Abstract
Summary
This study used the “functional muscle–bone unit” concept to investigate muscle–bone interaction of the lumbar spine in subjects of varying bone mineral density. It was found that unit bone mass corresponded to a relatively more muscle mass in subjects with reduced bone mineral density, indicating a relatively higher mechanical load from muscles exerted on trabecular bone.
Introduction
Bone is an architecturally adaptive tissue which responds to mechanical loading. This study is proposed to use “functional muscle–bone unit” to reflect this muscle–bone interaction at spine in subjects with different bone mineral density.
Methods
The study was carried out in young normal subjects (21 females; age, 29 ± 3) and elderly subjects (155 females; age, 73 ± 3.9) with varying bone mineral density. Cross-sectional area of paravertebral muscle groups was measured in MR images to indicate the muscle mass, while the bone mineral content by dual X-ray absorptiometry was used to represent the bone mass. The functional muscle–bone unit was calculated as the ratio between the bone mass to muscle mass.
Results
It showed that with aging, the muscle mass decreased with the bone mass losing. However, more pronounced reduction was found in bone mass than in muscle mass in the subjects with lower bone mineral density.
Conclusions
Muscle–bone interaction was changed in elderly, especially in those with osteoporosis. Unit bone mass corresponded to a higher muscle mass in subjects with reduced bone mineral density than those normal subjects. This may be contributory to the occurrence of nontraumatic vertebral fractures in elderly subjects with reduced bone mineral density.
Similar content being viewed by others
References
Frost HM (1997) Defining osteopenias and osteoporoses: another view (with insights from a new paradigm). Bone 20:385–391
Ferretti JL, Cointry GR, Capozza RF, Frost HM (2003) Bone mass, bone strength, muscle–bone interactions, osteopenias and osteoporoses. Mech Ageing Dev 124:269–279
Schoenau E, Neu CM, Beck B, Manz F, Rauch F (2002) Bone mineral content per muscle cross-sectional area as an index of the functional muscle-bone unit. J Bone Miner Res 17:1095–1101
Schoenau E (2005) From mechanostat theory to development of the "Functional Muscle-Bone-Unit". J Musculoskelet Neuronal Interact 5:232–238
Fricke O, Schoenau E (2007) The ‘Functional Muscle-Bone Unit’: probing the relevance of signals for bone development in children and adolescents. Growth Hormone & IGF Research 17:1–9
(1993) Consensus Development Conference: diagnosis, prophylaxis, and treatment of osteoporosis. Am J Med 94:646–650
Kanis JA (2002) Diagnosis of osteoporosis and assessment of fracture risk. Lancet 359:1929–1936
Johnell O, Kanis JA, Oden A, Johansson H, De Laet C, Delmas P, Eisman JA, Fujiwara S, Kroger H, Mellstrom D, Meunier PJ, Melton L Jr, O’Neill T, Pols H, Reeve J, Silman A, Tenenhouse A (2007) Predictive value of BMD for hip and other fractures. J Bone Miner Res 20:1185–1194
Bergstrom U, Bjornstig U, Stenlund H, Jonsson H, Svensson O (2008) Fracture mechanisms and fracture pattern in men and women aged 50 years and older: a study of a 12-year population-based injury register, Umea, Sweden. Osteoporos Int 9:1275
Riggs BL, Wahner HW, Seeman E, Offord KP, Dunn WL, Mazess RB, Johnson KA, Melton LJ 3rd (1982) Changes in bone mineral density of the proximal femur and spine with aging. Differences between the postmenopausal and senile osteoporosis syndromes. J Clin Invest 70:716–723
Weiss A, Arbell I, Steinhagen-Thiessen E, Silbermann M (1991) Structural changes in aging bone: osteopenia in the proximal femurs of female mice. Bone 12:165–172
Seeman E (2003) Pathogenesis of osteoporosis. J Appl Physiol 95:2142–2151
