Abstract

Benign joint hypermobility syndrome (BJHS) is associated with the early development of certain degenerative conditions, which may be associated with altered muscle activity. This pilot study compared muscle activation patterns during postural tasks between people with BJHS who do not have pain and people with normal flexibility (control group). Sixteen subjects aged 22–45 years (8 with BJHS) were selected from a population recruited to a larger study. Electromyographic activity of erector spinae (ES), gluteus medius (GM), and lower limb (rectus femoris (RF), semitendinosus (ST), tibialis anterior (TA) and gastrocnemius lateralis) muscles was assessed, and chosen based on the muscles being tested in the larger study. Subjects carried out 30 s of quiet standing (QS) and one-leg standing (OLS), both with eyes open (EO) and eyes closed (EC). Both groups had significantly more TA activity, and control subjects had significantly more GM activity, during OLS EC compared with QS. GM activity was not significantly different between groups. Compared with the BJHS group, control subjects had significantly less ST activation overall, significantly more ES activity during OLS EC and significantly less RF-ST co-contraction during QS. This study has noted differences in muscle activation patterns between pain-free hypermobile people and control subjects, specifically involving muscles surrounding the pelvis and hip. This pilot data suggests that strategies for stabilising the body during balancing tasks may be relevant to injury risk in people with BJHS. While results need to be verified with a larger subject sample, this study is important in developing new treatments for hypermobile people.

Highlights

  • Benign joint hypermobility syndrome (BJHS) is a hereditable collagen disorder that features excessive flexibility of joints and chronic pain

  • analysis of variance (ANOVA) revealed a significant effect of task on muscle activity (P < 0.001)

  • gluteus medius (GM) activity was significantly greater during task 4 compared with tasks 1 and 2 (P < 0.05; Fig. 1) within the control group only; it was observed to increase in the hypermobile group, this did not reach statistical significance

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Summary

Introduction

Benign joint hypermobility syndrome (BJHS) is a hereditable collagen disorder that features excessive flexibility of joints and chronic pain. It is closely associated with a genetic disorder, the hypermobile type of Ehlers Danlos Syndrome (EDS type III) (Grahame, 2008). This condition was considered an insignificant finding due in part to the absence of any nonmusculoskeletal symptoms. Other associations include increased incidence of anxiety disorders and delayed motor development in infants (Grahame, 1990)

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