
[3] Stat Consulting, Burgos, Spain
[4] Natl Res Ctr Human Evolut CENIEH, Palaeophysiol Res Grp, Burgos, Spain
关键词
Body composition; Huntington's disease; Body mass index; Skeletal muscle; Fat-free mass; Fat mass; Bioimpedancy; Energy;
D O I
10.1016/j.jns.2015.09.351
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Skeletal muscle wasting is likely to play an important role in the Huntington's disease (HD) pathogenesis. Our aim was to analyze the body composition, and specifically fat-free mass (FFM), as an indirect marker of skeletal muscle in patients with HD, and its association with HD severity and energy balance. Methods: Cross-sectional, case-control study. Body composition was analyzed using bioelectrical impedance. Information was collected as regards of the anthropometrics, disease severity [Unified Huntington Disease Rating (UHDRS) and Total functional capacity (TFC) scores], CAG repeats, protein catabolism, energy intake and energy expenditure. Results: Twenty two patients with HD [mean age 50.3 +/- 15.6, mean UHDRS of 27.9 +/- 23.7, median TFC of 11 (IQR: 7:13); median body mass index 23.6 (IQR: 26.8; 22.5)], and 18 controls were included. Both groups were similar in terms of age, gender, body mass index, body composition, physical activity level, and protein catabolism. FFM was correlated with energy intake (r = 0.73, p < 0.001), resting energy expenditure (r = 0.64, p = 0.001) and physical activity (r = 0.54, p = 0.003), but not with CAG repeats, or HD severity. Conclusions: Our results do not support the presence of significant muscle wasting in patients with early-moderate Huntington's disease. However, to prevent muscle wasting in HD, dietary strategies, in addition to physical exercise, should be further investigated. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:335 / 338
页数:4
相关论文
共 24 条
  • [11] Skeletal muscle mass abnormalities are associated with survival rates of institutionalized elderly nursing home residents
    Kimyagarov, S.
    Klid, R.
    Fleissig, Y.
    Kopel, B.
    Arad, M.
    Adunsky, A.
    [J]. JOURNAL OF NUTRITION HEALTH & AGING, 2012, 16 (05) : 432 - 436
  • [12] Behavioural problems in Huntington's disease using the problem behaviours assessment
    Kingma, Elisabeth M.
    van Duijn, Erik
    Timman, Reinier
    van der Mast, Rose C.
    Roos, Raymund A. C.
    [J]. GENERAL HOSPITAL PSYCHIATRY, 2008, 30 (02) : 155 - 161
  • [13] Body Adiposity Index Utilization in a Spanish Mediterranean Population: Comparison with the Body Mass Index
    Lopez, Angel A.
    Cespedes, Mey L.
    Vicente, Teofila
    Tomas, Matias
    Bennasar-Veny, Miguel
    Tauler, Pedro
    Aguilo, Antoni
    [J]. PLOS ONE, 2012, 7 (04):
  • [14] Skeletal Muscle Atrophy in R6/2 Mice - Altered Circulating Skeletal Muscle Markers and Gene Expression Profile Changes
    Magnusson-Lind, Anna
    Davidsson, Marcus
    Silajdzic, Edina
    Hansen, Christian
    McCourt, Andrew C.
    Tabrizi, Sarah J.
    Bjorkqvist, Maria
    [J]. JOURNAL OF HUNTINGTONS DISEASE, 2014, 3 (01) : 13 - 24
  • [15] Musculoskeletal health, frailty and functional decline
    Milte, R.
    Crotty, M.
    [J]. BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY, 2014, 28 (03): : 395 - 410
  • [16] Characteristics of individuals with Huntington disease in long-term care
    Nance, MA
    Sanders, G
    [J]. MOVEMENT DISORDERS, 1996, 11 (05) : 542 - 548
  • [17] Increased mitochondrial fission and neuronal dysfunction in Huntington's disease: implications for molecular inhibitors of excessive mitochondrial fission
    Reddy, P. Hemachandra
    [J]. DRUG DISCOVERY TODAY, 2014, 19 (07) : 951 - 955
  • [18] Techniques for the diagnosis of sarcopenia
    Rubbieri, Gaia
    Mossello, Enrico
    Di Bari, Mauro
    [J]. CLINICAL CASES IN MINERAL AND BONE METABOLISM, 2014, 11 (03) : 181 - 184
  • [19] Molecular characterization of skeletal muscle atrophy in the R6/2 mouse model of Huntington's disease
    She, Pengxiang
    Zhang, Zhiyou
    Marchionini, Deanna
    Diaz, William C.
    Jetton, Thomas J.
    Kimball, Scot R.
    Vary, Thomas C.
    Lang, Charles H.
    Lynch, Christopher J.
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2011, 301 (01): : E49 - E61
  • [20] Varela-Moreiras G., 2012, EUR J CLIN NUTR, V64, pS37