Muscle and Myotendinous Tissue Properties at the Distal Tibia as Assessed by High-Resolution Peripheral Quantitative Computed Tomography

Abstract High-resolution peripheral quantitative computed tomography (HR-pQCT) quantifies bone microstructure and density at the distal tibia where there is also a sizable amount of myotendinous (muscle and tendon) tissue (MT ); however, there is no method for the quantification of MT . This study a...

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Veröffentlicht in:Journal of clinical densitometry 2017-04, Vol.20 (2), p.226-232
Hauptverfasser: Erlandson, M.C, Wong, A.K.O, Szabo, E, Vilayphiou, N, Zulliger, M.A, Adachi, J.D, Cheung, A.M
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Sprache:eng
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Zusammenfassung:Abstract High-resolution peripheral quantitative computed tomography (HR-pQCT) quantifies bone microstructure and density at the distal tibia where there is also a sizable amount of myotendinous (muscle and tendon) tissue (MT ); however, there is no method for the quantification of MT . This study aimed (1) to assess the feasibility of using HR-pQCT distal tibia scans to estimate MT properties using a custom algorithm, and (2) to determine the relationship between MT properties at the distal tibia and mid-leg muscle density (MD) obtained from pQCT. Postmenopausal women from the Hamilton cohort of the Canadian Multicenter Osteoporosis Study had a single-slice (2.3 ± 0.5 mm) 66% site pQCT scan measuring muscle cross-sectional area (MCSA) and MD. A standard HR-pQCT scan was acquired at the distal tibia. HR-pQCT-derived MT cross-sectional area (MT CSA) and MT density (MT D) were calculated using a custom algorithm in which thresholds (34.22–194.32 mg HA/cm3 ) identified muscle seed volumes and were iteratively expanded. Pearson and Bland-Altman plots were used to assess correlations and systematic differences between pQCT- and HR-pQCT-derived muscle properties. Among 45 women (mean age: 74.6 ± 8.5 years, body mass index: 25.9 ± 4.3 kg/m2 ), MT D was moderately correlated with mid-leg MD across the 2 modalities (r = 0.69–0.70, p  
ISSN:1094-6950
1559-0747
DOI:10.1016/j.jocd.2016.10.005