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. 2015 Jun;15(2):154-60.

Gastrocnemius medialis muscle architecture and physiological cross sectional area in adult males with Duchenne muscular dystrophy

Affiliations

Gastrocnemius medialis muscle architecture and physiological cross sectional area in adult males with Duchenne muscular dystrophy

C I Morse et al. J Musculoskelet Neuronal Interact. 2015 Jun.

Abstract

Objectives: To describe muscle size and architecture of the gastrocnemius medialis (GM) muscle in eleven adult males with Duchenne Muscular Dystrophy (DMD, age 24.5±5.4 years), and a control group of eleven males without DMD (CTRL, age 22.1±0.9 years).

Methods: GM anatomical cross sectional area (ACSA), volume (VOL), physiological cross sectional area (PCSA), fascicle length (Lf) and pennation angle (θ) were assessed using B-Mode Ultrasonography. GM ACSA was measured at 25, 50 and 75% of muscle length (Lm), from which VOL was calculated. At 50% of Lm, sagittal plane images were analysed to determine GM Lf and θ. GM PCSA was calculated as: VOL/Lf. The ratio of Lf and Lm was also calculated.

Results: GM ACSA at 50% Lm, VOL and PCSA were smaller in DMD males compared to CTRL males by 36, 47 and 43%, respectively (P<0.01). There were no differences in Lf and θ. GM Lm was 29% shorter in DMD compared to CTRL. Lf/Lm was 29% longer in DMD (P<0.01).

Conclusions: Unlike previous data in children with DMD, our results show significant atrophy in adult males with DMD, and no change in Lf or θ. The shorter Lm may have implications for joint flexibility.

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Conflict of interest statement

The authors have no conflict of interest.

Figures

Figure 1
Figure 1
An example of the reconstructed GM ACSA at 50% of muscle length in a participant with DMD (A) and a control participant (B).
Figure 2
Figure 2
An example of a sagittal plane ultrasound scan at 50% of GM length in an individual with DMD (A) and a control participant (B).
Figure 3
Figure 3
Gastrocnemius medialis anatomical cross sectional area (GM ACSA) at 25, 50 and 75% of GM length from origin. Adult males with Duchenne muscular dystrophy are denoted with open circles, and the control participants are denoted with closed squares. * denotes significant difference from the control group (P<0.05).

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