Be’ery-Lipperman M, Gefen A (2005) Contribution of muscular weakness to osteoporosis: computational and animal models. Clin Biomech 20:984–997
Lanyon LE (1993) Osteocytes, strain detection, bone modeling and remodeling. Calcif Tissue Int 53:S102–S106
Frost HM, Ferretti JL, Jee WS (1998) Perspectives: some roles of mechanical usage, muscle strength, and the mechanostat in skeletal physiology, disease, and research. Calcif Tissue Int 62:1–7
Ferretti JL, Capozza RF, Cointry GR, Garcia SL, Plotkin H, Alvarez Filgueira ML, Zanchetta JR (1998) Gender-related differences in the relationship between densitometric values of whole-body bone mineral content and lean body mass in humans between 2 and 87 years of age. Bone 22:683–690
Luo ZP, Zhang L, Turner RT, An K-N (2000) Effects of mechanical stress/strain and estrogen on cancellous bone structure predicted by fuzzy decision. IEEE Trans Biomed Eng 47:344–351
Ferretti JL, Capozza RF, Cointry GR, Capiglioni R, Roldan EJ, Zanchetta JR (2000) Densitometric and tomographic analyses of musculoskeletal interactions in humans. J Musculoskelet Neuronal Interact 1:31–34
Seeman E, Delmas PD (2006) Bone quality—the material and structural basis of bone strength and fragility. N Engl J Med 354:2250–2261
Frost H (1987) Bone "mass" and the "mechanostat": a proposal. Anat Rec 219(1):1–9
Marotti G (2000) The osteocyte as a wiring transmission system. J Musculoskelet Neuronal Interact 1:133–136
Turner CH, Forwood MR, Rho JY, Yoshikawa T (1994) Mechanical loading thresholds for lamellar and woven bone formation. J Bone Miner Res 9:87–97
Riddle RC, Donahue HJ (2009) From streaming-potentials to shear stress: 25 years of bone cell mechanotransduction. J Orthop Res 27:143–149
Lang T, LeBlanc A, Evans H, Lu Y, Genant H, Yu A (2004) Cortical and trabecular bone mineral loss from the spine and hip in long-duration spaceflight. J Bone Miner Res 19:1006–1012
Frost HM (1990) Skeletal structural adaptations to mechanical usage (SATMU): 1. Redefining Wolff’s law: the bone modeling problem. Anat Rec 226:403–413
Frost HM (1990) Structural adaptations to mechanical usage (SATMU). 2. Redefining Wolff’s Law: the bone remodeling problem. Anat Rec 226:414–422
Reeve J, Walton J, Russell LJ, Lunt M, Wolman R, Abraham R, Justice J, Nicholls A, Wardley-Smith B, Green JR, Mitchell A (1999) Determinants of the first decade of bone loss after menopause at spine, hip and radius. QJM 92:261–273
Lang TF (2011) The bone–muscle relationship in men and women. J Osteoporos 2011:702735
Lee KC, Lanyon LE (2004) Mechanical loading influences bone mass through estrogen receptor alpha. Exerc Sport Sci Rev 32:64–68
Khoo BC, Brown K, Cann C, Zhu K, Henzell S, Low V, Gustafsson S, Price RI, Prince RL (2009) Comparison of QCT-derived and DXA-derived areal bone mineral density and T scores. Osteoporos Int 20:1539–1545
Li N, Li XM, Xu L, Sun WJ, Cheng XG, Tian W (2013) Comparison of QCT and DXA: osteoporosis detection rates in postmenopausal women. Int J Endocrinol 2013:895474
Acknowledgments
This study is supported by the National Natural Science Foundation of China (81000647), Basic Research Foundation (Outstanding Young Investigator Track) of Shenzhen (JC201005260124A), High-end Talent Oversea Returnees Foundation of Shenzhen (KQC201109020052A), and Research Grants Council of the Hong Kong Special Administrative Region, China (Project No. 465111).
Conflicts of interest
None.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Ma, H.T., Griffith, J.F., Xu, L. et al. The functional muscle–bone unit in subjects of varying BMD. Osteoporos Int 25, 999–1004 (2014). https://doi.org/10.1007/s00198-013-2482-7
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00198-013-2482-7