Force, falls and fear of falls in myotonic dystrophy type 1. Cross-sectional and longitudinal studies
Sammanfattning
ABSTRACT
Background: Myotonic dystrophy type 1 (DM1) is a neuromuscular multisystemic
disorder with slowly progressive muscle weakness. The overall
purpose of this thesis was, in adult patients with DM1, to investigate factors
of importance for functional balance skills and falls, and to investigate the
natural course of muscle force and functional balance impairments, with
reliable measurement methods.
Methods: In the first study we evaluated test-retest reliability in static and
dynamic balance tests and gait, with three assessment occasions spaced oneweek
apart, in ten patients with DM1. In the second study, which is a crosssectional
study, 51 patients were assessed for muscle strength, gait and
functional balance together with self-reported balance confidence, walking
ability and falls. A multivariate analysis of factors of importance for
functional balance impairment was performed. Of these 51 patients, 43 were
further analysed in a third five-year prospective study for changes in muscle
force, gait and functional balance together with self-reported balance
confidence, walking ability and falls.
Results: The test-retest reliability analysis results advocate dynamic balance
tests and timed gait before the static tests. The cross-sectional study shows
that falls are common in the weaker, but still ambulant, patients. A
combination of weak ankle muscles and a physical capability to accelerate to
fast walking increased the risk of falling. Over five years the distal muscles
of the leg have a more steep force decrease than the proximal muscles. There
was a tendency towards a greater worsening in males, and we found a
statistically significant difference between genders in the knee extensor and
flexor force change. All men had fallen within the previous year at the fiveyear
assessment. Injuries of the face and head were more frequent at five
years.
Conclusions: Test-retest reliable dynamic balance tests and isometric
muscle force measures showed that there is a statistically significant
decrease in functional balance skill and in leg muscle force after five years in
patients with DM1. The number of patients who had fallen had increased and
the fall injuries were worse. It is of great importance to prevent falls
especially in those who are at most risk for falls, by which we mean those
who have a more steep muscle force reduction. Regular assessments of gait,
functional balance and leg muscle force could be a way to determine who is
at most risk for falls. This would give the opportunity to intervene with
rehabilitation therapy and assistive devices as possible means for fall
prevention in patients with DM1.
Delarbeten
I. Hammarén E, Ohlsson JA, Lindberg C, Kjellby-Wendt G. Reliability of static and dynamic balance tests in subjects with myotonic dystrophy type 1. Adv Physiother 2012; 14: 48–54. With Appendix ::doi::10.3109/14038196.2012.675352 II. Hammarén E, Kjellby-Wendt G, Kowalski J, Lindberg C. Factors of importance for dynamic balance impairment and frequency of falls in individuals with myotonic dystrophy type 1 – A cross-sectional study – Including reference values of Timed Up & Go, 10 m walk and step test. Neuromuscul Disord 2014;24(3)207-15. ::PMID::24412157 III. Hammarén E, Kjellby-Wendt G, Lindberg C. Muscle force, balance and falls in muscular impaired individuals with myotonic dystrophy type 1 - A five-year prospective cohort study. Submitted
Examinationsnivå
Doctor of Philosophy (Medicine)
Universitet
University of Gothenburg. Sahlgrenska Academy
Institution
Institute of Neuroscience and Physiology. Department of Clinical Neuroscience and Rehabilitation
Disputation
Fredagen den 17 oktober 2014, kl 9.00, Hörsal Arvid Carlsson, Academicum, Medicinaregatan 3
Datum för disputation
2014-10-17
E-post
elisabet.hammaren@vgregion.se
Datum
2014-09-26Författare
Hammarén, Elisabet
Nyckelord
myotonic dystrophy
physiotherapy
muscle force
postural balance
gait
reliability
Publikationstyp
Doctoral thesis
ISBN
978-91-628-9098-8 (e-pub)
978-91-628-9077-3 (tryckt)
Språk
eng