Michael Perrins1,2, Michiel Simons2,3, Paul Kennedy4, Lisa Salisbury5, Colin Brown6, Timothy Walsh1,7, Edwin J.R. van Beek2, David Griffith1,7, and Neil Roberts2
1MRC Centre for Inflammation Research, University of Edinburgh, Edinburgh, United Kingdom, 2Edinburgh Imaging Facility, University of Edinburgh, Edinburgh, United Kingdom, 3Department of Clinical Surgery, University of Edinburgh, Edinburgh, United Kingdom, 4Department of Radiology, Icahn School of Medicine at Mount Sinai, Manhattan, NY, United States, 5Department of Physiotherapy, Queen Margaret University, Edinburgh, United Kingdom, 6The Mentholatum Company Ltd., East Kilbride, Glasgow, United Kingdom, 7Anaesthesia, Critical Care and Pain Medicine, University of Edinburgh, Edinburgh, United Kingdom
Synopsis
Age-related
weakness and strength has been shown to have an anatomical basis, with stability
of the knee being particularly prone to effects of ageing. Magnetic Resonance
Elastography (MRE) was used to obtain muscle size and stiffness measurements in
a ‘Younger’ and ‘Older’ group of participants. It was found that the Quadriceps
muscle group were primarily impacted by age related atrophy, whilst also
increasing in stiffness with age. Furthermore, the muscles along the medial
side of the leg showed significantly lower muscle stiffness in ‘Older’
participants which we determined to be a biomarker for age-related anatomical instability.
Introduction
Age-related
muscle atrophy primarily affects the Quadriceps muscle group when comparing 24
to 79 year olds1, with each of the four muscles within the
Quadriceps shown to atrophy at the same rate. Age-related muscle atrophy of
Vastus Lateralis has been suggested as an indicator for the whole quadriceps
muscle group1, beginning at the age of 25, with atrophy then
increasing incrementally with age2. Periods of immobility have been
shown to be detrimental to muscle morphology3, however decreases in
muscle size and strength seen in older individuals4 may be due to
age-related changes in muscle fibres5,6. These changes result in
gait instability7. Knee joint stability relies on static (joint
congruency and ligaments) and dynamic stabilisers (surrounding musculature)8
with Quadriceps strength (determined by size4) and medial
muscles playing a pivotal role9. Muscle recruitment patterns change
with instability leading to increased co-contraction of antagonist muscles10.
The purpose of the present study is to investigate age related changes to
muscle morphology and mechanical properties, by applying Magnetic Resonance
Elastography (MRE) to identify changes in the mechanical properties of middle
aged adults’ thigh muscles for biomarkers of gait instability. The hypothesis
of this study is that the Quadriceps will be primarily affected by age related
atrophy, and biomarkers for age related instability will occur down the medial
side of the thigh.Methods
Participants
were grouped into two groups depending on age, with a ‘Younger’ group (24.53[±4.10]
years old, n=15) and an ‘Older’ group
(49.33[±6.77] years old, n=6). Multi-frequency MRE11
was carried out (25, 37.5, 50, 62.5Hz) followed by ESP post-processing12.
Thighs were manually segmented into 12 individual muscles of four muscle groups:
Quadriceps (Rectus Femoris, Vastus
Lateralis, Vastus Intermedius and Vastus Medialis), Hamstrings (Biceps Femoris Long Head, Bicep Femoris
Short Head, Semimembranosus and Semitendinosus), Adductors (Adductor Magnus and Adductor Longus) and
the Medial rotator muscles (Gracilis and
Sartorius). Region of interest (ROI) analysis was performed for
cross-sectional area (CSA - cm2) and muscle stiffness (|G*| - kPa), across
ages (20-55 years old) and also between the two age groups. Multivariate ANOVA (MANOVA) was used to analyse ROI measurements between
age groups.Results
Overall
thigh CSA was 22% lower in the ‘Older’ group (Figure 1) compared to the ‘Younger’ group (p=.008). The Quadriceps were primarily affected by ageing, with the
‘Older’ group showing a 25% decrease in Quadriceps CSA compared to the ‘Younger’
group (p<.000), particularly in
the Vastus Lateralis (-33%; p=.004)
There were no significant differences between age groups in CSA (Figure 2) for
the Hamstrings (p=.999), Adductors (p=.489) and Medial muscles (p=.988). |G*| was significantly greater
in the ‘Older’ group compared to the ‘Younger’ group for the Quadriceps (+9%; p=.021; Figure 3). There was a significant
correlation for age (Figure 4) with Quadriceps CSA (r[82]=-.22; p=.049) and
|G*| (r[82]=.23; p=.033). Finally, |G*| was significantly lower in the Medial
muscles of the ‘Older’ group than the ‘Younger’ group (1.19[±.30] kPa vs
1.49[±.20] kPa; -20%; p=.001), with a
significant negative correlation co-efficient for this decrease across ages (r[40]=-.50; p=.001). Linear regression analysis showed that age had a
significant effect on Medial muscle |G*| (R2=.25, F[1,40]=13.08, p<.000).Discussion
The
findings of the present study support previous research which found that the
Quadriceps were primarily effected by ageing-effects1. The
quadriceps muscle did not atrophy uniformly with the greatest decrease
observed in Vastus Lateralis. Interestingly, muscle stiffness of the Quadriceps
increased with age, while muscle stiffness of the Medial muscles
decreased. Muscle MRE has been sensitive to muscle stiffness change with age
and has identified two potential signs of age related mechanical weakness. Firstly,
decreased Quadriceps muscle group size as this is an anatomical basis for muscle
strength4. Secondly, the reduction in the medial muscles stiffness could be seen
as an early biomarker for age related instability, since previous research has
shown the importance muscle co-activation10, particularly for the medial muscles9. The results shown here suggest
that the medial muscles would be considerably less stable in supporting the
‘Older’ group compared to the ‘Younger’ group. Conclusion
We
conclude that through the use of MRE we demonstrated evidence for detection of
age related weakness and anatomical instability in middle ages adults, due to
morphometric and mechanical changes in thigh muscle.Acknowledgements
No acknowledgement found.References
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